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12 pages, 2295 KiB  
Review
A Rare Parasite in Cats: Record of a Linguatula serrata Frölich, 1789 (Porocephalida, Linguatulidae) Nymphal Infestation in a Cat in Albania, with a Synopsis and Review of the Literature on L. serrata Infestation in Cats
by Enstela Vokshi, Martin Knaus and Steffen Rehbein
Biology 2024, 13(12), 1073; https://doi.org/10.3390/biology13121073 - 20 Dec 2024
Viewed by 178
Abstract
Linguatula serrata, commonly known as the dogs’ ‘tongue-worm’, is an arthropod endoparasite of the class Pentastomida infesting chiefly canids as definitive hosts and herbivores as intermediate hosts. Adult L. serrata usually reside in the upper respiratory tract, such as the nasal cavity [...] Read more.
Linguatula serrata, commonly known as the dogs’ ‘tongue-worm’, is an arthropod endoparasite of the class Pentastomida infesting chiefly canids as definitive hosts and herbivores as intermediate hosts. Adult L. serrata usually reside in the upper respiratory tract, such as the nasal cavity and sinuses, and the larval stages are encapsulated in various visceral organs, respectively. This report presents the first case of a L. serrata nymphal pulmonary infestation in a cat from Albania and adds to the description of the overall rare cases of this parasitic infestation in domestic cats. Discussion of this case together with a comprehensive review of the literature allows us to conclude that cats are susceptible to the infestation with L. serrata when ingesting the parasite’s eggs and allow for the development of the nymphal stage of the parasite in several visceral organs. Therefore, cats may serve as accidental intermediate hosts in the life cycle of L. serrata but are unlikely to be of epidemiological relevance. There is no evidence that domestic cats can act as definitive hosts of L. serrata. Full article
(This article belongs to the Special Issue Zoonotic Diseases)
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Figure 1
<p>Nymph of <span class="html-italic">Linguatula serrata</span> collected from the lungs of a cat.</p>
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<p>Anterior end of nymph of <span class="html-italic">Linguatula serrata</span> collected from the lungs of a cat, with central mouth opening flanked by two pairs of hooks (ventral view).</p>
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13 pages, 12629 KiB  
Case Report
Different Types of Co-Infection by Contagious Ecthyma Virus, Enteropathogenic Escherichia coli, Mycoplasma conjunctivae, Ecto- and Endo-Parasites in Four Young Alpine Ibex (Capra ibex)
by Lorenzo Domenis, Raffaella Spedicato, Cristina Guidetti, Emanuele Carella and Serena Robetto
Animals 2024, 14(24), 3666; https://doi.org/10.3390/ani14243666 - 19 Dec 2024
Viewed by 309
Abstract
The research aimed to investigate the perinatal pathology of Alpine ibex (Capra ibex) through the study of four young subjects (at the age of 3 to 4 months) found dead in Valle d’Aosta, a region of northwestern Italy. The carcasses were [...] Read more.
The research aimed to investigate the perinatal pathology of Alpine ibex (Capra ibex) through the study of four young subjects (at the age of 3 to 4 months) found dead in Valle d’Aosta, a region of northwestern Italy. The carcasses were submitted to necropsy followed by an examination of ecto- and endoparasites (ECP and ENP); samples from the gross lesions (in summary, cutaneous papilloma and crusts, ocular discharge, lobular haemorrhagic areas in the lungs, catarrhal–haemorrhagic enterocolitis) were analysed by bacteriological, histopathological, and biomolecular methods to define the etiological agent. The subjects, with various co-infection patterns, were affected by contagious ecthyma virus (ORFV) (agent of a highly diffusive pustular dermatitis transmissible to small ruminants and humans), Enteropathogenic Escherichia coli (EPEC) (major etiological agent of infantile diarrhoea especially in developing countries), Mycoplasma conjunctivae (MC) (cause of an ocular infection common to goats and sheep), various ECP (ticks and keds) and ENP (lung and intestinal nematodes, and coccidia). This study emphasises the potential role of the Alpine ibex in the transmission of infectious diseases to other animals such as to humans and, secondly, the need to apply diversified analytical approaches, with the commitment of various specialistic skills, in order to define, in detail, the various and frequently overlapping causes that led a free-ranging animal to the death. Full article
(This article belongs to the Special Issue Wildlife Diseases: Pathology and Diagnostic Investigation)
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Figure 1
<p>(<b>A</b>) Alpine ibex contagious ecthyma. Papillomatous proliferative lesion by ORFV, partially ulcerated and strongly hyperaemic, on the tongue (arrow) and upper lip (arrowhead)—(Subject 1). (<b>B</b>) Alpine ibex contagious ecthyma. Typical “cauliflower-like” papillomatous proliferative lesions (arrow) by ORFV, heavily crusted, at the extremities of the limbs, proximal to the nails—(Subject 1). (<b>C</b>) Alpine ibex contagious ecthyma. ORFV lesion in the tongue, characterised by epithelial proliferation with spongiosis (asterisk) and severe dilatation of the sub-epithelial vessel network (arrow)—(Subject 1). HE (10×). (<b>D</b>) Alpine ibex contagious ecthyma. Acidophilic intra-cytoplasmatic inclusion bodies by ORFV, with clear halo, inside epithelial spongiotic cells of the tongue mucosa (arrows)—(1). HE (100×). (<b>E</b>) Alpine ibex contagious ecthyma. Cutaneous proliferative lesions by ORFV, characterised by orthokeratotic hyperkeratosis (arrow), middle acanthosis (asterisk), dilatation of sub-epidermic vessel network, and mixed cells dermal phlogosis (triangle)—(Subject 2). HE (10×).</p>
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<p>(<b>A</b>) Alpine ibex contagious ecthyma. Papillomatous proliferative lesion by ORFV, partially ulcerated and strongly hyperaemic, on the tongue (arrow) and upper lip (arrowhead)—(Subject 1). (<b>B</b>) Alpine ibex contagious ecthyma. Typical “cauliflower-like” papillomatous proliferative lesions (arrow) by ORFV, heavily crusted, at the extremities of the limbs, proximal to the nails—(Subject 1). (<b>C</b>) Alpine ibex contagious ecthyma. ORFV lesion in the tongue, characterised by epithelial proliferation with spongiosis (asterisk) and severe dilatation of the sub-epithelial vessel network (arrow)—(Subject 1). HE (10×). (<b>D</b>) Alpine ibex contagious ecthyma. Acidophilic intra-cytoplasmatic inclusion bodies by ORFV, with clear halo, inside epithelial spongiotic cells of the tongue mucosa (arrows)—(1). HE (100×). (<b>E</b>) Alpine ibex contagious ecthyma. Cutaneous proliferative lesions by ORFV, characterised by orthokeratotic hyperkeratosis (arrow), middle acanthosis (asterisk), dilatation of sub-epidermic vessel network, and mixed cells dermal phlogosis (triangle)—(Subject 2). HE (10×).</p>
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<p>Alpine ibex ecto- and endo-parasites. <span class="html-italic">Ixodes ricinus</span> (<b>A</b>), <span class="html-italic">Melophagus rupicaprinus</span> (<b>B</b>), <span class="html-italic">Eimeria</span> spp., (<b>C</b>), <span class="html-italic">Nematodirus</span> spp. (<b>D</b>)—(Subjects 1, 2, 4).</p>
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<p>(<b>A</b>) Alpine ibex enteritis by EPEC. The intestine appears oedematous, dilated, and congested, with diarrhoeic haemorrhagic content (insert)—(Subject 4). (<b>B</b>) Alpine ibex enteritis by EPEC. Acute phlogosis with a severe dilatation of lamina propria and sub-mucosa vessel network—(Subject 4). HE (10×). (<b>C</b>) Alpine ibex enteritis by EPEC. Intestinal villi show loss of epithelial surface cells (arrow), oedema, and mixed phlogosis with macrophages, monocytes, and neutrophils (asterisk)—(Subject 4). HE (40×).</p>
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<p>(<b>A</b>) Alpine ibex verminous bronchopneumonia. Parasitic lesions inside caudal lung lobes, characterised by multiple-coloured grey foci of consolidated parenchyma (arrows)—(Subject 4). (<b>B</b>) Alpine ibex verminous bronchopneumonia. Multiple appreciable nematodes larvae inside alveolar lumina (arrows) and hyperplasia of BALT system (triangle)—(Subject 4). HE (10×).</p>
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10 pages, 2282 KiB  
Article
Bioactive Secondary Metabolites from Harposporium anguillulae Against Meloidogyne incognita
by Dong Li, Ling-Feng Bao, Hong-Mei Lei, Guang-Ke Zhang, Guo-Hong Li and Pei-Ji Zhao
Microorganisms 2024, 12(12), 2585; https://doi.org/10.3390/microorganisms12122585 - 13 Dec 2024
Viewed by 360
Abstract
Root-knot nematodes (RKNs) are pathogens that endanger a wide range of crops and cause serious global agricultural losses. In this study, we investigated metabolites of the endoparasitic fungus Harposporium anguillulae YMF1.01751, with the expectation of discovering valuable Meloidogyne incognita biocontrol compounds. Based on [...] Read more.
Root-knot nematodes (RKNs) are pathogens that endanger a wide range of crops and cause serious global agricultural losses. In this study, we investigated metabolites of the endoparasitic fungus Harposporium anguillulae YMF1.01751, with the expectation of discovering valuable Meloidogyne incognita biocontrol compounds. Based on results obtained by a liquid chromatograph coupled to a mass spectrometer (LC-MS) of crude extracts under five culture conditions and their nematicidal activity against M. incognita, corn meal agar (CMA) medium was determined as the scale-up fermentation medium. Twelve metabolites (112) were isolated from the fermentation products, and compound 1 was identified to be a new cyclic tetrapeptide. The activity assay results showed that phenylacetic acid (11) had good nematicidal activity at 400 μg/mL, and the mortalities of M. incognita were 89.76% and 96.05% at 12 and 24 h, respectively, while the mortality of canthin-6-one (2) against M. incognita was 44.26% at 72 h. In addition, the results of chemotaxis activity showed that 1-(1H-indol-3-yl)ethanone (10) possessed attraction activity towards M. incognita. At the tested concentrations, cyclo-(Arg-Pro) (4) and cyclo-(Val-Ile) (7) showed an avoidant response to M. incognita. This study provides insight into the nematode-active compounds of H. anguillulae origin and offers new opportunities for the development of RKN biocontrol products. Full article
(This article belongs to the Special Issue Secondary Metabolism of Microorganisms, 3rd Edition)
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Figure 1
<p>The LC-MS detection of extracts produced by <span class="html-italic">H. anguillulae</span> YMF1.01751 in five media. (<b>A</b>) Principal component analysis of the metabolites from <span class="html-italic">H. anguillulae</span> YMF1.01751 in different media. (<b>B</b>) LC-MS profiles of metabolites extracted from <span class="html-italic">H. anguillulae</span> YMF1.01751 in total ion chromatography.</p>
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<p>The COSY and key HMBC correlations of <b>1</b>.</p>
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<p>The metabolites isolated from <span class="html-italic">H. anguillulae</span> YMF1.01751.</p>
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<p>The nematicidal activity of compounds against <span class="html-italic">M. incognita</span>. In the same time period of data, two way-ANOVA statistical analysis indicates significant differences (* <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.005; *** <span class="html-italic">p</span> &lt; 0.003; **** <span class="html-italic">p</span> &lt; 0.001) compared with the control.</p>
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<p>The chemotactic activity of compounds towards <span class="html-italic">M. incognita</span>. (<b>A</b>) Schematic diagram of chemotactic activity. (<b>B</b>) The chemotactic activity of compounds. In the same time period of data, two way-ANOVA statistical analysis indicates significant differences (* <span class="html-italic">p</span> &lt; 0.05) compared with the control.</p>
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11 pages, 2381 KiB  
Article
Investigating Endoparasites in Captive Birds of Prey in Italy
by Carolina Allievi, Sergio A. Zanzani, Fulvio Bottura and Maria Teresa Manfredi
Animals 2024, 14(24), 3579; https://doi.org/10.3390/ani14243579 - 11 Dec 2024
Viewed by 326
Abstract
Birds of prey can be parasitised by several endoparasites that can coexist without clinical signs of disease or occur in conjunction with stressful events. Because the number of birds of prey kept in captivity is copiously increasing due to their use for bird [...] Read more.
Birds of prey can be parasitised by several endoparasites that can coexist without clinical signs of disease or occur in conjunction with stressful events. Because the number of birds of prey kept in captivity is copiously increasing due to their use for bird control, breeding programs, exhibition and falconry, the main endoparasites of 81 apparently healthy captive birds of prey from northern Italy were investigated by examining faecal and blood samples. Faeces were analysed by a quali-quantitative technique, i.e., the FLOTAC® basic technique, employing potassium iodomercurate flotation solution, while blood smears were stained to detect haemoparasites. Risk factors were further assessed. Considering gastrointestinal parasites, an overall prevalence of 41.7% was recorded, and 50% of Accipitriformes, 43% of Falconiformes and 33.3% of Strigiformes tested positive for at least one parasite taxon. Moreover, age and diet were associated with an increased risk of infection. As for haemoparasites, a prevalence of 18.2% was evidenced, and none of the risk factors were associated with prevalence. The results of this study highlighted the importance of monitoring the endoparasites of captive birds of prey with a highly sensitive copromicroscopic technique to target medical treatments, improve housing conditions and conduct epidemiological studies aimed at wildlife conservation and management. Full article
(This article belongs to the Section Wildlife)
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<p>Parasitic elements detected in the analysed faecal and blood samples in captive birds of prey in northern Italy. (<b>A</b>) Eggs of Ascarididae (100×); (<b>B</b>) egg of <span class="html-italic">Porrocaecum</span> spp. (100×); (<b>C</b>) egg of Spiruridae (200×); (<b>D</b>) egg of Capillariidae (400×); (<b>E</b>) egg of Cestoda with visible hooks of the embryo (400×); (<b>F</b>) eggs of Trematoda deformed by the contact with the FS8 flotation solution (100×); (<b>G</b>) oocysts of <span class="html-italic">Caryospora</span> spp. (100×); (<b>H</b>) Giemsa-stained blood smear with <span class="html-italic">Leucocytozoon</span> spp. (1000×). Scale bars: (<b>A</b>–<b>C</b>) 20 μm; (<b>D</b>–<b>F</b>,<b>H</b>) 10 μm; (<b>G</b>) 40 μm.</p>
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16 pages, 8319 KiB  
Article
Liver Lesions in Estuarine Dolphins in the Indian River Lagoon, Florida: Does Microcystin Play a Role?
by Ami Krasner, Wendy Noke Durden, Megan Stolen, Teresa Jablonski, Agatha Fabry, Annie Page, Wendy Marks, Cecilia Costa, H. C. D. Marley and Spencer Fire
Toxics 2024, 12(12), 858; https://doi.org/10.3390/toxics12120858 - 27 Nov 2024
Viewed by 590
Abstract
Microcystin (MC), a hepatotoxin produced by cyanobacteria, was introduced into the Indian River Lagoon (IRL), Florida, in 2005 through freshwater outflows. Since then, MC has been detected in humans, domestic animals, and wildlife in the lagoon. Potential public health effects associated with MC [...] Read more.
Microcystin (MC), a hepatotoxin produced by cyanobacteria, was introduced into the Indian River Lagoon (IRL), Florida, in 2005 through freshwater outflows. Since then, MC has been detected in humans, domestic animals, and wildlife in the lagoon. Potential public health effects associated with MC exposure along the IRL include an increased risk of non-alcoholic liver disease among area residents. Yet, there are limited studies characterizing liver disease, as well as the potential role of MC, in humans and animals in this region. Thus, histopathology reports (n = 133) were reviewed in the stranded common bottlenose dolphin (Tursiops truncatus truncatus) (n = 156, 2005–2024) to describe liver lesions in this important IRL sentinel. Liver and fecal samples (n = 161) from stranded individuals were screened for MC via an enzyme immunoassay (ELISA). These samples were then confirmed via the 2-methyl-3-methoxy-4-phenylbutyric acid technique (MMPB) to evaluate whether liver histopathologic lesions were linked to MC exposure. Minimally invasive MC screening methods were also assessed using respiratory swabs and vapor. Inflammation (24%, n = 32), fibrosis (23%, n = 31), lipidosis/vacuolation (11%, n = 15), and necrosis (11%, n = 14) were the most common liver anomalies observed. These non-specific lesions have been reported to be associated with MC exposure in numerous species in the peer-reviewed literature. Ten bottlenose dolphins tested positive for the toxin via ELISA, including two individuals with hepatic lipidosis, but none were confirmed by MMPB. Thus, this study did not provide evidence for MC-induced liver disease in IRL bottlenose dolphins. Other causes should be considered for the lesions observed (e.g., heavy metals, metabolic disease, and endoparasites). Respiratory swabs require further validation as a pre-mortem MC screening tool in free-ranging wildlife. Full article
(This article belongs to the Section Exposome Analysis and Risk Assessment)
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<p>Common bottlenose dolphin (<span class="html-italic">Tursiops truncatus truncatus</span>) strandings (black dots) within the Indian River Lagoon (IRL) that were screened for microcystin (MC) exposure and liver lesions from 2005–2024. The study site extends along the east coast of Florida (inset map) between Ponce Inlet (Spruce Creek) and Jupiter Inlet.</p>
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<p>Histologic features of an IRL common bottlenose dolphin (Dolphin 11) with liver dysfunction (unknown etiology) as a cause of mortality. Acute hemorrhagic infarcts (arrows) and necrosis (marked, centrilobular, midzonal to submassive, and multifocal to coalescing) were observed microscopically (H&amp;E; 300 dpi; 40×; scale bar = 40 µm). Image credit/histologic interpretation: Dr. David Rotstein.</p>
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<p>Histologic features of an IRL common bottlenose dolphin (Dolphin 12) with liver dysfunction (unknown etiology) as the cause of stranding. Periportal hepatitis (patchy and lymphoplasmacytic; asterisks), portal fibrosis (diffuse and moderate; star), and bile duct hyperplasia (arrows) were observed microscopically (H&amp;E; 300 dpi with a scale bar). (<b>a</b>) 10×; scale bar = 100 µm (<b>b</b>) 40×; scale bar = 20 µm. Image credit/histologic interpretation: Dr. David Rotstein.</p>
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<p>Histologic features of an IRL common bottlenose dolphin (Dolphin 12) with liver dysfunction (unknown etiology) as the cause of stranding. Periportal hepatitis (patchy and lymphoplasmacytic; asterisks), portal fibrosis (diffuse and moderate; star), and bile duct hyperplasia (arrows) were observed microscopically (H&amp;E; 300 dpi with a scale bar). (<b>a</b>) 10×; scale bar = 100 µm (<b>b</b>) 40×; scale bar = 20 µm. Image credit/histologic interpretation: Dr. David Rotstein.</p>
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<p>Histologic features of an IRL common bottlenose dolphin (Dolphin 13) with liver dysfunction (unknown etiology) as the cause of stranding and mortality. Portal hepatitis (mild, multifocal, chronic to active, lymphoplasmacytic, and neutrophilic), atrophy (mild and multifocal; arrow), and portal fibrosis (asterisks) were observed microscopically (H&amp;E; 300 dpi with a scale bar). (<b>a</b>) 10×; scale bar = 100 µm (<b>b</b>) 40×; scale bar = 20 µm. Image credit/histologic interpretation: Dr. David Rotstein.</p>
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<p>Histologic features of an IRL common bottlenose dolphin (Dolphin 13) with liver dysfunction (unknown etiology) as the cause of stranding and mortality. Portal hepatitis (mild, multifocal, chronic to active, lymphoplasmacytic, and neutrophilic), atrophy (mild and multifocal; arrow), and portal fibrosis (asterisks) were observed microscopically (H&amp;E; 300 dpi with a scale bar). (<b>a</b>) 10×; scale bar = 100 µm (<b>b</b>) 40×; scale bar = 20 µm. Image credit/histologic interpretation: Dr. David Rotstein.</p>
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16 pages, 5475 KiB  
Article
Helminthofauna Diversity in Synanthropic Rodents of the Emilia-Romagna Region (Italy): Implications for Public Health and Rodent Control
by Filippo Maria Dini, Carlotta Mazzoni Tondi and Roberta Galuppi
Vet. Sci. 2024, 11(11), 585; https://doi.org/10.3390/vetsci11110585 - 20 Nov 2024
Viewed by 613
Abstract
Synanthropic rodents are species well adapted to coexisting in anthropogenically influenced environments. This coexistence raises concerns about the potential risks of pathogen’s transmission due to their close proximity to human habitats. This study presents an epidemiological survey of the gastrointestinal helminth fauna in [...] Read more.
Synanthropic rodents are species well adapted to coexisting in anthropogenically influenced environments. This coexistence raises concerns about the potential risks of pathogen’s transmission due to their close proximity to human habitats. This study presents an epidemiological survey of the gastrointestinal helminth fauna in synanthropic rodents (Mus musculus, Rattus rattus, and Rattus norvegicus) from the Emilia-Romagna Region (Italy), aiming to provide updated data on the endoparasitic populations in these species. A total of 111 rodents, sampled from 2019 to 2021 during pest control programs, were examined for parasitic infections. Helminths were extracted through necropsy and microscopic analysis of gastrointestinal tracts and sediment, with species identification based on morphological characteristics. Overall, 72.1% of the rodents were found to be parasitized, with nematodes being the most prevalent. Syphacia muris, Aspiculuris tetraptera, Nippostrongylus brasiliensis, and Heterakis spumosa were the most frequently identified nematodes. Tapeworms, including Rodentolepis nana and Hymenolepis diminuta, were also detected, albeit in lower frequencies. The trematode Brachylaima recurva was recovered only in one R. rattus. Co-infection was common, particularly among rats, with 51.8% of black rats and 22% of brown rats harboring multiple parasitic species. Mice exhibited lower levels of polyparasitism, with only two individuals showing mixed infections. Interestingly, disparities between the detection of adult helminths and parasitic eggs were noted, especially in cases where no adults were observed, but eggs were found through sediment analysis. These findings suggest that traditional necropsy, especially with poorly preserved carcasses, may underestimate parasite prevalence. This highlights the importance of combining necropsy with microscopic techniques, such as flotation and sedimentation, for a more thorough assessment. Using these methods, nematodes with direct life cycles, such as Syphacia spp., Nippostrongylus brasiliensis, and Heterakis spumosa, have been confirmed as widespread and cosmopolitan among rodent populations. The detection of zoonotic parasites raises concerns about potential transmission to humans, particularly in areas with poor sanitation and high rodent densities. These findings underscore the need for integrated rodent control and environmental sanitation to reduce zoonotic risks. Full article
(This article belongs to the Section Veterinary Microbiology, Parasitology and Immunology)
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<p>Different municipalities of the provinces of Ravenna and Forlì-Cesena in which the samplings were carried out. Scale bar: 20 km.</p>
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<p>Anatomical details of <span class="html-italic">Syphacia</span> spp. and <span class="html-italic">Heterakis spumosa</span> in <span class="html-italic">R. norvegicus</span> and <span class="html-italic">M. musculus.</span> (<b>a</b>) <span class="html-italic">Syphacia obvelata</span>, male, tail; (<b>b</b>) <span class="html-italic">S. muris</span>, male, tail; (<b>c</b>) <span class="html-italic">Heterakis spumosa</span>, male, tale; (<b>d</b>) <span class="html-italic">H. spumosa</span>: female, vulvar opening.</p>
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<p>Anatomical details of <span class="html-italic">Aspiculuris tetraptera</span> and Strongylda from <span class="html-italic">R. norvegicus</span>. (<b>a</b>) <span class="html-italic">Aspiculuris tetraptera</span>, head; (<b>b</b>) <span class="html-italic">Heligmosomoides polygyrus</span>, male tail; (<b>c</b>) <span class="html-italic">H. polygyrus</span>, female tail; (<b>d</b>) <span class="html-italic">Nippostrongylus brasiliensis</span>, male tail; (<b>e</b>) <span class="html-italic">N. brasiliensis</span>, horizontal striations and longitudinal ridges.</p>
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<p>Eggs found at microscopic examination of sediment of both <span class="html-italic">Rattus</span> spp. and <span class="html-italic">M. musculus</span>. (<b>a</b>) <span class="html-italic">Trichuris</span> sp.; (<b>b</b>) <span class="html-italic">Capillaria</span> spp.; (<b>c</b>) <span class="html-italic">Rodentolepis nana</span> (upward), and <span class="html-italic">Hymenolepis diminuta</span> (down). Scale bar: 20 µm.</p>
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15 pages, 2090 KiB  
Article
Endoparasites of Red Deer (Cervus elaphus L.) and Roe Deer (Capreolus capreolus L.) in Serbian Hunting Grounds
by Nemanja M. Jovanovic, Tamas Petrović, Nenadovic Katarina, Dejan Bugarski, Zoran Stanimirovic, Milan Rajkovic, Marko Ristic, Jovan Mirceta and Tamara Ilic
Animals 2024, 14(21), 3120; https://doi.org/10.3390/ani14213120 - 30 Oct 2024
Viewed by 1256
Abstract
In this study, parasitological examinations were conducted from 2019 to 2023. Fecal samples were collected from 289 wild ruminants (158 red deer and 131 roe deer) from hunting grounds in Vojvodina, which belong to the public company Vojvodinašume. Using qualitative and quantitative coprological [...] Read more.
In this study, parasitological examinations were conducted from 2019 to 2023. Fecal samples were collected from 289 wild ruminants (158 red deer and 131 roe deer) from hunting grounds in Vojvodina, which belong to the public company Vojvodinašume. Using qualitative and quantitative coprological diagnostic methods, the presence of protozoa (coccidia and Buxtonella sulcata), nematodes (gastrointestinal strongyles, Trichuris spp., Capillaria spp., Dictyocaulus spp., and Muellerius spp.), cestodes (Moniezia spp.), and trematodes (Fasciola hepatica, Fascioloides magna, Paramphistomum spp., and Dicrocoelium dendriticum) in the form of single and mixed infections were confirmed. Coproculture was used to identify the infective larvae of gastrointestinal strongyles. The total prevalence of endoparasitic infections in hunting ground 1 was 89.77% in red deer and 92.85% in roe deer, while in hunting ground 2, it was 72.97% in red deer and 85.96% in roe deer. Knowledge of the prevalence and assessment of the intensity of parasitic infections in wild ruminants is necessary for designing health protection programs in hunting grounds and planning control strategies, which are significant for this branch of hunting and public health. Full article
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<p>Map of Serbia with administrative districts where the survey was conducted. The map was generated by using QGIS v3.36 [<a href="#B20-animals-14-03120" class="html-bibr">20</a>].</p>
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<p>Parasitic elements detected in fecal samples: (<b>A</b>) <span class="html-italic">Müellerius</span> spp. (100×); (<b>B</b>) <span class="html-italic">Dictyocaulus</span> spp. (100×); (<b>C</b>) coccidia oocyst (400×); (<b>D</b>) <span class="html-italic">Buxtonella sulcata</span> cyst (100×); (<b>E</b>) Strongylidae egg (400×); (<b>F</b>) <span class="html-italic">Trichuris</span> spp. eggs (400×); (<b>G</b>) <span class="html-italic">Capillaria</span> spp. egg (400×); (<b>H</b>) <span class="html-italic">Moniezia</span> spp. egg (400×); (<b>I</b>) <span class="html-italic">Fasciola hepatica</span> egg (100×); (<b>J</b>) <span class="html-italic">Paramphistomum</span> spp. egg (100×); (<b>K</b>) <span class="html-italic">Fascioloides magna</span> egg (100×); (<b>L</b>) <span class="html-italic">Dicrocoelium dendrticum</span> egg (400×).</p>
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<p>The third-stage larvae (L3) recovered using the corpoculture method (40×, 100×). (<b>A</b>,<b>B</b>) <span class="html-italic">Haemonchus contortus</span>; (<b>C</b>,<b>D</b>) <span class="html-italic">Chabertia ovina</span>; (<b>E</b>,<b>F</b>) <span class="html-italic">Oesophagostomum columbianum</span>; (<b>G</b>,<b>H</b>) <span class="html-italic">Trichostrongylus axei</span>. Morphological identification was performed according to total length, esophagus length, tail sheath length, and the number of intestinal cells [<a href="#B21-animals-14-03120" class="html-bibr">21</a>].</p>
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18 pages, 9790 KiB  
Article
Exploring Hidden Connections: Endophytic System and Flower Meristem Development of Pilostyles berteroi (Apodanthaceae) and Interaction with Its Host Adesmia trijuga (Fabaceae)
by Ana Maria Gonzalez, María Florencia Romero and Héctor A. Sato
Plants 2024, 13(21), 3010; https://doi.org/10.3390/plants13213010 - 28 Oct 2024
Viewed by 658
Abstract
Pilostyles, an endoparasitic genus within the Apodanthaceae family, grows inside host stems with flowers and fruits being the only external manifestations. Previous studies of P. berteroi growing on Adesmia trijuga provided limited details of the endophyte and omitted the origin of flowers [...] Read more.
Pilostyles, an endoparasitic genus within the Apodanthaceae family, grows inside host stems with flowers and fruits being the only external manifestations. Previous studies of P. berteroi growing on Adesmia trijuga provided limited details of the endophyte and omitted the origin of flowers and sinker structure. This study, using classical methods of optical microscopy applied to the analysis with scanning electron microscopy and confocal laser scanning microscopy, expands the understanding of the P. berteroi/A. trijuga complex. We find that P. berteroi develops isophasically with its host, forming endophytic patches between the host’s secondary phloem cells. The parasitized Adesmia stem’s cambium primarily produces xylem parenchyma, with limited vessel production and halting fiber formation. The radial polarization of endophytic patches led to the formation of floral meristems. Flowers develop endogenously and emerge by the breakthrough of the host stem. Flowers are connected to the host cambium via chimeric sinkers, combining P. berteroi parenchyma and tracheoids with Adesmia vessels. Unlike previous studies that show uniformity among Pilostyles species, our analysis reveals new insights into the structural interaction between P. berteroi and A. trijuga. Full article
(This article belongs to the Special Issue Advances in Plant Anatomy and Cell Biology)
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<p>Specimens of <span class="html-italic">A. trijuga</span>. (<b>A</b>) General aspect of the landscape with <span class="html-italic">A. trijuga</span> plants; (<b>B</b>) <span class="html-italic">A. trijuga</span> plants, where the zone of stem secondary structure is indicated by arrows and detailed in the inset; (<b>C</b>) <span class="html-italic">A. trijuga</span> plant parasitized by <span class="html-italic">P. berteroi</span> (arrows indicate the parasite’s flowers); (<b>D</b>–<b>F</b>) <span class="html-italic">P. berteroi</span> flowers emerging from host stems; (<b>E</b>) Detail of buds and flowers at anthesis; (<b>F</b>) Basal region with older staminate flowers and scarring from previous year’s flowers. Abbreviations: b: flower buds, f: flowers in blossom, mf: mature flowers; sf: scars of flower or fruits. Scales: (<b>B</b>,<b>C</b>): 10 cm; (<b>D</b>): 1.5 cm; (<b>E</b>,<b>F</b>): 0.5 cm.</p>
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<p>Anatomy of the non-parasitized stem of <span class="html-italic">A. trijuga</span> in transversal (<b>A</b>–<b>G</b>), and radial longitudinal sections (<b>H</b>,<b>I</b>) are analyzed with a light microscope (LM). (<b>A</b>) Transection of 2-year-old non-parasitized stem; (<b>B</b>,<b>C</b>) phloem and cambial zone in a stem with vessels in the process of formation (*); (<b>D</b>) periderm; (<b>E</b>) secondary phloem; (<b>F</b>) wood anatomy showing its diffuse porosity; (<b>G</b>) detail of vessels, paratracheal parenchyma and libriform fibers; the crystals in the area indicated with a square are shown in the inset (polarized light); (<b>H</b>) vessels, libriform fibers and rays; crystals in the inset; (<b>I</b>) vessels showing simple perforation plates; (<b>J</b>) detail of vestured pits. Abbreviations: as: air spaces; cc: companion cells; ck: cork; co: cortex; cr: prismatic crystals; cz: cambial zone; lf: libriform fibers; le: lenticels; p: phellogen; pe: periderm; pf: primary phloem fibers; ph: secondary phloem; pi: pith; pl: phelloderm; pp: simple perforation plate; ra: rays; se: sieve elements; ve: vessels; xy: xylem. Scales: (<b>A</b>) 0.5 mm; (<b>B</b>,<b>C</b>,<b>F</b>) 50 µm; (<b>D</b>,<b>H</b>) 20 µm; (<b>E</b>,<b>G</b>,<b>I</b>) 10 µm; (<b>J</b>) 2 µm.</p>
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<p>Stems of <span class="html-italic">A. trijuga</span> parasitized by <span class="html-italic">P. berteroi</span> in transverse (<b>A</b>–<b>D</b>,<b>G</b>–<b>J</b>), and radial longitudinal section (<b>E</b>,<b>F</b>), analyzed with LM. (<b>A</b>) Stem of <span class="html-italic">A. trijuga</span> with early stages of parasite development; the first endophytic patches (EPs) of <span class="html-italic">P. berteroi</span> cells are seen in the phloem (box); (<b>B</b>) detail of an EP of <span class="html-italic">P. berteroi</span> corresponding to the box in (<b>A</b>); (<b>C</b>) detail of EPs of <span class="html-italic">P. berteroi</span> and cells of secondary phloem of <span class="html-italic">A. trijuga</span>; (<b>D</b>–<b>F</b>) parasitized stems showing the presence of numerous EPs that occupied most of the secondary phloem. (<b>G</b>) EP stained with Safranin–Astra blue; (<b>H</b>–<b>J</b>) EP subjected to histochemical tests, combined with Astra blue to enhance cell wall identification: (<b>H</b>) lugol (black) for starch, (<b>I</b>) ferric chloride (brown) for phenol groups, (<b>J</b>) sudan black (blue–black) for lipids. Abbreviations: cc: companion cells; co: cortex; cz: cambial zone; hc: host cells; EP: endophytic patches; lra: lignified rays; nra: non-lignified rays; np: parasite nuclei; pe: periderm; ph: secondary phloem; pra: phloem rays; ra: rays; se: sieve elements; xy: secondary xylem. Scales:  (<b>A</b>,<b>F</b>) 100 µm; (<b>B</b>,<b>C</b>,<b>E</b>,<b>G</b>–<b>J</b>) 10 µm; (<b>D</b>) 50 µm.</p>
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<p>Flower development of <span class="html-italic">P. berteroi</span> in stems of <span class="html-italic">A. trijuga</span>, analyzed with LM (<b>A</b>–<b>D</b>,<b>G</b>), and CLSM for autofluorescence (<b>E</b>,<b>F</b>). (<b>A</b>,<b>B</b>,<b>E</b>,<b>G</b>) Cross-sections and (<b>C</b>,<b>D</b>,<b>F</b>) radial sections of infested <span class="html-italic">A. trijuga</span> stems. (<b>A</b>) Origin of the <span class="html-italic">P. berteroi</span> floral meristem from an EP (box); (<b>B</b>) Close-up of box in (<b>A</b>) showing the polarity of EP with vegetative and reproductive cells surrounded by collapsed host cells; (<b>C</b>) floral meristem; (<b>D</b>) meristem with first bract whorl; (<b>E</b>–<b>G</b>) <span class="html-italic">P. berteroi</span> staminate flowers at various stages of development, with some already emerging through the periderm of the stem of <span class="html-italic">A. trijuga</span>. Abbreviations: ch: collapsed host cells; co: cortex; cz: cambial zone; EP: endophytic patches; fb: floral bud; fm: floral meristem; pe: periderm; ph: phloem; rc: reproductive cells; sf: staminate flower; sk: sinker; vc: vegetative cells; xy: xylem. Scales: (<b>A</b>) 200 µm; (<b>B</b>) 20 µm; (<b>C</b>) 100 µm; (<b>D</b>,<b>E</b>) 200 µm; (<b>F</b>,<b>G</b>) 1 mm.</p>
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<p>Sinker formation in <span class="html-italic">P. berteroi</span> flowers in transverse (<b>A</b>,<b>B</b>) and longitudinal radial section (<b>C</b>–<b>F</b>), analyzed with LM. (<b>A</b>–<b>D</b>) Flowers of <span class="html-italic">P. berteroi</span> and their sinkers; (<b>B</b>) detail of the sinker showing parasite and host tracheary elements separated by parenchymal cells, corresponding to the box indicated in photo (<b>A</b>); (<b>D</b>) close-up of the plate in the radial longitudinal section of the stem, corresponding to the boxed area in (<b>C</b>); (<b>E</b>) detail of the cambial zone showing the sinker with the <span class="html-italic">A. trijuga</span> tracheary elements and the tracheoids of <span class="html-italic">P. berteroi</span>; (<b>F</b>) another detail showing the <span class="html-italic">A. trijuga</span> vessels of the axial system and the tracheary elements entering the sinker. The tracheary elements of <span class="html-italic">A. trijuga</span> and the tracheoids of <span class="html-italic">P. berteroi</span> are in contact. Abbreviations: ahx: axial host xylem; cz: cambial zone; EP: endophytic patches; he: host tracheary elements; pc: parenchyma cell; pt: parasite tracheoid; ra: rays; xy: xylem. Scales: (<b>A</b>) 200 µm; (<b>B</b>,<b>E</b>,<b>F</b>) 20 µm; (<b>C</b>) 500 µm; (<b>D</b>) 100 µm.</p>
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<p>Host vessels and parasite tracheoids of sinkers analyzed with SEM (<b>A</b>–<b>F</b>), and CLSM maximum images projection of 30 optical sections at 0.95-µm intervals (<b>G</b>–<b>I</b>). (<b>A</b>,<b>B</b>) Parasite tracheoids and host tracheary elements separated by parenchymatic cells; (<b>C</b>) parasite tracheoids and parenchymatic cells; (<b>D</b>) detail of tracheoid with smooth ridges; (<b>E</b>,<b>F</b>) host tracheary elements with vestured pits; (<b>G</b>,<b>H</b>) CLSM merged two channels images, green: ex/em 503/508–633; red: 627/635–750; (<b>G</b>) detail of sinker highlighting elements of the parasite and host xylem; (<b>H</b>) tracheoids from the flower of <span class="html-italic">P. berteroi</span>; (<b>I</b>) detail of macerated host stem secondary xylem axial elements from a region not invaded by the parasite, CLSM green: 503/508–633 nm. Abbreviations: ahv: axial host vessel; lf: libriform fibers; he: host tracheary elements; ht: helical thickenings; pc: parenchyma cell; pt: parasite tracheoids; rc: rays cells; vp: vestured pits. Scales: (<b>A</b>,<b>B</b>,<b>E</b>) 10 µm; (<b>C</b>) 5 µm; (<b>D</b>,<b>F</b>) 2 µm; (<b>G</b>–<b>I</b>) 20 µm.</p>
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13 pages, 2159 KiB  
Article
Parasites Diversity, Abundance, Prevalence, and Richness Infecting Didelphis aurita (Didelphimorphia: Didelphidae) in the Atlantic Rainforest, Brazil
by Carolina Romeiro Fernandes Chagas, Cauê Monticelli, Caio Filipe da Motta Lima and Patrícia Locosque Ramos
Pathogens 2024, 13(9), 806; https://doi.org/10.3390/pathogens13090806 - 18 Sep 2024
Viewed by 834
Abstract
Parasites are key players in ecosystems, influencing population sizes and food webs, yet the impact of environmental factors on their diversity is not well understood. The Atlantic rainforest in Brazil, particularly the Parque Estadual das Fontes do Ipiranga (PEFI), exemplifies a biodiversity hotspot [...] Read more.
Parasites are key players in ecosystems, influencing population sizes and food webs, yet the impact of environmental factors on their diversity is not well understood. The Atlantic rainforest in Brazil, particularly the Parque Estadual das Fontes do Ipiranga (PEFI), exemplifies a biodiversity hotspot facing significant deforestation, housing diverse animal species such as the synanthropic Brazilian common opossum (Didelphis aurita), which serves as a reservoir for multiple zoonotic pathogens. In this study, we investigated parasite diversity, abundance, prevalence, and richness in free-living D. aurita in the PEFI, São Paulo, Brazil. From January 2015 to January 2017, 101 fecal samples of D. aurita were collected in two areas of PEFI, at the Instituto de Pesquisas Ambientais (IPA) and the Parque de Ciência e Tecnologia (Cientec), and analyzed using three different parasitological methods. In total, 99% of the samples were positive for at least one parasite. The most prevalent parasite belonged to the order Strongylida (82%), followed by Cruzia sp. (77%), the latter having a significantly higher prevalence at IPA. In contrast, Acanthocephala showed greater prevalence at Cientec. Co-infections were common, with some individuals harboring up to seven different parasites. Our findings reveal significant parasite diversity in the D. aurita population at PEFI, including both helminths and protozoan trophozoites, some of which are reported for the first time in this host species. Further research is essential for accurate species identification of the observed parasites. Full article
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<p>Study site showing the location of the Parque Estadual das Fontes do Ipiranga (PEFI) within South American and in the São Paulo state. Traps were set in the Instituto de Pesquisas Ambientais (IPA) and Parque de Ciência e Tecnologia (Cientec).</p>
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<p>Helminth eggs (<b>A</b>–<b>C</b>,<b>F</b>–<b>I</b>,<b>K</b>) and coccidian oocysts (<b>D</b>,<b>E</b>,<b>L</b>) and sporocyst (<b>J</b>) found in <span class="html-italic">Didelphis aurita</span> feces sampled in the Parque Estadual das Fontes do Ipiranga (PEFI), São Paulo, Brazil. Strongylida (<b>A</b>), <span class="html-italic">Cruzia</span> sp. (<b>B</b>), Trematoda (<b>C</b>), <span class="html-italic">Eimeria</span> sp. (<b>D</b>,<b>E</b>), Trichuridae (<b>F</b>), Strongyloididae (<b>G</b>), Acanthocephala (<b>H</b>), Ascaridida (<b>I</b>), <span class="html-italic">Sarcocystis</span> sp. (<b>J</b>), Oxyuroidea (<b>K</b>), Adeleidae (<b>L</b>). Images were taken with the same magnification (400×), except for (<b>E</b>) (100×).</p>
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<p>Parasite richness in fecal samples collected from <span class="html-italic">Didelphis aurita</span> in the Instituto de Pesquisas Ambientais (IPA)—in blue, and the Parque de Ciência e Tecnologia (Cientec)—in red, in Parque Estadual das Fontes do Ipiranga (PEFI), São Paulo, Brazil. Richness was considered as the number of different parasite types per sample. The parasite richness distributions of the two study sites are represented by a dot-boxplot (<b>a</b>) and a histogram (<b>b</b>).</p>
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8 pages, 1355 KiB  
Article
First Record of Two Nasal Mites Genus Rhinonyssus (Mesostigmata, Rhinonyssidae) Parasitizing Birds from Estonia
by Ivan Dimov
Parasitologia 2024, 4(3), 288-295; https://doi.org/10.3390/parasitologia4030025 - 3 Sep 2024
Viewed by 755
Abstract
Rhinonyssids are obligate hematophagous mites that parasitize the nasal cavity of domestic and wilds birds worldwide. For the first time, two species of nasal mites of the genus Rhinonyssus from Estonia are described. One species of nasal mite, Rhinonyssus pluvialis Fain et Johnston, [...] Read more.
Rhinonyssids are obligate hematophagous mites that parasitize the nasal cavity of domestic and wilds birds worldwide. For the first time, two species of nasal mites of the genus Rhinonyssus from Estonia are described. One species of nasal mite, Rhinonyssus pluvialis Fain et Johnston, 1966, is described and illustrated based on material from Pluvialis apricaria Linnaeus, 1758 (Charadriiformes, Charadriidae). Another species of nasal mite, Rhinonyssus tringae Fain, 1963, is described and illustrated based on material from Tringa glareola Linnaeus, 1758 (Charadriiformes, Scolopacidae). The bird hosts were collected in Estonia, Puhato järv. Full article
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<p><span class="html-italic">Rhinonyssus pluvialis</span> female dorsum.</p>
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<p><span class="html-italic">Rhinonyssus pluvialis</span> female venter.</p>
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<p><span class="html-italic">Rhinonyssus pluvialis</span> female tarsal receptor complex.</p>
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<p><span class="html-italic">Rhinonyssus pluvialis</span> female palpal receptor complex.</p>
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<p><span class="html-italic">Rhinonyssus tringae</span> female dorsum.</p>
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<p><span class="html-italic">Rhinonyssus tringae</span> female venter.</p>
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<p><span class="html-italic">Rhinonyssus tringae</span> female tarsal receptor complex.</p>
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<p><span class="html-italic">Rhinonyssus tringae</span> female palpal receptor complex.</p>
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12 pages, 2575 KiB  
Article
Morphological and Molecular Characterization of the Potato Rot Nematode, Ditylenchus destructor, Parasitizing Garlic in Korea
by Sungchan Huh, Sohee Park, Hwanseok Je, Namsook Park, Donggeun Kim, Insoo Choi and Heonil Kang
Horticulturae 2024, 10(9), 902; https://doi.org/10.3390/horticulturae10090902 - 26 Aug 2024
Viewed by 722
Abstract
A survey of plant parasitic nematodes was carried out in 650 garlic fields in Korea from 2020 to 2022. Migratory endoparasite nematodes (Ditylenchus sp.) were recovered from 6% of the garlic samples, with an average density of 494 individuals per garlic bulb. [...] Read more.
A survey of plant parasitic nematodes was carried out in 650 garlic fields in Korea from 2020 to 2022. Migratory endoparasite nematodes (Ditylenchus sp.) were recovered from 6% of the garlic samples, with an average density of 494 individuals per garlic bulb. The morphological characteristics of males and females from the 2022 survey were very similar to D. destructor, but D. dipsaci was not found. The Korean population traits have a lateral field containing six incisures, and the posterior esophagus part overlaps the intestine dorsally. PCR and DNA sequencing were performed for the D2/D3 region of the ribosomal DNA 28S and the ITS region, and the phylogenetic analysis strongly supports the monophyly of D. destructor. This is the first report of D. destructor parasitizing garlic in the Republic of Korea. In Korea, due to changes in agricultural or environmental conditions, the most damaging potential PPNs changed from D. dipsaci to D. destructor in garlic cultivation. Full article
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<p>Damage symptoms of garlic bulb (<b>A</b>) and the garlic peel infected by <span class="html-italic">Ditylenchus destructor</span> (<b>B</b>). Scale bars: (<b>B</b>) = 100 μm.</p>
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<p>Photographs of females of <span class="html-italic">Ditylenchus destructor</span>. Entire body (<b>A</b>); lateral line (<b>B</b>); anterior region (<b>C</b>); posterior region (<b>D</b>); posterior esophagus part (<b>E</b>). Scale bars: (<b>A</b>) = 100 μm, (<b>B</b>) = 2 μm, (<b>C</b>–<b>E</b>) = 10 μm.</p>
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<p>Photographs of vulva and tail region of <span class="html-italic">Ditylenchus destructor</span>. Tail of female (<b>A</b>,<b>B</b>); vulva region (<b>C</b>). Scale bars: (<b>A</b>,<b>B</b>) = 50 μm, (<b>C</b>) = 20 μm.</p>
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<p>Photographs of spicule and tail region of <span class="html-italic">Ditylenchus destructor</span>. Tail of female (<b>A</b>,<b>B</b>); spicule region (<b>C</b>). Scale bars: (<b>A</b>) = 20 μm, (<b>B</b>,<b>C</b>) = 10 μm.</p>
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<p>Phylogenetic relationships within population and species of <span class="html-italic">Ditylenchus</span>. Bayesian 50% majority rule consensus tree from two runs, as inferred from the analysis of the D2D3 of 28S rDNA gene sequences under the GTR + I + G model. Posterior probability values more than 50% are given in appropriate clades. Newly sequenced samples are indicated in bold font.</p>
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<p>Phylogenetic relationships within population and species of <span class="html-italic">Ditylenchus</span>. Bayesian 50% majority rule consensus tree from two runs, as inferred from the analysis of the ITS rRNA gene sequences under the GTR + I + G model. Posterior probability values more than 50% are given in appropriate clades. Newly sequenced samples are indicated in bold font.</p>
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11 pages, 2482 KiB  
Protocol
Parasitological Examination of the Digestive System of Wild Boar from a Practical Point of View—Endoparasitological Sampling under Field Conditions
by Csaba Farkas, Alexandra Juhász, Balázs Fekete and Borisz Egri
Methods Protoc. 2024, 7(4), 65; https://doi.org/10.3390/mps7040065 - 21 Aug 2024
Viewed by 707
Abstract
From 2015 to 2023, we conducted a comprehensive study in the 11,893-hectare hunting area managed by the Marcal-Bitvaközi Hunting Company, characterised by its substantial wild boar population. The research was carried out across various settings, including a free-range wild boar garden during large-scale [...] Read more.
From 2015 to 2023, we conducted a comprehensive study in the 11,893-hectare hunting area managed by the Marcal-Bitvaközi Hunting Company, characterised by its substantial wild boar population. The research was carried out across various settings, including a free-range wild boar garden during large-scale hunts and free-living areas during individual hunts. We examined 216 wild boars in total, with 173 individuals from free-living areas and 43 from free-range areas. Throughout the sample collection process, we encountered numerous technical challenges that are infrequently detailed in the professional literature, often mentioned only tangentially. This oversight in existing publications neglects the significance of addressing field sampling difficulties, which are crucial for ensuring the precision and accuracy of research. This paper details the equipment requirements, sampling methodologies, and practical solutions to streamline fieldwork. While our primary focus was on endoparasitic infections of the stomach and small intestine, the described methodologies and findings are broadly applicable to research involving all internal organs. Full article
(This article belongs to the Special Issue Feature Papers in Methods and Protocols 2024)
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<p>Only the organs we need are found in the middle of the spread foil (Original).</p>
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<p>Our thumb is placed in one end of the washed intestinal section and the end of the intestinal section is continuously pulled, and the upper part of the intestinal wall is torn open at the tip of our finger (Original).</p>
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<p>Spreading a sample containing <span class="html-italic">A. suum</span> on a glass table illuminated from below (Original).</p>
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13 pages, 1690 KiB  
Article
Extrinsic and Intrinsic Competition between Chouioa cunea Yang and Tetrastichus septentrionalis (Hymenoptera: Eulophidae), Two Pupal Parasitoids of the Fall Webworm, Hyphantria cunea (Lepidoptera: Erebidae)
by Zhixin Li, Liyuan Yang, Xi Ma, Xudan Liu, Yiran Cheng and Shouhui Sun
Insects 2024, 15(8), 617; https://doi.org/10.3390/insects15080617 - 15 Aug 2024
Viewed by 902
Abstract
The endoparasitoids Chouioa cunea Yang and Tetrastichus septentrionalis Yang (Hymenoptera: Eulophidae) are both gregarious pupal parasitoids of the fall webworm, Hyphantria cunea (Drury) (Lepidoptera: Erebidae). In order to analyze the competitive interactions between both parasitoids exploiting H. cunea, we assessed both extrinsic [...] Read more.
The endoparasitoids Chouioa cunea Yang and Tetrastichus septentrionalis Yang (Hymenoptera: Eulophidae) are both gregarious pupal parasitoids of the fall webworm, Hyphantria cunea (Drury) (Lepidoptera: Erebidae). In order to analyze the competitive interactions between both parasitoids exploiting H. cunea, we assessed both extrinsic and intrinsic competition. The search time, oviposition duration, and oviposition frequency were used as evaluation criteria for extrinsic competition. The number of survival days, female ratio, and number of parasitoids emerging from the host were used as evaluation criteria for intrinsic competition. The results indicated that both parasitoid species were able to parasitize hosts that were already parasitized by competitors. The first released species consistently emerged as the superior competitor in multiparasitized hosts. Both parasitoid release orders and time intervals between oviposition affect the competition of parasitoids and the parasitic efficiency. The results emphasize the parasitic abilities of both parasitoid species and provide a basis for future research on competition mechanisms and biological control of H. cunea. Full article
(This article belongs to the Section Insect Physiology, Reproduction and Development)
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<p><span class="html-italic">Chouioa cunea</span> and <span class="html-italic">Tetrastichus septentrionalis</span> parasitize the same pupa of <span class="html-italic">Hyphantria cunea</span>. Annotation: upper side of the picture is <span class="html-italic">T. septentrionalis</span> and the lower side is <span class="html-italic">C. cunea</span>.</p>
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<p>The differences in oviposition frequency between <span class="html-italic">Chouioa cunea</span> and <span class="html-italic">Tetrastichus septentrionalis</span> were observed in <span class="html-italic">Hyphantria cunea</span>. Annotation: Data are presented as mean ± SEM. Control, where only <span class="html-italic">C. cunea</span> or <span class="html-italic">T. septentrionalis</span> was released; 0 h, where <span class="html-italic">C. cunea</span> and <span class="html-italic">T. septentrionalis</span> were introduced simultaneously; Ts-Cc 24 h, Ts-Cc 48 h, and Ts-Cc 72 h, where <span class="html-italic">T. septentrionalis</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">C. cunea</span>; Cc-Ts 24 h, Cc-Ts 48 h, and Cc-Ts 72 h, where <span class="html-italic">C. cunea</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">T. septentrionalis</span>. * indicates a difference and ** indicates a strong difference (<span class="html-italic">p</span> &lt; 0.05; <span class="html-italic">p</span> &lt; 0.01). The number of repetitions is 10.</p>
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<p>The differences in oviposition duration between <span class="html-italic">Chouioa cunea</span> and <span class="html-italic">Tetrastichus septentrionalis</span> were observed in <span class="html-italic">Hyphantria cunea</span>. Annotation: Data are presented as mean ± SEM. Control, where only <span class="html-italic">C. cunea</span> or <span class="html-italic">T. septentrionalis</span> was released; 0 h, where <span class="html-italic">C. cunea</span> and <span class="html-italic">T. septentrionalis</span> were introduced simultaneously; Ts-Cc 24 h, Ts-Cc 48 h, and Ts-Cc 72 h, where <span class="html-italic">T. septentrionalis</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">C. cunea</span>; Cc-Ts 24 h, Cc-Ts 48 h, and Cc-Ts 72 h, where <span class="html-italic">C. cunea</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">T. septentrionalis</span>. The number of repetitions is 10.</p>
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<p>The differences in search time between <span class="html-italic">Chouioa cunea</span> and <span class="html-italic">Tetrastichus septentrionalis</span> was observed in <span class="html-italic">Hyphantria cunea</span>. Annotation: Data are presented as mean ± SEM. Control, where only <span class="html-italic">C. cunea</span> or <span class="html-italic">T. septentrionalis</span> was released; 0 h, where <span class="html-italic">C. cunea</span> and <span class="html-italic">T. septentrionalis</span> were introduced simultaneously; Ts-Cc 24 h, Ts-Cc 48 h, and Ts-Cc 72 h, where <span class="html-italic">T. septentrionalis</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">C. cunea</span>; Cc-Ts 24 h, Cc-Ts 48 h, and Cc-Ts 72 h, where <span class="html-italic">C. cunea</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">T. septentrionalis</span>. ** indicates a strong difference (<span class="html-italic">p</span> &lt; 0.05). The number of repetitions is 10.</p>
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<p>The differences in female ratio of offspring between <span class="html-italic">Chouioa cunea</span> and <span class="html-italic">Tetrastichus septentrionalis</span> were observed in <span class="html-italic">Hyphantria cunea</span>. Annotation: Data are presented as mean ± SEM. Control, where only <span class="html-italic">C. cunea</span> or <span class="html-italic">T. septentrionalis</span> was released; 0 h, where <span class="html-italic">C. cunea</span> and <span class="html-italic">T. septentrionalis</span> were introduced simultaneously; Ts-Cc 24 h, Ts-Cc 48 h, and Ts-Cc 72 h, where <span class="html-italic">T. septentrionalis</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">C. cunea</span>; Cc-Ts 24 h, Cc-Ts 48 h, and Cc-Ts 72 h, where <span class="html-italic">C. cunea</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">T. septentrionalis</span>. The values displayed at the base of each column indicate the number of replicates.</p>
Full article ">Figure 6
<p>The differences in female ratio, number of survival days, and number of offspring of <span class="html-italic">Chouioa cunea</span> and <span class="html-italic">Tetrastichus septentrionalis</span> under the different conditions. Annotation: Data are presented as mean ± SEM. Cc alone, where only <span class="html-italic">C. cunea</span> was released; Ts alone, where only <span class="html-italic">T. septentrionalis</span> was released; 0 h, where <span class="html-italic">C. cunea</span> and <span class="html-italic">T. septentrionalis</span> were introduced simultaneously; Ts-Cc 24 h, Ts-Cc 48 h, and Ts-Cc 72 h, where <span class="html-italic">T. septentrionalis</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">C. cunea</span>; Cc-Ts 24 h, Cc-Ts 48 h, and Cc-Ts 72 h, where <span class="html-italic">C. cunea</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">T. septentrionalis</span>. * indicates a difference and ** indicates a strong difference (<span class="html-italic">p</span> &lt; 0.05; <span class="html-italic">p</span> &lt; 0.01).</p>
Full article ">Figure 7
<p>The differences in number of survival days of offspring between <span class="html-italic">Chouioa cunea</span> and <span class="html-italic">Tetrastichus septentrionalis</span> were observed in <span class="html-italic">Hyphantria cunea</span>. Annotation: Data are presented as mean ± SEM. Control, where only <span class="html-italic">C. cunea</span> or <span class="html-italic">T. septentrionalis</span> was released; 0 h, where <span class="html-italic">C. cunea</span> and <span class="html-italic">T. septentrionalis</span> were introduced simultaneously; Ts-Cc 24 h, Ts-Cc 48 h, and Ts-Cc 72 h, where <span class="html-italic">T. septentrionalis</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">C. cunea</span>; Cc-Ts 24 h, Cc-Ts 48 h, and Cc-Ts 72 h, where <span class="html-italic">C. cunea</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">T. septentrionalis</span>. The values displayed at the base of each column indicate the number of replicates. * indicates a difference and ** indicates a strong difference (<span class="html-italic">p</span> &lt; 0.05; <span class="html-italic">p</span> &lt; 0.01).</p>
Full article ">Figure 8
<p>The differences in number of offspring between <span class="html-italic">Chouioa cunea</span> and <span class="html-italic">Tetrastichus septentrionalis</span> were observed in <span class="html-italic">Hyphantria cunea</span>. Annotation: Data are presented as mean ± SEM. Control, where only <span class="html-italic">C. cunea</span> or <span class="html-italic">T. septentrionalis</span> was released; 0 h, where <span class="html-italic">C. cunea</span> and <span class="html-italic">T. septentrionalis</span> were introduced simultaneously; Ts-Cc 24 h, Ts-Cc 48 h, and Ts-Cc 72 h, where <span class="html-italic">T. septentrionalis</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">C. cunea</span>; Cc-Ts 24 h, Cc-Ts 48 h, and Cc-Ts 72 h, where <span class="html-italic">C. cunea</span> was released 24 h, 48 h, and 72 h before <span class="html-italic">T. septentrionalis</span>. The values displayed at the base of each column indicate the number of replicates. * indicates a difference and ** indicates a strong difference (<span class="html-italic">p</span> &lt; 0.05; <span class="html-italic">p</span> &lt; 0.01).</p>
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10 pages, 277 KiB  
Review
Endoparasitic Diseases in Breeding Kennels: A Frequent and Complex Problem Requiring a Holistic Approach
by Aurélien Grellet and Hanna Mila
Animals 2024, 14(16), 2357; https://doi.org/10.3390/ani14162357 - 15 Aug 2024
Viewed by 972
Abstract
Parasitic infestations in dogs are frequent, particularly in breeding kennels, being a cause of suffering in animals and economic loss for breeders. In breeding bitches, some parasites may cause abortion, and in puppies they may be responsible for neonatal mortality, weaning diarrhea, or [...] Read more.
Parasitic infestations in dogs are frequent, particularly in breeding kennels, being a cause of suffering in animals and economic loss for breeders. In breeding bitches, some parasites may cause abortion, and in puppies they may be responsible for neonatal mortality, weaning diarrhea, or neurological clinical signs. This review aims to investigate the factors of predisposition, diagnostics, and control in relation to the most frequent parasitic diseases in breeding kennels. It highlights that the control of parasitic diseases in dogs at the population level is complex. A holistic multidisciplinary and pluritechnical approach is thus needed to deal with endoparasitoses. Full article
(This article belongs to the Section Companion Animals)
12 pages, 1586 KiB  
Article
Zoonotic Enteric Nematodes and Dermatophytes in Cat Cafés: An Investigation in the Bangkok Metropolitan Area, Thailand
by Phakjira Sanguansook, Siwaporn Tuangpermsub, Boonyakorn Leelakarnsakul, Sutida Phaisansomsuk, Vachira Hunprasit, Laura Del Río, Waree Niyomtham, Nuvee Prapasarakul and Woraporn Sukhumavasi
Vet. Sci. 2024, 11(8), 358; https://doi.org/10.3390/vetsci11080358 - 7 Aug 2024
Viewed by 2096
Abstract
Cat cafés have gained significant popularity worldwide, offering a unique interface between humans and cats. The present study aims to assess the prevalence of potentially zoonotic endoparasites and dermatophytes from cats living in cat cafés situated in the Bangkok metropolitan area in 2017–2018. [...] Read more.
Cat cafés have gained significant popularity worldwide, offering a unique interface between humans and cats. The present study aims to assess the prevalence of potentially zoonotic endoparasites and dermatophytes from cats living in cat cafés situated in the Bangkok metropolitan area in 2017–2018. Cat fecal samples were subjected to microscopic examination employing centrifugal flotation and centrifugal sedimentation techniques. The hair samples from every cat were cultured on a dermatophyte test medium and Sabouraud dextrose agar and subsequently confirmed by visualization of the typical colony and macroconidia morphology. Findings from 11 cat cafés indicated an 18.2% (2/11) prevalence of gastrointestinal parasites, including Toxocara spp., Ancylostoma spp., Physaloptera spp., and Eucoleus aerophilus. Dermatophytes were prevalent in 16.2% (32/198) of the total number of cats tested, with Microsporum canis being the sole species identified. Notably, the presence of dermatophyte was significantly correlated with the presence of skin lesions and the cats’ origin. In summary, the findings of this study have provided evidence of potentially zoonotic endoparasites and dermatophytes in cats residing in cat cafés. Therefore, it is imperative to heighten awareness and encourage preventive measures among cat café owners and customers to halt the dissemination of these pathogens. Full article
(This article belongs to the Section Veterinary Microbiology, Parasitology and Immunology)
Show Figures

Figure 1

Figure 1
<p>Geographical distribution of the selected 11 cat cafés for this study located in Bangkok metropolitan area, Thailand, 2017–2018.</p>
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<p>Microscopic findings of endoparasite eggs isolated from cat feces of positive cat café taken at 400× magnification: (<b>A</b>) <span class="html-italic">Toxocara</span> spp. (<b>B</b>) <span class="html-italic">Ancylostoma</span> spp. (<b>C</b>) <span class="html-italic">Physaloptera</span> spp. (<b>D</b>) <span class="html-italic">Eucoleus aerophilus</span>.</p>
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<p><span class="html-italic">Demodex gatoi</span> found in cat feces recovered by the centrifugal flotation technique, 400× magnification: (<b>A</b>) from cat café no. 03 (<b>B</b>) from cat café no. 06.</p>
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<p>Example of dermatophytes cultured from hair samples of cats residing in cat cafés: (<b>A</b>) The growth of typical white fluffy colony on DTM media that changed to purple color after 14 days incubation. (<b>B</b>) Several spindle-shaped macroconidia of <span class="html-italic">M. canis</span> stained in lactophenol cotton blue from subculture on SDA for 21 days, 400× magnification.</p>
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