Wonderling Laura, Pearce Rachel, Wallace F Morgan, Call Jeffrey E, Feder Ingrid, Tamplin Mark, Luchansky John B
Eastern Regional Research Center, Agricultural Research Service, U.S. Department of Agriculture, 600 E. Mermaid Lane, Wyndmoor, PA 19038, USA.
Appl Environ Microbiol. 2003 Jul;69(7):4177-82. doi: 10.1128/AEM.69.7.4177-4182.2003.
Salmonella enterica isolates were recovered from swine at a collaborating processing plant over a 2-month period in the spring of 2000. In the present study, molecular subtyping by pulsed-field gel electrophoresis (PFGE) was performed on the 581 confirmed Salmonella isolates from the 84 Salmonella-positive samples obtained from the previous study. A total of 32 different PFGE pulsotypes were observed visually, and a BioNumerics software analysis clustered those pulsotypes into 12 PFGE groups. The B, F, and G groups predominated throughout the sampling period and were isolated from 39, 22, and 13% of the swine, respectively. In addition, multiple isolates were obtained from 67 of the 84 Salmonella-positive samples, and subtyping revealed multiple PFGE profiles in 35 of these 67 (62%) samples. Both carcass and fecal isolates of Salmonella were recovered from 13 swine, resulting in "matched" samples. Molecular typing of the 252 isolates recovered from the matched samples revealed that 7 (54%) of the 13 carcasses were contaminated with Salmonella pulsotypes that were not isolated from the feces of the same animal. Conversely, from 6 of the 13 (46%) matched animals, Salmonella clonal types were isolated from the feces that were not isolated from the carcass of the same animal. These data establish that each lot of swine introduces new contaminants into the plant environment and that swine feces from one animal can contaminate many carcasses. In addition, these results indicate that the examination of multiple Salmonella isolates from positive samples is necessary to determine the variety of potential contaminants of swine carcasses during slaughter and processing.
2000年春季,在一家合作加工厂的猪群中,在两个月的时间里分离出了肠炎沙门氏菌。在本研究中,对先前研究中从84份沙门氏菌阳性样本中获得的581株确诊沙门氏菌分离株进行了脉冲场凝胶电泳(PFGE)分子分型。通过肉眼观察,共观察到32种不同的PFGE脉冲型,BioNumerics软件分析将这些脉冲型聚类为12个PFGE组。B、F和G组在整个采样期间占主导地位,分别从39%、22%和13%的猪中分离得到。此外,在84份沙门氏菌阳性样本中的67份中获得了多个分离株,亚型分析显示在这67份样本中的35份(62%)中存在多种PFGE图谱。从13头猪中同时分离出了沙门氏菌的胴体和粪便分离株,从而得到了“匹配”样本。对从匹配样本中回收的252株分离株进行分子分型显示,13头胴体中有7头(54%)被沙门氏菌脉冲型污染,而这些脉冲型未从同一动物的粪便中分离出来。相反,在13头匹配动物中的6头(46%)中,从粪便中分离出的沙门氏菌克隆型未从同一动物的胴体中分离出来。这些数据表明,每批猪都会将新的污染物引入工厂环境,并且一只动物的猪粪便可以污染许多胴体。此外,这些结果表明,对阳性样本中的多个沙门氏菌分离株进行检测对于确定屠宰和加工过程中猪胴体潜在污染物的种类是必要的。