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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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