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Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans

We previously showed that chromosome 8 of A/J mice was associated with susceptibility to S. aureus infection. However, the specific genes responsible for this susceptibility are unknown. Chromosome substitution strain 8 (CSS8) mice, which have chromosome 8 from A/J but an otherwise C57BL/6J genome,...

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Autores principales: Yan, Qin, Ahn, Sun Hee, Medie, Felix Mba, Sharma-Kuinkel, Batu K., Park, Lawrence P., Scott, William K., Deshmukh, Hitesh, Tsalik, Ephraim L., Cyr, Derek D., Woods, Christopher W., Yu, Chen-Hsin Albert, Adams, Carlton, Qi, Robert, Hansen, Brenda, Fowler, Vance G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5464679/
https://www.ncbi.nlm.nih.gov/pubmed/28594911
http://dx.doi.org/10.1371/journal.pone.0179033
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author Yan, Qin
Ahn, Sun Hee
Medie, Felix Mba
Sharma-Kuinkel, Batu K.
Park, Lawrence P.
Scott, William K.
Deshmukh, Hitesh
Tsalik, Ephraim L.
Cyr, Derek D.
Woods, Christopher W.
Yu, Chen-Hsin Albert
Adams, Carlton
Qi, Robert
Hansen, Brenda
Fowler, Vance G.
author_facet Yan, Qin
Ahn, Sun Hee
Medie, Felix Mba
Sharma-Kuinkel, Batu K.
Park, Lawrence P.
Scott, William K.
Deshmukh, Hitesh
Tsalik, Ephraim L.
Cyr, Derek D.
Woods, Christopher W.
Yu, Chen-Hsin Albert
Adams, Carlton
Qi, Robert
Hansen, Brenda
Fowler, Vance G.
author_sort Yan, Qin
collection PubMed
description We previously showed that chromosome 8 of A/J mice was associated with susceptibility to S. aureus infection. However, the specific genes responsible for this susceptibility are unknown. Chromosome substitution strain 8 (CSS8) mice, which have chromosome 8 from A/J but an otherwise C57BL/6J genome, were used to identify the genetic determinants of susceptibility to S. aureus on chromosome 8. Quantitative trait loci (QTL) mapping of S. aureus-infected N2 backcross mice (F1 [C8A] × C57BL/6J) identified a locus 83180780–88103009 (GRCm38/mm10) on A/J chromosome 8 that was linked to S. aureus susceptibility. All genes on the QTL (n~ 102) were further analyzed by three different strategies: 1) different expression in susceptible (A/J) and resistant (C57BL/6J) mice only in response to S. aureus, 2) consistently different expression in both uninfected and infected states between the two strains, and 3) damaging non-synonymous SNPs in either strain. Eleven candidate genes from the QTL region were significantly differently expressed in patients with S. aureus infection vs healthy human subjects. Four of these 11 genes also exhibited significantly different expression in S. aureus-challenged human neutrophils: Ier2, Crif1, Cd97 and Lyl1. CD97 ligand binding was evaluated within peritoneal neutrophils from A/J and C57BL/6J. CD97 from A/J had stronger CD55 but weaker integrin α5β1 ligand binding as compared with C57BL/6J. Because CD55/CD97 binding regulates immune cell activation and cytokine production, and integrin α5β1 is a membrane receptor for fibronectin, which is also bound by S. aureus, strain-specific differences could contribute to susceptibility to S. aureus. Down-regulation of Crif1 with siRNA was associated with increased host cell apoptosis among both naïve and S. aureus-infected bone marrow-derived macrophages. Specific genes in A/J chromosome 8, including Cd97 and Crif1, may play important roles in host defense against S. aureus.
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spelling pubmed-54646792017-06-22 Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans Yan, Qin Ahn, Sun Hee Medie, Felix Mba Sharma-Kuinkel, Batu K. Park, Lawrence P. Scott, William K. Deshmukh, Hitesh Tsalik, Ephraim L. Cyr, Derek D. Woods, Christopher W. Yu, Chen-Hsin Albert Adams, Carlton Qi, Robert Hansen, Brenda Fowler, Vance G. PLoS One Research Article We previously showed that chromosome 8 of A/J mice was associated with susceptibility to S. aureus infection. However, the specific genes responsible for this susceptibility are unknown. Chromosome substitution strain 8 (CSS8) mice, which have chromosome 8 from A/J but an otherwise C57BL/6J genome, were used to identify the genetic determinants of susceptibility to S. aureus on chromosome 8. Quantitative trait loci (QTL) mapping of S. aureus-infected N2 backcross mice (F1 [C8A] × C57BL/6J) identified a locus 83180780–88103009 (GRCm38/mm10) on A/J chromosome 8 that was linked to S. aureus susceptibility. All genes on the QTL (n~ 102) were further analyzed by three different strategies: 1) different expression in susceptible (A/J) and resistant (C57BL/6J) mice only in response to S. aureus, 2) consistently different expression in both uninfected and infected states between the two strains, and 3) damaging non-synonymous SNPs in either strain. Eleven candidate genes from the QTL region were significantly differently expressed in patients with S. aureus infection vs healthy human subjects. Four of these 11 genes also exhibited significantly different expression in S. aureus-challenged human neutrophils: Ier2, Crif1, Cd97 and Lyl1. CD97 ligand binding was evaluated within peritoneal neutrophils from A/J and C57BL/6J. CD97 from A/J had stronger CD55 but weaker integrin α5β1 ligand binding as compared with C57BL/6J. Because CD55/CD97 binding regulates immune cell activation and cytokine production, and integrin α5β1 is a membrane receptor for fibronectin, which is also bound by S. aureus, strain-specific differences could contribute to susceptibility to S. aureus. Down-regulation of Crif1 with siRNA was associated with increased host cell apoptosis among both naïve and S. aureus-infected bone marrow-derived macrophages. Specific genes in A/J chromosome 8, including Cd97 and Crif1, may play important roles in host defense against S. aureus. Public Library of Science 2017-06-08 /pmc/articles/PMC5464679/ /pubmed/28594911 http://dx.doi.org/10.1371/journal.pone.0179033 Text en © 2017 Yan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yan, Qin
Ahn, Sun Hee
Medie, Felix Mba
Sharma-Kuinkel, Batu K.
Park, Lawrence P.
Scott, William K.
Deshmukh, Hitesh
Tsalik, Ephraim L.
Cyr, Derek D.
Woods, Christopher W.
Yu, Chen-Hsin Albert
Adams, Carlton
Qi, Robert
Hansen, Brenda
Fowler, Vance G.
Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans
title Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans
title_full Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans
title_fullStr Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans
title_full_unstemmed Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans
title_short Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans
title_sort candidate genes on murine chromosome 8 are associated with susceptibility to staphylococcus aureus infection in mice and are involved with staphylococcus aureus septicemia in humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5464679/
https://www.ncbi.nlm.nih.gov/pubmed/28594911
http://dx.doi.org/10.1371/journal.pone.0179033
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