Breitenwieser Franziska, Doll Etienne V, Clavel Thomas, Scherer Siegfried, Wenning Mareike
Milchprüfring Baden-Württemberg e.V., Kirchheim unter Teck, Germany.
Chair for Microbial Ecology, Weihenstephan School of Life Sciences, Technische Universität München, Freising, Germany.
Front Microbiol. 2020 Jul 9;11:1557. doi: 10.3389/fmicb.2020.01557. eCollection 2020.
Raw milk microbiota are complex communities with a significant impact on the hygienic, sensory and technological quality of milk products. However, there is a lack of knowledge on factors determining their composition. In the present study, four bulk tank milk samples of two farms at two different time points were analyzed in detail for their microbiota using cultivation and 16S rRNA amplicon sequencing. Diversity in samples from the first time point was assessed via cultivation of 500 aerobic mesophilic bacterial isolates in each sample. A high biodiversity of 70 and 110 species per sample was determined, of which 25-28% corresponded to yet unknown taxa. The isolates were dominated by Gram-positive members of the genera , or , whilst and were most abundant among the Gram-negative taxa. At the second time point, samples of the same farms were analyzed via both cultivation (1,500 individual colonies each) and high-throughput 16S rRNA gene amplicon sequencing. The latter revealed a threefold higher biodiversity at the genus level, as anaerobic or fastidious species were also detected. However, cultivation identified genera not captured by sequencing, indicating that both approaches are complementary. Using amplicon sequencing, the relative abundance of a few genera was distorted, which seems to be an artifact of sample preparation. Therefore, attention needs to be paid to the library preparation procedure with special emphasis on cell lysis and PCR.
生牛奶微生物群是复杂的群落,对乳制品的卫生、感官和工艺质量有重大影响。然而,对于决定其组成的因素仍缺乏了解。在本研究中,使用培养和16S rRNA扩增子测序对两个农场在两个不同时间点采集的四个大罐牛奶样本的微生物群进行了详细分析。通过培养每个样本中的500个需氧嗜温细菌分离株,评估了第一个时间点样本的多样性。确定每个样本具有70至110种的高生物多样性,其中25%-28%对应于未知分类群。分离株以革兰氏阳性菌属、或为主,而革兰氏阴性菌属中最丰富的是和。在第二个时间点,通过培养(每个样本1500个单菌落)和高通量16S rRNA基因扩增子测序对相同农场的样本进行了分析。后者在属水平上揭示了高三倍的生物多样性,因为还检测到了厌氧或苛求菌。然而,培养鉴定出了测序未捕获的属,表明这两种方法是互补的。使用扩增子测序时,少数属的相对丰度被扭曲,这似乎是样本制备的假象。因此,需要注意文库制备程序,特别强调细胞裂解和PCR。