A nontyphoidal Salmonella serovar domestication accompanying enhanced niche adaptation

Abstract Invasive nontyphoidal Salmonella (iNTS) causes extraintestinal infections with ~15% case fatality in many countries. However, the mechanism by which iNTS emerged in China remains unaddressed. We conducted clinical investigations of iNTS infection with recurrent treatment failure, caused by...

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Main Authors: Yan Li, Lin Teng, Xuebin Xu, Xiaomeng Li, Xianqi Peng, Xiao Zhou, Jiaxin Du, Yanting Tang, Zhijie Jiang, Zining Wang, Chenghao Jia, Anja Müller, Corinna Kehrenberg, Haoqiu Wang, Beibei Wu, François‐Xavier Weill, Min Yue
Format: Article
Language:English
Published: Springer Nature 2022-09-01
Series:EMBO Molecular Medicine
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Online Access:https://doi.org/10.15252/emmm.202216366
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author Yan Li
Lin Teng
Xuebin Xu
Xiaomeng Li
Xianqi Peng
Xiao Zhou
Jiaxin Du
Yanting Tang
Zhijie Jiang
Zining Wang
Chenghao Jia
Anja Müller
Corinna Kehrenberg
Haoqiu Wang
Beibei Wu
François‐Xavier Weill
Min Yue
author_facet Yan Li
Lin Teng
Xuebin Xu
Xiaomeng Li
Xianqi Peng
Xiao Zhou
Jiaxin Du
Yanting Tang
Zhijie Jiang
Zining Wang
Chenghao Jia
Anja Müller
Corinna Kehrenberg
Haoqiu Wang
Beibei Wu
François‐Xavier Weill
Min Yue
author_sort Yan Li
collection DOAJ
description Abstract Invasive nontyphoidal Salmonella (iNTS) causes extraintestinal infections with ~15% case fatality in many countries. However, the mechanism by which iNTS emerged in China remains unaddressed. We conducted clinical investigations of iNTS infection with recurrent treatment failure, caused by underreported Salmonella enterica serovar Livingstone (SL). Genomic epidemiology demonstrated five clades in the SL population and suggested that the international animal feed trade was a likely vehicle for their introduction into China, as evidenced by multiple independent transmission incidents. Importantly, isolates from Clade‐5‐I‐a/b, predominant in China, showed an invasive nature in mice, chicken and zebrafish infection models. The antimicrobial susceptibility testing revealed most isolates (> 96%) in China are multidrug‐resistant (MDR). Overall, we offer exploiting genomics in uncovering international transmission led by the animal feed trade and highlight an emerging hypervirulent clade with increased resistance to frontline antibiotics.
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publishDate 2022-09-01
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spelling doaj-art-e1c57f62f37048ffb52a63f3c1fcfd6a2025-08-20T03:43:14ZengSpringer NatureEMBO Molecular Medicine1757-46761757-46842022-09-01141111010.15252/emmm.202216366A nontyphoidal Salmonella serovar domestication accompanying enhanced niche adaptationYan Li0Lin Teng1Xuebin Xu2Xiaomeng Li3Xianqi Peng4Xiao Zhou5Jiaxin Du6Yanting Tang7Zhijie Jiang8Zining Wang9Chenghao Jia10Anja Müller11Corinna Kehrenberg12Haoqiu Wang13Beibei Wu14François‐Xavier Weill15Min Yue16Hainan Institute of Zhejiang UniversityInstitute of Preventive Veterinary Science & Department of Veterinary Medicine, Zhejiang University College of Animal SciencesShanghai Municipal Center for Disease Control and PreventionInstitute of Preventive Veterinary Science & Department of Veterinary Medicine, Zhejiang University College of Animal SciencesInstitute of Preventive Veterinary Science & Department of Veterinary Medicine, Zhejiang University College of Animal SciencesInstitute of Preventive Veterinary Science & Department of Veterinary Medicine, Zhejiang University College of Animal SciencesInstitute of Preventive Veterinary Science & Department of Veterinary Medicine, Zhejiang University College of Animal SciencesInstitute of Preventive Veterinary Science & Department of Veterinary Medicine, Zhejiang University College of Animal SciencesInstitute of Preventive Veterinary Science & Department of Veterinary Medicine, Zhejiang University College of Animal SciencesHainan Institute of Zhejiang UniversityHainan Institute of Zhejiang UniversityInstitute for Veterinary Food Science, Faculty of Veterinary Medicine, Justus‐Liebig University GiessenInstitute for Veterinary Food Science, Faculty of Veterinary Medicine, Justus‐Liebig University GiessenHangzhou Center for Disease Control and PreventionZhejiang Province Center for Disease Control and PreventionDepartment of Global Health, Institut PasteurHainan Institute of Zhejiang UniversityAbstract Invasive nontyphoidal Salmonella (iNTS) causes extraintestinal infections with ~15% case fatality in many countries. However, the mechanism by which iNTS emerged in China remains unaddressed. We conducted clinical investigations of iNTS infection with recurrent treatment failure, caused by underreported Salmonella enterica serovar Livingstone (SL). Genomic epidemiology demonstrated five clades in the SL population and suggested that the international animal feed trade was a likely vehicle for their introduction into China, as evidenced by multiple independent transmission incidents. Importantly, isolates from Clade‐5‐I‐a/b, predominant in China, showed an invasive nature in mice, chicken and zebrafish infection models. The antimicrobial susceptibility testing revealed most isolates (> 96%) in China are multidrug‐resistant (MDR). Overall, we offer exploiting genomics in uncovering international transmission led by the animal feed trade and highlight an emerging hypervirulent clade with increased resistance to frontline antibiotics.https://doi.org/10.15252/emmm.202216366antimicrobial resistanceevolutionhost adaptationinvasive nontyphoidal SalmonellaLivingstone
spellingShingle Yan Li
Lin Teng
Xuebin Xu
Xiaomeng Li
Xianqi Peng
Xiao Zhou
Jiaxin Du
Yanting Tang
Zhijie Jiang
Zining Wang
Chenghao Jia
Anja Müller
Corinna Kehrenberg
Haoqiu Wang
Beibei Wu
François‐Xavier Weill
Min Yue
A nontyphoidal Salmonella serovar domestication accompanying enhanced niche adaptation
EMBO Molecular Medicine
antimicrobial resistance
evolution
host adaptation
invasive nontyphoidal Salmonella
Livingstone
title A nontyphoidal Salmonella serovar domestication accompanying enhanced niche adaptation
title_full A nontyphoidal Salmonella serovar domestication accompanying enhanced niche adaptation
title_fullStr A nontyphoidal Salmonella serovar domestication accompanying enhanced niche adaptation
title_full_unstemmed A nontyphoidal Salmonella serovar domestication accompanying enhanced niche adaptation
title_short A nontyphoidal Salmonella serovar domestication accompanying enhanced niche adaptation
title_sort nontyphoidal salmonella serovar domestication accompanying enhanced niche adaptation
topic antimicrobial resistance
evolution
host adaptation
invasive nontyphoidal Salmonella
Livingstone
url https://doi.org/10.15252/emmm.202216366
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