Integrons: an antibiotic resistance gene capture and expression system

被引:68
作者
Ploy, MC
Lambert, T
Couty, JP
Denis, F
机构
[1] CHU Dupuytren, Lab Bacteriol Virol Hyg, F-87042 Limoges, France
[2] Fac Pharm, Microbiol Lab, Chatenay Malabry, France
关键词
integron; antibiotic resistance; dissemination;
D O I
10.1515/CCLM.2000.070
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Bacteria can transfer genetic information to provide themselves with protection against most antibiotics. The acquisition of resistance gene arrays involves genetic mobile elements like plasmids and transposons. Another class of genetic structures, termed integrons, have been described and contain one or more gene cassettes located at a specific site. Integrons are defined by an intl gene encoding an integrase, a recombination site attl and a strong promoter. At least six classes of integrons have been determined according to their intl gene. Classes 1, 2 and 3 are the most studied and are largely implicated in the dissemination of antibiotic resistance. A gene cassette includes an open reading frame and, at the 3'-end, a recombination site attC. Integration or excision of cassettes occur by a site-specific recombination mechanism catalyzed by the integrase. However, insertion can occur, albeit rarely, at non-specific sites leading to a stable situation for the cassette. Cassettes are transcribed from the common promoter located in the 5'-conserved segment and expression of distal genes is reduced by the presence of upstream cassettes. Most gene cassettes encode antibiotic resistant determinants but antiseptic resistant genes have also been described. Integrons seem to have a major role in the spread of multidrug resistance in Gram-negative bacteria but integrons in Gram-positive bacteria were described recently. Moreover, the finding of super-integrons with gene-cassettes coding for other determinants (biochemical functions, virulence factors) in Vibrio isolates dating from 1888 suggests the likely implication of: this multicomponent cassette-integron system in bacterial genome evolution before the antibiotic era and to a greater extent than initially believed.
引用
收藏
页码:483 / 487
页数:5
相关论文
共 28 条
[1]   A NOVEL INTEGRON-LIKE ELEMENT CARRYING THE METALLO-BETA-LACTAMASE GENE BLA(IMP) [J].
ARAKAWA, Y ;
MURAKAMI, M ;
SUZUKI, K ;
ITO, H ;
WACHAROTAYANKUN, R ;
OHSUKA, S ;
KATO, N ;
OHTA, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (07) :1612-1615
[2]   CHARACTERIZATION OF THE NONENZYMATIC CHLORAMPHENICOL RESISTANCE (CMLA) GENE OF THE IN4 INTEGRON OF TN1696 - SIMILARITY OF THE PRODUCT TO TRANSMEMBRANE TRANSPORT PROTEINS [J].
BISSONNETTE, L ;
CHAMPETIER, S ;
BUISSON, JP ;
ROY, PH .
JOURNAL OF BACTERIOLOGY, 1991, 173 (14) :4493-4502
[3]   The integrons In0, In2, and In5 are defective transposon derivatives [J].
Brown, HJ ;
Stokes, HW ;
Hall, RM .
JOURNAL OF BACTERIOLOGY, 1996, 178 (15) :4429-4437
[4]   Extended-spectrum β-lactamase-producing strain of Acinetobacter baumannii isolated from a patient in France [J].
Poirel, L ;
Karim, A ;
Mercat, A ;
Le Thomas, I ;
Vahaboglu, H ;
Richard, C ;
Nordmann, P .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 43 (01) :157-158
[5]   EXPRESSION OF ANTIBIOTIC-RESISTANCE GENES IN THE INTEGRATED CASSETTES OF INTEGRONS [J].
COLLIS, CM ;
HALL, RM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (01) :155-162
[6]   GENE CASSETTES FROM THE INSERT REGION OF INTEGRONS ARE EXCISED AS COVALENTLY CLOSED CIRCLES [J].
COLLIS, CM ;
HALL, RM .
MOLECULAR MICROBIOLOGY, 1992, 6 (19) :2875-2885
[7]   SITE-SPECIFIC DELETION AND REARRANGEMENT OF INTEGRON INSERT GENES CATALYZED BY THE INTEGRON DNA INTEGRASE [J].
COLLIS, CM ;
HALL, RM .
JOURNAL OF BACTERIOLOGY, 1992, 174 (05) :1574-1585
[8]   Cholera in Vietnam:: Changes in genotypes and emergence of class I integrons containing aminoglycoside resistance gene cassettes in Vibrio cholerae O1 strains isolated from 1979 to 1996 [J].
Dalsgaard, A ;
Forslund, A ;
Tam, NV ;
Vinh, DX ;
Cam, PD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (03) :734-741
[9]   INACTIVATION OF ANTIBIOTICS AND THE DISSEMINATION OF RESISTANCE GENES [J].
DAVIES, J .
SCIENCE, 1994, 264 (5157) :375-382
[10]   SECONDARY SITES FOR INTEGRATION MEDIATED BY THE TN21 INTEGRASE [J].
FRANCIA, MV ;
DELACRUZ, F ;
LOBO, JMG .
MOLECULAR MICROBIOLOGY, 1993, 10 (04) :823-828