Susceptibility of mouse mammary glands to murine gammaherpesvirus 72 (MHV-72) infection: evidence of MHV-72 transmission via breast milk
Murine gammaherpesvirus 72 (MHV-72) is a virus of wild rodents and serves as a convenient small animal model to understand the pathogenesis of Epstein–Barr virus (EBV) and human herpesvirus 8 (HHV8) infection. In laboratory mice MHV-72 causes an acute infection of lung epithelial cells and establish...
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Veröffentlicht in: | Microbial pathogenesis 2001-08, Vol.31 (2), p.47-58 |
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description | Murine gammaherpesvirus 72 (MHV-72) is a virus of wild rodents and serves as a convenient small animal model to understand the pathogenesis of Epstein–Barr virus (EBV) and human herpesvirus 8 (HHV8) infection. In laboratory mice MHV-72 causes an acute infection of lung epithelial cells and establishes the latency in B lymphocytes. In this study, we investigated athymic nude and immunocompetent mice for distribution of virus in organs after infection with MHV-72. Ten days following subcutaneous dorsal injection of nude mice, virus replicated in lungs, lymphoid organs, salivary glands and also in mammary glands. The virus titre decreased by day 21 post-infection in former tissues, but increased in mammary glands. Presence of virus DNA sequences was detected in the lymphoid and non-lymphoid tissues until the death of the animals (about 1 month post-infection). Infection of immunocompetent mice with MHV-72 induced replication of virus up to 42 days post-infection in mammary glands reaching the highest level of infectious virus at day 8 post-infection. These data show that there is latent infection in mice never detected before. Moreover, virus DNA was detected using nested PCR (by amplification of a portion of gp150 gene sequence) in the mammary glands and the milk of mouse mothers infected with MHV-72 2 days before delivery. We demonstrated the presence of virus DNA also in the milk removed from the stomach of non-infected newborn mice, which were nourished by infected mothers (wet-nurses) for 1 or 2 days. The failure to detect the virus DNA in newborn mice lungs confirmed that they did not become infected from wet-nurses by the intranasal route. This suggests that MHV may be naturally transmitted to newborn mice via breast milk. |
doi_str_mv | 10.1006/mpat.2001.0441 |
format | Article |
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In laboratory mice MHV-72 causes an acute infection of lung epithelial cells and establishes the latency in B lymphocytes. In this study, we investigated athymic nude and immunocompetent mice for distribution of virus in organs after infection with MHV-72. Ten days following subcutaneous dorsal injection of nude mice, virus replicated in lungs, lymphoid organs, salivary glands and also in mammary glands. The virus titre decreased by day 21 post-infection in former tissues, but increased in mammary glands. Presence of virus DNA sequences was detected in the lymphoid and non-lymphoid tissues until the death of the animals (about 1 month post-infection). Infection of immunocompetent mice with MHV-72 induced replication of virus up to 42 days post-infection in mammary glands reaching the highest level of infectious virus at day 8 post-infection. These data show that there is latent infection in mice never detected before. Moreover, virus DNA was detected using nested PCR (by amplification of a portion of gp150 gene sequence) in the mammary glands and the milk of mouse mothers infected with MHV-72 2 days before delivery. We demonstrated the presence of virus DNA also in the milk removed from the stomach of non-infected newborn mice, which were nourished by infected mothers (wet-nurses) for 1 or 2 days. The failure to detect the virus DNA in newborn mice lungs confirmed that they did not become infected from wet-nurses by the intranasal route. This suggests that MHV may be naturally transmitted to newborn mice via breast milk.</description><identifier>ISSN: 0882-4010</identifier><identifier>EISSN: 1096-1208</identifier><identifier>DOI: 10.1006/mpat.2001.0441</identifier><identifier>PMID: 11453700</identifier><identifier>CODEN: MIPAEV</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Animals, Suckling ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antifungal agents ; Biological and medical sciences ; Breast - virology ; Disease Models, Animal ; DNA, Viral - analysis ; Experimental mycoses and models ; Female ; Fundamental and applied biological sciences. Psychology ; Gammaherpesvirinae ; Gammaherpesvirinae - isolation & purification ; Gammaherpesvirinae - physiology ; Herpesviridae Infections - transmission ; Herpesviridae Infections - virology ; Immunocompetence ; Infectious Disease Transmission, Vertical ; Infectious diseases ; Lung - virology ; Lymph Nodes - virology ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Microbiology ; Milk - virology ; Murine gammaherpesvirus 72 ; murine herpesvirus 4 (MHV) strain 72, murine gammaherpesvirus, nude mice, milk, virus transmission, mammary glands ; Mycoses ; Pharmacology. 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In laboratory mice MHV-72 causes an acute infection of lung epithelial cells and establishes the latency in B lymphocytes. In this study, we investigated athymic nude and immunocompetent mice for distribution of virus in organs after infection with MHV-72. Ten days following subcutaneous dorsal injection of nude mice, virus replicated in lungs, lymphoid organs, salivary glands and also in mammary glands. The virus titre decreased by day 21 post-infection in former tissues, but increased in mammary glands. Presence of virus DNA sequences was detected in the lymphoid and non-lymphoid tissues until the death of the animals (about 1 month post-infection). Infection of immunocompetent mice with MHV-72 induced replication of virus up to 42 days post-infection in mammary glands reaching the highest level of infectious virus at day 8 post-infection. These data show that there is latent infection in mice never detected before. Moreover, virus DNA was detected using nested PCR (by amplification of a portion of gp150 gene sequence) in the mammary glands and the milk of mouse mothers infected with MHV-72 2 days before delivery. We demonstrated the presence of virus DNA also in the milk removed from the stomach of non-infected newborn mice, which were nourished by infected mothers (wet-nurses) for 1 or 2 days. The failure to detect the virus DNA in newborn mice lungs confirmed that they did not become infected from wet-nurses by the intranasal route. This suggests that MHV may be naturally transmitted to newborn mice via breast milk.</description><subject>Animals</subject><subject>Animals, Suckling</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antifungal agents</subject><subject>Biological and medical sciences</subject><subject>Breast - virology</subject><subject>Disease Models, Animal</subject><subject>DNA, Viral - analysis</subject><subject>Experimental mycoses and models</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gammaherpesvirinae</subject><subject>Gammaherpesvirinae - isolation & purification</subject><subject>Gammaherpesvirinae - physiology</subject><subject>Herpesviridae Infections - transmission</subject><subject>Herpesviridae Infections - virology</subject><subject>Immunocompetence</subject><subject>Infectious Disease Transmission, Vertical</subject><subject>Infectious diseases</subject><subject>Lung - virology</subject><subject>Lymph Nodes - virology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Microbiology</subject><subject>Milk - virology</subject><subject>Murine gammaherpesvirus 72</subject><subject>murine herpesvirus 4 (MHV) strain 72, murine gammaherpesvirus, nude mice, milk, virus transmission, mammary glands</subject><subject>Mycoses</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymerase Chain Reaction</subject><subject>Pregnancy</subject><subject>Salivary Glands - virology</subject><subject>Time Factors</subject><subject>Virus Latency</subject><issn>0882-4010</issn><issn>1096-1208</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTtvFTEQhS0EIjeBlhK5AUGxl7HX-zAdighBCqLg0VpeezYY1ruL7b1S_gE_G1v3SqkQ1RTzzdGccwh5xmDPANo3ftVpzwHYHoRgD8iOgWwrxqF_SHbQ97wSwOCMnMf4EwCkqOVjcsaYaOoOYEf-fNmiwTW5wU0u3dFlpH7ZIlKvvdfhjt5OeraRpoX6LbgZ6W1Z_MCwYjy4sEXacfrq0_X3quOvqZtHNMkt81uKB2dxNlgkj2uagp6jdzFmgB6cpkNAHRP1bvr1hDwa9RTx6WlekG9X779eXlc3nz98vHx3U5lsJFUSLAeuQTSyb1ps2NAYxkdmoMM2ezey6QTYuh24qW1tQTNj-5YbqEfR6L6-IC-PumtYfm8Yk8oPGZyyTczGVVdilQ38F2SdhK5nPIP7I2jCEmPAUa3BlewUA1XUVClJlZJUKSkfPD8pb4NHe4-fWsnAixOgo9HTmGMzLt5zgrXAZZ25_shhDuzgMKhoXMncupBrUHZx__rhL_EHrMs</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>Raslova, Hana</creator><creator>Berebbi, Monique</creator><creator>Rajcani, Julius</creator><creator>Sarasin, Alain</creator><creator>Matis, Jan</creator><creator>Kudelova, Marcela</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</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>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20010801</creationdate><title>Susceptibility of mouse mammary glands to murine gammaherpesvirus 72 (MHV-72) infection: evidence of MHV-72 transmission via breast milk</title><author>Raslova, Hana ; Berebbi, Monique ; Rajcani, Julius ; Sarasin, Alain ; Matis, Jan ; Kudelova, Marcela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-90d202a0459856e51b5c12f1c07e6109c95740d36b2c3d3d0a1cd862c03f45a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Animals, Suckling</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antifungal agents</topic><topic>Biological and medical sciences</topic><topic>Breast - virology</topic><topic>Disease Models, Animal</topic><topic>DNA, Viral - analysis</topic><topic>Experimental mycoses and models</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gammaherpesvirinae</topic><topic>Gammaherpesvirinae - isolation & purification</topic><topic>Gammaherpesvirinae - physiology</topic><topic>Herpesviridae Infections - transmission</topic><topic>Herpesviridae Infections - virology</topic><topic>Immunocompetence</topic><topic>Infectious Disease Transmission, Vertical</topic><topic>Infectious diseases</topic><topic>Lung - virology</topic><topic>Lymph Nodes - virology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Microbiology</topic><topic>Milk - virology</topic><topic>Murine gammaherpesvirus 72</topic><topic>murine herpesvirus 4 (MHV) strain 72, murine gammaherpesvirus, nude mice, milk, virus transmission, mammary glands</topic><topic>Mycoses</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymerase Chain Reaction</topic><topic>Pregnancy</topic><topic>Salivary Glands - virology</topic><topic>Time Factors</topic><topic>Virus Latency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raslova, Hana</creatorcontrib><creatorcontrib>Berebbi, Monique</creatorcontrib><creatorcontrib>Rajcani, Julius</creatorcontrib><creatorcontrib>Sarasin, Alain</creatorcontrib><creatorcontrib>Matis, Jan</creatorcontrib><creatorcontrib>Kudelova, Marcela</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Microbial pathogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raslova, Hana</au><au>Berebbi, Monique</au><au>Rajcani, Julius</au><au>Sarasin, Alain</au><au>Matis, Jan</au><au>Kudelova, Marcela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Susceptibility of mouse mammary glands to murine gammaherpesvirus 72 (MHV-72) infection: evidence of MHV-72 transmission via breast milk</atitle><jtitle>Microbial pathogenesis</jtitle><addtitle>Microb Pathog</addtitle><date>2001-08-01</date><risdate>2001</risdate><volume>31</volume><issue>2</issue><spage>47</spage><epage>58</epage><pages>47-58</pages><issn>0882-4010</issn><eissn>1096-1208</eissn><coden>MIPAEV</coden><abstract>Murine gammaherpesvirus 72 (MHV-72) is a virus of wild rodents and serves as a convenient small animal model to understand the pathogenesis of Epstein–Barr virus (EBV) and human herpesvirus 8 (HHV8) infection. In laboratory mice MHV-72 causes an acute infection of lung epithelial cells and establishes the latency in B lymphocytes. In this study, we investigated athymic nude and immunocompetent mice for distribution of virus in organs after infection with MHV-72. Ten days following subcutaneous dorsal injection of nude mice, virus replicated in lungs, lymphoid organs, salivary glands and also in mammary glands. The virus titre decreased by day 21 post-infection in former tissues, but increased in mammary glands. Presence of virus DNA sequences was detected in the lymphoid and non-lymphoid tissues until the death of the animals (about 1 month post-infection). Infection of immunocompetent mice with MHV-72 induced replication of virus up to 42 days post-infection in mammary glands reaching the highest level of infectious virus at day 8 post-infection. These data show that there is latent infection in mice never detected before. Moreover, virus DNA was detected using nested PCR (by amplification of a portion of gp150 gene sequence) in the mammary glands and the milk of mouse mothers infected with MHV-72 2 days before delivery. We demonstrated the presence of virus DNA also in the milk removed from the stomach of non-infected newborn mice, which were nourished by infected mothers (wet-nurses) for 1 or 2 days. The failure to detect the virus DNA in newborn mice lungs confirmed that they did not become infected from wet-nurses by the intranasal route. This suggests that MHV may be naturally transmitted to newborn mice via breast milk.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>11453700</pmid><doi>10.1006/mpat.2001.0441</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Animals, Suckling Antibiotics. Antiinfectious agents. Antiparasitic agents Antifungal agents Biological and medical sciences Breast - virology Disease Models, Animal DNA, Viral - analysis Experimental mycoses and models Female Fundamental and applied biological sciences. Psychology Gammaherpesvirinae Gammaherpesvirinae - isolation & purification Gammaherpesvirinae - physiology Herpesviridae Infections - transmission Herpesviridae Infections - virology Immunocompetence Infectious Disease Transmission, Vertical Infectious diseases Lung - virology Lymph Nodes - virology Medical sciences Mice Mice, Inbred BALB C Mice, Nude Microbiology Milk - virology Murine gammaherpesvirus 72 murine herpesvirus 4 (MHV) strain 72, murine gammaherpesvirus, nude mice, milk, virus transmission, mammary glands Mycoses Pharmacology. Drug treatments Polymerase Chain Reaction Pregnancy Salivary Glands - virology Time Factors Virus Latency |
title | Susceptibility of mouse mammary glands to murine gammaherpesvirus 72 (MHV-72) infection: evidence of MHV-72 transmission via breast milk |
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