首页> 外文期刊>Acta Veterinaria Hungarica >PHENOTYPING AND GENOTYPING OF STREPTOCOCCI IN BOVINE MILK IN ARGENTINEAN DAIRY HERDS
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PHENOTYPING AND GENOTYPING OF STREPTOCOCCI IN BOVINE MILK IN ARGENTINEAN DAIRY HERDS

机译:阿根廷奶牛场牛乳中链球菌的表型和基因分型

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Most veterinary and milk hygiene laboratories identify streptococci and enterococci based on serological and biochemical tests. The analysis of 16S rDNA was suggested to be used for more exact identification; however, its use has not been considered so far in monitoring studies. The objective of the present study was to compare a conventional phenotypic method with restriction fragment length polymorphism analysis of 16S rDNA (16S rDNA RFLP) for identification of streptococci isolated from composite milk samples collected in connection with intramammary infection (IMI) in six Argentinean dairy farms. Composite milk samples (n = 1223) from cows belonging to six herds were collected for bacteriological analysis. Twelve reference strains and fifty streptococci or streptococcus-like isolates were identified to species level by the API 20 Strep system, conventional biochemical tests and 16S rDNA RFLP in a blind assay. The remaining streptococci or streptococcus-like isolates (n = 40) were identified to the species level both by 16S rDNA RFLP and conventional biochemical tests. As indicated by Kappa values, agreement between the 16S rDNA RFLP and the conventional scheme for identification of Streptococcus agalactiae, S. dysgalactiae, S. uberis, S. equinus and Enterococcus faecalis was 0.91, 0.73, 0.92, 0.81 and 0.85, respectively. Together with the less frequently isolated streptococcal species, the conventional scheme correctly identified 77 out of 90 isolates (85.5%). Thus, the use of 16S rDNA RFLP is considered valuable for monitoring studies due to its affordable cost for standard laboratories.
机译:大多数兽医和牛奶卫生实验室根据血清学和生化测试来鉴定链球菌和肠球菌。建议将16S rDNA分析用于更准确的鉴定。但是,到目前为止,在监测研究中尚未考虑使用它。本研究的目的是将常规表型方法与16S rDNA的限制性片段长度多态性分析(16S rDNA RFLP)进行比较,以鉴定从六个阿根廷奶牛场与乳房内感染(IMI)相关的复合牛奶样品中分离的链球菌。收集来自六个牛群的奶牛的复合乳样品(n = 1223)进行细菌学分析。通过API 20 Strep系统,常规生化测试和16S rDNA RFLP在盲法测定中鉴定出十二种参考菌株和五十种链球菌或类链球菌样分离株。通过16S rDNA RFLP和常规生化测试,将剩余的链球菌或类链球菌分离物(n = 40)鉴定到物种水平。如Kappa值所示,16S rDNA RFLP与鉴定无乳链球菌,痢疾链球菌,乳房链球菌,马齿链球菌和粪肠球菌的常规方案之​​间的一致性分别为0.91、0.73、0.92、0.81和0.85。常规方案与较少分离的链球菌一起,可正确鉴定出90种分离物中的77种(85.5%)。因此,由于16S rDNA RFLP对于标准实验室来说价格可承受,因此被认为对监测研究有价值。

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