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      Intestine and spleen microbiota composition in healthy and diseased tilapia

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          Abstract

          Symbiotic bacteria within the gut microbiome of various organisms, including fish, provide the host with several functions that improve the immune system. Although the spleen plays an important role in the modulation of immune responses, the role of spleen microbiota in shaping the immune system is unclear. Our study aimed at understanding the relationship between fish health and microbiota composition in the intestine and spleen. Our model organism was the hybrid tilapia ( Oreochromis aureus ×  Oreochromis niloticus). We sampled intestine and spleen from healthy and diseased adult tilapia and determined their microbiota composition by sequencing the 16S rRNA gene. Significant differences were found between the intestine and the spleen microbiota composition of healthy compared to diseased fish as well as between intestines and spleens of fish with the same health condition. The microbiota diversity of healthy fish compared to diseased fish was significantly different as well. In the intestine of healthy fish, Cetobacterium was the most abundant genus while Mycoplasma was the most abundant genus in the spleen. Vibrio was the most abundant genus in the intestine and spleen of diseased fish. Moreover, it seems that there is a co-infection interaction between Vibrio and Aeromonas, which was reflected in the spleen of diseased fish. While Vibrio, Aeromonas and Streptococcus were the probable pathogens in the diseased fish, the role of Mycoplasma as a pathogen of cultured hybrid tilapia remains uncertain. We conclude that the intestine and spleen microbiota composition is strongly related to the health condition of the fish.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s42523-022-00201-z.

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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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            Ultrastructural Characterization of the Lower Motor System in a Mouse Model of Krabbe Disease

            Krabbe disease (KD) is a neurodegenerative disorder caused by the lack of β- galactosylceramidase enzymatic activity and by widespread accumulation of the cytotoxic galactosyl-sphingosine in neuronal, myelinating and endothelial cells. Despite the wide use of Twitcher mice as experimental model for KD, the ultrastructure of this model is partial and mainly addressing peripheral nerves. More details are requested to elucidate the basis of the motor defects, which are the first to appear during KD onset. Here we use transmission electron microscopy (TEM) to focus on the alterations produced by KD in the lower motor system at postnatal day 15 (P15), a nearly asymptomatic stage, and in the juvenile P30 mouse. We find mild effects on motorneuron soma, severe ones on sciatic nerves and very severe effects on nerve terminals and neuromuscular junctions at P30, with peripheral damage being already detectable at P15. Finally, we find that the gastrocnemius muscle undergoes atrophy and structural changes that are independent of denervation at P15. Our data further characterize the ultrastructural analysis of the KD mouse model, and support recent theories of a dying-back mechanism for neuronal degeneration, which is independent of demyelination.
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              Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms

              DNA sequencing continues to decrease in cost with the Illumina HiSeq2000 generating up to 600 Gb of paired-end 100 base reads in a ten-day run. Here we present a protocol for community amplicon sequencing on the HiSeq2000 and MiSeq Illumina platforms, and apply that protocol to sequence 24 microbial communities from host-associated and free-living environments. A critical question as more sequencing platforms become available is whether biological conclusions derived on one platform are consistent with what would be derived on a different platform. We show that the protocol developed for these instruments successfully recaptures known biological results, and additionally that biological conclusions are consistent across sequencing platforms (the HiSeq2000 versus the MiSeq) and across the sequenced regions of amplicons.
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                Author and article information

                Contributors
                tamirofek2@gmail.com
                maya.lalzar@gmail.com
                izhaki@research.haifa.ac.il
                mhalpern@research.haifa.ac.il
                Journal
                Anim Microbiome
                Anim Microbiome
                Animal Microbiome
                BioMed Central (London )
                2524-4671
                13 August 2022
                13 August 2022
                2022
                : 4
                Affiliations
                [1 ]GRID grid.18098.38, ISNI 0000 0004 1937 0562, Department of Evolutionary and Environmental Biology, Faculty of Natural Sciences, , University of Haifa, ; 3498838 Haifa, Israel
                [2 ]GRID grid.425807.c, ISNI 0000 0004 0604 7918, Central Fish Health Laboratory, Fishery and Aquaculture Department, , Ministry of Agriculture and Rural Development, ; 1080300 Nir David, Israel
                [3 ]GRID grid.18098.38, ISNI 0000 0004 1937 0562, Bioinformatics Service Unit, , University of Haifa, ; 3498838 Haifa, Israel
                [4 ]GRID grid.18098.38, ISNI 0000 0004 1937 0562, Department of Biology and Environment, Faculty of Natural Sciences, , University of Haifa, ; 3600600 Oranim, Tivon, Israel
                Article
                201
                10.1186/s42523-022-00201-z
                9375283
                35964144
                1978d0f5-ce25-4ea0-a522-6a74c25ae2e9
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100006221, United States - Israel Binational Science Foundation;
                Award ID: 2015103
                Award Recipient :
                Funded by: India-Israel Joint UGC-ISF
                Award ID: 2728/17
                Award Recipient :
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                © The Author(s) 2022

                hybrid tilapia,intestine and spleen microbiota composition,intensive freshwater aquaculture,pathogenic bacteria,bacterial co-infection

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