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The use of PCR for the identification and characterisation of bacteriocin genes from bacterial strains isolated from rumen or caecal contents of cattle and sheep

机译:PCR在鉴定和表征牛和绵羊瘤胃或盲肠内容物中分离的细菌菌株中细菌素基因的应用

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PCR primers were designed to amplify the gene that encodes bovicin 255 from Streptococcus gallolyticus LRC0255 and the bacteriocin genes from Butyrivibrio fibrisolvens strains AR10 and OR79A (bviD and bvi79A) in order to screen for their incidence in rumen and caecal B. fibrisolvens and Streptococcus bovis-like isolates from New Zealand and North American ruminants. None of the B. fibrisolvens-like strains (n = 34) isolated from New Zealand or North America had the genes encoding for butyrivibriocins AR10 (bviD) or OR79 (bvi79A). However, seven S. bovis isolates from New Zealand ruminants and three from North American animals had the bovicin 255 gene. Sequence comparison of cloned bovicin 255 PCR products indicated a 92.9-95.7% similarity to that of the corresponding bovicin 255 gene sequence of S. gallolyticus. Four of the New Zealand bovicin 255 positive S. bovis isolates were from the caecal contents of the same sheep and had identical PFGE profiles. Two other S. bovis isolates sharing the same PFGE profile were isolated from a separate animal from the same flock. PFGE analysis of the North American strains indicated that all three were closely related as two of three had identical PFGE profiles with the remaining isolate differing only by a single band position. The 16S rRNA gene sequences of the 10 isolates were at least 99.8% identical to S. bovis. All 10 S. bovis isolates having the gene for bovicin 255 produced bacteriocin activity that inhibited the growth of Peptostreptococcus anaerobius D1 in a deferred antagonism plating (DAP) assay. Certain S. bovis isolates obtained from ruminants have bacteriocin activity associated with a distinct bovicin 255 gene sequence but it appears that bacteriocin production by the rumen anaerobe B. fibrisolvens may be uncommon in strains isolated from cattle and sheep in New Zealand. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
机译:设计PCR引物以扩增来自解毒链球菌LRC0255的鲍维菌素255的基因和来自纤维溶解丁酸弧菌AR10和OR79A的细菌素基因(bviD和bvi79A),以筛选它们在瘤胃和盲肠弯曲杆菌中的发生率。如来自新西兰和北美反刍动物的分离株。从新西兰或北美分离出的B. fibrisolvens样菌株(n = 34)均没有编码丁酸新霉素AR10(bviD)或OR79(bvi79A)的基因。然而,来自新西兰反刍动物的7个牛链球菌分离株和来自北美动物的3个牛分离株具有bovicin 255基因。克隆的鲍维菌素255 PCR产物的序列比较表明,与解毒链球菌的相应鲍维菌素255基因序列具有92.9-95.7%的相似性。新西兰bovicin 255阳性葡萄球菌的四株来自同一只绵羊的盲肠内容物,并且具有相同的PFGE图谱。从同一羊群的另一只动物中分离出具有相同PFGE谱的另外两个牛链球菌。北美菌株的PFGE分析表明,所有三个菌株都密切相关,因为三个菌株中的两个具有相同的PFGE图谱,其余分离株仅在单个条带位置上存在差异。 10个分离株的16S rRNA基因序列与牛链球菌至少99.8%相同。在延缓拮抗作用平板(DAP)分析中,所有具有鲍维霉素255基因的10株牛链球菌都产生了细菌素活性,抑制了厌氧消化链球菌D1的生长。从反刍动物获得的某些牛链球菌分离物具有与独特的bovicin 255基因序列相关的细菌素活性,但似乎在新西兰牛和绵羊分离的菌株中,瘤胃厌氧杆菌纤维状解纤菌产生细菌素的情况并不常见。 (C)2004年欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。

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