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.

dc.contributor.author

Yan, Qin

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Ahn, Sun Hee

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Medie, Felix Mba

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Sharma-Kuinkel, Batu K

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Park, Lawrence P

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Scott, William K

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Deshmukh, Hitesh

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Tsalik, Ephraim L

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Cyr, Derek D

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Woods, Christopher W

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Yu, Chen-Hsin Albert

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Adams, Carlton

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Qi, Robert

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Hansen, Brenda

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Fowler, Vance G

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Robinson, D Ashley

dc.date.accessioned

2023-04-01T16:24:53Z

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2023-04-01T16:24:53Z

dc.date.issued

2017-01

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2023-04-01T16:24:51Z

dc.description.abstract

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.

dc.identifier

PONE-D-17-14057

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1932-6203

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1932-6203

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https://hdl.handle.net/10161/26959

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eng

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Public Library of Science (PLoS)

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PloS one

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10.1371/journal.pone.0179033

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Neutrophils

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Chromosomes, Mammalian

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Macrophages

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Bone Marrow

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Animals

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Mice, Inbred C57BL

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Humans

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Staphylococcus aureus

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Staphylococcal Infections

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Sepsis

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Genetic Predisposition to Disease

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Cell Cycle Proteins

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Nuclear Proteins

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RNA, Small Interfering

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Antigens, CD

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Ligands

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Reproducibility of Results

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Chromosome Mapping

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Apoptosis

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Gene Expression Regulation

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Polymorphism, Single Nucleotide

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Alleles

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Quantitative Trait Loci

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Genetic Association Studies

dc.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.

dc.type

Journal article

duke.contributor.orcid

Tsalik, Ephraim L|0000-0002-6417-2042

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Woods, Christopher W|0000-0001-7240-2453

duke.contributor.orcid

Fowler, Vance G|0000-0002-8048-0897

pubs.begin-page

e0179033

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6

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Duke

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School of Medicine

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School of Nursing

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Nursing

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Basic Science Departments

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Clinical Science Departments

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Institutes and Centers

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Biostatistics & Bioinformatics

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Molecular Genetics and Microbiology

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Medicine

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Pathology

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Medicine, Cardiology

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Medicine, Infectious Diseases

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Duke Cancer Institute

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Duke Clinical Research Institute

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Duke Human Vaccine Institute

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Institutes and Provost's Academic Units

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University Institutes and Centers

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Duke Global Health Institute

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Duke Center for Applied Genomics and Precision Medicine

pubs.publication-status

Published

pubs.volume

12

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