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Cynomolgus macaque IL37 polymorphism and control of SIV infection
The association between gene polymorphisms and plasma virus load at the set point (SP-PVL) was investigated in Mauritian macaques inoculated with SIV. Among 44 macaques inoculated with 50 AID50, six individuals were selected: three with SP-PVL among the highest and three with SP-PVL among the lowest...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538695/ https://www.ncbi.nlm.nih.gov/pubmed/31138840 http://dx.doi.org/10.1038/s41598-019-44235-x |
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author | Shiina, Takashi Suzuki, Shingo Congy-Jolivet, Nicolas Aarnink, Alice Garchon, Henri-Jean Dereuddre-Bosquet, Nathalie Vaslin, Bruno Tchitchek, Nicolas Desjardins, Delphine Autran, Brigitte Lambotte, Olivier Theodorou, Ioannis Le Grand, Roger Blancher, Antoine |
author_facet | Shiina, Takashi Suzuki, Shingo Congy-Jolivet, Nicolas Aarnink, Alice Garchon, Henri-Jean Dereuddre-Bosquet, Nathalie Vaslin, Bruno Tchitchek, Nicolas Desjardins, Delphine Autran, Brigitte Lambotte, Olivier Theodorou, Ioannis Le Grand, Roger Blancher, Antoine |
author_sort | Shiina, Takashi |
collection | PubMed |
description | The association between gene polymorphisms and plasma virus load at the set point (SP-PVL) was investigated in Mauritian macaques inoculated with SIV. Among 44 macaques inoculated with 50 AID50, six individuals were selected: three with SP-PVL among the highest and three with SP-PVL among the lowest. The exons of 390 candidate genes of these six animals were sequenced. Twelve non-synonymous single nucleotide polymorphisms (NS-SNPs) lying in nine genes potentially associated with PVL were genotyped in 23 animals. Three NS-SNPs with probabilities of association with PVL less than 0.05 were genotyped in a total of 44 animals. One NS-SNP lying in exon 1 of the IL37 gene displayed a significant association (p = 3.33 × 10(−4)) and a strong odds ratio (19.52). Multiple linear regression modeling revealed three significant predictors of SP-PVL, including the IL37 exon 1 NS-SNP (p = 0.0004) and the MHC Class IB haplotypes M2 (p = 0.0007) and M6 (p = 0.0013). These three factors in conjunction explained 48% of the PVL variance (p = 4.8 × 10(−6)). The potential role of IL37 in the control of SIV infection is discussed. |
format | Online Article Text |
id | pubmed-6538695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65386952019-06-07 Cynomolgus macaque IL37 polymorphism and control of SIV infection Shiina, Takashi Suzuki, Shingo Congy-Jolivet, Nicolas Aarnink, Alice Garchon, Henri-Jean Dereuddre-Bosquet, Nathalie Vaslin, Bruno Tchitchek, Nicolas Desjardins, Delphine Autran, Brigitte Lambotte, Olivier Theodorou, Ioannis Le Grand, Roger Blancher, Antoine Sci Rep Article The association between gene polymorphisms and plasma virus load at the set point (SP-PVL) was investigated in Mauritian macaques inoculated with SIV. Among 44 macaques inoculated with 50 AID50, six individuals were selected: three with SP-PVL among the highest and three with SP-PVL among the lowest. The exons of 390 candidate genes of these six animals were sequenced. Twelve non-synonymous single nucleotide polymorphisms (NS-SNPs) lying in nine genes potentially associated with PVL were genotyped in 23 animals. Three NS-SNPs with probabilities of association with PVL less than 0.05 were genotyped in a total of 44 animals. One NS-SNP lying in exon 1 of the IL37 gene displayed a significant association (p = 3.33 × 10(−4)) and a strong odds ratio (19.52). Multiple linear regression modeling revealed three significant predictors of SP-PVL, including the IL37 exon 1 NS-SNP (p = 0.0004) and the MHC Class IB haplotypes M2 (p = 0.0007) and M6 (p = 0.0013). These three factors in conjunction explained 48% of the PVL variance (p = 4.8 × 10(−6)). The potential role of IL37 in the control of SIV infection is discussed. Nature Publishing Group UK 2019-05-28 /pmc/articles/PMC6538695/ /pubmed/31138840 http://dx.doi.org/10.1038/s41598-019-44235-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shiina, Takashi Suzuki, Shingo Congy-Jolivet, Nicolas Aarnink, Alice Garchon, Henri-Jean Dereuddre-Bosquet, Nathalie Vaslin, Bruno Tchitchek, Nicolas Desjardins, Delphine Autran, Brigitte Lambotte, Olivier Theodorou, Ioannis Le Grand, Roger Blancher, Antoine Cynomolgus macaque IL37 polymorphism and control of SIV infection |
title | Cynomolgus macaque IL37 polymorphism and control of SIV infection |
title_full | Cynomolgus macaque IL37 polymorphism and control of SIV infection |
title_fullStr | Cynomolgus macaque IL37 polymorphism and control of SIV infection |
title_full_unstemmed | Cynomolgus macaque IL37 polymorphism and control of SIV infection |
title_short | Cynomolgus macaque IL37 polymorphism and control of SIV infection |
title_sort | cynomolgus macaque il37 polymorphism and control of siv infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538695/ https://www.ncbi.nlm.nih.gov/pubmed/31138840 http://dx.doi.org/10.1038/s41598-019-44235-x |
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