Pathogenicity island integrase cross-talk: a potential new tool for virulence modulation

被引:22
作者
Manson, Janet M.
Gilmore, Michael S. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Ophthalmol, Boston, MA 02115 USA
[2] Schepens Eye Res Inst, Boston, MA USA
关键词
D O I
10.1111/j.1365-2958.2006.05262.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Instability and excision of pathogenicity islands (PAIs) have already been described in Escherichia coli 536. In this edition of Molecular Microbiology, Bianca Hochhut and colleagues from the University of Wurzburg in Germany have shown that the instability of four of the E. coli 536 PAIs is mediated by a P4-type integrase encoded within the specific PAI by a site-specific recombination mechanism. The integrase encoded on PAI II536 is able to mediate excision and integration of both PAI II536, and also PAI V-536. The att sites of both these PAIs have a region of sequence similarity, which is also found in several other PAIs and in tRNA genes in several bacterial species. The cross-PAI activity of this integrase (Int(PAI II)) suggests that it plays an important role in both genome evolution and horizontal transfer of pathogenicity elements, possibly even across species barriers. Deletion of PAIs that carry genes for adhesins and other traits might lead to a phase variation-like phenomenon. Differential regulation of integrase activity or production might add a further level of fine-tuning during bacterial infection.
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收藏
页码:555 / 559
页数:5
相关论文
共 19 条
[1]   Analyses of the cag pathogenicity island of Helicobacter pylori [J].
Akopyants, NS ;
Clifton, SW ;
Kersulyte, D ;
Crabtree, JE ;
Youree, BE ;
Reece, CA ;
Bukanov, NO ;
Drazek, ES ;
Roe, BA ;
Berg, DE .
MOLECULAR MICROBIOLOGY, 1998, 28 (01) :37-53
[2]   EXCISION OF LARGE DNA REGIONS TERMED PATHOGENICITY ISLANDS FROM TRANSFER-RNA-SPECIFIC LOCI IN THE CHROMOSOME OF AN ESCHERICHIA-COLI WILD-TYPE PATHOGEN [J].
BLUM, G ;
OTT, M ;
LISCHEWSKI, A ;
RITTER, A ;
IMRICH, H ;
TSCHAPE, H ;
HACKER, J .
INFECTION AND IMMUNITY, 1994, 62 (02) :606-614
[3]   The 102-kilobase unstable region of Yersinia pestis comprises a high-pathogenicity island linked to a pigmentation segment which undergoes internal rearrangement [J].
Buchrieser, C ;
Prentice, M ;
Carniel, E .
JOURNAL OF BACTERIOLOGY, 1998, 180 (09) :2321-2329
[4]   Genetic structure and distribution of four pathogenicity islands (PAI I536 to PAI IV536) of uropathogenic Escherichia coli strain 536 [J].
Dobrindt, U ;
Blum-Oehler, G ;
Nagy, G ;
Schneider, G ;
Johann, A ;
Gottschalk, G ;
Hacker, J .
INFECTION AND IMMUNITY, 2002, 70 (11) :6365-6372
[5]   Genomic islands in pathogenic and environmental microorganisms [J].
Dobrindt, U ;
Hochhut, B ;
Hentschel, U ;
Hacker, J .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (05) :414-424
[6]  
HOCHHUT B, 2006, MOL MICROBIOL, DOI DOI 10.1111/J.1365-2958.05255.X.
[7]   Demonstration of regulatory cross-talk between P fimbriae and type 1 fimbriae in uropathogenic Escherichia coli [J].
Holden, NJ ;
Totsika, M ;
Mahler, E ;
Roe, AJ ;
Catherwood, K ;
Lindner, K ;
Dobrindt, U ;
Gally, DL .
MICROBIOLOGY-SGM, 2006, 152 :1143-1153
[8]   Switches, cross-talk and memory in Escherichia coli adherence [J].
Holden, NJ ;
Gally, DL .
JOURNAL OF MEDICAL MICROBIOLOGY, 2004, 53 (07) :585-593
[9]   LARGE, UNSTABLE INSERTS IN THE CHROMOSOME AFFECT VIRULENCE PROPERTIES OF UROPATHOGENIC ESCHERICHIA-COLI O6 STRAIN 536 [J].
KNAPP, S ;
HACKER, J ;
JARCHAU, T ;
GOEBEL, W .
JOURNAL OF BACTERIOLOGY, 1986, 168 (01) :22-30
[10]   Instability of pathogenicity islands in uropathogenic Escherichia coli 536 [J].
Middendorf, B ;
Hochhut, B ;
Leipold, K ;
Dobrindt, U ;
Blum-Oehler, G ;
Hacker, J .
JOURNAL OF BACTERIOLOGY, 2004, 186 (10) :3086-3096