Molecular characterization of Vibrio cholerae outbreak strains with altered El Tor biotype from southern India

被引:52
作者
Goel, A. K. [1 ,2 ]
Jain, M. [1 ]
Kumar, P. [1 ]
Jiang, S. C. [2 ]
机构
[1] Def Res & Dev Estab, Div Biotechnol, Gwalior 474002, India
[2] Univ Calif Irvine, Dept Civil & Environm Engn, Irvine, CA 92697 USA
关键词
Vibrio cholerae; Molecular characterization; Antibiogram; Toxin gene; Evolution; POLYMERASE-CHAIN-REACTION; MOBILE GENE CASSETTES; RTX TOXIN GENE; HOSPITALIZED-PATIENTS; RESISTANCE GENE; O1; STRAINS; ACUTE DIARRHEA; EMERGENCE; INTEGRON; BANGLADESH;
D O I
10.1007/s11274-009-0171-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Forty-four Vibrio cholerae isolates collected over a 7-month period in Chennai, India in 2004 were characterized for gene traits, antimicrobial susceptibility and genomic fingerprints. All 44 isolates were identified as O1 El Tor Ogawa, positive for various toxigenic and pathogenic genes viz. ace, ctxB, hlyA, ompU, ompW, rfbO1, rtx, tcpA, toxR and zot. Nucleotide sequencing revealed the presence of cholera toxin B of classical biotype in all the El Tor isolates, suggesting infection of isolates by classical CTXI broken vertical bar. Antibiogram analysis showed a broad-spectrum antibiotic resistance that was also confirmed by the presence of resistant genes in the genomes. All isolates contained a class 1 integron and an SXT constin. However, isolates were sensitive to chloramphenicol and tested negative for the chloramphenicol resistant gene suggesting a deletion in SXT constin. Fingerprinting analysis of isolates by ERIC- and Box PCR revealed similar DNA patterns indicating the clonal dissemination of a single predominant V. cholerae O1 strain throughout the 2004 outbreak in Chennai.
引用
收藏
页码:281 / 287
页数:7
相关论文
共 38 条
[1]   Cholera in Mozambique, variant of Vibrio cholerae [J].
Ansaruzzaman, M ;
Bhuiyan, NA ;
Nair, GB ;
Sack, DA ;
Lucas, M ;
Deen, JL ;
Ampuero, J ;
Chaignat, CL .
EMERGING INFECTIOUS DISEASES, 2004, 10 (11) :2057-2059
[2]   Identification of operators and promoters that control SXT conjugative transfer [J].
Beaber, JW ;
Waldor, MK .
JOURNAL OF BACTERIOLOGY, 2004, 186 (17) :5945-5949
[3]   Genomic and functional analyses of SXT, an integrating antibiotic resistance gene transfer element derived from Vibrio cholerae [J].
Beaber, JW ;
Hochhut, B ;
Waldor, MK .
JOURNAL OF BACTERIOLOGY, 2002, 184 (15) :4259-4269
[4]   Detection of RTX toxin gene in Vibrio cholerae by PCR [J].
Chow, KH ;
Ng, TK ;
Yuen, KY ;
Yam, WC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (07) :2594-2597
[5]  
Clinical and Laboratory Standards Institute (CLSI), 2007, M100S17 CLSI
[6]   SITE-SPECIFIC DELETION AND REARRANGEMENT OF INTEGRON INSERT GENES CATALYZED BY THE INTEGRON DNA INTEGRASE [J].
COLLIS, CM ;
HALL, RM .
JOURNAL OF BACTERIOLOGY, 1992, 174 (05) :1574-1585
[8]   Class 1 integron-borne, multiple-antibiotic resistance encoded by a 150-kilobase conjugative plasmid in epidemic Vibrio cholerae O1 strains isolated in Guinea-Bissau [J].
Dalsgaard, A ;
Forslund, A ;
Petersen, A ;
Brown, DJ ;
Dias, F ;
Monteiro, S ;
Molbak, K ;
Aaby, P ;
Rodrigues, A ;
Sandström, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (10) :3774-3779
[9]  
Faruque ASG, 2007, J HEALTH POPUL NUTR, V25, P241
[10]   Emergence and evolution of Vibrio cholerae O139 [J].
Faruque, SM ;
Sack, DA ;
Sack, RB ;
Colwell, RR ;
Takeda, Y ;
Nair, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :1304-1309