Song Jaeyong, Choi Hyuck, Jeong Jin Young, Lee Seul, Lee Hyun Jung, Baek Youlchang, Ji Sang Yun, Kim Minseok
Animal Nutrition and Physiology Team, National Institute of Animal science, Rural Development Administration, Wanju 55365, Republic of Korea.
Department of Pet Science, Seojeong College, Yangju 11429, Republic of Korea.
J Microbiol Biotechnol. 2018 Oct 28;28(10):1700-1705. doi: 10.4014/jmb.1803.03002.
We evaluated the influence of sampling technique (cannulation vs. stomach tube) and site (dorsal sac vs. ventral sac) on the rumen microbiome and fermentation parameters in Hanwoo steers. Rumen samples were collected from three cannulated Hanwoo steers via both a stomach tube and cannulation, and 16S rRNA gene amplicons were sequenced on the MiSeq platform to investigate the rumen microbiome composition among samples obtained via 1) the stomach tube, 2) dorsal sac via rumen cannulation, and 3) ventral sac via rumen cannulation. A total of 722,001 high-quality 16S rRNA gene sequences were obtained from the three groups and subjected to phylogenetic analysis. There was no significant difference in the composition of the major taxa or alpha diversity among the three groups (> 0.05). Bacteroidetes and Firmicutes represented the first and second most dominant phyla, respectively, and their abundances did not differ among the three groups (> 0.05). Beta diversity principal coordinate analysis also did not separate the rumen microbiome based on the three sample groups. Moreover, there was no effect of sampling site or method on fermentation parameters, including pH and volatile fatty acids ( > 0.05). Overall, this study demonstrates that the rumen microbiome and fermentation parameters are not affected by different sampling techniques and sampling sites. Therefore, a stomach tube can be a feasible alternative method to collect representative rumen samples rather than the standard and more invasive method of rumen cannulation in Hanwoo steers.
我们评估了采样技术(插管法与胃管法)和采样部位(背囊与腹囊)对韩牛阉牛瘤胃微生物群和发酵参数的影响。通过胃管和插管法从三头装有瘤胃插管的韩牛阉牛采集瘤胃样本,并在MiSeq平台上对16S rRNA基因扩增子进行测序,以研究通过以下方式获得的样本间的瘤胃微生物群组成:1)胃管;2)通过瘤胃插管采集的背囊;3)通过瘤胃插管采集的腹囊。从三组样本中总共获得了722,001条高质量的16S rRNA基因序列,并进行了系统发育分析。三组之间主要分类群的组成或α多样性没有显著差异(>0.05)。拟杆菌门和厚壁菌门分别是最主要的第一和第二优势菌门,它们在三组中的丰度没有差异(>0.05)。β多样性主坐标分析也没有根据三个样本组区分瘤胃微生物群。此外,采样部位或方法对包括pH值和挥发性脂肪酸在内的发酵参数没有影响(>0.05)。总体而言,本研究表明瘤胃微生物群和发酵参数不受不同采样技术和采样部位的影响。因此,对于韩牛阉牛,胃管可以作为一种可行的替代方法来采集具有代表性的瘤胃样本,而无需采用标准且侵入性更强的瘤胃插管法。