New insights into Acinetobacter baumannii pathogenesis revealed by high-density pyrosequencing and transposon mutagenesis

Genes and Development - Tập 21 Số 5 - Trang 601-614 - 2007
Michael G. Smith1, Tara A. Gianoulis2,3, Stefan Pukatzki4, John J. Mekalanos4, L. Nicholas Ornston1, Mark Gerstein2,3, M Snyder2,1
1Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA
2Department of Molecular Biochemistry and Biophysics Yale University New Haven, Connecticut 06520 USA
3Program in Computational Biology and Bioinformatics, Yale University, New Haven, Connecticut 06520, USA
4Harvard Medical School Department of Microbiology and Molecular Genetics Boston, Massachusetts 02115, USA

Tóm tắt

Acinetobacter baumannii has emerged as an important and problematic human pathogen as it is the causative agent of several types of infections including pneumonia, meningitis, septicemia, and urinary tract infections. We explored the pathogenic content of this harmful pathogen using a combination of DNA sequencing and insertional mutagenesis. The genome of this organism was sequenced using a strategy involving high-density pyrosequencing, a novel, rapid method of high-throughput sequencing. Excluding the rDNA repeats, the assembled genome is 3,976,746 base pairs (bp) and has 3830 ORFs. A significant fraction of ORFs (17.2%) are located in 28 putative alien islands, indicating that the genome has acquired a large amount of foreign DNA. Consistent with its role in pathogenesis, a remarkable number of the islands (16) contain genes implicated in virulence, indicating the organism devotes a considerable portion of its genes to pathogenesis. The largest island contains elements homologous to the Legionella/Coxiella Type IV secretion apparatus. Type IV secretion systems have been demonstrated to be important for virulence in other organisms and thus are likely to help mediate pathogenesis of A. baumannii. Insertional mutagenesis generated avirulent isolates of A. baumannii and verified that six of the islands contain virulence genes, including two novel islands containing genes that lacked homology with others in the databases. The DNA sequencing approach described in this study allows the rapid elucidation of the DNA sequence of any microbe and, when combined with genetic screens, can identify many novel genes important for microbial pathogenesis.

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Tài liệu tham khảo

10.1038/436758a

10.1046/j.1462-5822.2003.00287.x

10.1006/jmbi.1990.9999

10.1093/nar/25.17.3389

10.1007/s00203-003-0616-6

Avery, L. Thomas, J.H. (1997) in C. elegans II, Feeding and defecation, ed Riddle, D.L. (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY), pp 679–716.

10.1093/nar/gkh910

Baumann,, 1968, Study of the Moraxella group. I. Genus Moraxella and the Neisseria catarrhalis group, J. Bacteriol., 95, 58, 10.1128/jb.95.1.58-73.1968

Baumann,, 1968, A study of the Moraxella group. II. Oxidative-negative species (genus Acinetobacter), J. Bacteriol., 95, 1520, 10.1128/jb.95.5.1520-1541.1968

Bergogne-Berezin,, 1996, Acinetobacter spp. as nosocomial pathogens: Microbiological, clinical, and epidemiological features, Clin. Microbiol. Rev., 9, 148, 10.1128/CMR.9.2.148

10.1086/502335

10.1034/j.1600-0854.2001.002005311.x

10.1093/bioinformatics/bti553

2004, Acinetobacter baumannii infections among patients at military medical facilities treating injured U.S. service members, 2002–2004, MMWR Morb. Mortal Wkly. Rep., 53, 1063

Chastre,, 2000, Problem pathogens (Pseudomonas aeruginosa and Acinetobacter), Semin. Respir. Infect., 15, 287, 10.1053/srin.2000.20944

10.1111/j.1462-5822.2005.00538.x

10.1093/nar/27.23.4636

10.1128/AEM.68.12.6353-6360.2002

10.1128/JCM.41.9.4188-4193.2003

10.1099/mic.0.27371-0

10.1016/j.plasmid.2006.01.004

10.1371/journal.pgen.0020007

10.1073/pnas.0604351103

10.1128/IAI.00210-06

10.1146/annurev.mi.32.100178.002025

10.1093/nar/gkj102

10.1016/S0966-842X(01)02079-0

Koulenti,, 2006, Gram-negative bacterial pneumonia: Aetiology and management, Curr. Opin. Pulm. Med., 12, 198

10.1016/S1046-2023(02)00226-8

La Scola,, 2004, Acinetobacter baumannii in human body louse, Emerg. Infect. Dis., 10, 1671, 10.3201/eid1009.040242

Margulies,, 2005, Genome sequencing in microfabricated high-density picolitre reactors, Nature, 437, 376, 10.1038/nature03959

Olivera-Severo,, 2006, Ureases display biological effects independent of enzymatic activity: Is there a connection to diseases caused by urease-producing bacteria?, Braz. J. Med. Biol. Res., 39, 851, 10.1590/S0100-879X2006000700002

Piechaud,, 1951, [Studies of 26 strains of Moraxella Iwoffi.], Ann. Inst. Pasteur (Paris), 80, 97

10.1073/pnas.052704399

10.1093/nar/18.10.2887

10.1093/nar/gki366

10.1128/MCB.24.9.3874-3884.2004

10.1099/00221287-43-2-159

Sulston, J. Hodgkin, J. (1988) in The nematode Caenorhabditis elegans, Methods, ed Wood, W.B. (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York), pp 587–606.

Sussman,, 1987, Cultivation and synchronous morphogenesis of Dictyostelium under controlled experimental conditions, Methods Cell Biol., 28, 9, 10.1016/S0091-679X(08)61635-0

10.1093/bioinformatics/17.12.1123

10.1126/science.278.5338.631

10.1099/mic.0.26541-0

10.1146/annurev.micro.59.051905.105823