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Keywords = mycoredoxins

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10 pages, 1310 KiB  
Communication
A Novel Screening Strategy Reveals ROS-Generating Antimicrobials That Act Synergistically against the Intracellular Veterinary Pathogen Rhodococcus equi
by Álvaro Mourenza, José A. Gil, Luís M. Mateos and Michal Letek
Antioxidants 2020, 9(2), 114; https://doi.org/10.3390/antiox9020114 - 28 Jan 2020
Cited by 7 | Viewed by 3322
Abstract
: Rhodococcus equi is a facultative intracellular pathogen that causes infections in foals and many other animals such as pigs, cattle, sheep, and goats. Antibiotic resistance is rapidly rising in horse farms, which makes ineffective current antibiotic treatments based on a combination of [...] Read more.
: Rhodococcus equi is a facultative intracellular pathogen that causes infections in foals and many other animals such as pigs, cattle, sheep, and goats. Antibiotic resistance is rapidly rising in horse farms, which makes ineffective current antibiotic treatments based on a combination of macrolides and rifampicin. Therefore, new therapeutic strategies are urgently needed to treat R. equi infections caused by antimicrobial resistant strains. Here, we employed a R. equi mycoredoxin-null mutant strain highly susceptible to oxidative stress to screen for novel ROS-generating antibiotics. Then, we used the well-characterized Mrx1-roGFP2 biosensor to confirm the redox stress generated by the most promising antimicrobial agents identified in our screening. Our results suggest that different combinations of antibacterial compounds that elicit oxidative stress are promising anti-infective strategies against R. equi. In particular, the combination of macrolides with ROS-generating antimicrobial compounds such as norfloxacin act synergistically to produce a potent antibacterial effect against R. equi. Therefore, our screening approach could be applied to identify novel ROS-inspired therapeutic strategies against intracellular pathogens. Full article
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Figure 1

Figure 1
<p>Screening results for the identification of ROS-generating antimicrobials active against <span class="html-italic">R. equi</span>. (<b>A</b>) Antimicrobial susceptibility of <span class="html-italic">R. equi</span> 103S<sup>+</sup> (clear grey) and <span class="html-italic">R. equi Δmrx1Δmrx2Δmrx3</span> mutant (dark grey) to different antibacterial compounds: Chloramphenicol (Chl), clindamycin (Cli), erythromycin (Ery), rifampicin (Rif), and vancomycin (Van). The concentration used of each antibiotic is shown in brackets (µg/mL). The diameter of the growth inhibition zones was measured to the nearest millimetre, and the mean ± SD of three independent experiments was plotted. A Kruskall-Wallis non-parametric analysis was performed to test for statistical significance across comparisons of the wild type strain and the triple <span class="html-italic">mrx</span>-null mutant. <span class="html-italic">p</span>-value &lt; 0.05 (*) or <span class="html-italic">p</span>-value &lt; 0.01 (**). (<b>B</b>) Ratiometric response of the Mrx1-roGFP2 biosensor. Fluorescence 405/490 ratio was calculated by confocal microscopy at different time points in response to very low doses of rifampicin, erythromycin, and vancomycin. The results show the mean ± SD of three independent experiments.</p>
Full article ">Figure 2
<p>Identification of other ROS-generating antimicrobials against <span class="html-italic">R. equi</span>. (<b>A</b>) Antimicrobial susceptibility of <span class="html-italic">R. equi</span> 103S<sup>+</sup> (clear grey) and <span class="html-italic">R. equi Δmrx1Δmrx2Δmrx3</span> mutant (dark grey) to clofazimine (Clo) and norfloxacin (Nor). The concentration of each antibiotic used is shown in brackets (µg/ml). The diameter of the growth inhibition zones was measured to the nearest millimetre, and the mean ± SD of three independent experiments was plotted. Two-way ANOVA and post-hoc Tukey´s multiple comparison tests were performed to assess for statistical significance across comparisons of the wild type strain and the triple <span class="html-italic">mrx</span>-null mutant. <span class="html-italic">p</span>-value &lt; 0.05 (*). (<b>B</b>) Ratiometric response of the Mrx1-roGFP2 biosensor. Fluorescence 405/490 ratio was calculated by confocal microscopy at different time points in presence of 10 µg/mL of norfloxacin. The results show the mean ± SD of three independent experiments.</p>
Full article ">Figure 3
<p>Antimicrobial susceptibility of <span class="html-italic">R. equi</span> 103S<sup>+</sup> to 5 µg of different combinations of antimicrobial compounds, including clofazimine (Clo), erythromycin (Ery), norfloxacin (Nor), rifampicin (Rif), and vancomycin (Van). The diameter of the growth inhibition zones was measured to the nearest millimetre, and the mean ± SD of three independent experiments was plotted. Two-way ANOVA and post-hoc Tukey´s multiple comparison tests were performed to assess for statistical significance across conditions. N.s.: Not significant.</p>
Full article ">Figure 4
<p>Antimicrobial effect of different combinatorial antibiotherapies against intracellular <span class="html-italic">R. equi</span> 103S<sup>+</sup> infecting J774.A1 murine macrophages. Percentages of survival were quantified after 8 h of infection. Different combinations of rifampicin (Rif), erythromycin (Ery), norfloxacin (Nor), and vancomycin (Van) were compared against a negative control with gentamicin (C). The concentration of some drug combinations was increased 5-fold (5×) or 20-fold (20×) their MIC. Two-way ANOVA and post-hoc Tukey’s multiple comparison tests were performed to assess for statistical significance related to the number of CFU recovered from the negative control (C). <span class="html-italic">p</span>-value &lt; 0.05 (*).</p>
Full article ">
15 pages, 1697 KiB  
Communication
Mycoredoxins Are Required for Redox Homeostasis and Intracellular Survival in the Actinobacterial Pathogen Rhodococcus equi
by Álvaro Mourenza, Natalia Bravo-Santano, Inés Pradal, Jose A. Gil, Luis M. Mateos and Michal Letek
Antioxidants 2019, 8(11), 558; https://doi.org/10.3390/antiox8110558 - 15 Nov 2019
Cited by 8 | Viewed by 4100
Abstract
Rhodococcus equi is a facultative intracellular pathogen that can survive within macrophages of a wide variety of hosts, including immunosuppressed humans. Current antibiotherapy is often ineffective, and novel therapeutic strategies are urgently needed to tackle infections caused by this pathogen. In this study, [...] Read more.
Rhodococcus equi is a facultative intracellular pathogen that can survive within macrophages of a wide variety of hosts, including immunosuppressed humans. Current antibiotherapy is often ineffective, and novel therapeutic strategies are urgently needed to tackle infections caused by this pathogen. In this study, we identified three mycoredoxin-encoding genes (mrx) in the genome of R. equi, and we investigated their role in virulence. Importantly, the intracellular survival of a triple mrx-null mutant (Δmrx1Δmrx2Δmrx3) in murine macrophages was fully impaired. However, each mycoredoxin alone could restore the intracellular proliferation rate of R. equi Δmrx1Δmrx2Δmrx3 to wild type levels, suggesting that these proteins could have overlapping functions during host cell infection. Experiments with the reduction-oxidation sensitive green fluorescent protein 2 (roGFP2) biosensor confirmed that R. equi was exposed to redox stress during phagocytosis, and mycoredoxins were involved in preserving the redox homeostasis of the pathogen. Thus, we studied the importance of each mycoredoxin for the resistance of R. equi to different oxidative stressors. Interestingly, all mrx genes did have overlapping roles in the resistance to sodium hypochlorite. In contrast, only mrx1 was essential for the survival against high concentrations of nitric oxide, while mrx3 was not required for the resistance to hydrogen peroxide. Our results suggest that all mycoredoxins have important roles in redox homeostasis, contributing to the pathogenesis of R. equi and, therefore, these proteins may be considered interesting targets for the development of new anti-infectives. Full article
(This article belongs to the Section Antioxidant Enzyme Systems)
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Figure 1

Figure 1
<p>Macrophage infection assays. Intracellular survival in J774.A macrophages of the wild type <span class="html-italic">R. equi</span> 103S<sup>+</sup> strain, the virulence plasmid cured <span class="html-italic">R. equi</span> 103S<sup>−</sup> strain, the triple <span class="html-italic">Δmrx1Δmrx2Δmrx3</span> mutant, and <span class="html-italic">R. equi Δmrx1Δmrx2Δmrx3</span> strain individually complemented with each <span class="html-italic">mrx</span> gene. Bacterial viability was measured by quantifying the number of colony-forming units (CFUs) of each strain at 48 h, and data were normalized by the percentage of <span class="html-italic">R. equi</span> 103S<sup>+</sup> CFUs. Data are expressed as means ± SD of three independent experiments. One-way ANOVA and post hoc Tukey´s multiple comparison tests were performed to assess for statistical significance related to the wild type strain. ** <span class="html-italic">p</span>-value &lt; 0.01.</p>
Full article ">Figure 2
<p>In vitro viability of <span class="html-italic">R. equi</span> strains after 3 h in trypticase soy broth (TSB) supplemented with either 10 mM H<sub>2</sub>O<sub>2</sub> (<b>A</b>) or 5 mM sodium hypochlorite NaClO (<b>B</b>). Control: <span class="html-italic">R. equi</span> 103S<sup>+</sup> cultured on plain TSB. Bacterial viability was measured by quantifying the number of CFUs of each strain at 3 h, and data were normalized by the percentage of <span class="html-italic">R. equi</span> 103S<sup>+</sup> CFUs recovered from plain TSB. Data are expressed as means ± SD of three independent experiments. One-way ANOVA and post hoc Tukey´s multiple comparison tests were performed to assess for statistical significance across conditions. <span class="html-italic">p</span>-value &lt; 0.05 (*) or <span class="html-italic">p</span>-value &lt; 0.01 (**).</p>
Full article ">Figure 3
<p>DETA NONOate susceptibility test. Analysis of the susceptibility to the oxidative agent DETA NONOate of the triple <span class="html-italic">R. equi Δmrx1Δmrx2Δmrx3</span> mutant and its <span class="html-italic">mrx</span>-complemented derivative strains in comparison to the wild type strain. Results are expressed as means ± SD of three independent experiments. One-way ANOVA and post hoc Tukey’s multiple comparison tests were performed to assess for statistical significance across conditions. <span class="html-italic">p</span>-value &lt; 0.01 (**) or &lt; 0.001 (***).</p>
Full article ">Figure 4
<p>Fluorescence analysis of <span class="html-italic">R. equi</span> strains expressing the reduction-oxidation sensitive green fluorescent protein (roGFP2) biosensor under the control of the constitutive promoter P<span class="html-italic"><sub>kan</sub></span>. All Mrxs-roGFP2 fusions were expressed in <span class="html-italic">R. equi Δmrx1Δmrx2Δmrx3</span>. The 405/490 ratio fluorescence of ≈200 cells was evaluated at different time points during treatments with 5 mM H<sub>2</sub>O<sub>2</sub> (<b>A</b>), 5 mM NaClO (<b>B</b>), or 5 mM DETA NONOate (<b>C</b>), and during macrophage infection (<b>D</b>); fluorescence 405/490 ratio was calculated by confocal microscopy at different time points. Data are expressed as means ± SD of ≈200 cells from three independent experiments.</p>
Full article ">
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