Phase variation and microevolution at homopolymeric tracts in Bordetella pertussis

被引:25
作者
Gogol, Emily B.
Cummings, Craig A. [1 ]
Burns, Ryan C.
Relman, David A.
机构
[1] Stanford Univ, Dept Microbiol & Immunol, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Med, Sch Med, Stanford, CA 94305 USA
[3] VA Palo Alto Hlth Care Syst, Palo Alto, CA 94304 USA
关键词
D O I
10.1186/1471-2164-8-122
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
Background: Bordetella pertussis, the causative agent of whooping cough, is a highly clonal pathogen of the respiratory tract. Its lack of genetic diversity, relative to many bacterial pathogens, could limit its ability to adapt to a hostile and changing host environment. This limitation might be overcome by phase variation, as observed for other mucosal pathogens. One of the most common mechanisms of phase variation is reversible expansion or contraction of homopolymeric tracts (HPTs). Results: The genomes of B. pertussis and the two closely related species, B. bronchiseptica and B. parapertussis, were screened for homopolymeric tracts longer than expected on the basis of chance, given their nucleotide compositions. Sixty-nine such HPTs were found in total among the three genomes, 74% of which were polymorphic among the three species. Nine HPTs were genotyped in a collection of 90 geographically and temporally diverse B. pertussis strains using the polymerase chain reaction/ligase detection reaction (PCR/LDR) assay. Six HPTs were polymorphic in this collection of B. pertussis strains. Of note, one of these polymorphic HPTs was found in the fimX promoter, where a single base insertion variant was present in seven strains, all of which were isolated prior to introduction of the pertussis vaccine. Transcript abundance of fimX was found to be 3.8-fold lower in strains carrying the longer allele. HPTs in three other genes, tcfA, bapC, and BP3651, varied widely in composition across the strain collection and displayed allelic polymorphism within single cultures. Conclusion: Allelic polymorphism at homopolymeric tracts is common within the B. pertussis genome. Phase variability may be an important mechanism in B. pertussis for evasion of the immune system and adaptation to different niches in the human host. High sensitivity and specificity make the PCR/LDR assay a powerful tool for investigating allelic variation at HPTs. Using this method, allelic diversity and phase variation were demonstrated at several B. pertussis loci.
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页数:16
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共 55 条
[1]   BORDETELLA-PARAPERTUSSIS AND BORDETELLA-BRONCHISEPTICA CONTAIN TRANSCRIPTIONALLY SILENT PERTUSSIS TOXIN GENES [J].
ARICO, B ;
RAPPUOLI, R .
JOURNAL OF BACTERIOLOGY, 1987, 169 (06) :2847-2853
[2]   Significant gene order and expression differences in Bordetella pertussis despite limited gene content variation [J].
Brinig, MM ;
Cummings, CA ;
Sanden, GN ;
Stefanelli, P ;
Lawrence, A ;
Relman, DA .
JOURNAL OF BACTERIOLOGY, 2006, 188 (07) :2375-2382
[3]   ACT: the Artemis comparison tool [J].
Carver, TJ ;
Rutherford, KM ;
Berriman, M ;
Rajandream, MA ;
Barrell, BG ;
Parkhill, J .
BIOINFORMATICS, 2005, 21 (16) :3422-3423
[4]   Polymorphism in Bordetella pertussis pertactin and pertussis toxin virulence factors in the United States, 1935-1999 [J].
Cassiday, P ;
Sanden, G ;
Heuvelman, K ;
Mooi, F ;
Bisgard, KM ;
Popovic, T .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (05) :1402-1408
[5]  
*CDCP, 1995, MMWR-MORBID MORTAL W, V44, P525
[6]   Species- and strain-specific control of a complex, flexible regulon by Bordetella BvgAS [J].
Cummings, CA ;
Bootsma, HJ ;
Relman, DA ;
Miller, JF .
JOURNAL OF BACTERIOLOGY, 2006, 188 (05) :1775-1785
[7]   Bordetella species are distinguished by patterns of substantial gene loss and host adaptation [J].
Cummings, CA ;
Brinig, MM ;
Lepp, PW ;
van de Pas, S ;
Relman, DA .
JOURNAL OF BACTERIOLOGY, 2004, 186 (05) :1484-1492
[8]   Bordetella pertussis, the causative agent of whooping cough, evolved from a distinct, human-associated lineage of B-bronchiseptica [J].
Diavatopoulos, Dimitri A. ;
Cummings, Craig A. ;
Schouls, Leo M. ;
Brinig, Mary M. ;
Relman, David A. ;
Mooi, Frits R. .
PLOS PATHOGENS, 2005, 1 (04) :373-383
[9]   Whole genome plasticity in pathogenic bacteria [J].
Dobrindt, U ;
Hacker, J .
CURRENT OPINION IN MICROBIOLOGY, 2001, 4 (05) :550-557
[10]   Strain variation among Bordetella pertussis isolates in Finland, where the whole-cell pertussis vaccine has been used for 50 years [J].
Elomaa, A ;
Advani, A ;
Donnelly, D ;
Antila, M ;
Mertsola, J ;
Hallander, H ;
He, QS .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (08) :3681-3687