Evidence for a conjugation-like mechanism of DNA transfer in Helicobacter pylori

被引:62
作者
Kuipers, EJ
Israel, DA
Kusters, JG
Blaser, MJ [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Div Infect Dis, Med Ctr N A3310, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Vet Affairs Med Ctr, Nashville, TN 37212 USA
[3] Free Univ Amsterdam Hosp, Dept Gastroenterol, Amsterdam, Netherlands
[4] Free Univ Amsterdam Hosp, Dept Med Microbiol, Amsterdam, Netherlands
关键词
D O I
10.1128/JB.180.11.2901-2905.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Many strains of Helicobacter pylori are naturally competent for transformation in vitro. Since there is a high degree of genetic variation among H. pylori strains, we sought to determine whether mechanisms of DNA exchange other than transformation exist in these organisms. Studies were done with H. pylori cells that each were resistant to two different antibiotics; the procedure used involved mating of cells on plates or in broth, in the absence or presence of DNase. In each experiment, such matings produced progeny with the markers of both parents. Examination of the full resistance profile and random arbitrarily primed DNA PCR (RAPD-PCR) profiles of the progeny indicated that DNA transfer was bidirectional. DNase treatment reduced but did not eliminate transfer; only the presence of both DNase and a membrane separating the cells did so. For progeny derived from matings in the presence of DNase, antibiotic resistance and RAPD profiles indicated that transfer was unidirectional. DNase-treated cell free supernatants also did not transform, ruling out transduction. These experiments indicate that both a DNase-sensitive mechanism (transformation) and a DNase-resistant conjugation-like mechanism involving cell-to-cell contact may contribute to DNA transfer between H. pylori cells.
引用
收藏
页码:2901 / 2905
页数:5
相关论文
共 36 条
[1]  
Akopyants N. S., 1995, Gut, V37, pA1
[2]   DNA DIVERSITY AMONG CLINICAL ISOLATES OF HELICOBACTER-PYLORI DETECTED BY PCR-BASED RAPD FINGERPRINTING [J].
AKOPYANZ, N ;
BUKANOV, NO ;
WESTBLOM, TU ;
KRESOVICH, S ;
BERG, DE .
NUCLEIC ACIDS RESEARCH, 1992, 20 (19) :5137-5142
[3]   MOSAICISM IN VACUOLATING CYTOTOXIN ALLELES OF HELICOBACTER-PYLORI - ASSOCIATION OF SPECIFIC VACA TYPES WITH CYTOTOXIN PRODUCTION AND PEPTIC-ULCERATION [J].
ATHERTON, JC ;
CAO, P ;
PEEK, RM ;
TUMMURU, MKR ;
BLASER, MJ ;
COVER, TL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (30) :17771-17777
[4]   PARASITISM BY THE SLOW BACTERIUM HELICOBACTER-PYLORI LEADS TO ALTERED GASTRIC HOMEOSTASIS AND NEOPLASIA [J].
BLASER, MJ ;
PARSONNET, J .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) :4-8
[5]  
Blaser MJ, 1996, HELICOBACTER PYLORI, P33
[6]  
CATLIN BW, 1981, GENETIC EXCHANGE CEL, P310
[7]   cag, a pathogenicity island of Helicobacter pylori, encodes type I-specific and disease-associated virulence factors [J].
Censini, S ;
Lange, C ;
Xiang, ZY ;
Crabtree, JE ;
Ghiara, P ;
Borodovsky, M ;
Rappuoli, R ;
Covacci, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14648-14653
[8]   MOLECULAR CHARACTERIZATION OF THE 128-KDA IMMUNODOMINANT ANTIGEN OF HELICOBACTER-PYLORI-ASSOCIATED WITH CYTOTOXICITY AND DUODENAL-ULCER [J].
COVACCI, A ;
CENSINI, S ;
BUGNOLI, M ;
PETRACCA, R ;
BURRONI, D ;
MACCHIA, G ;
MASSONE, A ;
PAPINI, E ;
XIANG, ZY ;
FIGURA, N ;
RAPPUOLI, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) :5791-5795
[9]   CONSTRUCTION OF DNA RECOGNITION SITES ACTIVE IN HEMOPHILUS TRANSFORMATION [J].
DANNER, DB ;
SMITH, HO ;
NARANG, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (07) :2393-2397
[10]  
FROSCH M, 1992, FEMS MICROBIOL LETT, V100, P345, DOI 10.1016/0378-1097(92)90231-C