Nayak R, Stewart T, Wang R-F, Lin J, Cerniglia C E, Kenney P B
Division of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR 72079, USA.
Int J Food Microbiol. 2004 Feb 15;91(1):51-62. doi: 10.1016/S0168-1605(03)00330-1.
This study evaluated the molecular diversity of 29 Salmonella serotypes isolated from turkey ceca and the production environment. Isolates were resistant to bacitracin (100%), erythromycin (100%), novobiocin (100%), rifampin (100%), streptomycin (62%), gentamicin (52%), spectinomycin (48%), tetracycline (31%), sulfamethoxazole/trimethoprim (SXT) (3%) and tobramycin (3%). The minimum inhibitory concentration (MIC) values ranged from 32 to >/=1024 microg/ml. The pulsed-field gel electrophoresis (PFGE) and ribotyping patterns were identical within each of the serotypes Heidelberg, Worthington and Muenster. The plasmid profiles were identical within each of the Salmonella serotypes. Two different clones of Salmonella anatum were differentiated by PFGE typing but not by ribotyping. Heidelberg isolates from nine turkey ceca and three drinker samples had identical antibiotic resistance, PFGE, ribotype and plasmid patterns, suggesting that transmission of this particular clone may have occurred between the birds and the drinkers. Identical PFGE, ribotype and plasmid patterns were observed in one Salmonella worthington isolate from turkey ceca in one flock and two S. worthington isolates from feeder contents and drinkers from a subsequent flock, suggesting transmission of this pathogen between flocks. Individual and multiple polymerase chain reaction (PCR) analyses revealed the presence of the virulence genes invA, aceK and sopB and the absence of the h-1i gene in all isolates. A combination of genotypic and phenotypic markers can be useful in studying genetic variation among natural salmonellae populations in turkey production and delineating possible transmission pathways.
本研究评估了从火鸡盲肠和生产环境中分离出的29种沙门氏菌血清型的分子多样性。分离菌株对杆菌肽(100%)、红霉素(100%)、新生霉素(100%)、利福平(100%)、链霉素(62%)、庆大霉素(52%)、壮观霉素(48%)、四环素(31%)、磺胺甲恶唑/甲氧苄啶(SXT)(3%)和妥布霉素(3%)耐药。最低抑菌浓度(MIC)值范围为32至≥1024微克/毫升。在海德堡、沃辛顿和明斯特血清型的每一种内,脉冲场凝胶电泳(PFGE)和核糖体分型图谱均相同。沙门氏菌各血清型内的质粒图谱相同。通过PFGE分型可区分出两种不同的鸭沙门氏菌克隆,但核糖体分型无法区分。来自9个火鸡盲肠和3个饮水器样本的海德堡分离株具有相同的抗生素耐药性、PFGE、核糖体分型和质粒图谱,这表明该特定克隆可能在禽类和饮水器之间发生了传播。在一个鸡群的火鸡盲肠中分离出的一株沃辛顿沙门氏菌与后续鸡群的饲料和饮水器中分离出的两株沃辛顿沙门氏菌观察到相同的PFGE、核糖体分型和质粒图谱,这表明该病原体在鸡群之间发生了传播。单独和多重聚合酶链反应(PCR)分析显示,所有分离株中均存在毒力基因invA、aceK和sopB,且不存在h-1i基因。基因型和表型标记的组合有助于研究火鸡生产中自然沙门氏菌种群的遗传变异,并描绘可能的传播途径。