Characterization of the semen microbiota of healthy stud dogs using 16S RNA sequencing
The reproductive microbiota of male dogs has never been investigated using culture-independent sequencing techniques. The purpose of the present study was to get seminal knowledge on the microbiota of the ejaculate. Specifically, factors as the fraction of the ejaculate, the sperm quality (normosper...
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description | The reproductive microbiota of male dogs has never been investigated using culture-independent sequencing techniques. The purpose of the present study was to get seminal knowledge on the microbiota of the ejaculate. Specifically, factors as the fraction of the ejaculate, the sperm quality (normospermia, teratozoospermia), and the living environment were evaluated. The sperm-rich and the prostatic fractions of the ejaculate were collected from healthy stud dogs. Following the sperm analysis, samples from twenty animals (normospermic n = 10 and teratozoospermic n = 10) were stored at – 80 °C until further processing including DNA extraction and 16S rRNA sequencing. Alpha- (Shannon index) and beta- (Bray-Curtis, Unweighted UniFrac) diversities were assessed and compared (PERMANOVA) based on the group of samples (biological samples from the ejaculate and controls), the fraction of the ejaculate (sperm-rich and prostatic fractions), the animal group (normospermia and teratozoospermia), and the living environment of the animal (kennel or pet living in-house). The most abundant bacterial phyla in canine semen samples were Proteobacteria, Firmicutes, and Actinobacteria. Overall, the dominant bacterial family was that of Pasteurellaceae The genus Mycoplasma was never detected. No differences in terms of bacterial composition were found based on the fraction of the ejaculate and based on the animal group (P > 0.05). On the other hand, differences in alpha and beta diversities were highlighted based on the living environment (P = 0.001).
Overall, the results of the present study provide preliminary insights on dog semen microbiota, opening a new chapter in the field of canine andrology. Our results suggest that the environment may play a role in influencing the reproductive microbiota of male dogs and that the prostatic fraction of the ejaculate can be used for further research as a representative of the semen microbiota.
•The living environment shapes the semen microbiota of male dogs.•The sperm-rich and prostatic fraction of canine ejaculates share the microbiota.•The semen microbiota of healthy dogs has low bacterial abundance. |
doi_str_mv | 10.1016/j.theriogenology.2023.12.018 |
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Overall, the results of the present study provide preliminary insights on dog semen microbiota, opening a new chapter in the field of canine andrology. Our results suggest that the environment may play a role in influencing the reproductive microbiota of male dogs and that the prostatic fraction of the ejaculate can be used for further research as a representative of the semen microbiota.
•The living environment shapes the semen microbiota of male dogs.•The sperm-rich and prostatic fraction of canine ejaculates share the microbiota.•The semen microbiota of healthy dogs has low bacterial abundance.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/j.theriogenology.2023.12.018</identifier><identifier>PMID: 38141548</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>16S rRNA sequencing ; Actinobacteria ; animal reproduction ; Animals ; Bacteria - genetics ; Canine ; DNA ; Dog Diseases ; Dogs ; family ; Firmicutes ; genus ; kennels ; Male ; males ; Microbiota ; microorganisms ; Mycoplasma ; Pasteurellaceae ; Reproductive microbiota ; RNA ; RNA, Ribosomal, 16S - genetics ; Semen ; Sequence Analysis, RNA - veterinary ; Sperm ; sperm quality ; Teratozoospermia - veterinary</subject><ispartof>Theriogenology, 2024-03, Vol.216, p.1-7</ispartof><rights>2023 The Author(s)</rights><rights>Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-b4cbe416093fbec348d44c0c669963d1694c3bfefecced73412eaea652b2763b3</citedby><cites>FETCH-LOGICAL-c440t-b4cbe416093fbec348d44c0c669963d1694c3bfefecced73412eaea652b2763b3</cites><orcidid>0000-0001-6061-4889</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0093691X23004958$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38141548$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Banchi, P.</creatorcontrib><creatorcontrib>Bertolotti, L.</creatorcontrib><creatorcontrib>Spanoghe, L.</creatorcontrib><creatorcontrib>Ali Hassan, H.</creatorcontrib><creatorcontrib>Lannoo, J.</creatorcontrib><creatorcontrib>Domain, G.</creatorcontrib><creatorcontrib>Henzel, K.S.</creatorcontrib><creatorcontrib>Gaillard, V.</creatorcontrib><creatorcontrib>Rota, A.</creatorcontrib><creatorcontrib>Van Soom, A.</creatorcontrib><title>Characterization of the semen microbiota of healthy stud dogs using 16S RNA sequencing</title><title>Theriogenology</title><addtitle>Theriogenology</addtitle><description>The reproductive microbiota of male dogs has never been investigated using culture-independent sequencing techniques. The purpose of the present study was to get seminal knowledge on the microbiota of the ejaculate. Specifically, factors as the fraction of the ejaculate, the sperm quality (normospermia, teratozoospermia), and the living environment were evaluated. The sperm-rich and the prostatic fractions of the ejaculate were collected from healthy stud dogs. Following the sperm analysis, samples from twenty animals (normospermic n = 10 and teratozoospermic n = 10) were stored at – 80 °C until further processing including DNA extraction and 16S rRNA sequencing. Alpha- (Shannon index) and beta- (Bray-Curtis, Unweighted UniFrac) diversities were assessed and compared (PERMANOVA) based on the group of samples (biological samples from the ejaculate and controls), the fraction of the ejaculate (sperm-rich and prostatic fractions), the animal group (normospermia and teratozoospermia), and the living environment of the animal (kennel or pet living in-house). The most abundant bacterial phyla in canine semen samples were Proteobacteria, Firmicutes, and Actinobacteria. Overall, the dominant bacterial family was that of Pasteurellaceae The genus Mycoplasma was never detected. No differences in terms of bacterial composition were found based on the fraction of the ejaculate and based on the animal group (P > 0.05). On the other hand, differences in alpha and beta diversities were highlighted based on the living environment (P = 0.001).
Overall, the results of the present study provide preliminary insights on dog semen microbiota, opening a new chapter in the field of canine andrology. Our results suggest that the environment may play a role in influencing the reproductive microbiota of male dogs and that the prostatic fraction of the ejaculate can be used for further research as a representative of the semen microbiota.
•The living environment shapes the semen microbiota of male dogs.•The sperm-rich and prostatic fraction of canine ejaculates share the microbiota.•The semen microbiota of healthy dogs has low bacterial abundance.</description><subject>16S rRNA sequencing</subject><subject>Actinobacteria</subject><subject>animal reproduction</subject><subject>Animals</subject><subject>Bacteria - genetics</subject><subject>Canine</subject><subject>DNA</subject><subject>Dog Diseases</subject><subject>Dogs</subject><subject>family</subject><subject>Firmicutes</subject><subject>genus</subject><subject>kennels</subject><subject>Male</subject><subject>males</subject><subject>Microbiota</subject><subject>microorganisms</subject><subject>Mycoplasma</subject><subject>Pasteurellaceae</subject><subject>Reproductive microbiota</subject><subject>RNA</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Semen</subject><subject>Sequence Analysis, RNA - veterinary</subject><subject>Sperm</subject><subject>sperm quality</subject><subject>Teratozoospermia - veterinary</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEFr3DAQhUVJ6W7S_oWiQw-52NFYstaGXsKSTQIhhaQtvQlZHu9qsa2NJAe2vz5aNink1tPA8N68eR8h34DlwEBebPO4QW_dGkfXu_U-L1jBcyhyBtUHModqUWe84HBC5ozVPJM1_JmR0xC2jDEuJXwiM16BgFJUc_J7udFem5gu_tXRupG6jqYAGnDAkQ7WeNdYF_Vhv0Hdx82ehji1tHXrQKdgxzUF-Ugf7i-T52nC0aTVZ_Kx033AL6_zjPxaXf1c3mR3P65vl5d3mRGCxawRpkEBMv3ZNWi4qFohDDNS1rXkLchaGN502KEx2C64gAI1alkWTbGQvOFn5Px4d-ddyg5RDTYY7Hs9opuC4lDyspaMlUn6_ShNjULw2Kmdt4P2ewVMHciqrXpPVh3IKihUIpvsX1-TpmbA9p_5DWUSrI4CTH2fLXoVjE00sLUeTVSts_-X9ALoYZQF</recordid><startdate>20240301</startdate><enddate>20240301</enddate><creator>Banchi, P.</creator><creator>Bertolotti, L.</creator><creator>Spanoghe, L.</creator><creator>Ali Hassan, H.</creator><creator>Lannoo, J.</creator><creator>Domain, G.</creator><creator>Henzel, K.S.</creator><creator>Gaillard, V.</creator><creator>Rota, A.</creator><creator>Van Soom, A.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0001-6061-4889</orcidid></search><sort><creationdate>20240301</creationdate><title>Characterization of the semen microbiota of healthy stud dogs using 16S RNA sequencing</title><author>Banchi, P. ; Bertolotti, L. ; Spanoghe, L. ; Ali Hassan, H. ; Lannoo, J. ; Domain, G. ; Henzel, K.S. ; Gaillard, V. ; Rota, A. ; Van Soom, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-b4cbe416093fbec348d44c0c669963d1694c3bfefecced73412eaea652b2763b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>16S rRNA sequencing</topic><topic>Actinobacteria</topic><topic>animal reproduction</topic><topic>Animals</topic><topic>Bacteria - genetics</topic><topic>Canine</topic><topic>DNA</topic><topic>Dog Diseases</topic><topic>Dogs</topic><topic>family</topic><topic>Firmicutes</topic><topic>genus</topic><topic>kennels</topic><topic>Male</topic><topic>males</topic><topic>Microbiota</topic><topic>microorganisms</topic><topic>Mycoplasma</topic><topic>Pasteurellaceae</topic><topic>Reproductive microbiota</topic><topic>RNA</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Semen</topic><topic>Sequence Analysis, RNA - veterinary</topic><topic>Sperm</topic><topic>sperm quality</topic><topic>Teratozoospermia - veterinary</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Banchi, P.</creatorcontrib><creatorcontrib>Bertolotti, L.</creatorcontrib><creatorcontrib>Spanoghe, L.</creatorcontrib><creatorcontrib>Ali Hassan, H.</creatorcontrib><creatorcontrib>Lannoo, J.</creatorcontrib><creatorcontrib>Domain, G.</creatorcontrib><creatorcontrib>Henzel, K.S.</creatorcontrib><creatorcontrib>Gaillard, V.</creatorcontrib><creatorcontrib>Rota, A.</creatorcontrib><creatorcontrib>Van Soom, A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Theriogenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Banchi, P.</au><au>Bertolotti, L.</au><au>Spanoghe, L.</au><au>Ali Hassan, H.</au><au>Lannoo, J.</au><au>Domain, G.</au><au>Henzel, K.S.</au><au>Gaillard, V.</au><au>Rota, A.</au><au>Van Soom, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of the semen microbiota of healthy stud dogs using 16S RNA sequencing</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>2024-03-01</date><risdate>2024</risdate><volume>216</volume><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>The reproductive microbiota of male dogs has never been investigated using culture-independent sequencing techniques. The purpose of the present study was to get seminal knowledge on the microbiota of the ejaculate. Specifically, factors as the fraction of the ejaculate, the sperm quality (normospermia, teratozoospermia), and the living environment were evaluated. The sperm-rich and the prostatic fractions of the ejaculate were collected from healthy stud dogs. Following the sperm analysis, samples from twenty animals (normospermic n = 10 and teratozoospermic n = 10) were stored at – 80 °C until further processing including DNA extraction and 16S rRNA sequencing. Alpha- (Shannon index) and beta- (Bray-Curtis, Unweighted UniFrac) diversities were assessed and compared (PERMANOVA) based on the group of samples (biological samples from the ejaculate and controls), the fraction of the ejaculate (sperm-rich and prostatic fractions), the animal group (normospermia and teratozoospermia), and the living environment of the animal (kennel or pet living in-house). The most abundant bacterial phyla in canine semen samples were Proteobacteria, Firmicutes, and Actinobacteria. Overall, the dominant bacterial family was that of Pasteurellaceae The genus Mycoplasma was never detected. No differences in terms of bacterial composition were found based on the fraction of the ejaculate and based on the animal group (P > 0.05). On the other hand, differences in alpha and beta diversities were highlighted based on the living environment (P = 0.001).
Overall, the results of the present study provide preliminary insights on dog semen microbiota, opening a new chapter in the field of canine andrology. Our results suggest that the environment may play a role in influencing the reproductive microbiota of male dogs and that the prostatic fraction of the ejaculate can be used for further research as a representative of the semen microbiota.
•The living environment shapes the semen microbiota of male dogs.•The sperm-rich and prostatic fraction of canine ejaculates share the microbiota.•The semen microbiota of healthy dogs has low bacterial abundance.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38141548</pmid><doi>10.1016/j.theriogenology.2023.12.018</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6061-4889</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 16S rRNA sequencing Actinobacteria animal reproduction Animals Bacteria - genetics Canine DNA Dog Diseases Dogs family Firmicutes genus kennels Male males Microbiota microorganisms Mycoplasma Pasteurellaceae Reproductive microbiota RNA RNA, Ribosomal, 16S - genetics Semen Sequence Analysis, RNA - veterinary Sperm sperm quality Teratozoospermia - veterinary |
title | Characterization of the semen microbiota of healthy stud dogs using 16S RNA sequencing |
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