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J Appl Microbiol. 2017 Jun;122(6):1456-1470. doi: 10.1111/jam.13456. Epub 2017 May 3.
2
Bacterial and fungal core microbiomes associated with small grain silages during ensiling and aerobic spoilage.在青贮和有氧变质过程中与小粒谷物青贮饲料相关的细菌和真菌核心微生物群。
BMC Microbiol. 2017 Mar 3;17(1):50. doi: 10.1186/s12866-017-0947-0.
3
A Perspective Study of Koumiss Microbiome by Metagenomics Analysis Based on Single-Cell Amplification Technique.基于单细胞扩增技术的宏基因组学分析对马奶酒微生物组的前瞻性研究。
Front Microbiol. 2017 Feb 7;8:165. doi: 10.3389/fmicb.2017.00165. eCollection 2017.
4
Bacterial microbiota of Kazakhstan cheese revealed by single molecule real time (SMRT) sequencing and its comparison with Belgian, Kalmykian and Italian artisanal cheeses.通过单分子实时(SMRT)测序揭示的哈萨克斯坦奶酪的细菌微生物群及其与比利时、卡尔梅克和意大利手工奶酪的比较。
BMC Microbiol. 2017 Jan 9;17(1):13. doi: 10.1186/s12866-016-0911-4.
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Using PacBio Long-Read High-Throughput Microbial Gene Amplicon Sequencing To Evaluate Infant Formula Safety.利用 PacBio 长读长高通量微生物基因扩增子测序评估婴儿配方奶粉安全性。
J Agric Food Chem. 2016 Sep 21;64(37):6993-7001. doi: 10.1021/acs.jafc.6b01817. Epub 2016 Sep 9.
6
Assessing quality of Medicago sativa silage by monitoring bacterial composition with single molecule, real-time sequencing technology and various physiological parameters.通过使用单分子实时测序技术监测细菌组成和各种生理参数来评估紫花苜蓿青贮饲料的质量。
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7
Use of propidium monoazide for selective profiling of viable microbial cells during Gouda cheese ripening.使用碘化丙啶单叠氮化物选择性分析高达干酪成熟过程中活菌细胞的组成。
Int J Food Microbiol. 2016 Jul 2;228:1-9. doi: 10.1016/j.ijfoodmicro.2016.03.027. Epub 2016 Mar 25.
8
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10
Fermentation characteristics and lactic Acid bacteria succession of total mixed ration silages formulated with peach pomace.用桃渣配制的全混合日粮青贮饲料的发酵特性及乳酸菌演替
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利用单分子实时测序技术对发酵饲料中的活菌细菌和真菌微生物群落进行分析。

Profiling of the viable bacterial and fungal microbiota in fermented feeds using single-molecule real-time sequencing.

机构信息

Department of Laboratory Animal Science, College of Basic Medical Sciences, Third Military Medical University, Chongqing, China.

Key Laboratory of Dairy Biotechnology and Engineering, Ministry of Education, Key Laboratory of Dairy Products Processing, Ministry of Agriculture, Inner Mongolia Agricultural University, Huhhot, China.

出版信息

J Anim Sci. 2020 Feb 1;98(2). doi: 10.1093/jas/skaa029.

DOI:10.1093/jas/skaa029
PMID:32017844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7036599/
Abstract

Fermented concentrated feed has been widely recognized as an ideal feed in the animal industry. In this study, we used a powerful method, coupling propidium monoazide (PMA) pretreatment with single-molecule real-time (SMRT) sequencing technology to compare the bacterial and fungal composition of feeds before and after fermentation with four added lactic acid bacteria (LAB) inoculants (one Lactobacillus casei strain and three L. plantarum strains). Five feed samples consisting of corn, soybean meal, and wheat bran were fermented with LAB additives for 3 d. Following anaerobic fermentation, the pH rapidly decreased, and the mean numbers of LAB increased from 106 to 109 colony-forming units (cfu)/g fresh matter. SMRT sequencing results showed that the abundance and diversity of bacteria and fungi in the feed were significantly higher before fermentation than after fermentation. Fifteen bacterial species and eight fungal genera were significantly altered following fermentation, and L. plantarum was the dominant species (relative abundance 88.94%) in the post-fermentation group. PMA treatment revealed that the bacteria Bacillus cereus, B. circulans, Alkaliphilus oremlandii, Cronobacter sakazakii, Paenibacillus barcinonensis, and P. amylolyticus (relative abundance >1%) were viable in the raw feed. After fermentation, their relative abundances decreased sharply to <0.2%; however, viable L. plantarum was still the dominant species post fermentation. We inferred that our LAB additives grew rapidly and inhibited harmful microorganisms and further improved feed quality. In addition, coupling PMA treatment with the Pacific Biosciences SMRT sequencing technology was a powerful tool for providing accurate live microbiota profiling data in this study.

摘要

发酵浓缩饲料在动物产业中已被广泛认为是一种理想的饲料。在这项研究中,我们使用了一种强大的方法,即将吖啶橙单加处理(PMA)与单分子实时(SMRT)测序技术相结合,以比较在添加四种乳酸菌(LAB)接种物(一种干酪乳杆菌菌株和三种植物乳杆菌菌株)前后发酵的饲料的细菌和真菌组成。使用 LAB 添加剂对包含玉米、豆粕和麦麸的五种饲料样品进行了 3 天的发酵。在厌氧发酵后,pH 值迅速下降,LAB 的平均数量从 106 增加到 109 个菌落形成单位(cfu)/g 新鲜物质。SMRT 测序结果表明,发酵前饲料的细菌和真菌丰度和多样性显著高于发酵后。发酵后有 15 种细菌物种和 8 种真菌属发生了显著变化,植物乳杆菌是发酵后组中的优势物种(相对丰度 88.94%)。PMA 处理表明,原始饲料中存在活的芽孢杆菌、环杆菌、嗜碱古菌、阪崎克罗诺杆菌、拜氏芽孢杆菌和淀粉芽孢杆菌(相对丰度>1%)。发酵后,它们的相对丰度急剧下降至<0.2%;然而,活的植物乳杆菌仍然是发酵后的主要物种。我们推断,我们的 LAB 添加剂生长迅速,抑制了有害微生物,进一步提高了饲料质量。此外,将 PMA 处理与太平洋生物科学公司的 SMRT 测序技术相结合,是本研究中提供准确的活微生物组分析数据的有力工具。