Prevalence of cdtABC genes encoding cytolethal distending toxin among Haemophilus ducreyi and Actinobacillus actinomycetemcomitans strains

被引:47
作者
Ahmed, HJ
Svensson, LA
Cope, LD
Latimer, JL
Hansen, EJ
Ahlman, K
Bayat-Turk, J
Klamer, D
Lagergård, T
机构
[1] Gothenburg Univ, Dept Med Microbiol & Immunol, S-41346 Gothenburg, Sweden
[2] Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX USA
关键词
D O I
10.1099/0022-1317-50-10-860
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The aim of this study was to investigate the presence of the three cdtABC genes responsible for production of cytolethal, distending toxin (CDT) in Haemophilus ducreyi and Actinobacillus actinomycetemcoinitans strains. Of 100 H. ducreyi strains from the culture collection of the University of Goteborg (CCUG), 27 strains with low or intermediate cytotoxic titre (<1 in 10(4)) and 23 of the remaining isolates with a high cytotoxic titre (greater than or equal to1 in 10(4)) were selected. Twenty-nine strains of H. ducreyi were isolated recently from patients with chancroid and 50 A. actinomycetemcomitans strains from patients with periodontitis. The cytotoxic activity on HEp-2 cells and the presence of cdtABC genes were studied by cytotoxicity assay of bacterial sonicates and PCR with primers specific for individual cdtA, B. and C genes of H. ducreyi in bacterial DNA preparations, respectively. All strains that manifested a cytotoxic titre in sonicate greater than or equal to1 in 100 possessed all the three cdt genes. Eighteen of the 50 strains selected from the culture collection were negative and 32 positive for cdt genes. As all strains with a high cytotoxic titre gave positive PCR results, it, can be assumed that the remaining 50 strains, which have high cytotoxic titre, would have been positive as well. Thus, it can be estimated that 82% of the culture collection strains had cdtABC genes. Similarly, 24 (83%) of 29 recent H. ducreyi isolates expressed the CDT activity and displayed all cdtABC genes. Forty-three (86%) of 50, strains of the closely related A. actinomycetemcomitans, expressing a cytotoxic activity greater than or equal to1 in 100, also possessed all three genes. Furthermore, the nucleotide sequence of the cdtABC genes was highly conserved among H. ducreyi strains from different geographic areas. These results indicate that the majority of pathogenic H. ducreyi and A. actinomycetemcomitans strains express a CDT activity encoded by all three cdtABC.
引用
收藏
页码:860 / 864
页数:5
相关论文
共 35 条
[1]   MONOCLONAL-ANTIBODIES AGAINST HAEMOPHILUS-DUCREYI LIPOOLIGOSACCHARIDE AND THEIR DIAGNOSTIC USEFULNESS [J].
AHMED, HJ ;
BORRELLI, S ;
JONASSON, J ;
ERIKSSON, L ;
HANSON, S ;
HOJER, B ;
SUNKUNTU, M ;
MUSABA, E ;
ROGGEN, EL ;
LAGERGARD, T ;
LINDBERG, AA .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1995, 14 (10) :892-898
[2]   Escherichia coli cytolethal distending toxin blocks the HeLa cell cycle at the G(2)/M transition by preventing cdc2 protein kinase dephosphorylation and activation [J].
Comayras, C ;
Tasca, C ;
Peres, SY ;
Ducommun, B ;
Oswald, E ;
DeRycke, J .
INFECTION AND IMMUNITY, 1997, 65 (12) :5088-5095
[3]   A diffusible cytotoxin of Haemophilus ducreyi [J].
Cope, LD ;
Lumbley, S ;
Latimer, JL ;
KlesneyTait, J ;
Stevens, MK ;
Johnson, LS ;
Purven, M ;
Munson, RS ;
Lagergard, T ;
Radolf, JD ;
Hansen, EJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :4056-4061
[4]   The cytolethal distending toxin from the chancroid bacterium Haemophilus ducreyi induces cell-cycle arrest in the G2 phase [J].
Cortes-Bratti, X ;
Chaves-Olarte, E ;
Lagergård, T ;
Thelestam, M .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (01) :107-115
[5]   The Haemophilus ducreyi cytolethal distending toxin induces cell cycle arrest and apoptosis via the DNA damage checkpoint pathways [J].
Cortes-Bratti, X ;
Karlsson, C ;
Lagergård, T ;
Thelestam, M ;
Frisan, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (07) :5296-5302
[6]  
DESCHRYVER A, 1990, B WORLD HEALTH ORGAN, V68, P639
[7]   CHANCROID EPIDEMIOLOGY IN NEW-ORLEANS MEN [J].
DICARLO, RP ;
ARMENTOR, BS ;
MARTIN, DH .
JOURNAL OF INFECTIOUS DISEASES, 1995, 172 (02) :446-452
[8]   DNase I homologous residues in CdtB are critical for cytolethal distending toxin-mediated cell cycle arrest [J].
Elwell, CA ;
Dreyfus, LA .
MOLECULAR MICROBIOLOGY, 2000, 37 (04) :952-963
[9]  
FRISK A, IN PRESS MICROB PATH
[10]  
Gelfanova V, 1999, INFECT IMMUN, V67, P6394