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Phenotypic and genotypic characterization of Enterococcus spp. from yolk sac infections in broiler chicks with a focus on virulence factors

机译:肠球菌SPP的表型和基因型表征。从肉鸡小鸡中的卵黄囊感染重点是毒力因子

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摘要

Bacterial infections of yolk sacs contribute to increased mortality of chicks, chronic infections during their rearing, or increased selection in the flock, which in turn leads to high economic losses in poultry production worldwide. The aim of this study was a phenotypic and genotypic characterization of enterococci isolated from yolk sac infections (YSI) of broiler chickens from Poland and the Netherlands. Biochemical, matrix-assisted laser desorption/ionization (MALDI)–time-of-flight (TOF) MS, and rpoA gene sequencing identification was performed. Moreover, phenotypic and genotypic characterization of virulence factors and analysis of the clonal relationship of isolates by MALDI-TOF MS and enterobacterial repetitive intergenic consensus—polymerase chain reaction (ERIC-PCR) were performed. The biochemical test identified 70 isolates as Enterococcus faecalis and 6 as Enterococcus mundtii. The results of MALDI-TOF MS were 100% concordant with those obtained by rpoA gene sequencing, and all 76 isolates were identified as E. faecalis. Differences were noted in the β-glucuronidase, β-glucosidase, α-galactosidase, phosphatase, melibiose, lactose, and raffinose tests that is going about the results of biochemical identification. None of the isolates were beta-hemolytic on blood agar in aerobic conditions, but all but one were gelatinase positive. Among biofilm-forming isolates (30/76; 39.5%), as many as 66.7% (20/30) were Polish E. faecalis strains. Most of the isolates carried virulence genes, that is gelE, ace, asa1, efaAfs, fsrA, fsrB, fsrC, cob, cpd, and ccf, but none had the hyl gene. Some isolates harbored cyl operon genes. One Polish strain (ST16) had all of the tested cyl genes and the esp gene, considered clinically important, and showed the highest biofilm-forming ability. Nearly 50% of the isolates showed close genetic relatedness in ERIC typing. In contrast with MALDI-TOF MS cluster analysis, ERIC-PCR results did not show a relationship with the origin of the strains. Using MALDI-TOF MS, 7 peaks were found in Polish and Dutch isolates, which may type them as species-specific biomarkers in E. faecalis from YSI.
机译:卵黄囊的细菌感染他们饲养过程中造成的小鸡,慢性感染的死亡率增加,或增加羊群选择,而这又导致家禽生产全球高昂的经济损失。本研究的目的是表型和肠球菌从波兰和荷兰肉鸡的卵黄囊感染(YSI)分离的基因型表征。进行生化,基质辅助激光解吸/电离(MALDI)-time飞行(TOF)MS和RPOA基因测序鉴定。此外,进行的毒力因子,并通过MALDI-TOF MS和肠细菌间重复一致 - 聚合酶链反应(ERIC-PCR)分离株的克隆关系的分析表型和基因型特征。生物化学试验identi音响编70个分离株如粪肠球菌和6作为肠球菌mundtii。 MALDI-TOF MS的结果分别为100%一致与由RPOA基因测序获得的那些,并且所有76株被鉴定为粪肠球菌。差异在β葡糖苷酸酶,β葡糖苷酶,α半乳糖苷酶,磷酸酶,蜜二糖,乳糖,和打算约的生化鉴定结果棉子糖试验指出。分离株中没有一个对血液的β-溶血性琼脂在有氧条件下,但所有,但一个是明胶酶阳性。中形成生物膜的分离株(76分之30; 39.5%),多达66.7%(20/30)是波兰粪肠球菌菌株。大多数致病基因携带的菌株,即歌乐山,王牌,ASA1,efaAfs的FSRA,fsrB,金管会,COB,CPD和CCF,但什么都没有了HYL基因。有些菌株窝藏缸操纵子的基因。一个波兰株(ST16)把所有的测试共青团基因和ESP基因,认为是临床上重要的,显示出最高的生物膜形成能力。该菌株的近50%,表明在ERIC打字密切遗传相关。与MALDI-TOF MS聚类分析对比度,ERIC-PCR结果没有显示出与菌株的原点的关系。使用MALDI-TOF MS,7个峰波兰和荷兰分离物中发现,其可以输入它们在大肠杆菌物种特异性生物标志物从粪YSI。

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