Paillard D, McKain N, Rincon M T, Shingfield K J, Givens D I, Wallace R J
Rowett Research Institute, Aberdeen, UK.
J Appl Microbiol. 2007 Oct;103(4):1251-61. doi: 10.1111/j.1365-2672.2007.03349.x.
All members of the ruminal Butyrivibrio group convert linoleic acid (cis-9,cis-12-18:2) via conjugated 18:2 metabolites (mainly cis-9,trans-11-18:2, conjugated linoleic acid) to vaccenic acid (trans-11-18:1), but only members of a small branch, which includes Clostridium proteoclasticum, of this heterogeneous group further reduce vaccenic acid to stearic acid (18:0, SA). The aims of this study were to develop a real-time polymerase chain reaction (PCR) assay that would detect and quantify these key SA producers and to use this method to detect diet-associated changes in their populations in ruminal digesta of lactating cows.
The use of primers targeting the 16S rRNA gene of Cl. proteoclasticum was not sufficiently specific when only binding dyes were used for detection in real-time PCR. Their sequences were too similar to some nonproducing strains. A molecular beacon probe was designed specifically to detect and quantify the 16S rRNA genes of the Cl. proteoclasticum subgroup. The probe was characterized by its melting curve and validated using five SA-producing and ten nonproducing Butyrivibrio-like strains and 13 other common ruminal bacteria. Analysis of ruminal digesta collected from dairy cows fed different proportions of starch and fibre indicated a Cl. proteoclasticum population of 2-9% of the eubacterial community. The influence of diet on numbers of these bacteria was less than variations between individual cows.
A molecular beacon approach in qPCR enables the detection of Cl. proteoclasticum in ruminal digesta. Their numbers are highly variable between individual animals.
SA producers are fundamental to the flow of polyunsaturated fatty acid and vaccenic acid from the rumen. The method described here enabled preliminary information to be obtained about the size of this population. Further application of the method to digesta samples from cows fed diets of more variable composition should enable us to understand how to control these bacteria in order to enhance the nutritional characteristics of ruminant-derived foods, including milk and beef.
瘤胃丁酸弧菌属的所有成员都能将亚油酸(顺式-9,顺式-12-18:2)通过共轭18:2代谢物(主要是顺式-9,反式-11-18:2,共轭亚油酸)转化为vaccenic酸(反式-11-18:1),但在这个异质菌群中,只有包括解蛋白质梭菌在内的一个小分支的成员能进一步将vaccenic酸还原为硬脂酸(18:0,SA)。本研究的目的是开发一种实时聚合酶链反应(PCR)检测方法,用于检测和定量这些关键的SA产生菌,并使用该方法检测泌乳奶牛瘤胃消化物中与饮食相关的这些菌数量的变化。
当在实时PCR中仅使用结合染料进行检测时,针对解蛋白质梭菌16S rRNA基因的引物特异性不足。它们的序列与一些不产生SA的菌株过于相似。设计了一种分子信标探针,专门用于检测和解蛋白质梭菌亚群16S rRNA基因的定量。该探针通过熔解曲线进行表征,并使用5株产生SA的和10株不产生SA的类丁酸弧菌菌株以及13种其他常见瘤胃细菌进行了验证。对饲喂不同淀粉和纤维比例的奶牛收集的瘤胃消化物进行分析表明,解蛋白质梭菌数量占真细菌群落的2%-9%。饮食对这些细菌数量的影响小于个体奶牛之间的差异。
实时定量PCR中的分子信标方法能够检测瘤胃消化物中的解蛋白质梭菌。它们的数量在个体动物之间差异很大。
SA产生菌对于瘤胃中多不饱和脂肪酸和vaccenic酸的流动至关重要。这里描述的方法能够获得有关该菌群大小的初步信息。将该方法进一步应用于饲喂成分更具变化性日粮的奶牛的消化物样本,应该能使我们了解如何控制这些细菌,以提高反刍动物源性食品(包括牛奶和牛肉)的营养特性。