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Research Article
- Enoxacin adversely affects Salmonella enterica virulence and host pathogenesis through interference with type III secretion system type II (T3SS-II) and disruption of translocation of Salmonella Pathogenicity Island-2 (SPI2) effectors
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El-Sayed Khafagy, Gamal A. Soliman, Maged S. Abdel-Kader, Mahmoud M. Bendary, Wael A. H. Hegazy, Momen Askoura
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J. Microbiol. 2025;63(2):e2410015. Published online February 27, 2025
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DOI: https://doi.org/10.71150/jm.2410015
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Abstract
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- Salmonella enterica is a clinically significant oro-fecal pathogen that causes a wide variety of illnesses and can lead to epidemics. S. enterica expresses a lot of virulence factors that enhance its pathogenesis in host. For instance, S. enterica employs a type three secretion system (T3SS) to translocate a wide array of effector proteins that could change the surrounding niche ensuring suitable conditions for the thrive of Salmonella infection. Many antimicrobials have been recently introduced to overcome the annoying bacterial resistance to antibiotics. Enoxacin is member of the second-generation quinolones that possesses a considerable activity against S. enterica. The present study aimed to evaluate the effect of enoxacin at sub-minimum inhibitory concentration (sub-MIC) on S. enterica virulence capability and pathogenesis in host. Enoxacin at sub-MIC significantly diminished both Salmonella invasion and intracellular replication within the host cells. The observed inhibitory effect of enoxacin on S. enterica internalization could be attributed to its ability to interfere with translocation of the T3SS effector proteins. These results were further confirmed by the finding that enoxacin at sub-MIC down-regulated the expression of the genes encoding for T3SS-type II (T3SS-II). Moreover, enoxacin at sub-MIC lessened bacterial adhesion to abiotic surface and biofilm formation which indicates a potential anti-virulence activity. Importantly, in vivo results showed a significant ability of enoxacin to protect mice against S. enterica infection and decreased bacterial colonization within animal tissues. In nutshell, current findings shed light on an additional mechanism of enoxacin at sub-MIC by interfering with Salmonella intracellular replication. The outcomes presented herein could be further invested in conquering bacterial resistance and open the door for additional effective clinical applications.
Journal Article
- Genetic Characteristics and Phylogeographic Dynamics of Echovirus
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Yan Wang , Pir Tariq Shah , Yue Liu , Amina Nawal Bahoussi , Li Xing
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J. Microbiol. 2023;61(9):865-877. Published online September 15, 2023
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DOI: https://doi.org/10.1007/s12275-023-00078-w
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Abstract
- Echoviruses belong to the genus Enterovirus in the Picornaviridae family, forming a large group of Enterovirus B (EVB)
within the Enteroviruses. Previously, Echoviruses were classified based on the coding sequence of VP1. In this study,
we performed a reliable phylogenetic classification of 277 sequences isolated from 1992 to 2019 based on the full-length
genomes of Echovirus. In this report, phylogenetic, phylogeographic, recombination, and amino acid variability landscape
analyses were performed to reveal the evolutional characteristics of Echovirus worldwide. Echoviruses were clustered into
nine major clades, e.g., G1–G9. Phylogeographic analysis showed that branches G2–G9 were linked to common strains,
while the branch G1 was only linked to G5. In contrast, strains E12, E14, and E16 clustered separately from their G3 and
G7 clades respectively, and became a separate branch. In addition, we identified a total of 93 recombination events, where
most of the events occurred within the VP1-VP4 coding regions. Analysis of amino acid variation showed high variability in
the a positions of VP2, VP1, and VP3. This study updates the phylogenetic and phylogeographic information of Echovirus
and indicates that extensive recombination and significant amino acid variation in the capsid proteins drove the emergence
of new strains.
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