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Characterization of Salmonella enterica Serotype Newport Isolated from Humans and Food Animals

机译:从人类和食用动物中分离出沙门氏菌血清型新港的特征

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摘要

Salmonella enterica serotype Newport isolates resistant to at least nine antimicrobials (including extended-spectrum cephalosporins), known as serotype Newport MDR-AmpC isolates, have been rapidly emerging as pathogens in both animals and humans throughout the United States. Resistance to extended-spectrum cephalosporins is associated with clinical failures, including death, in patients with systemic infections. In this study, 87 Salmonella serotype Newport strains were characterized by pulsed-field gel electrophoresis (PFGE) and antimicrobial susceptibility testing and examined for the presence of class 1 integrons and blaCMY genes. Thirty-five PFGE patterns were observed with XbaI, and three of these patterns were indistinguishable among isolates from humans and animals. Fifty-three (60%) Salmonella serotype Newport isolates were identified as serotype Newport MDR-AmpC, including 16 (53%) of 30 human isolates, 27 (93%) of 29 cattle isolates, 7 (70%) of 10 swine isolates, and 3 (30%) of 10 chicken isolates. However, 28 (32%) Salmonella serotype Newport isolates were susceptible to all 16 antimicrobials tested. The blaCMY gene was present in all serotype Newport MDR-AmpC isolates. Furthermore, the plasmid-mediated blaCMY gene was transferable via conjugation to an Escherichia coli strain. The transconjugant showed the MDR-AmpC resistance profile. Thirty-five (40%) of the isolates possessed class 1 integrons. Sequence analyses of the integrons showed that they contained aadA, which confers resistance to streptomycin, or aadA and dhfr, which confer resistance to trimethoprim-sulfamethoxazole. One integron from a swine isolate contained the sat-1 gene, which encodes resistance to streptothricin, an antimicrobial agent that has never been approved for use in the United States. In conclusion, Salmonella serotype Newport MDR-AmpC was commonly identified among Salmonella serotype Newport isolates recovered from humans and food animals. These findings support the possibility of transmission of this organism to humans through the food chain.
机译:沙门氏菌血清型纽波特分离株对至少九种抗微生物剂(包括广谱头孢菌素)耐药,被称为血清型纽波特MDR-AmpC分离株,已在美国和美国迅速成为动物和人类的病原体。全身感染患者对广谱头孢菌素的耐药性与包括死亡在内的临床失败有关。在这项研究中,通过脉冲场凝胶电泳(PFGE)和抗菌药敏试验对87株沙门氏菌血清型Newport菌株进行了表征,并检查了1类整合素和blaCMY基因的存在。用XbaI观察到了35种PFGE模式,其中三种模式在人和动物的分离株中没有区别。已鉴定出53株(60%)沙门氏菌血清型Newport分离株为纽波特MDR-AmpC血清型,包括30株人类分离株中的16株(53%),29株牛分离株中的27株(93%),10株猪分离物中的7株(70%) ,以及10株鸡中的3株(占30%)。但是,有28种(32%)血清型纽波特沙门氏菌对所有16种抗微生物药敏感。 blaCMY基因存在于所有血清型的纽波特MDR-AmpC分离株中。此外,质粒介导的blaCMY基因可通过缀合转移至大肠杆菌菌株。转导结合剂显示出MDR-AmpC的抗性曲线。分离物中的三十五(40%)个具有1类整合素。整合素的序列分析表明它们含有aadA,赋予对链霉素的抗性,或aadA和dhfr,赋予对甲氧苄氨嘧啶-磺胺甲恶唑的抗性。来自猪分离株的一个整合子含有sat-1基因,该基因编码对链霉菌素的抗药性,该药从未在美国获准使用。总之,沙门氏菌血清型纽波特MDR-AmpC通常在从人类和食用动物中回收的沙门氏菌血清型纽波特分离株中被鉴定。这些发现支持了这种生物通过食物链传播给人类的可能性。

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