{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,23]],"date-time":"2026-08-23T17:37:39Z","timestamp":1787506659376,"version":"build-2736575974"},"reference-count":59,"publisher":"American Society for Microbiology","issue":"11","license":[{"start":{"date-parts":[[2023,11,16]],"date-time":"2023-11-16T00:00:00Z","timestamp":1700092800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/doi.org\/10.1128\/ASMCopyrightv2"},{"start":{"date-parts":[[2023,11,16]],"date-time":"2023-11-16T00:00:00Z","timestamp":1700092800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Infect Immun"],"published-print":{"date-parts":[[2023,11,16]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    Extraintestinal pathogenic\n                    <jats:italic>Escherichia coli<\/jats:italic>\n                    (ExPEC) is responsible for severe bloodstream infections in humans and animals. However, the mechanisms underlying ExPEC\u2019s serum resistance remain incompletely understood. Through the transposon-directed insertion-site sequencing approach, our previous study identified\n                    <jats:italic>nhaA<\/jats:italic>\n                    , the gene encoding a Na\n                    <jats:sup>+<\/jats:sup>\n                    \/H\n                    <jats:sup>+<\/jats:sup>\n                    antiporter, as a crucial factor for infection\n                    <jats:italic>in vivo<\/jats:italic>\n                    . In this study, we investigated the role of NhaA in ExPEC virulence utilizing both\n                    <jats:italic>in vitro<\/jats:italic>\n                    models and systemic infection models involving avian and mammalian animals. Genetic mutagenesis analysis revealed that\n                    <jats:italic>nhaA<\/jats:italic>\n                    deletion resulted in filamentous bacterial morphology and rendered the bacteria more susceptible to sodium dodecyl sulfate, suggesting the role of\n                    <jats:italic>nhaA<\/jats:italic>\n                    in maintaining cell envelope integrity. The\n                    <jats:italic>nhaA<\/jats:italic>\n                    mutant also displayed heightened sensitivity to complement-mediated killing compared to the wild-type strain, attributed to augmented deposition of complement components (C3b and C9). Remarkably, NhaA played a more crucial role in virulence compared to several well-known factors, including Iss, Prc, NlpI, and OmpA. Our findings revealed that NhaA significantly enhanced virulence across diverse human ExPEC prototype strains within B2 phylogroups, suggesting widespread involvement in virulence. Given its pivotal role, NhaA could serve as a potential drug target for tackling ExPEC infections.\n                  <\/jats:p>","DOI":"10.1128\/iai.00039-23","type":"journal-article","created":{"date-parts":[[2023,10,10]],"date-time":"2023-10-10T09:03:46Z","timestamp":1696928626000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":8,"title":["NhaA facilitates the maintenance of bacterial envelope integrity and the evasion of complement attack contributing to extraintestinal pathogenic\n                    <i>Escherichia coli<\/i>\n                    virulence"],"prefix":"10.1128","volume":"91","author":[{"given":"Zhao","family":"Mao","sequence":"first","affiliation":[{"name":"Key Laboratory of Veterinary Public Health of Ministry of Agriculture, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences , Harbin, 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