Comparison of gyrA mutations, cyclohexane resistance, and the presence of class I integrons in Salmonella enterica from farm animals in England and Wales

被引:51
作者
Liebana, E
Clouting, C
Cassar, CA
Randall, LP
Walker, RA
Threlfall, EJ
Clifton-Hadley, FA
Ridley, AM
机构
[1] Vet Labs Agcy Weybridge, Dept Bacterial Dis, Addlestone KT15 3NB, Surrey, England
[2] Cent Publ Hlth Lab, Lab Enter Pathogens, London NW9 5HT, England
关键词
D O I
10.1128/JCM.40.4.1481-1486.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This study is focused on real-time detection of gyrA mutations and of the presence of class I integrons in a panel of 100 veterinary isolates of Salmonella enterica from farm animals. The isolates were selected on the basis of resistance to nalidixic acid, representing a variety of the most prevalent serotypes in England and Wales. In addition, organic solvent (cyclohexane) resistance in these isolates was investigated in an attempt to elucidate the presence of efflux pump mechanisms. The most prevalent mutation among the isolates studied was Asp87-Asn (n = 42), followed by Ser83-Phe (n = 38), Ser83-Tyr (n = 12), Asp87-Tyr (n = 4), and Asp87-Gly (n = 3). Two distinct subpopulations were identified, separated at the 1-mg/liter breakpoint for ciprofloxacin: 86% of isolates with mutations in codon 83 showed MICs of greater than or equal to1 mg/liter, while 89.8% of isolates with mutations in codon 87 presented MICs of less than or equal to0.5 mg/liter. Cyclohexane resistance was more prevalent among Ser83 mutants than among Asp87 mutants (34.7 and 4%, respectively), and in 79% of isolates that presented both gyrA mutations and cyclohexane resistance, the level of ciprofloxacin resistance was greater than or equal to2.0 mg/liter. Thirty-four isolates contained class I integrons, with 71% of the S. enterica serovar Typhimurium isolates and 6.9% of isolates belonging to other serotypes containing such elements. The methods used represent sensitive ways of investigating the presence of gyrA mutations and of detecting class-I integrons in Salmonella isolates. The results can be obtained in less than 1 h from single colonies without the need for purifying DNA.
引用
收藏
页码:1481 / 1486
页数:6
相关论文
共 34 条
[1]   Organic solvent tolerance and antibiotic resistance increased by overexpression of marA in Escherichia coli [J].
Asako, H ;
Nakajima, H ;
Kobayashi, K ;
Kobayashi, M ;
Aono, R .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (04) :1428-1433
[2]  
Asako H, 1999, APPL ENVIRON MICROB, V65, P294
[3]   Preventing antibiotic resistance through rapid genotypic identification of bacteria and of their antibiotic resistance genes in the clinical microbiology laboratory [J].
Bergeron, MG ;
Ouellette, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (08) :2169-2172
[4]  
Cambau E, 1993, Drugs, V45 Suppl 3, P15
[5]   Nalidixic acid resistance in salmonellae isolated from turkeys and other livestock in Great Britain [J].
Davies, RH ;
Teale, CJ ;
Wray, C ;
McLaren, IH ;
Jones, YE ;
Chappell, S ;
Kidd, S .
VETERINARY RECORD, 1999, 144 (12) :320-322
[6]  
EVANS S, 1999, SALMONELLA LIVESTOCK, P127
[7]   AMPLIFIABLE RESISTANCE TO TETRACYCLINE, CHLORAMPHENICOL, AND OTHER ANTIBIOTICS IN ESCHERICHIA-COLI - INVOLVEMENT OF A NONPLASMID-DETERMINED EFFLUX OF TETRACYCLINE [J].
GEORGE, AM ;
LEVY, SB .
JOURNAL OF BACTERIOLOGY, 1983, 155 (02) :531-540
[8]   Comparative studies of mutations in animal isolates and experimental in vitro- and in vivo-selected mutants of Salmonella spp. suggest a counterselection of highly fluoroquinolone-resistant strains in the field [J].
Giraud, E ;
Brisabois, A ;
Martel, JL ;
Chaslus-Dancla, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (09) :2131-2137
[9]   Evidence for active efflux as the primary mechanism of resistance to ciprofloxacin in Salmonella enterica serovar typhimurium [J].
Giraud, E ;
Cloeckaert, A ;
Kerboeuf, D ;
Chaslus-Dancla, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (05) :1223-1228
[10]   Mutations in gyrA gene of quinolone-resistant Salmonella serotypes isolated from humans and animals [J].
Griggs, DJ ;
Gensberg, K ;
Piddock, LJV .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (04) :1009-1013