A decline in taxonomic diversity of milk microbiome is linked to clinical mastitis and physiological states of cow

IF 1 Q4 GENETICS & HEREDITY
I.L. Maslennikova , Y.I. Nechaeva , L.A. Ilina , G.Y. Laptev , E.S. Ponomareva , I.N. Zhdanova , M.V. Kuznetsova
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Abstract

Using 16S rRNA gene amplicon sequencing, longitudinal shifts in the microbial composition during dry-off, calving, the early, middle and late lactation state of healthy and mastitis cows were examined. Compared to healthy cow milk, fewer bacteria taxa were found for mastitis cow milk. Throughout the dry-off, calving, the early, middle, and late lactation phases, the taxonomic diversity of bacteria in both groups were declined. At dry-off, post-calving, early, middle, and late lactation periods, the percentage of bacteria species that were shared by milk samples of healthy and mastitis cows was 71.1, 65.8, 80.3, 52.6, and 44.3 %, respectively. From dry-off to late lactation periods, the core unique bacteria species of mastitis cow milk rose from 13 to 34 taxa, while the core unique species for healthy cow milk declined from 31 to 20 taxa. In the milk samples of healthy/mastitis cows the majority of microorganisms were represented by the phylum Proteobacteria as 52.9/9.1 %; 38.5/95.4 %; 24.0/19.2 %; 92.9/43.5 %; 46.8/57.1 %; the phylum Firmicutes as 16.5/50.7 %; 35.9/1.4 %; 28.6/11.3 %; 3.1/11.4 %; 7.0/2.7 % at dry-off, post-calving, early, middle and late lactation period, respectively. Taxonomic profile of 40 most abundant bacterial genera of milk samples were comparable in the both group of healthy and mastitis animals at all physiological states. There are prevalence of positive/negative correlation between the number of microorganisms of clinically important species in milk of healthy/mastitis cows, respectively, from dry-off to the late lactation periods.

Abstract Image

牛奶微生物组分类多样性的下降与奶牛的临床乳腺炎和生理状态有关
采用16S rRNA基因扩增子测序技术,研究了健康奶牛和乳腺炎奶牛在干乳、产犊、泌乳早、中、后期微生物组成的纵向变化。与健康牛奶相比,乳腺炎牛奶中发现的细菌类群较少。在干枯期、产犊期和泌乳期的前、中、后期,两组细菌的分类多样性均呈下降趋势。在干乳期、产犊后期、泌乳早期、中期和后期,健康奶牛和乳腺炎奶牛的乳样中共有细菌的比例分别为71.1、65.8、80.3、52.6和44.3%。从干乳期到泌乳后期,乳腺炎乳的核心独特细菌种类从13个增加到34个,而健康乳的核心独特细菌种类从31个减少到20个。在健康奶牛/乳腺炎奶牛乳样品中,以变形杆菌门为代表的微生物最多,占52.9/ 9.1%;38.5/95.4 %;24.0/19.2 %;92.9/43.5 %;46.8/57.1 %;厚壁门占16.5/ 50.7%;35.9/1.4 %;28.6/11.3 %;3.1/11.4 %;干乳期、产犊后、泌乳前期、中期和后期分别为7.0% / 2.7%。在所有生理状态下,健康动物和乳腺炎动物的乳样品中40个最丰富的细菌属的分类特征具有可比性。健康奶牛/乳腺炎奶牛乳汁中临床重要菌种的数量从干乳期到泌乳期后期分别呈正相关/负相关。
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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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