Microarray Identification of Clostridium difficile Core Components and Divergent Regions Associated with Host Origin

被引:63
作者
Janvilisri, Tavan [1 ,5 ]
Scaria, Joy [1 ]
Thompson, Angela D. [2 ]
Nicholson, Ainsley [2 ]
Limbago, Brandi M. [2 ]
Arroyo, Luis G. [3 ]
Songer, J. Glenn [4 ]
Groehn, Yrjoe T. [1 ]
Chang, Yung-Fu [1 ]
机构
[1] Cornell Univ, Coll Vet Med, Dept Populat Med & Diagnost Sci, Ithaca, NY 14853 USA
[2] Ctr Dis Control & Prevent, Div Healthcare Qual Promot, Atlanta, GA 30333 USA
[3] Univ Guelph, Ontario Vet Coll, Dept Clin Studies, Guelph, ON N1G 2W1, Canada
[4] Univ Arizona, Dept Vet Sci & Microbiol, Tucson, AZ 85721 USA
[5] Mahidol Univ, Fac Sci, Dept Biol, Bangkok 10400, Thailand
基金
美国国家卫生研究院;
关键词
FRAGMENT LENGTH POLYMORPHISM; FIELD GEL-ELECTROPHORESIS; MOLECULAR CHARACTERIZATION; ESCHERICHIA-COLI; BINARY TOXIN; STRAINS; BACTERIA; EXPRESSION; INFECTION; EPIDEMIC;
D O I
10.1128/JB.00222-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Clostridium difficile is a gram-positive, spore-forming enteric anaerobe which can infect humans and a wide variety of animal species. Recently, the incidence and severity of human C. difficile infection has markedly increased. In this study, we evaluated the genomic content of 73 C. difficile strains isolated from humans, horses, cattle, and pigs by comparative genomic hybridization with microarrays containing coding sequences from C. difficile strains 630 and QCD-32g58. The sequenced genome of C. difficile strain 630 was used as a reference to define a candidate core genome of C. difficile and to explore correlations between host origins and genetic diversity. Approximately 16% of the genes in strain 630 were highly conserved among all strains, representing the core complement of functional genes defining C. difficile. Absent or divergent genes in the tested strains were distributed across the entire C. difficile 630 genome and across all the predicted functional categories. Interestingly, certain genes were conserved among strains from a specific host species, but divergent in isolates with other host origins. This information provides insight into the genomic changes which might contribute to host adaptation. Due to a high degree of divergence among C. difficile strains, a core gene list from this study offers the first step toward the construction of diagnostic arrays for C. difficile.
引用
收藏
页码:3881 / 3891
页数:11
相关论文
共 49 条
[31]   A MOLECULAR CHARACTERIZATION OF CLOSTRIDIUM-DIFFICILE ISOLATES FROM HUMANS, ANIMALS AND THEIR ENVIRONMENTS [J].
ONEILL, G ;
ADAMS, JE ;
BOWMAN, RA ;
RILEY, TV .
EPIDEMIOLOGY AND INFECTION, 1993, 111 (02) :257-264
[32]   Differentiation of Escherichia coli pathotypes by oligonucleotide spotted array [J].
Palaniappan, RUM ;
Zhang, Y ;
Chiu, D ;
Torres, A ;
DebRoy, C ;
Whittam, TS ;
Chang, YF .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (04) :1495-1501
[33]   Iron metabolism in pathogenic bacteria [J].
Ratledge, C ;
Dover, LG .
ANNUAL REVIEW OF MICROBIOLOGY, 2000, 54 :881-941
[34]   A novel toxinotyping scheme and correlation of toxinotypes with serogroups of Clostridium difficile isolates [J].
Rupnik, M ;
Avesani, V ;
Janc, M ;
von Eichel-Streiber, C ;
Delmée, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (08) :2240-2247
[35]   Characterization of polymorphisms in the toxin A and B genes of Clostridium difficile [J].
Rupnik, M ;
Braun, V ;
Soehn, F ;
Janc, M ;
Hofstetter, M ;
LaufenbergFeldmann, R ;
vonEichelStreiber, C .
FEMS MICROBIOLOGY LETTERS, 1997, 148 (02) :197-202
[36]   Heterogeneity of large clostridial toxins:: importance of Clostridium difficile toxinotypes [J].
Rupnik, Maja .
FEMS MICROBIOLOGY REVIEWS, 2008, 32 (03) :541-555
[37]   Transcription and analysis of polymorphism in a cluster of genes encoding surface-associated proteins of Clostridium difficile [J].
Savariau-Lacomme, MP ;
Lebarbier, C ;
Karjalainen, T ;
Collignon, A ;
Janoir, C .
JOURNAL OF BACTERIOLOGY, 2003, 185 (15) :4461-4470
[38]   Microbial Diagnostic Array Workstation (MDAW): a web server for diagnostic array data storage, sharing and analysis [J].
Scaria, Joy ;
Sreedharan, Aswathy ;
Chang, Yung-Fu .
SOURCE CODE FOR BIOLOGY AND MEDICINE, 2008, 3 (01)
[39]   Microarray for molecular typing of Salmonella enterica serovars [J].
Scaria, Joy ;
Palaniappan, Raghavan U. M. ;
Chiu, David ;
Phan, Julie Ann ;
Ponnala, Lalit ;
McDonough, Patrick ;
Grohn, Yrjo T. ;
Porwollik, Steffen ;
McClelland, Michael ;
Chiou, Chien-Shun ;
Chu, Chishih ;
Chang, Yung-Fu .
MOLECULAR AND CELLULAR PROBES, 2008, 22 (04) :238-243
[40]   The multidrug-resistant human pathogen Clostridium difficile has a highly mobile, mosaic genome [J].
Sebaihia, Mohammed ;
Wren, Brendan W. ;
Mullany, Peter ;
Fairweather, Neil F. ;
Minton, Nigel ;
Stabler, Richard ;
Thomson, Nicholas R. ;
Roberts, Adam P. ;
Cerdeno-Tarrraga, Ana M. ;
Wang, Hongmei ;
Holden, Matthew T. G. ;
Wright, Anne ;
Churcher, Carol ;
Quail, Michael A. ;
Baker, Stephen ;
Bason, Nathalie ;
Brooks, Karen ;
Chillingworth, Tracey ;
Cronin, Ann ;
Davis, Paul ;
Dowd, Linda ;
Fraser, Audrey ;
Feltwell, Theresa ;
Hance, Zahra ;
Holroyd, Simon ;
Jagels, Kay ;
Moule, Sharon ;
Mungall, Karen ;
Price, Claire ;
Rabbinowitsch, Ester ;
Sharp, Sarah ;
Simmonds, Mark ;
Stevens, Kim ;
Unwin, Louise ;
Whithead, Sally ;
Dupuy, Bruno ;
Dougan, Gordon ;
Barrell, Bart ;
Parkhill, Julian .
NATURE GENETICS, 2006, 38 (07) :779-786