Significant gene order and expression differences in Bordetella pertussis despite limited gene content variation

被引:62
作者
Brinig, MM
Cummings, CA
Sanden, GN
Stefanelli, P
Lawrence, A
Relman, DA
机构
[1] VAPAHCS, Palo Alto, CA 94304 USA
[2] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[4] Ctr Dis Control & Prevent, Atlanta, GA 30333 USA
[5] Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy
[6] Womens & Childrens Hosp, Adelaide, SA 5006, Australia
关键词
D O I
10.1128/JB.188.7.2375-2382.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bordetella pertussis, an obligate human pathogen and the agent of whooping cough, is a clonal species, despite the dynamic selection pressures imposed by host immunity and vaccine usage. Because the generation of variation is critical for species evolution, we employed a variety of approaches to examine features of B. pertussis genetic variation. We found a high level of conservation of gene content among 137 B. pertussis strains with different geographical, temporal, and epidemiological associations, using comparative genomic hybridization. The limited number of regions of difference were frequently located adjacent to copies of the insertion element IS481, which is present in high numbers in the B. pertussis chromosome. This repeated sequence appears to provide targets for homologous recombination, resulting in deletion of intervening sequences. Using subtractive hybridization, we searched for previously undetected genes in diverse clinical isolates but did not detect any new genes, indicating that gene acquisition is rare in B. pertussis. In contrast, we found evidence of altered gene order in the several strains that were examined and again found an association of IS481 with sites of rearrangement. Finally, we compared whole-genome expression profiles of different strains and found significant changes in transcript abundance, even in the same strain after as few as 12 laboratory passages. This combination of approaches provides a detailed picture of a pathogenic species with little gene loss or gain but with the capacity to generate variation by rearranging its chromosome and altering gene expression. These findings have broad implications for host adaptation by microbial pathogens.
引用
收藏
页码:2375 / 2382
页数:8
相关论文
共 42 条
[22]   Black holes and bacterial pathogenicity:: A large genomic deletion that enhances the virulence of Shigella spp. and enteroinvasive Escherichia coli [J].
Maurelli, AT ;
Fernández, RE ;
Bloch, CA ;
Rode, CK ;
Fasano, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3943-3948
[23]   Representational difference analysis identifies a strain-specific LPS biosynthesis locus in Bordetella spp. [J].
Middendorf, B ;
Gross, R .
MOLECULAR AND GENERAL GENETICS, 1999, 262 (01) :189-198
[24]   Microarray transcription analysis of clinical Staphylococcus aureus isolates resistant to vancomycin [J].
Mongodin, E ;
Finan, J ;
Climo, MW ;
Rosato, A ;
Gill, S ;
Archer, GL .
JOURNAL OF BACTERIOLOGY, 2003, 185 (15) :4638-4643
[25]   Epidemiological typing of Bordetella pertussis isolates:: Recommendations for a standard methodology [J].
Mooi, FR ;
Hallander, H ;
von König, CHW ;
Hoet, B ;
Guiso, N .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2000, 19 (03) :174-181
[26]  
MUSSER JM, 1986, J BACTERIOL, V166, P230, DOI 10.1128/jb.166.1.230-237.1986
[27]   Structural flexibility in the Burkholderia mallei genome [J].
Nierman, WC ;
DeShazer, D ;
Kim, HS ;
Tettelin, H ;
Nelson, KE ;
Feldblyum, T ;
Ulrich, RL ;
Ronning, CM ;
Brinkac, LM ;
Daugherty, SC ;
Davidsen, TD ;
Deboy, RT ;
Dimitrov, G ;
Dodson, RJ ;
Durkin, AS ;
Gwinn, ML ;
Haft, DH ;
Khouri, H ;
Kolonay, JF ;
Madupu, R ;
Mohammoud, Y ;
Nelson, WC ;
Radune, D ;
Romero, CM ;
Sarria, S ;
Selengut, J ;
Shamblin, C ;
Sullivan, SA ;
White, O ;
Yu, Y ;
Zafar, N ;
Zhou, LW ;
Fraser, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (39) :14246-14251
[28]   Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica [J].
Parkhill, J ;
Sebaihia, M ;
Preston, A ;
Murphy, LD ;
Thomson, N ;
Harris, DE ;
Holden, MTG ;
Churcher, CM ;
Bentley, SD ;
Mungall, KL ;
Cerdeño-Tárraga, AM ;
Temple, L ;
James, K ;
Harris, B ;
Quail, MA ;
Achtman, M ;
Atkin, R ;
Baker, S ;
Basham, D ;
Bason, N ;
Cherevach, I ;
Chillingworth, T ;
Collins, M ;
Cronin, A ;
Davis, P ;
Doggett, J ;
Feltwell, T ;
Goble, A ;
Hamlin, N ;
Hauser, H ;
Holroyd, S ;
Jagels, K ;
Leather, S ;
Moule, S ;
Norberczak, H ;
O'Neil, S ;
Ormond, D ;
Price, C ;
Rabbinowitsch, E ;
Rutter, S ;
Sanders, M ;
Saunders, D ;
Seeger, K ;
Sharp, S ;
Simmonds, M ;
Skelton, J ;
Squares, R ;
Squares, S ;
Stevens, K ;
Unwin, L .
NATURE GENETICS, 2003, 35 (01) :32-40
[29]   Host adaptation and immune modulation are mediated by homologous recombination in Helicobacter pylori [J].
Robinson, K ;
Loughlin, MF ;
Potter, R ;
Jenks, PJ .
JOURNAL OF INFECTIOUS DISEASES, 2005, 191 (04) :579-587
[30]   A whole-genome microarray reveals genetic diversity among Helicobacter pylori strains [J].
Salama, N ;
Guillemin, K ;
McDaniel, TK ;
Sherlock, G ;
Tompkins, L ;
Falkow, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14668-14673