[go: up one dir, main page]
More Web Proxy on the site http://driver.im/
You seem to have javascript disabled. Please note that many of the page functionalities won't work as expected without javascript enabled.
 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (164)

Search Parameters:
Keywords = interspecies transmission

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
15 pages, 4710 KiB  
Review
Comparative Insights into Acute Gastroenteritis in Cattle Caused by Bovine Rotavirus A and Bovine Coronavirus
by Vjekoslava Kostanić, Valentina Kunić, Marina Prišlin Šimac, Marica Lolić, Tomislav Sukalić and Dragan Brnić
Vet. Sci. 2024, 11(12), 671; https://doi.org/10.3390/vetsci11120671 (registering DOI) - 21 Dec 2024
Viewed by 272
Abstract
Acute gastroenteritis (AGE) in cattle significantly impacts the economy due to relatively high morbidity and mortality and decreased production. Its multifactorial nature drives its global persistence, involving enteric viruses, bacteria, protozoa, and environmental factors. Bovine Rotavirus A (BoRVA) and bovine coronavirus (BCoV) are [...] Read more.
Acute gastroenteritis (AGE) in cattle significantly impacts the economy due to relatively high morbidity and mortality and decreased production. Its multifactorial nature drives its global persistence, involving enteric viruses, bacteria, protozoa, and environmental factors. Bovine Rotavirus A (BoRVA) and bovine coronavirus (BCoV) are among the most important enteric RNA viruses causing AGE in cattle. These viruses infect intestinal enterocytes, leading to cell damage and consequently to malabsorption and diarrhea. BoRVA primarily affects calves under 14 days old with gastrointestinal clinical signs, while BCoV affects all ages, causing gastrointestinal and respiratory distress. The economic impact of BoRVA and BCoV, along with their interspecies transmission potential, warrants attention. This concise review discusses the molecular structure, epidemiology, pathogenesis, clinical signs, diagnosis, treatment, and preventive measures of BoRVA and BCoV while providing a comparative analysis. By offering practical guidance on managing such viral infections in cattle, these comparative insights may prove valuable for veterinarians in clinical practice. Full article
(This article belongs to the Section Veterinary Microbiology, Parasitology and Immunology)
Show Figures

Figure 1

Figure 1
<p>(<b>a</b>) Negative-staining electron microscopy reveals the characteristic wheel-like morphology of RV [<a href="#B20-vetsci-11-00671" class="html-bibr">20</a>]. (<b>b</b>) A negative-staining electron micrograph of a CoV virion [<a href="#B21-vetsci-11-00671" class="html-bibr">21</a>].</p>
Full article ">Figure 2
<p>(<b>a</b>) A schematic of a triple-layered RV particle featuring the inner capsid (VP1, VP2, VP3), middle capsid (VP6), outer capsid (VP7), and spike protein (VP4) [<a href="#B22-vetsci-11-00671" class="html-bibr">22</a>]. (<b>b</b>) A diagram of the CoV virion’s structure, featuring the nucleocapsid (N) protein and viral RNA genome at its core, encased in an envelope containing the spike (S), hemagglutinin–esterase (HE), membrane (M), and envelope (E) proteins [<a href="#B23-vetsci-11-00671" class="html-bibr">23</a>].</p>
Full article ">Figure 3
<p>(<b>a</b>) A one-week-old calf exhibiting gastrointestinal signs, showing an example of yellowish diarrhea caused by BCoV [<a href="#B40-vetsci-11-00671" class="html-bibr">40</a>]. (<b>b</b>) Hemorrhagic diarrhea resulting from BCoV infection [<a href="#B40-vetsci-11-00671" class="html-bibr">40</a>]. Both images are courtesy of Cabinet Vétérinaire de Riom-es-Montagnes, Cantal, France.</p>
Full article ">Figure 4
<p>(<b>a</b>) A section of an intestine from a calf infected with RV, stained with H&amp;E, reveals villous exfoliation, engorged capillary plexuses, and moderate infiltration of the lamina propria in the ileum [<a href="#B58-vetsci-11-00671" class="html-bibr">58</a>]. (<b>b</b>) An intestinal section from a calf infected with BCoV presents thick homogeneous necrotic material covering the ulcerated mucosa of the colon, as indicated by the arrows [<a href="#B58-vetsci-11-00671" class="html-bibr">58</a>].</p>
Full article ">
13 pages, 7705 KiB  
Communication
Novel Betaherpesviruses in Neotropical Bats on the Caribbean Island of St. Kitts: First Report from Antillean Tree Bats (Ardops nichollsi) and Evidence for Cross-Species Transmission
by Jessica L. Kulberg, Sarah Hooper, Yashpal S. Malik and Souvik Ghosh
Microorganisms 2024, 12(12), 2603; https://doi.org/10.3390/microorganisms12122603 - 16 Dec 2024
Viewed by 577
Abstract
To date, limited information is available on herpesviruses in bats from the Caribbean region. We report here high detection rates (24.24%, n = 66) of herpesviruses in oral samples from apparently healthy bats (Ardops nichollsi (75%, 9/12) and Molossus molossus (28%, 7/25)) [...] Read more.
To date, limited information is available on herpesviruses in bats from the Caribbean region. We report here high detection rates (24.24%, n = 66) of herpesviruses in oral samples from apparently healthy bats (Ardops nichollsi (75%, 9/12) and Molossus molossus (28%, 7/25)) on the Lesser Antillean Island of St. Kitts. Based on analysis of partial DNA polymerase (DPOL) sequences (~225 amino acid (aa) residues), we identified two distinct groups of herpesviruses (BO-I and -II) that were unique to A. nichollsi and M. molossus, respectively. Within the subfamily Betaherpesvirinae, the BO-I DPOL sequences shared low deduced aa identities (<70%) with other herpesviruses, and phylogenetically, they formed a distinct cluster, representing a putative novel betaherpesvirus. The BO-II DPOL sequences were closely related to a putative novel betaherpesvirus from a M. molossus in Lesser Antillean Island of Martinique, indicating possible transmission of herpesviruses by bat movement between the Caribbean Islands. Phylogenetically, the BO-I and -II betaherpesviruses exhibited species-specific (A. nichollsi and M. molossus, respectively) as well as family-specific (Phyllostomidae and Molossidae, respectively) clustering patterns, corroborating the hypothesis on host specificity of betaherpesviruses. Interestingly, a single M. molossus betaherpesvirus strain clustered with the A. nichollsi betaherpesviruses, indicating possible interspecies transmission of herpesviruses between Phyllostomidae and Molossidae. To our knowledge, this is the first report on detection of herpesviruses from Antillean tree bats (A. nichollsi), expanding the host range of betaherpesviruses. Taken together, the present study identified putative novel betaherpesviruses that might be unique to chiropteran species (A. nichollsi and M. molossus), indicating virus–host coevolution, and provided evidence for interspecies transmission of betaherpesviruses between chiropteran families. Full article
(This article belongs to the Special Issue New Progress in Animal Herpesviruses)
Show Figures

Figure 1

Figure 1
<p>Map of the Caribbean Island of St. Kitts showing the capture locations of BO group-I and -II herpesvirus-positive bats (shown with red and blue pins, respectively). Bat BO27 (capture site shown with a black pin) yielded a low-quality (Phred value &lt; 40) putative DNA polymerase sequence and was excluded from further analysis. The map of St. Kitts was adapted from <a href="https://www.google.com/maps" target="_blank">https://www.google.com/maps</a> (accessed on 2 October 2024) (<b>a</b>). In the present study, <span class="html-italic">Ardops nichollsi</span> (<b>b</b>) and <span class="html-italic">Molossus molossus</span> (<b>c</b>) tested positive for herpesviruses. The photographs were taken during sampling by Dr. Sarah Hooper, RUSVM (<b>b</b>,<b>c</b>).</p>
Full article ">Figure 1 Cont.
<p>Map of the Caribbean Island of St. Kitts showing the capture locations of BO group-I and -II herpesvirus-positive bats (shown with red and blue pins, respectively). Bat BO27 (capture site shown with a black pin) yielded a low-quality (Phred value &lt; 40) putative DNA polymerase sequence and was excluded from further analysis. The map of St. Kitts was adapted from <a href="https://www.google.com/maps" target="_blank">https://www.google.com/maps</a> (accessed on 2 October 2024) (<b>a</b>). In the present study, <span class="html-italic">Ardops nichollsi</span> (<b>b</b>) and <span class="html-italic">Molossus molossus</span> (<b>c</b>) tested positive for herpesviruses. The photographs were taken during sampling by Dr. Sarah Hooper, RUSVM (<b>b</b>,<b>c</b>).</p>
Full article ">Figure 2
<p>(<b>A</b>,<b>B</b>). Phylogenetic analysis of the partial deduced amino acid (aa) sequences (~225 aa, and ~150 aa putative DPOL sequences were analyzed in figure (<b>A</b>) and (<b>B</b>), respectively) of putative DNA polymerases of the BO-I and -II herpesviruses (shown with red and blue circles, respectively) from bats in St. Kitts with cognate sequences of other betaherpesviruses. (<b>A</b>): The <span class="html-italic">Ardops nichollsi</span>, <span class="html-italic">Molossus molossus</span>, and other chiropteran species are shown with red, blue, and black bat emojis, respectively. The bat emojis were obtained from <a href="https://creazilla.com/media/silhouette/7977573/bat" target="_blank">https://creazilla.com/media/silhouette/7977573/bat</a> (accessed on 10 October 2024) under a CC0 license. (<b>B</b>): The chiropteran families are mentioned to the upper left and highlighted with different colored boxes. (<b>A</b>,<b>B</b>): The recognized genera within the subfamily <span class="html-italic">Betaherpesvirinae</span> are shown with <span class="html-italic">italic</span> font. The ‘name of the virus/bat-species/country/year of sampling’ has been mentioned for the BO herpesviruses, whilst the name of the virus, the isolate, or the strain/host species/GenBank accession number is shown for the other betaherpesviruses. A member of the subfamily <span class="html-italic">Gammaherpesvirinae</span> (ClGHV3/CJ0149/AF319782) was used as the outgroup sequence. Bootstrap values &lt; 70% are not shown. Scale bar, 0.1 substitutions per aa residue.</p>
Full article ">Figure 2 Cont.
<p>(<b>A</b>,<b>B</b>). Phylogenetic analysis of the partial deduced amino acid (aa) sequences (~225 aa, and ~150 aa putative DPOL sequences were analyzed in figure (<b>A</b>) and (<b>B</b>), respectively) of putative DNA polymerases of the BO-I and -II herpesviruses (shown with red and blue circles, respectively) from bats in St. Kitts with cognate sequences of other betaherpesviruses. (<b>A</b>): The <span class="html-italic">Ardops nichollsi</span>, <span class="html-italic">Molossus molossus</span>, and other chiropteran species are shown with red, blue, and black bat emojis, respectively. The bat emojis were obtained from <a href="https://creazilla.com/media/silhouette/7977573/bat" target="_blank">https://creazilla.com/media/silhouette/7977573/bat</a> (accessed on 10 October 2024) under a CC0 license. (<b>B</b>): The chiropteran families are mentioned to the upper left and highlighted with different colored boxes. (<b>A</b>,<b>B</b>): The recognized genera within the subfamily <span class="html-italic">Betaherpesvirinae</span> are shown with <span class="html-italic">italic</span> font. The ‘name of the virus/bat-species/country/year of sampling’ has been mentioned for the BO herpesviruses, whilst the name of the virus, the isolate, or the strain/host species/GenBank accession number is shown for the other betaherpesviruses. A member of the subfamily <span class="html-italic">Gammaherpesvirinae</span> (ClGHV3/CJ0149/AF319782) was used as the outgroup sequence. Bootstrap values &lt; 70% are not shown. Scale bar, 0.1 substitutions per aa residue.</p>
Full article ">
10 pages, 1747 KiB  
Case Report
Fatal Feline Leukemia Virus-Associated Enteritis in a Wild Eurasian Lynx (Lynx lynx) in Germany
by Katharina M. Gregor, Monica Mirolo, Florian Brandes, Sonja T. Jesse, Franziska Kaiser, Jutta Verspohl, Sybille Wölfl, Albert D. M. E. Osterhaus, Wolfgang Baumgärtner, Martin Ludlow and Andreas Beineke
Biology 2024, 13(12), 997; https://doi.org/10.3390/biology13120997 - 30 Nov 2024
Viewed by 482
Abstract
The Eurasian lynx (Lynx lynx), a widespread wild felid on the Eurasian continent, is currently classified as “critically endangered” in Germany. Understanding the impact of infectious agents is of particular importance for the continued conservation of these animals, especially regarding pathogens [...] Read more.
The Eurasian lynx (Lynx lynx), a widespread wild felid on the Eurasian continent, is currently classified as “critically endangered” in Germany. Understanding the impact of infectious agents is of particular importance for the continued conservation of these animals, especially regarding pathogens with broad host ranges and risk of interspecies transmission. Feline leukemia virus (FeLV) is known to infect wild and domestic felids worldwide, including several species of lynx, but it has not been reported thus far in the Eurasian lynx. In September 2020, a 16-month-old female Eurasian lynx from the Bavarian Forest, Germany, showed a sudden onset of gastrointestinal signs such as anorexia, diarrhea, and vomiting, and died within one week. Macroscopic and histologic examination revealed hemorrhagic-necrotizing enteritis and typhlocolitis, with the degeneration of crypts and crypt abscesses, as well as depleted Peyer’s patches. In addition, the animal showed lymphoid depletion (lymph nodes, thymus, and spleen) and hypocellularity of the bone marrow. FeLV infection was confirmed by immunohistochemistry and next generation sequencing. A secondary bacterial infection with hemolytic Escherichia coli and Clostridium perfringens type A was present in the intestine. This is the first report of FeLV-associated enteritis, lymphoid depletion and bone marrow suppression with associated secondary bacterial infection in a Eurasian lynx. Full article
(This article belongs to the Section Infection Biology)
Show Figures

Figure 1

Figure 1
<p>Macroscopic findings in a Eurasian lynx (<span class="html-italic">Lynx lynx</span>). The jejunum is diffusely red and filled with blood-tinged digesta.</p>
Full article ">Figure 2
<p>Histologic and immunohistochemical findings in small intestine and mesenteric lymph node of a Eurasian lynx (<span class="html-italic">Lynx lynx</span>). (<b>a</b>) Severe, diffuse, subacute, hemorrhagic-necrotizing enteritis with loss of intestinal crypts, crypt dilatation (star), and crypt epithelial degeneration. Hematoxylin–eosin (HE). Bar = 100 µm. Insert. Dilatation of a single intestinal crypt with crypt epithelial degeneration (arrows) and luminal accumulation of cellular debris (crypt abscess). HE. Bar = 20 µm. (<b>b</b>) Lymphatic depletion and blood resorption in mesenteric lymph node. HE. Bar = 100 µm. (<b>c</b>) Immunolabeling of feline leukemia virus gp85/gp70 envelope protein in the intestinal crypt epithelium (arrows) and infiltrating mononuclear cells (arrowheads). Bars = 50 µm. (<b>d</b>) Immunolabeling of feline leukemia virus gp85/gp70 envelope protein in mononuclear cells (arrowheads) in mesenteric lymph node. Bar = 50 µm.</p>
Full article ">Figure 3
<p>Phylogenetic analysis based on the complete coding sequence of feline leukemia virus (FeLV). The tree was constructed using the maximum likelihood method and the GTR + G was used as best fit model to shape evolutionary rates across sites with 1000 bootstraps. Bootstrap values are presented at nodes. The scale bar indicates the number of nucleotide changes per site. Taxon names are presented by the GenBank accession number, virus name and strain. Genome sequences belonging to different FeLV clades were downloaded from GenBank (<a href="#app1-biology-13-00997" class="html-app">Table S4</a>).</p>
Full article ">
16 pages, 8810 KiB  
Article
Streptococcus agalactiae Infection in Wild Trahira (Hoplias malabaricus) and Farmed Arapaima (Arapaima gigas) in Brazil: An Interspecies Transmission in Aquatic Environments Shared with Nile Tilapia (Oreochromis niloticus)
by Carlos Augusto Gomes Leal, Rafael Gariglio Clark Xavier, Guilherme Alves de Queiroz, Tarcísio Martins França Silva, Júnia Pacheco Teixeira, Flávia Figueira Aburjaile and Guilherme Campos Tavares
Microorganisms 2024, 12(12), 2393; https://doi.org/10.3390/microorganisms12122393 - 22 Nov 2024
Viewed by 476
Abstract
Streptococcus agalactiae is an important pathogen responsible for cases of high mortality in farmed and wild fish worldwide. In Brazil, this bacterium has been commonly associated with outbreaks in Nile tilapia farms, but other native fish species are also susceptible. Since floating cages [...] Read more.
Streptococcus agalactiae is an important pathogen responsible for cases of high mortality in farmed and wild fish worldwide. In Brazil, this bacterium has been commonly associated with outbreaks in Nile tilapia farms, but other native fish species are also susceptible. Since floating cages are one of the most common culture systems used in the country, the close contact between farmed tilapia and native fish species presents a risk concerning the transmission of this pathogen. In this study, we characterized a mortality outbreak in free-living trahira and in farmed arapaima, as well as the genetic and antimicrobial susceptibility patterns of the isolates obtained. During the outbreaks, moribund fish were sampled and subjected to bacterial examination, after which the isolates were identified via MALDI-ToF analysis. Genotyping was evaluated using repetitive sequence-based PCR (REP-PCR) and multilocus sequence typing (MLST). Antimicrobial susceptibility was evaluated using disc diffusion assays. In addition, whole-genome analysis also was performed. S. agalactiae was identified in all diseased fish, all of which belonged to serotype Ib; however, trahira strains were classified as non-typeable lineages in the MLST assay, while arapaima strains were classified as ST260. These isolates were shown to be similar to the main genotype found in Nile tilapia in Brazil, using REP-PCR, MLST and phylogenomic analysis. The pathogenicity of the bacterium was confirmed by Koch’s postulates for both fish species. The antimicrobial susceptibility assay showed variable results to the same antibiotics among the isolates, prompting four of the isolates to be classified as multidrug-resistant. This study represents the first report of a natural outbreak of Streptococcus agalactiae infection in wild trahira and farmed arapaima inhabiting the same aquatic environment as Nile tilapia. Full article
(This article belongs to the Special Issue Infectious Diseases in Aquaculture)
Show Figures

Figure 1

Figure 1
<p>Natural <span class="html-italic">Streptococcus agalactiae</span> infection in native fish species. (<b>A</b>) Diseased wild trahira with exophthalmia (arrow) found dead during the outbreak; (<b>B</b>) Diseased arapaima with exophtalmia and corneal opacity, alive in the tank.</p>
Full article ">Figure 2
<p>REP-PCR results for five <span class="html-italic">Streptococcus agalactiae</span> strains isolated from trahira, arapaima, Amazon catfish and Nile tilapia. The dendrogram was constructed using Dice’s coefficient and the UPGMA method.</p>
Full article ">Figure 3
<p>Whole-genome sequence RA × ML phylogenetic tree constructed using SA32-17 and SA45-17 strains together other Brazilian <span class="html-italic">Streptococcus agalactiae</span> strains deposited in the GenBank database (bootstrap test, 1000 replicates). Two distantly related groups of isolates are visualized one on the right side (CC260, marked with *) and one on the left side (NT) of the figure. Bootstrap values are presented as color gradients at the branches for better visualization.</p>
Full article ">Figure 4
<p>Mortality rate of the trahira and arapaima challenged with <span class="html-italic">Streptococcus agalactiae</span> during the experimental period.</p>
Full article ">Figure 5
<p>Histology of challenged trahira (<b>a</b>–<b>c</b>) and arapaima (<b>d</b>). (<b>a</b>) Brain—meningitis was and obvious sign characterized by thickening with congested blood vessels and inflammatory cells infiltration; (<b>b</b>) Liver—congestion and thrombosis of portal blood vessel accompanied with hepatic sinusoids with marked vacuolar degeneration change of hepatocytes; (<b>c</b>) Heart—Accumulation of inflammatory cells (arrows) and hemorrhagic areas in myocardium and pericardium; (<b>d</b>) Spleen—cellular necrosis (picnosis = arrow) in white pulp associated with the presence of Gram-positive bacteria (arrow head).</p>
Full article ">
10 pages, 1995 KiB  
Article
New Genotype G3 P[8] of Rotavirus Identified in a Mexican Gastroenteric Rabbit
by Emmanuel Reynoso-Utrera, Linda Guiliana Bautista-Gómez, Salvador Fonseca-Coronado, Juan Diego Pérez-de la Rosa, Valeria Jazmín Rodríguez-Villavicencio, Camilo Romero-Núñez, Ariadna Flores-Ortega, Pedro Abel Hernández-García and José Simón Martínez-Castañeda
Viruses 2024, 16(11), 1729; https://doi.org/10.3390/v16111729 - 2 Nov 2024
Viewed by 1309
Abstract
Rotavirus species A (RVA) is a major cause of acute viral gastroenteritis in young humans and diverse animal species. The study of the genetic characteristics of RVAs that infect rabbits (Oryctolagus cuniculus) (lapine strain [LRV]) has been limited, and, to date, the most [...] Read more.
Rotavirus species A (RVA) is a major cause of acute viral gastroenteritis in young humans and diverse animal species. The study of the genetic characteristics of RVAs that infect rabbits (Oryctolagus cuniculus) (lapine strain [LRV]) has been limited, and, to date, the most common and epidemiologically important combinations of G/P genotypes in rabbits have been reported to be G3 P[14] and G3 P[22]. In this study, a rotavirus species A detected from an outbreak of enteritis in a Mexican commercial rabbitry was genotypically characterized. Based on sequence and phylogenetic analysis of the VP7 and VP4 genes, the strain identified in this study (C-3/15) demonstrated a G3 P[8] genotype of rotavirus, which had not previously been reported in rabbits. Moreover, both genes were closely related to human, not lapine, rotaviruses. The G3 genotype has been reported in a wide variety of hosts, including humans and rabbits, whereas the P[8] genotype has only been reported in humans. Because this combination of genotypes has never been identified in rabbits, it is proposed that the finding presented here is possibly the result of an interspecies transmission event. This is the first work to study the molecular characteristics of rotaviruses in rabbits in Mexico, as well as the identification of human G3 and P[8] genotypes in a rabbit with enteric disease. Full article
(This article belongs to the Section Animal Viruses)
Show Figures

Figure 1

Figure 1
<p>Phylogenetic tree of the VP4 nucleotide sequence based on the neighbor joining method with a bootstrap of 1000 replicates, showing the sequence associations of different P genotypes of RV. C-3/15-VP4 is reported in this study.</p>
Full article ">Figure 2
<p>Phylogenetic tree of VP7 nucleotide sequence based on the neighbor joining method with a bootstrap of 1000 replicates, where the relationships between the C-3/15-VP7 strain and RVA strains with G3 genotype are shown.</p>
Full article ">Figure 3
<p>Phylogenetic tree of VP7 nucleotide sequence based on the neighbor joining method with a bootstrap of 1000 replicates, showing the associations of different G genotypes of RVA. C-3/15-VP7 is reported in this study.</p>
Full article ">Figure 4
<p>Phylogenetic tree of VP7 and VP4 nucleotide sequences, by the neighbor joining method with a bootstrap of 1000 replicates. The relationships of P and G genotypes of different strains of RVA are shown. C-3/15 is reported in this study.</p>
Full article ">
25 pages, 1848 KiB  
Review
Influenza A Viruses in the Swine Population: Ecology and Geographical Distribution
by Nailya Klivleyeva, Nurbol Saktaganov, Tatyana Glebova, Galina Lukmanova, Nuray Ongarbayeva and Richard Webby
Viruses 2024, 16(11), 1728; https://doi.org/10.3390/v16111728 - 1 Nov 2024
Viewed by 1988
Abstract
Despite the efforts of practical medicine and virology, influenza viruses remain the most important pathogens affecting human and animal health. Swine are exposed to infection with all types of influenza A, B, C, and D viruses. Influenza viruses have low pathogenicity for swine, [...] Read more.
Despite the efforts of practical medicine and virology, influenza viruses remain the most important pathogens affecting human and animal health. Swine are exposed to infection with all types of influenza A, B, C, and D viruses. Influenza viruses have low pathogenicity for swine, but in the case of co-infection with other pathogens, the outcome can be much more serious, even fatal. Having a high zoonotic potential, swine play an important role in the ecology and spread of influenza to humans. In this study, we review the state of the scientific literature on the zoonotic spread of swine influenza A viruses among humans, their circulation in swine populations worldwide, reverse zoonosis from humans to swine, and their role in interspecies transmission. The analysis covers a long period to trace the ecology and evolutionary history of influenza A viruses in swine. The following databases were used to search the literature: Scopus, Web of Science, Google Scholar, and PubMed. In this review, 314 papers are considered: n = 107 from Asia, n = 93 from the U.S., n = 86 from Europe, n = 20 from Africa, and n = 8 from Australia. According to the date of publication, they are conditionally divided into three groups: contemporary, released from 2011 to the present (n = 121); 2000–2010 (n = 108); and 1919–1999 (n = 85). Full article
(This article belongs to the Section Animal Viruses)
Show Figures

Figure 1

Figure 1
<p>Influenza A, B, C, and D in different species of mammals.</p>
Full article ">Figure 2
<p>Influenza subtypes of viruses H1–H18 and N1–N11 in different species of mammals.</p>
Full article ">Figure 3
<p>The geographical distribution of swine influenza viruses. The locations where influenza viruses were detected in pigs are marked in pink. The world map was created online at <a href="https://mapchart.net" target="_blank">https://mapchart.net</a> (accessed on 11 October 2024).</p>
Full article ">
19 pages, 1138 KiB  
Review
Emerging Threats of Highly Pathogenic Avian Influenza A (H5N1) in US Dairy Cattle: Understanding Cross-Species Transmission Dynamics in Mammalian Hosts
by Chithra C. Sreenivasan, Feng Li and Dan Wang
Viruses 2024, 16(11), 1703; https://doi.org/10.3390/v16111703 - 30 Oct 2024
Viewed by 2853
Abstract
The rapid geographic spread of the highly pathogenic avian influenza (HPAI) A(H5N1) virus in poultry, wild birds, and other mammalian hosts, including humans, raises significant health concerns globally. The recent emergence of HPAI A(H5N1) in agricultural animals such as cattle and goats indicates [...] Read more.
The rapid geographic spread of the highly pathogenic avian influenza (HPAI) A(H5N1) virus in poultry, wild birds, and other mammalian hosts, including humans, raises significant health concerns globally. The recent emergence of HPAI A(H5N1) in agricultural animals such as cattle and goats indicates the ability of the virus to breach unconventional host interfaces, further expanding the host range. Among the four influenza types—A, B, C, and D, cattle are most susceptible to influenza D infection and serve as a reservoir for this seven-segmented influenza virus. It is generally thought that bovines are not hosts for other types of influenza viruses, including type A. However, this long-standing viewpoint has been challenged by the recent outbreaks of HPAI A(H5N1) in dairy cows in the United States. To date, HPAI A(H5N1) has spread into fourteen states, affecting 299 dairy herds and causing clinical symptoms such as reduced appetite, fever, and a sudden drop in milk production. Infected cows can also transmit the disease through raw milk. This review article describes the current epidemiological landscape of HPAI A(H5N1) in US dairy cows and its interspecies transmission events in other mammalian hosts reported across the globe. The review also discusses the viral determinants of tropism, host range, adaptative mutations of HPAI A(H5N1) in various mammalian hosts with natural and experimental infections, and vaccination strategies. Finally, it summarizes some immediate questions that need to be addressed for a better understanding of the infection biology, transmission, and immune response of HPAI A(H5N1) in bovines. Full article
(This article belongs to the Special Issue Bovine Influenza)
Show Figures

Figure 1

Figure 1
<p>Current status of HPAI A(H5N1) virus spread in the US dairy cow herds. As of 14 October 2024, HPAI A(H5N1) virus was detected in 299 dairy cow herds in fourteen states of the US. The number of herds affected in each state was color-coded and shown. Data were obtained from USDA website (<a href="https://www.aphis.usda.gov/livestock-poultry-disease/avian/avian-influenza/hpai-detections/livestock" target="_blank">https://www.aphis.usda.gov/livestock-poultry-disease/avian/avian-influenza/hpai-detections/livestock</a>, accessed on 15 August 2024). Map image was downloaded from <a href="https://inkpx.com" target="_blank">https://inkpx.com</a>, accessed on 15 August 2024.</p>
Full article ">Figure 2
<p>Cross-species transmission and host range of HPAI A(H5N1). Wild aquatic birds are the reservoir hosts for type A avian influenza viruses. Wild birds, wild mammals, poultry, and domestic/pet animals were affected by HPAI A(H5N1). The bold dark blue arrows denote frequent spillover events, while the gray arrows denote sporadic/infrequent spillover. Sustained human-to-human transmission has not been reported. Vector images were downloaded from Freepik (<a href="http://www.freepik.com" target="_blank">www.freepik.com</a>, accessed on 15 August 2024), vecteezy (<a href="https://www.vecteezy.com/" target="_blank">https://www.vecteezy.com/</a>, accessed on 15 October 2024), and Microsoft Office icons.</p>
Full article ">
19 pages, 620 KiB  
Review
Zoonotic Paramyxoviruses: Evolution, Ecology, and Public Health Strategies in a Changing World
by Francesco Branda, Grazia Pavia, Alessandra Ciccozzi, Angela Quirino, Nadia Marascio, Giovanni Matera, Chiara Romano, Chiara Locci, Ilenia Azzena, Noemi Pascale, Daria Sanna, Marco Casu, Giancarlo Ceccarelli, Massimo Ciccozzi and Fabio Scarpa
Viruses 2024, 16(11), 1688; https://doi.org/10.3390/v16111688 - 29 Oct 2024
Viewed by 1445
Abstract
The family Paramyxoviridae includes a number of negative RNA viruses known for their wide host range and significant zoonotic potential. In recent years, there has been a surge in the identification of emerging zoonotic paramyxoviruses, particularly those hosted by bat species, which serve [...] Read more.
The family Paramyxoviridae includes a number of negative RNA viruses known for their wide host range and significant zoonotic potential. In recent years, there has been a surge in the identification of emerging zoonotic paramyxoviruses, particularly those hosted by bat species, which serve as key reservoirs. Among these, the genera Henipavirus and Pararubulavirus are of particular concern. Henipaviruses, including the highly pathogenic Hendra and Nipah viruses, have caused severe outbreaks with high mortality rates in both humans and animals. In contrast, zoonotic pararubulaviruses such as the Menangle virus typically induce mild symptoms or remain asymptomatic in human hosts. This review summarizes current knowledge on the evolution, ecology, and epidemiology of emerging zoonotic paramyxoviruses, focusing on recently discovered viruses and their potential to cause future epidemics. We explore the molecular mechanisms underlying host-switching events, viral replication strategies, and immune evasion tactics that facilitate interspecies transmission. In addition, we discuss ecological factors influencing virus emergence, including changes in bat populations and habitats and the role of wildlife–human interfaces. We also examine the public health impact of these emerging viruses, underlining the importance of enhanced surveillance, developing improved diagnostic tools, and implementing proactive strategies to prevent potential outbreaks. By providing a comprehensive overview of recent advances and gaps in knowledge, this review aims to inform future research directions and public health policies related to zoonotic paramyxoviruses. Full article
(This article belongs to the Special Issue Emerging Zoonotic Paramyxoviruses)
Show Figures

Figure 1

Figure 1
<p>Primary evolutionary theories involved in the generation of new emerging zoonotic paramyxoviruses with epidemic potential.</p>
Full article ">Figure 2
<p>The ecological, environmental, and anthropogenic factors for predicting and mitigating zoonotic risks.</p>
Full article ">
21 pages, 4834 KiB  
Article
Assessment of PPMV-1 Genotype VI Virulence in Pigeons and Chickens and Protective Effectiveness of Paramyxovirus Vaccines in Pigeons
by Esraa E. Hamouda, Amal A. M. Eid, Hagar F. Gouda, Amina A. Dessouki, Ayman H. El-Deeb, Rebecca Daines, Munir Iqbal and Reham M. ElBakrey
Viruses 2024, 16(10), 1585; https://doi.org/10.3390/v16101585 - 9 Oct 2024
Viewed by 1464
Abstract
Pigeon paramyxovirus serotype 1 (PPMV-1), an antigenic and host variant of avian paramyxovirus Newcastle disease virus (NDV), primarily originating from racing pigeons, has become a global panzootic. Egypt uses both inactivated PPMV-1 and conventional NDV vaccines to protect pigeons from disease and mortality. [...] Read more.
Pigeon paramyxovirus serotype 1 (PPMV-1), an antigenic and host variant of avian paramyxovirus Newcastle disease virus (NDV), primarily originating from racing pigeons, has become a global panzootic. Egypt uses both inactivated PPMV-1 and conventional NDV vaccines to protect pigeons from disease and mortality. However, the impact of prevalent strains and the effectiveness of available vaccines in pigeons in Egypt are unclear. This study investigates the virulence of PPMV-1 (Pigeon/Egypt/Sharkia-19/2015/KX580988) and evaluates available paramyxovirus vaccines in protecting pigeons against a PPMV-1 challenge. Ten-day-old specific-pathogen-free (SPF) embryonated chicken eggs infected with this strain exhibited a mean death time (MDT) of 86.4 ± 5.88 h. The intracerebral pathogenicity index (ICPI) in day-old chickens was 0.8, while pigeons experienced an ICPI of 0.96 and an intravenous pathogenicity index (IVPI) of 2.11. These findings classify the strain as virulent and velogenic. Experimental infection of pigeons with this PPMV-1 strain at 106 EID50/0.1 mL resulted in a 62.5% mortality rate, displaying nervous and enteric distress. The virus caused extensive lesions in visceral organs, with strong immunohistochemistry signals in all examined organs, indicating the systemic spread of the virus concurrent to its neurotropic and viscerotropic tropism. Furthermore, vaccination using an inactivated PPMV-1 and live NDV LaSota vaccine regimen protected 100% of pigeons against mortality, while with a single NDV LaSota vaccine, it was 62.5%. The PPMV alone or combined with NDV LaSota induced protective levels of haemagglutination inhibition (HI) antibody titres and reduced virus shedding from buccal and cloacal cavities. Based on generalised linear gamma model analysis, both PPMV-1 and NDV LaSota are antigenically comparable by HI. These findings suggest that using both inactivated PPMV-1 (G-VI) and live attenuated NDV (LaSota) vaccines is an effective prophylactic regimen for preventing and controlling PPMV-1 and NDV in pigeons, thereby reducing the risk of interspecies transmission. Full article
(This article belongs to the Special Issue Newcastle Disease and Other Avian Orthoavulaviruses 1)
Show Figures

Figure 1

Figure 1
<p>Summary of the experimental design: (<b>a</b>) Design of pathogenicity characterisation. (<b>b</b>) Design of vaccines’ assessment against those challenged with a field strain of PPMV-1, “Pigeon/Egypt/Sharkia-19/2015/KX580988”. G1a, G2a, G3a, and G4a were kept as control groups to monitor any natural infection exposure from the environment to these pigeons. G1b, G2b, G3b, and G4b were challenged with the PPMV-1 strain.</p>
Full article ">Figure 2
<p>Virulence (ICPI and IVPI) assessment of the PPMV-1 strain (Pigeon/Egypt/Sharkia-19/2015/KX580988) in pigeons and chickens. The birds were inoculated via intracerebral (I/C) and intravenous (I/V) routes to 1-day-old chickens and 5-week-old pigeons. The clinical scores were recorded until 10 days post-infection (dpi). The clinical scores are represented as healthy (green), displaying variable clinical signs, such as ruffled feathers, depression, anorexia, and greenish diarrhoea (light blue, except nervous signs in dark blue), and dead (red). A1–A10 are numbers of chickens in the I/C group (G4C), B1–B10 are numbers of pigeons in the I/C group (G1P), and C1–C10 are numbers of pigeons in the I/V group (G2P).</p>
Full article ">Figure 3
<p>Survival rates and clinical indices post-challenge with PPMV-1. (<b>a</b>) Survival curves of vaccinated pigeons with the tested vaccines post-challenge. (<b>b</b>) Clinical indices of vaccinated pigeons with the tested vaccines post-challenge. G1b: vaccinated with NDV LaSota/challenged with PPMV-1; G2b: vaccinated with PPMV/challenged with PPMV-1; G3b: dual-vaccinated with LaSota and PPMV/challenged with PPMV-1; G4a: non-vaccinated/non-challenged; G4b: non-vaccinated/challenged.</p>
Full article ">Figure 4
<p>Clinical and post-mortem findings of pigeons vaccinated/challenged with PPMV-1 strain. (<b>A</b>) Torticollis in non-vaccinated/challenged pigeon (G4b). (<b>B</b>) Wing paralysis in non-vaccinated/challenged pigeon (G4b). (<b>C</b>) Complete paralysis in non-vaccinated/challenged pigeon (G4b). (<b>D</b>) Severe greenish diarrhoea in non-vaccinated/challenged pigeon (G4b). (<b>E</b>) Opisthotonos position in pigeon of NDV LaSota vaccinated/challenged (G1b). (<b>F</b>) Greenish diarrhoea in pigeon of NDV LaSota vaccinated/challenged (G1b). (<b>G</b>) Severe congested and haemorrhagic brain in non-vaccinated/challenged pigeon (G4b). (<b>H</b>) Congested heart with minute petechial haemorrhages in non-vaccinated/challenged pigeon (G4b). (<b>I</b>) Enlarged and severe congested spleen with haemorrhages in non-vaccinated/challenged pigeon (G4b). (<b>J</b>) Pancreatitis with punctate haemorrhages in non-vaccinated/challenged pigeon (G4b). (<b>K</b>) Severe nephrosis in non-vaccinated/challenged pigeon (G4b). (<b>L</b>) Haemorrhages at junction between oesophagus and proventriculus with greenish content in the gizzard of non-vaccinated/challenged pigeon (G4b). (<b>M</b>) Moderate congestion in brain of pigeon in NDV LaSota vaccinated/challenged group (G1b). (<b>N</b>) Mild congestion (apparently normal) of heart in pigeon of NDV LaSota vaccinated/challenged group (G1b). (<b>O</b>) Enlarged spleen with few haemorrhages in pigeon of NDV LaSota vaccinated/challenged group (G1b). (<b>P</b>) Pancreatitis with necrosis in pigeon of NDV LaSota vaccinated/challenged group (G1b). (<b>Q</b>) Moderate nephrosis in pigeon of NDV LaSota group (G1b).</p>
Full article ">Figure 5
<p>Histopathological lesions in different tissue organs of non-vaccinated infected pigeons with PPMV-1. H&amp;E X400, bar indicates 50 μm. Brain: (<b>a</b>) Congestion of brain capillaries (long arrows). (<b>b</b>) Sub-meningeal haemorrhages (H). (<b>c</b>) Multifocal degeneration and swelling of neurons gliosis (arrow heads) and degenerated neurons (short arrows). Pancreas: (<b>d</b>) Severe congestion (stars). (<b>e</b>) Multifocal haemorrhages (H) with degeneration and necrosis of pancreatic acini (N). (<b>f</b>) Multifocal aggregations of lymphocytic infiltrations (arrowhead). Spleen: (<b>g</b>) Severe congestion of sinusoids and splenic blood vessels (stars), with multifocal haemorrhages (H). (<b>h</b>) Multifocal haemorrhages (H) and severe depletion of subcapsular lymphoid follicles (long arrows), with necrosis (N), and congested blood vessels (star). (<b>i</b>) Severe depletion of subcapsular lymphoid follicles (long arrows), and necrosis (N). (<b>j</b>) Liver: severe congestion, focal degeneration (long arrow), and discrete necrosis of some hepatic cells, along with mild leukocytes around bile duct (arrowhead). (<b>k</b>) Kidneys: intratubular haemorrhages (H), degeneration of renal tubular epithelium (long arrow), and focal necrosis (N) with leukocyte infiltration (arrowhead). (<b>l</b>) Heart: intermuscular congestion (long arrows) and haemorrhages (H).</p>
Full article ">Figure 6
<p>Photomicrograph of immunohistochemistry (IHC) of PPMV-1 presence in different tissue organs of non-vaccinated/challenged pigeons. (<b>a</b>) Brain: positive expression in degenerated neurons. (<b>b</b>) Trachea: positive expression in the tracheal epithelium and in the inflammatory cells of the propria submucosa. (<b>c</b>) Lung: positive expression in air capillaries. (<b>d</b>) Pancreas: positive expression in the exocrine epithelial cells. (<b>e</b>) Spleen: positive expression in the splenic parenchyma. (<b>f</b>) Heart: positive expression in the cardiac muscle. (<b>g</b>) Proventriculus: positive expression in the glandular epithelium and desquamated epithelial cells. (<b>h</b>) Intestine: positive expression in intestinal mucosa. (<b>i</b>) Kidneys: positive expression in the renal tubular epithelium.</p>
Full article ">Figure 7
<p>(<b>a</b>) Density plot showing the positive skewness in the HI titre distribution. (<b>b</b>) Model selection criteria for linear and generalised linear designs based on the Akaike Information Criterion (AIC). N = number of collected serum samples from all experiment pigeon groups throughout the experiment periods.</p>
Full article ">
6 pages, 1697 KiB  
Brief Report
Whole Genome Sequences of the Wildtype AU-1 Rotavirus A Strain: The Prototype of the AU-1-like Genotype Constellation
by Chantal Ama Agbemabiese, Francis Ekow Dennis, Belinda Larteley Lartey, Susan Afua Damanka, Toyoko Nakagomi, Osamu Nakagomi and George Enyimah Armah
Viruses 2024, 16(10), 1529; https://doi.org/10.3390/v16101529 - 27 Sep 2024
Viewed by 676
Abstract
Most human rotaviruses belong to the Wa-like, DS-1-like, or AU-1-like genotype constellation. The AU-1-like constellation, albeit minor, captured attention because its prototype strain AU-1 originated from feline rotavirus, leading to the concept of interspecies transmission of rotavirus. The AU-1 genome sequence determined by [...] Read more.
Most human rotaviruses belong to the Wa-like, DS-1-like, or AU-1-like genotype constellation. The AU-1-like constellation, albeit minor, captured attention because its prototype strain AU-1 originated from feline rotavirus, leading to the concept of interspecies transmission of rotavirus. The AU-1 genome sequence determined by various laboratories over the years has documented two conflicting VP7 sequences in the GenBank. As culture-adaptation may introduce changes in the viral genome, the original fecal (wild-type) and the seed stock of culture-adapted AU-1 genomes were sequenced using the Illumina’s MiSeq platform to determine the authentic AU-1 sequence and to identify what mutational changes were selected during cell-culture adaptation. The wild-type and culture-adapted AU-1 genomes were identical except for one VP4-P475L substitution. Their VP7 gene was 99.9% identical to the previously reported AU-1 VP7 under accession number AB792641 but only 92.5% to that under accession number D86271. Thus, the wild-type sequences determined in this study (accession numbers OR727616-OR727626) should be used as the reference. The VP4-P475L mutation was more likely incidental than inevitable during cell-culture adaptation. This was the first study in which the whole genomes of both wild-type and cultured RVA strains were simultaneously determined by deep sequencing. Full article
(This article belongs to the Special Issue The 9th Edition of the European Rotavirus Biology Meeting (ERBM-9))
Show Figures

Figure 1

Figure 1
<p>Comparison of the raw sequence reads around aa position 475 of AU-1-wt and AU-1-tc VP4 gene. Full genome sequences of AU-1-wt and AU-1-tc were generated by Illumina Miseq sequencing. FASTQ files were viewed using Geneious Prime software v2023.2.1.</p>
Full article ">
4 pages, 193 KiB  
Brief Report
Bovine Highly Pathogenic Avian Influenza Virus Stability and Inactivation in the Milk Byproduct Lactose
by Taeyong Kwon, Jordan T. Gebhardt, Eu Lim Lyoo, Mohammed Nooruzzaman, Natasha N. Gaudreault, Igor Morozov, Diego G. Diel and Juergen A. Richt
Viruses 2024, 16(9), 1451; https://doi.org/10.3390/v16091451 - 12 Sep 2024
Cited by 2 | Viewed by 1591
Abstract
The recent incursion of highly pathogenic influenza viruses into dairy cattle opens new insights for influenza virus ecology and its interspecies transmission and may have a significant impact on public health and agriculture. The aim of this study was to determine the stability [...] Read more.
The recent incursion of highly pathogenic influenza viruses into dairy cattle opens new insights for influenza virus ecology and its interspecies transmission and may have a significant impact on public health and agriculture. The aim of this study was to determine the stability of a bovine highly pathogenic avian influenza H5N1 virus isolate in the milk byproduct lactose and to evaluate two inactivation methods using industrial procedures. The bovine isolate of the highly pathogenic avian influenza H5N1 virus was stable for 14 days in a concentrated lactose solution under refrigerated conditions. Heat or citric acid treatments successfully inactivated the virus in lactose. This study highlights the persistence of HPAIV in lactose and its efficient inactivation under industrial standards. Full article
(This article belongs to the Special Issue Bovine Influenza)
Show Figures

Figure 1

Figure 1
<p>The stability of the bovine isolate of HPAI H5N1 clade 2.3.4.4b in a concentrated lactose solution. The virus was mixed with whole milk and lactose at 1:10 dilution and incubated at a refrigerated temperature. At each time point, the samples were titrated on MDCK cells. Dash line represents the limit of detection, 4.64 TCID<sub>50</sub>/mL.</p>
Full article ">
15 pages, 1068 KiB  
Article
Multidrug-Resistant Staphylococcus aureus Colonizing Pigs and Farm Workers in Rio de Janeiro State, Brazil: Potential Interspecies Transmission of Livestock-Associated MRSA (LA-MRSA) ST398
by Joana Talim, Ianick Martins, Cassio Messias, Hellen Sabino, Laura Oliveira, Tatiana Pinto, Julia Albuquerque, Aloysio Cerqueira, Ítalo Dolores, Beatriz Moreira, Renato Silveira, Felipe Neves and Renata Rabello
Antibiotics 2024, 13(8), 767; https://doi.org/10.3390/antibiotics13080767 - 14 Aug 2024
Viewed by 1154
Abstract
Multidrug-resistant (MDR) Staphylococcus aureus has been increasingly isolated from pigs and people in close contact with them, especially livestock-associated methicillin-resistant S. aureus (LA-MRSA). In this cross-sectional study, we investigated S. aureus colonization in pigs and farm workers, their resistance profile, and genetic background [...] Read more.
Multidrug-resistant (MDR) Staphylococcus aureus has been increasingly isolated from pigs and people in close contact with them, especially livestock-associated methicillin-resistant S. aureus (LA-MRSA). In this cross-sectional study, we investigated S. aureus colonization in pigs and farm workers, their resistance profile, and genetic background to estimate interspecies transmission potential within farms from Rio de Janeiro state, Brazil, between 2014 and 2019. We collected nasal swabs from 230 pigs and 27 workers from 16 and 10 farms, respectively. Five MDR strains were subjected to whole genome sequencing. Fourteen (6.1%) pigs and seven (25.9%) humans were colonized with S. aureus, mostly (64–71%) MDR strains. Resistance to clindamycin, erythromycin, penicillin, and tetracycline was the most common among the pig and human strains investigated. MDR strains shared several resistance genes [blaZ, dfrG, fexA, lsa(E), and tet(M)]. Pig and human strains recovered from the same farm shared the same genetic background and antimicrobial resistance profile. LA-MRSA ST398-SCCmecV-t011 was isolated from pigs in two farms and from a farm worker in one of them, suggesting interspecies transmission. The association between pig management practices and MDR S. aureus colonization might be investigated in additional studies. Full article
(This article belongs to the Special Issue Use of Antibiotics in Animals and Antimicrobial Resistance)
Show Figures

Figure 1

Figure 1
<p>Distribution of the pig farms, pigs and farm workers investigated and colonized with <span class="html-italic">Staphylococcus aureus</span> by regions (I–V) of the Rio de Janeiro state from 2014 to 2019. Farms: C, G, K, M, O and P (I); A, B, D and E (II); F, L and N (III); H, I and J (IV). * Farms in regions I and II were attended by the same veterinarian, and his sample was collected only once. No sample collection was done in farms from cities of the region V. MRSA strains were recovered from pig farms located in cities from regions marked with a star (driving distance of 225 km between the cities). This figure was created from the map made by Allice Hunter—File: Brazil Rio de Janeiro location map.svg, CC BY-SA 4.0, <a href="https://commons.wikimedia.org/w/index.php?curid=70980877" target="_blank">https://commons.wikimedia.org/w/index.php?curid=70980877</a>, accessed on 6 June 2024.</p>
Full article ">Figure 2
<p>Single nucleotide polymorphism (SNP)-based neighbor-joining tree generated using the Pathogenwatch web application based on core genome of seven <span class="html-italic">Staphylococcus aureus</span> ST398 strains from human and animal source in Brazil. The five study multidrug-resistant strains (circle) are presented together with two Brazilian <span class="html-italic">S. aureus</span> isolates (square) available at Pathogenwatch website (SAMN15214618 from swine nasal swab and SAMN15216868 from goat milk). SNP differences between strains are shown in blue.</p>
Full article ">
12 pages, 606 KiB  
Article
A Newly Incompatibility F Replicon Allele (FIB81) in Extensively Drug-Resistant Escherichia coli Isolated from Diseased Broilers
by Ahmed M. Ammar, Norhan K. Abd El-Aziz, Mohamed G. Aggour, Adel A. M. Ahmad, Adel Abdelkhalek, Florin Muselin, Laura Smuleac, Raul Pascalau and Fatma A. Attia
Int. J. Mol. Sci. 2024, 25(15), 8347; https://doi.org/10.3390/ijms25158347 - 30 Jul 2024
Cited by 1 | Viewed by 951
Abstract
Multiple drug resistance (MDR) has gained pronounced attention among Enterobacterales. The transfer of multiple antimicrobial resistance genes, frequently carried on conjugative incompatibility F (IncF) plasmids and facilitating interspecies resistance transmission, has been linked to Salmonella spp. and E. coli in broilers. In [...] Read more.
Multiple drug resistance (MDR) has gained pronounced attention among Enterobacterales. The transfer of multiple antimicrobial resistance genes, frequently carried on conjugative incompatibility F (IncF) plasmids and facilitating interspecies resistance transmission, has been linked to Salmonella spp. and E. coli in broilers. In Egypt, the growing resistance is exacerbated by the limited clinical efficacy of many antimicrobials. In this study, IncF groups were screened and characterized in drug-resistant Salmonella spp. and E. coli isolated from broilers. The antimicrobial resistance profile, PCR-based replicon typing of bacterial isolates pre- and post-plasmid curing, and IncF replicon allele sequence typing were investigated. Five isolates of E. coli (5/31; 16.13%) and Salmonella spp. (5/36; 13.89%) were pan-susceptible to the examined antimicrobial agents, and 85.07% of tested isolates were MDR and extensively drug-resistant (XDR). Twelve MDR and XDR E. coli and Salmonella spp. isolates were examined for the existence of IncF replicons (FII, FIA, and FIB). They shared resistance to ampicillin, ampicillin/sulbactam, amoxicillin/clavulanate, doxycycline, cefotaxime, and colistin. All isolates carried from one to two IncF replicons. The FII-FIA-FIB+ and FII-FIA+FIB- were the predominant replicon patterns. FIB was the most frequently detected replicon after plasmid curing. Three XDR E. coli isolates that were resistant to 12–14 antimicrobials carried a newly FIB replicon allele with four nucleotide substitutions: C99→A, G112→T, C113→T, and G114→A. These findings suggest that broilers are a significant reservoir of IncF replicons with highly divergent IncF-FIB plasmid incompatibility groups circulating among XDR Enterobacterales. Supporting these data with additional comprehensive epidemiological studies involving replicons other than the IncF can provide insights for implementing efficient policies to prevent the spreading of new replicons to humans. Full article
(This article belongs to the Special Issue Antimicrobial Resistance—New Insights, 3rd Edition)
Show Figures

Figure 1

Figure 1
<p>Phylogenetic circle tree of the FIB replicon alleles. The dendrogram was constructed using the neighbor-joining algorithm. Bootstrap values for 1000 replicates are indicated. The distribution of FIB alleles according to point mutations previously revealed eighty alleles. The new allele (FIB81) was examined in <span class="html-italic">E. coli</span> (O125) isolates (accession number OR453940) isolated from broiler; it is closely related to the FIB51 allele isolated from a human in France.</p>
Full article ">
14 pages, 1735 KiB  
Article
Prevalence and Genetic Diversity of Bat Hepatitis B Viruses in Bat Species Living in Gabon
by Danielle S. Koumba Mavoungou, Linda Bohou Kombila, Neil M. Longo Pendy, Schedy E. Koumba Moukouama, Sonia Etenna Lekana-Douki, Gaël D. Maganga, Eric M. Leroy, Avelin F. Aghokeng and Nadine N’dilimabaka
Viruses 2024, 16(7), 1015; https://doi.org/10.3390/v16071015 - 25 Jun 2024
Viewed by 1099
Abstract
Hepatitis B virus (HBV) infection leads to around 800,000 deaths yearly and is considered to be a major public health problem worldwide. However, HBV origins remain poorly understood. Here, we looked for bat HBV (BtHBV) in different bat species in Gabon to investigate [...] Read more.
Hepatitis B virus (HBV) infection leads to around 800,000 deaths yearly and is considered to be a major public health problem worldwide. However, HBV origins remain poorly understood. Here, we looked for bat HBV (BtHBV) in different bat species in Gabon to investigate the role of these animals as carriers of ancestral hepadnaviruses because these viruses are much more diverse in bats than in other host species. DNA was extracted from 859 bat livers belonging to 11 species collected in caves and villages in the southeast of Gabon and analyzed using PCRs targeting the surface gene. Positive samples were sequenced using the Sanger method. BtHBV DNA was detected in 64 (7.4%) individuals belonging to eight species mainly collected in caves. Thirty-six (36) sequences among the 37 obtained after sequencing were phylogenetically close to the RBHBV strain recently isolated in Gabonese bats, while the remaining sequence was close to a rodent HBV strain isolated in America. The generalized linear mixed model showed that the variable species best explained the occurrence of BtHBV infection in bats. The discovery of a BtHBV strain homologous to a rodent strain in bats raises the possibility that these animals may be carriers of ancestral hepadnaviruses. Full article
(This article belongs to the Section Animal Viruses)
Show Figures

Figure 1

Figure 1
<p>Distribution of bat collection sites in eastern Gabon. The black dots represent the collection sites.</p>
Full article ">Figure 2
<p>Migration of second-round PCR products obtained after amplifying a portion of the S gene. Sixty, 64, 65: positive samples; 61, 62, 63, 66, 67, 68, 69, 70, 71, 72: negative samples; PM: 100 bp molecular weight marker; C+: positive control; C-: negative control; bp: base pair.</p>
Full article ">Figure 3
<p>(<b>a</b>) Distribution of BtHBV PCR-positive and -negative bats according to collection sites. (<b>b</b>) Distribution of BtHBV PCR-positive bat species by collection site.</p>
Full article ">Figure 4
<p>Maximum likelihood phylogenetic analysis based on the partial nucleotide sequence of the S gene. Multiple sequence alignment was performed using the ClustalW algorithm implemented in the MEGA XI software package version 11.0.13. Phylogenetic trees were constructed using the maximum likelihood method and 1000 bootstrap replicates. Only bootstrap values greater than 50% are shown on the branches. Sequences from this study are represented in red and orange, while previous ones from GenBank are represented in black.</p>
Full article ">
18 pages, 4521 KiB  
Article
Emergence of a Novel G4P[6] Porcine Rotavirus with Unique Sequence Duplication in NSP5 Gene in China
by Xia Zhou, Xueyan Hou, Guifa Xiao, Bo Liu, Handuo Jia, Jie Wei, Xiaoyun Mi, Qingyong Guo, Yurong Wei and Shao-Lun Zhai
Animals 2024, 14(12), 1790; https://doi.org/10.3390/ani14121790 - 14 Jun 2024
Cited by 1 | Viewed by 1151
Abstract
Rotavirus is a major causative agent of diarrhoea in children, infants, and young animals around the world. The associated zoonotic risk necessitates the serious consideration of the complete genetic information of rotavirus. A segmented genome makes rotavirus prone to rearrangement and the formation [...] Read more.
Rotavirus is a major causative agent of diarrhoea in children, infants, and young animals around the world. The associated zoonotic risk necessitates the serious consideration of the complete genetic information of rotavirus. A segmented genome makes rotavirus prone to rearrangement and the formation of a new viral strain. Monitoring the molecular epidemiology of rotavirus is essential for its prevention and control. The quantitative RT-PCR targeting the NSP5 gene was used to detect rotavirus group A (RVA) in pig faecal samples, and two pairs of universal primers and protocols were used for amplifying the G and P genotype. The genotyping and phylogenetic analysis of 11 genes were performed by RT-PCR and a basic bioinformatics method. A unique G4P[6] rotavirus strain, designated S2CF (RVA/Pig-tc/CHN/S2CF/2023/G4P[6]), was identified in one faecal sample from a piglet with severe diarrhoea in Guangdong, China. Whole genome sequencing and analysis suggested that the 11 segments of the S2CF strain showed a unique Wa-like genotype constellation and a typical porcine RVA genomic configuration of G4-P[6]-I1-R1-C1-M1-A8-N1-T1-E1-H1. Notably, 4 of the 11 gene segments (VP4, VP6, VP2, and NSP5) clustered consistently with human-like RVAs, suggesting independent human-to-porcine interspecies transmission. Moreover, a unique 344-nt duplicated sequence was identified for the first time in the untranslated region of NSP5. This study further reveals the genetic diversity and potential inter-species transmission of porcine rotavirus. Full article
(This article belongs to the Section Pigs)
Show Figures

Figure 1

Figure 1
<p>Visualised agarose gel electrophoretic diagram of NSP5 segments. M, DL2,000 DNA marker; 1, positive control; 2, S2CF strain; 3, negative control.</p>
Full article ">Figure 2
<p>The schematic representation of the duplication events. The duplicated sequence in each of the strains was shown in dark grey.</p>
Full article ">Figure 3
<p>Maximum likelihood phylogenetic tree based on VP7 coding sequences, calculated with 1000 bootstrap replicates under the GTR + G + I model. Node labels representing bootstrap values ≥ 70% are shown. The S2CF strain isolated in this study is marked with red. Abbreviation: GTR = General Time Reversible, G = Gamme sites, I = Invariant sites.</p>
Full article ">Figure 4
<p>Phylogenetic dendrograms of the segment encoding VP4 was estimated using genetic distances calculated by maximum likelihood with 1000 bootstrap replicates under the GTR + G + I model. The bootstrap values ≥ 70% are indicated at each branch node represents substitutions per nucleotide site. The S2CF strain isolated in this study was marked in red.</p>
Full article ">Figure 5
<p>Phylogenetic tree constructed based on the segments of NSP5 was constructed using neighbour-joining method with 1000 bootstrap replicates. Node labels representing bootstrap values ≥ 70% are shown. The S2CF strain isolated in this study is marked with red.</p>
Full article ">
Back to TopTop