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Cooperation of Adhesin Alleles in Salmonella-Host Tropism

Allelic combinations and host specificities for three fimbrial adhesins, FimH, BcfD, and StfH, were compared for 262 strains of Salmonella enterica serovar Newport, a frequent human and livestock pathogen. Like FimH, BcfD had two major alleles (designated A and B), whereas StfH had two allelic group...

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Autores principales: De Masi, Leon, Yue, Min, Hu, Changmin, Rakov, Alexey V., Rankin, Shelley C., Schifferli, Dieter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343171/
https://www.ncbi.nlm.nih.gov/pubmed/28289725
http://dx.doi.org/10.1128/mSphere.00066-17
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author De Masi, Leon
Yue, Min
Hu, Changmin
Rakov, Alexey V.
Rankin, Shelley C.
Schifferli, Dieter M.
author_facet De Masi, Leon
Yue, Min
Hu, Changmin
Rakov, Alexey V.
Rankin, Shelley C.
Schifferli, Dieter M.
author_sort De Masi, Leon
collection PubMed
description Allelic combinations and host specificities for three fimbrial adhesins, FimH, BcfD, and StfH, were compared for 262 strains of Salmonella enterica serovar Newport, a frequent human and livestock pathogen. Like FimH, BcfD had two major alleles (designated A and B), whereas StfH had two allelic groups, each with two alleles (subgroup A1 and A2 and subgroup B1 and B2). The most prevalent combinations of FimH/BcfD/StfH alleles in S. Newport were A/A/A1 and B/B/B1. The former set was most frequently found in bovine and porcine strains, whereas the latter combination was most frequently found in environmental and human isolates. Bacteria genetically engineered to express Fim, Bcf, or Stf fimbriae on their surface were tested with the different alleles for binding to human, porcine, and bovine intestinal epithelial cells. The major allelic combinations with bovine and porcine strains (A/A/A1) or with human isolates (B/B/B1) provided at least two alleles capable of binding significantly better than the other alleles to an intestinal epithelial cell line from the respective host(s). However, each combination of alleles kept at least one allele mediating binding to an intestinal epithelial cell from another host. These findings indicated that allelic variation in multiple adhesins of S. Newport contributes to bacterial adaptation to certain preferential hosts without losing the capacity to maintain a broad host range. IMPORTANCE Salmonella enterica remains a leading foodborne bacterial pathogen in the United States; infected livestock serve often as the source of contaminated food products. A study estimated that over a billion Salmonella gastroenteritis cases and up to 33 million typhoid cases occur annually worldwide, with 3.5 million deaths. Although many Salmonella strains with a broad host range present preferential associations with certain host species, it is not clear what determines the various levels of host adaptation. Here, causal properties of host associations were determined with allelic variants of three colonization factors of S. enterica serovar Newport, a most frequent zoonotic serovar. This is the first study that related not only individual but also a small group of host-associated gene variants with functional properties that cooperate to determine the level of host-adapted virulence. The detected associations should help to identify sources of Salmonella infections in both humans and animals.
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spelling pubmed-53431712017-03-13 Cooperation of Adhesin Alleles in Salmonella-Host Tropism De Masi, Leon Yue, Min Hu, Changmin Rakov, Alexey V. Rankin, Shelley C. Schifferli, Dieter M. mSphere Research Article Allelic combinations and host specificities for three fimbrial adhesins, FimH, BcfD, and StfH, were compared for 262 strains of Salmonella enterica serovar Newport, a frequent human and livestock pathogen. Like FimH, BcfD had two major alleles (designated A and B), whereas StfH had two allelic groups, each with two alleles (subgroup A1 and A2 and subgroup B1 and B2). The most prevalent combinations of FimH/BcfD/StfH alleles in S. Newport were A/A/A1 and B/B/B1. The former set was most frequently found in bovine and porcine strains, whereas the latter combination was most frequently found in environmental and human isolates. Bacteria genetically engineered to express Fim, Bcf, or Stf fimbriae on their surface were tested with the different alleles for binding to human, porcine, and bovine intestinal epithelial cells. The major allelic combinations with bovine and porcine strains (A/A/A1) or with human isolates (B/B/B1) provided at least two alleles capable of binding significantly better than the other alleles to an intestinal epithelial cell line from the respective host(s). However, each combination of alleles kept at least one allele mediating binding to an intestinal epithelial cell from another host. These findings indicated that allelic variation in multiple adhesins of S. Newport contributes to bacterial adaptation to certain preferential hosts without losing the capacity to maintain a broad host range. IMPORTANCE Salmonella enterica remains a leading foodborne bacterial pathogen in the United States; infected livestock serve often as the source of contaminated food products. A study estimated that over a billion Salmonella gastroenteritis cases and up to 33 million typhoid cases occur annually worldwide, with 3.5 million deaths. Although many Salmonella strains with a broad host range present preferential associations with certain host species, it is not clear what determines the various levels of host adaptation. Here, causal properties of host associations were determined with allelic variants of three colonization factors of S. enterica serovar Newport, a most frequent zoonotic serovar. This is the first study that related not only individual but also a small group of host-associated gene variants with functional properties that cooperate to determine the level of host-adapted virulence. The detected associations should help to identify sources of Salmonella infections in both humans and animals. American Society for Microbiology 2017-03-08 /pmc/articles/PMC5343171/ /pubmed/28289725 http://dx.doi.org/10.1128/mSphere.00066-17 Text en Copyright © 2017 De Masi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
De Masi, Leon
Yue, Min
Hu, Changmin
Rakov, Alexey V.
Rankin, Shelley C.
Schifferli, Dieter M.
Cooperation of Adhesin Alleles in Salmonella-Host Tropism
title Cooperation of Adhesin Alleles in Salmonella-Host Tropism
title_full Cooperation of Adhesin Alleles in Salmonella-Host Tropism
title_fullStr Cooperation of Adhesin Alleles in Salmonella-Host Tropism
title_full_unstemmed Cooperation of Adhesin Alleles in Salmonella-Host Tropism
title_short Cooperation of Adhesin Alleles in Salmonella-Host Tropism
title_sort cooperation of adhesin alleles in salmonella-host tropism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343171/
https://www.ncbi.nlm.nih.gov/pubmed/28289725
http://dx.doi.org/10.1128/mSphere.00066-17
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