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      Health-associated changes of the fecal microbiota in dairy heifer calves during the pre-weaning period

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          Abstract

          Introduction

          Neonatal calf diarrhea is a multifactorial condition that occurs in early life when calves are particularly susceptible to enteric infection and dysbiosis of the gut microbiome. Good calf health is dependent on successful passive transfer of immunity from the dam through colostrum. There are limited studies on the developing gut microbiota from birth to weaning in calves.

          Methodology

          Therefore, the objective of this study was to examine the effect of immune status and diarrheal incidence on the development of the fecal microbiota in Jersey ( n = 22) and Holstein ( n = 29) heifer calves throughout the pre-weaning period. Calves were hand-fed a colostrum volume equivalent to 8.5% of their birthweight, from either the calf’s dam ( n = 28) or re-heated mixed colostrum (≤2 cows, ≤1d; n = 23) within 2 h of birth. All calves were clinically assessed using a modified Wisconsin–Madison calf health scoring system and rectal temperature at day (d) 0, d7, d21, or disease manifestation (DM) and weaning (d83). Weights were recorded at d0, d21, and d83. Calf blood samples were collected at d7 for the determination of calf serum IgG (sIgG). Fecal samples were obtained at d7, d21/DM [mean d22 (SE 0.70)], and at weaning for 16S rRNA amplicon sequencing of the fecal microbiota. Data were processed in R using DADA2; taxonomy was assigned using the SILVA database and further analyzed using Phyloseq and MaAsLin 2.

          Results and discussion

          Significant amplicon sequence variants (ASVs) and calf performance data underwent a Spearman rank-order correlation test. There was no effect ( p > 0.05) of colostrum source or calf breed on serum total protein. An effect of calf breed ( p < 0.05) was observed on sIgG concentrations such that Holstein calves had 6.49 (SE 2.99) mg/ml higher sIgG than Jersey calves. Colostrum source and calf breed had no effect ( p > 0.05) on health status or the alpha diversity of the fecal microbiota. There was a relationship between health status and time interaction ( p < 0.001), whereby alpha diversity increased with time; however, diarrheic calves had reduced microbial diversity at DM. No difference ( p > 0.05) in beta diversity of the microbiota was detected at d7 or d83. At the genus level, 33 ASVs were associated (adj. p < 0.05) with health status over the pre-weaning period.

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          Most cited references70

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          DADA2: High resolution sample inference from Illumina amplicon data

          We present DADA2, a software package that models and corrects Illumina-sequenced amplicon errors. DADA2 infers sample sequences exactly, without coarse-graining into OTUs, and resolves differences of as little as one nucleotide. In several mock communities DADA2 identified more real variants and output fewer spurious sequences than other methods. We applied DADA2 to vaginal samples from a cohort of pregnant women, revealing a diversity of previously undetected Lactobacillus crispatus variants.
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            phyloseq: An R Package for Reproducible Interactive Analysis and Graphics of Microbiome Census Data

            Background The analysis of microbial communities through DNA sequencing brings many challenges: the integration of different types of data with methods from ecology, genetics, phylogenetics, multivariate statistics, visualization and testing. With the increased breadth of experimental designs now being pursued, project-specific statistical analyses are often needed, and these analyses are often difficult (or impossible) for peer researchers to independently reproduce. The vast majority of the requisite tools for performing these analyses reproducibly are already implemented in R and its extensions (packages), but with limited support for high throughput microbiome census data. Results Here we describe a software project, phyloseq, dedicated to the object-oriented representation and analysis of microbiome census data in R. It supports importing data from a variety of common formats, as well as many analysis techniques. These include calibration, filtering, subsetting, agglomeration, multi-table comparisons, diversity analysis, parallelized Fast UniFrac, ordination methods, and production of publication-quality graphics; all in a manner that is easy to document, share, and modify. We show how to apply functions from other R packages to phyloseq-represented data, illustrating the availability of a large number of open source analysis techniques. We discuss the use of phyloseq with tools for reproducible research, a practice common in other fields but still rare in the analysis of highly parallel microbiome census data. We have made available all of the materials necessary to completely reproduce the analysis and figures included in this article, an example of best practices for reproducible research. Conclusions The phyloseq project for R is a new open-source software package, freely available on the web from both GitHub and Bioconductor.
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              Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample.

              The ongoing revolution in high-throughput sequencing continues to democratize the ability of small groups of investigators to map the microbial component of the biosphere. In particular, the coevolution of new sequencing platforms and new software tools allows data acquisition and analysis on an unprecedented scale. Here we report the next stage in this coevolutionary arms race, using the Illumina GAIIx platform to sequence a diverse array of 25 environmental samples and three known "mock communities" at a depth averaging 3.1 million reads per sample. We demonstrate excellent consistency in taxonomic recovery and recapture diversity patterns that were previously reported on the basis of metaanalysis of many studies from the literature (notably, the saline/nonsaline split in environmental samples and the split between host-associated and free-living communities). We also demonstrate that 2,000 Illumina single-end reads are sufficient to recapture the same relationships among samples that we observe with the full dataset. The results thus open up the possibility of conducting large-scale studies analyzing thousands of samples simultaneously to survey microbial communities at an unprecedented spatial and temporal resolution.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2433944/overviewRole: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/1282417/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/944693/overviewRole: Role: Role: Role: Role: Role:
                Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/425637/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role:
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                26 April 2024
                2024
                : 15
                : 1359611
                Affiliations
                [1] 1Animal and Bioscience Research Department, Animal and Grassland Research and Innovation Centre, Teagasc Grange , Meath, Ireland
                [2] 2School of Veterinary Medicine, University College Dublin , Dublin, Ireland
                [3] 3School of Biological and Chemical Sciences, University of Galway , Galway, Ireland
                Author notes

                Edited by: Kun Li, Nanjing Agricultural University, China

                Reviewed by: Jana Koscova, University of Veterinary Medicine and Pharmacy in Košice, Slovakia

                Yu Ping, University of California, Irvine, United States

                Houqiang Luo, Wenzhou Vocational College of Science and Technology, China

                *Correspondence: Sinéad M. Waters, sinead.waters@ 123456universityofgalway.ie
                Article
                10.3389/fmicb.2024.1359611
                11082272
                1df8a7ce-40ff-4100-acf4-232b4d08c39b
                Copyright © 2024 Scully, Earley, Smith, McAloon and Waters.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 21 December 2023
                : 01 April 2024
                Page count
                Figures: 5, Tables: 7, Equations: 0, References: 70, Pages: 21, Words: 14838
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was funded by the European Union Horizons 2020 “HoloRuminant” grant (grant agreement number: 101000213). SS was funded by a Teagasc Walsh Scholarship (RMIS 1286).
                Categories
                Microbiology
                Original Research
                Custom metadata
                Microorganisms in Vertebrate Digestive Systems

                Microbiology & Virology
                dairy,calf health,diarrhea,microbiota,colostrum,16s rrna sequencing
                Microbiology & Virology
                dairy, calf health, diarrhea, microbiota, colostrum, 16s rrna sequencing

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