A novel multiple locus variable number of tandem repeat (VNTR) analysis (MLVA) method for Propionibacterium acnes

被引:4
作者
Hauck, Yolande [1 ]
Soler, Charles [2 ]
Gerome, Patrick [3 ]
Vong, Rithy [2 ]
Macnab, Christine [2 ]
Appere, Geraldine [2 ]
Vergnaud, Gilles [1 ,4 ]
Pourcel, Christine [1 ]
机构
[1] Univ Paris Saclay, Univ Paris 11, Inst Integrat Biol Cell I2BC, CEA,CNRS, F-91405 Orsay, France
[2] NIA Percy, Lab Biol Clin, Clamart, France
[3] HIA Desgenettes, Serv Biol Med, F-69275 Lyon 03, France
[4] Univ Paris Saclay, ENSTA ParisTech, F-91762 Palaiseau, France
关键词
VNTR; Genotyping; In silico MLVA; CRISPR; Post-surgery infection; HUMAN SKIN; PHYLOGENETIC ANALYSIS; ANTIBIOTIC-RESISTANT; TYPING SCHEME; SEQUENCE; PCR; IDENTIFICATION; COMMENSAL; PATHOGEN; STRAINS;
D O I
10.1016/j.meegid.2015.05.009
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Propionibacterium acnes plays a central role in the pathogenesis of acne and is responsible for severe opportunistic infections. Numerous typing schemes have been developed that allow the identification of phylotypes, but they are often insufficient to differentiate subtypes. To better understand the genetic diversity of this species and to perform epidemiological analyses, high throughput discriminant genotyping techniques are needed. Here we describe the development of a multiple locus variable number of tandem repeats (VNTR) analysis (MLVA) method. Thirteen VNTRs were identified in the genome of P. acnes and were used to genotype a collection of clinical isolates. In addition, publically available sequencing data for 102 genomes were analyzed in silico, providing an MLVA genotype. The clustering of MLVA data was in perfect congruence with whole genome based clustering. Analysis of the clustered regularly interspaced short palindromic repeat (CRISPR) element uncovered new spacers, a supplementary source of genotypic information. The present MLVA(13) scheme and associated internet database represents a first line genotyping assay to investigate large number of isolates. Particular strains may then be submitted to full genome sequencing in order to better analyze their pathogenic potential. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:233 / 241
页数:9
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