揭示牛乳微生物组的复杂性:通过使用全长 16S 元胞编码进行肠道分型了解乳腺炎。

IF 4.9 Q1 MICROBIOLOGY Animal microbiome Pub Date : 2024-10-22 DOI:10.1186/s42523-024-00345-0
Leire Urrutia-Angulo, Medelin Ocejo, Beatriz Oporto, Gorka Aduriz, José Luís Lavín, Ana Hurtado
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引用次数: 0

摘要

背景:乳腺炎(乳腺炎症)是奶牛的主要疾病,也是使用抗菌素的主要原因。虽然主要由细菌感染引起,但传统的微生物培养方法往往无法确定病原体。本研究旨在检测牛乳腺微生物群的变化是否会导致乳腺炎的发生或发展:方法:使用牛津-纳米孔长读数测序技术生成全长 16S rRNA 基因读数(16S-metabarcoding),以描述根据乳腺炎病史和胎次将奶牛分为五组的健康和患病乳房中牛奶微生物群的特征:结果:样本被分为六个肠型,每个肠型都有一个标记属和几个不同的富集属。两个肠型完全由临床乳腺炎样本组成,表现出明显的菌群失调,其中一个致病菌属占主导地位并取代了内源性细菌群。其他乳腺炎样本(全部为亚临床样本,一半为临床样本)与来自健康动物的样本聚集成三种肠型,可能反映了健康与疾病之间的中间状态。临床乳腺炎发作后,临床恢复和微生物组重建并不总是同步进行的,这表明乳房健康状况的临床定义并不能一致地反映微生物概况:这些结果表明,乳腺炎是一个乳房微生物群不断变化的动态过程,这突出了确定乳腺炎的独特微生物群特征的复杂性。
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Unravelling the complexity of bovine milk microbiome: insights into mastitis through enterotyping using full-length 16S-metabarcoding.

Background: Mastitis, inflammation of the mammary gland, is a major disease of dairy cattle and the main cause for antimicrobial use. Although mainly caused by bacterial infections, the aetiological agent often remains unidentified by conventional microbiological culture methods. The aim of this study was to test whether shifts in the bovine mammary gland microbiota can result in initiation or progression of mastitis.

Methods: Oxford-Nanopore long-read sequencing was used to generate full-length 16S rRNA gene reads (16S-metabarcoding) to characterise the microbial population of milk from healthy and diseased udder of cows classified into five groups based on their mastitis history and parity.

Results: Samples were classified into six enterotypes, each characterised by a marker genus and several differentially-abundant genera. Two enterotypes were exclusively composed of clinical mastitis samples and displayed a marked dysbiosis, with a single pathogenic genus predominating and displacing the endogenous bacterial population. Other mastitis samples (all subclinical and half of the clinical) clustered with those from healthy animals into three enterotypes, probably reflecting intermediate states between health and disease. After an episode of clinical mastitis, clinical recovery and microbiome reconstitution do not always occur in parallel, indicating that the clinical definition of the udder health status does not consistently reflect the microbial profile.

Conclusions: These results show that mastitis is a dynamic process in which the udder microbiota constantly changes, highlighting the complexity of defining a unique microbiota profile indicative of mastitis.

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