Deletion of toxin-antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogen

Pathogenic Shigella spp. are the leading cause of bacterial dysentery, with Shigella flexneri and Shigella sonnei accounting for around 90% of cases worldwide. Although S. flexneri causes most disease in low-income countries (following ingestion of contaminated food and/or water), S. sonnei predomin...

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Main Authors: McVicker, G, Tang, C
Format: Journal article
Published: Nature Publishing Group 2016
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author McVicker, G
Tang, C
author_facet McVicker, G
Tang, C
author_sort McVicker, G
collection OXFORD
description Pathogenic Shigella spp. are the leading cause of bacterial dysentery, with Shigella flexneri and Shigella sonnei accounting for around 90% of cases worldwide. Although S. flexneri causes most disease in low-income countries (following ingestion of contaminated food and/or water), S. sonnei predominates in wealthy countries and is mainly spread from person to person. Although both species contain a large virulence plasmid, pINV, that is essential for the organism to cause disease, little is known about its maintenance. Here, using a counterselectable marker within the virulence-encoding region of pINV, we show that the S. sonnei plasmid is less stable than that of S. flexneri, especially at environmental temperatures. GmvAT, a toxin–antitoxin system, is responsible for the difference in stability and is present in pINV from S. flexneri but absent in S. sonnei pINV. GmvT is an acetyltransferase toxin that inhibits protein translation. Loss of GmvAT and a second toxin–antitoxin system, CcdAB, from pINV reduces S. sonnei plasmid stability outside the host, reflecting the host-adapted lifestyle and person-to-person transmission of this species and differences in its epidemiology.
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spelling oxford-uuid:d877f583-6976-458a-919f-1c584fca85e52022-03-27T08:48:53ZDeletion of toxin-antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogenJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d877f583-6976-458a-919f-1c584fca85e5Symplectic Elements at OxfordNature Publishing Group2016McVicker, GTang, CPathogenic Shigella spp. are the leading cause of bacterial dysentery, with Shigella flexneri and Shigella sonnei accounting for around 90% of cases worldwide. Although S. flexneri causes most disease in low-income countries (following ingestion of contaminated food and/or water), S. sonnei predominates in wealthy countries and is mainly spread from person to person. Although both species contain a large virulence plasmid, pINV, that is essential for the organism to cause disease, little is known about its maintenance. Here, using a counterselectable marker within the virulence-encoding region of pINV, we show that the S. sonnei plasmid is less stable than that of S. flexneri, especially at environmental temperatures. GmvAT, a toxin–antitoxin system, is responsible for the difference in stability and is present in pINV from S. flexneri but absent in S. sonnei pINV. GmvT is an acetyltransferase toxin that inhibits protein translation. Loss of GmvAT and a second toxin–antitoxin system, CcdAB, from pINV reduces S. sonnei plasmid stability outside the host, reflecting the host-adapted lifestyle and person-to-person transmission of this species and differences in its epidemiology.
spellingShingle McVicker, G
Tang, C
Deletion of toxin-antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogen
title Deletion of toxin-antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogen
title_full Deletion of toxin-antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogen
title_fullStr Deletion of toxin-antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogen
title_full_unstemmed Deletion of toxin-antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogen
title_short Deletion of toxin-antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogen
title_sort deletion of toxin antitoxin systems in the evolution of shigella sonnei as a host adapted pathogen
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