1 Division of Veterinary Public Health, ICAR-Indian Veterinary Research Institute, Izatnagar, India.
2 ICAR-National Research Centre on Meat, Hyderabad, India.
Foodborne Pathog Dis. 2019 Mar;16(3):214-220. doi: 10.1089/fpd.2018.2494. Epub 2019 Jan 11.
The occurrence of Listeria monocytogenes was studied by using cultural and serological methods in cattle housed in a particular gaushala (cattle shelter) and organized dairy farm.
A total of 1201 samples from cattle comprising blood (n = 207), milk (n = 203), vaginal swabs (n = 210), and serum (n = 207) from an organized farm (n = 210) and blood (n = 100), milk (n = 74), vaginal swabs (n = 100), and serum (n = 100) from a gaushala (n = 100) were collected and analyzed for L. monocytogenes. All samples excluding serum were analyzed for isolation and identification of L. monocytogenes, while the serum samples were screened for seropositivity. The isolates were further subjected to assess their virulence potential (in vitro and in vivo), biofilm formation ability, and antibiotic susceptibility patterns.
Four L. monocytogenes strains were isolated from the cattle; three (0.48%) from the organized farm and one (0.36%) from the gaushala. On serological screening of cattle from the organized dairy farm, 16.42% were found to be positive for antibodies against listeriolysin O, while cattle from the gaushala revealed 36% seropositivity. Furthermore, on characterization of the isolates for their pathogenic potential and biofilm-forming ability, all were found to be pathogenic by both in vitro and in vivo assays and were weak to moderate biofilm formers. The minimum inhibition concentration (MIC) of recovered isolates revealed resistance for ampicillin by two L. monocytogenes isolates (MIC >256 μg/mL), whereas three L. monocytogenes isolates were intermediately resistant (MIC >4 μg/mL) and one resistant against amoxicillin (MIC >8 μg/mL). However, all four isolates were susceptible to gentamicin, cotrimoxazole, and erythromycin.
Isolation of virulent and antibiotic-resistant strains of L. monocytogenes warrants the need for epidemiological surveillance, antimicrobial susceptibility, and implementation of control measures to combat the occurrence of L. monocytogenes infection in animals as well as humans.
使用文化和血清学方法研究了特定的牛棚(牛舍)和组织奶牛场中李斯特菌的发生情况。
共采集了来自组织农场(n=210)和牛棚(n=100)的 1201 份牛样本,包括血液(n=207)、牛奶(n=203)、阴道拭子(n=210)和血清(n=207),血液(n=100)、牛奶(n=74)、阴道拭子(n=100)和血清(n=100)。分析所有样本(血清除外)以分离和鉴定李斯特菌,而血清样本则用于检测血清阳性。进一步对分离株进行评估,以确定其毒力潜力(体外和体内)、生物膜形成能力和抗生素敏感性模式。
从牛中分离出 4 株李斯特菌,其中 3 株(0.48%)来自组织农场,1 株(0.36%)来自牛棚。在对组织奶牛场的牛进行血清学筛查时,发现 16.42%的牛对李斯特菌溶血素 O 的抗体呈阳性,而来自牛棚的牛的血清阳性率为 36%。此外,在对分离株的致病性和生物膜形成能力进行特征分析时,所有分离株均通过体外和体内试验被证明具有致病性,且均为弱至中度生物膜形成者。回收分离株的最小抑菌浓度(MIC)显示,2 株李斯特菌对氨苄西林的耐药性(MIC>256μg/mL),而 3 株李斯特菌对氨苄西林中度耐药(MIC>4μg/mL),1 株对阿莫西林耐药(MIC>8μg/mL)。然而,所有 4 株分离株均对庆大霉素、复方新诺明和红霉素敏感。
分离出的李斯特菌毒力强且对抗生素耐药,这就需要进行流行病学监测、抗生素敏感性检测以及实施控制措施,以防治动物和人类李斯特菌感染的发生。