Abstract

In the Mauritian macaque experimentally inoculated with SIV, gene polymorphisms potentially associated with the plasma virus load at a set point, approximately 100 days post inoculation, were investigated. Among the 42 animals inoculated with 50 AID50 of the same strain of SIV, none of which received any preventive or curative treatment, nine individuals were selected: three with a plasma virus load (PVL) among the lowest, three with intermediate PVL values and three among the highest PVL values. The complete genomes of these nine animals were then analyzed. Initially, attention was focused on variants with a potential functional impact on protein encoding genes (non-synonymous SNPs (NS-SNPs) and splicing variants). Thus, 424 NS-SNPs possibly associated with PVL were detected. The 424 candidates SNPs were genotyped in these 42 SIV experimentally infected animals (including the nine animals subjected to whole genome sequencing). The genes containing variants most probably associated with PVL at a set time point are analyzed herein.

Details

Title
Whole genome sequencing in the search for genes associated with the control of SIV infection in the Mauritian macaque model
Author
Marc de Manuel 1 ; Shiina, Takashi 2 ; Suzuki, Shingo 2 ; Dereuddre-Bosquet, Nathalie 3 ; Henri-Jean Garchon 4 ; Tanaka, Masayuki 5 ; Congy-Jolivet, Nicolas 6 ; Aarnink, Alice 7 ; Roger Le Grand 3 ; Marques-Bonet, Tomas 1   VIAFID ORCID Logo  ; Blancher, Antoine 6 

 Institute of Evolutionary Biology, UPF-CSIC, PRBB, Dr. Aiguader 88, Barcelona, Spain; Catalan Institution of Research and Advanced Studies, ICREA, Passeig de Lluís Companys, 23, Barcelona, Spain; CNAG-CRG, Centre for Genomic Regulation, CRG, Barcelona Institute of Science and Technology (BIST, Baldiri i Reixac 4, Barcelona, Spain 
 Department of Molecular Life Science, Division of Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, Isehara, Kanagawa, Japan 
 CEA – Université Paris-Sud 11 – INSERM U1184, Immunology of Viral Infections and Autoimmune Diseases, IDMIT Department, IBFJ, Fontenay-aux-Roses, France 
 Inserm U1173, Simone Veil School of Health Sciences, University of Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux, France; Genetics Division, Ambroise Paré Hospital (AP-HP), Boulogne-Billancourt, France 
 Support Center for Medical Research and Education, Tokai University, Isehara, Kanagawa, Japan 
 Laboratoire d’immunogénétique moléculaire (LIMT, EA 3034, Faculté de médecine Purpan, Université Toulouse 3 (Université Paul Sabatier, UPS), Toulouse, France; Laboratoire d’immunologie, CHU de Toulouse, France 
 Laboratoire d’immunogénétique moléculaire (LIMT, EA 3034, Faculté de médecine Purpan, Université Toulouse 3 (Université Paul Sabatier, UPS), Toulouse, France 
Pages
1-9
Publication year
2018
Publication date
May 2018
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2036389973
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.