Extreme divergence of Wolbachia tropism for the stem-cell-niche in the Drosophila testis
Microbial tropism, the infection of specific cells and tissues by a microorganism, is a fundamental aspect of host-microbe interactions. The intracellular bacteria Wolbachia have a peculiar tropism for the stem cell niches in the Drosophila ovary, the microenvironments that support the cells produci...
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description | Microbial tropism, the infection of specific cells and tissues by a microorganism, is a fundamental aspect of host-microbe interactions. The intracellular bacteria Wolbachia have a peculiar tropism for the stem cell niches in the Drosophila ovary, the microenvironments that support the cells producing the eggs. The molecular underpinnings of Wolbachia stem cell niche tropism are unknown. We have previously shown that the patterns of tropism in the ovary show a high degree of conservation across the Wolbachia lineage, with closely related Wolbachia strains usually displaying the same pattern of stem cell niche tropism. It has also been shown that tropism to these structures in the ovary facilitates both vertical and horizontal transmission, providing a strong selective pressure towards evolutionary conservation of tropism. Here we show great disparity in the evolutionary conservation and underlying mechanisms of stem cell niche tropism between male and female gonads. In contrast to females, niche tropism in the male testis is not pervasive, present in only 45% of niches analyzed. The patterns of niche tropism in the testis are not evolutionarily maintained across the Wolbachia lineage, unlike what was shown in the females. Furthermore, hub tropism does not correlate with cytoplasmic incompatibility, a Wolbachia-driven phenotype imprinted during spermatogenesis. Towards identifying the molecular mechanism of hub tropism, we performed hybrid analyses of Wolbachia strains in non-native hosts. These results indicate that both Wolbachia and host derived factors play a role in the targeting of the stem cell niche in the testis. Surprisingly, even closely related Wolbachia strains in Drosophila melanogaster, derived from a single ancestor only 8,000 years ago, have significantly different tropisms to the hub, highlighting that stem cell niche tropism is rapidly diverging in males. These findings provide a powerful system to investigate the mechanisms and evolution of microbial tissue tropism. |
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The intracellular bacteria Wolbachia have a peculiar tropism for the stem cell niches in the Drosophila ovary, the microenvironments that support the cells producing the eggs. The molecular underpinnings of Wolbachia stem cell niche tropism are unknown. We have previously shown that the patterns of tropism in the ovary show a high degree of conservation across the Wolbachia lineage, with closely related Wolbachia strains usually displaying the same pattern of stem cell niche tropism. It has also been shown that tropism to these structures in the ovary facilitates both vertical and horizontal transmission, providing a strong selective pressure towards evolutionary conservation of tropism. Here we show great disparity in the evolutionary conservation and underlying mechanisms of stem cell niche tropism between male and female gonads. In contrast to females, niche tropism in the male testis is not pervasive, present in only 45% of niches analyzed. The patterns of niche tropism in the testis are not evolutionarily maintained across the Wolbachia lineage, unlike what was shown in the females. Furthermore, hub tropism does not correlate with cytoplasmic incompatibility, a Wolbachia-driven phenotype imprinted during spermatogenesis. Towards identifying the molecular mechanism of hub tropism, we performed hybrid analyses of Wolbachia strains in non-native hosts. These results indicate that both Wolbachia and host derived factors play a role in the targeting of the stem cell niche in the testis. Surprisingly, even closely related Wolbachia strains in Drosophila melanogaster, derived from a single ancestor only 8,000 years ago, have significantly different tropisms to the hub, highlighting that stem cell niche tropism is rapidly diverging in males. 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This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Testis. 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The intracellular bacteria Wolbachia have a peculiar tropism for the stem cell niches in the Drosophila ovary, the microenvironments that support the cells producing the eggs. The molecular underpinnings of Wolbachia stem cell niche tropism are unknown. We have previously shown that the patterns of tropism in the ovary show a high degree of conservation across the Wolbachia lineage, with closely related Wolbachia strains usually displaying the same pattern of stem cell niche tropism. It has also been shown that tropism to these structures in the ovary facilitates both vertical and horizontal transmission, providing a strong selective pressure towards evolutionary conservation of tropism. Here we show great disparity in the evolutionary conservation and underlying mechanisms of stem cell niche tropism between male and female gonads. In contrast to females, niche tropism in the male testis is not pervasive, present in only 45% of niches analyzed. The patterns of niche tropism in the testis are not evolutionarily maintained across the Wolbachia lineage, unlike what was shown in the females. Furthermore, hub tropism does not correlate with cytoplasmic incompatibility, a Wolbachia-driven phenotype imprinted during spermatogenesis. Towards identifying the molecular mechanism of hub tropism, we performed hybrid analyses of Wolbachia strains in non-native hosts. These results indicate that both Wolbachia and host derived factors play a role in the targeting of the stem cell niche in the testis. Surprisingly, even closely related Wolbachia strains in Drosophila melanogaster, derived from a single ancestor only 8,000 years ago, have significantly different tropisms to the hub, highlighting that stem cell niche tropism is rapidly diverging in males. These findings provide a powerful system to investigate the mechanisms and evolution of microbial tissue tropism.</description><subject>Animal reproduction</subject><subject>Animals</subject><subject>Bacteria</subject><subject>Biology and Life Sciences</subject><subject>Competition</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - microbiology</subject><subject>Eggs</subject><subject>Female</subject><subject>Females</subject><subject>Health aspects</subject><subject>Infections</subject><subject>Insects</subject><subject>Male</subject><subject>Males</subject><subject>Microbiological research</subject><subject>Ovary - microbiology</subject><subject>Phenotype</subject><subject>Phylogeny</subject><subject>Research and Analysis Methods</subject><subject>Sex Factors</subject><subject>Sperm</subject><subject>Stem Cell Niche - physiology</subject><subject>Stem cell research</subject><subject>Stem cells</subject><subject>Testis - microbiology</subject><subject>Tropical diseases</subject><subject>Tropism - physiology</subject><subject>Tropisms</subject><subject>Wolbachia</subject><subject>Wolbachia - physiology</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVkktv1DAUhSMEoqXwDxBEYgOLDH7EdrJBqkppR6pA4iHYWY4fGY-SONhOVf49TietGokNyiL29XdOrk9ulr2EYAMxg-_3bvKD6DbjKOIGAlASxh5lx5AQXDDMyscP1kfZsxD2iYEY0qfZESIEQQrr4-zX-U30ute5stfat3qQOncm_-m6RsidFXn0brShz43zedzpPETdF1J3XTFYmfZ2uC1_9C64cWe7pNAh2vA8e2JEF_SL5X2S_fh0_v3ssrj6crE9O70qJMU4FqSEEmhTmcakPolRGJaYCNSUDSFVZZQEAimCASSQIgqVFAoDVqm0oqJB-CR7ffAdOxf4EkrgkFYE1YAymojtgVBO7PnobS_8H-6E5bcF51sufLSy0xwr2KiGGlkbUTaobphmjNVYlQxVDInk9WH52tT0Wkk9RC-6len6ZLA73rprXiIGklEyeLsYePd7Sknx3oY5TjFoN81947pmVUXKhL45oK1IrdnBuOQoZ5yf4ppSSEA9327zDyo9SvdWukEbm-orwbuVIDFR38RWTCHw7bev_8F-XrPlgZVpFILX5j4VCPg8sXc_h88Ty5eJTbJXDxO9F92NKP4LEwDnxQ</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Toomey, Michelle E</creator><creator>Frydman, Horacio M</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20141201</creationdate><title>Extreme divergence of Wolbachia tropism for the stem-cell-niche in the Drosophila testis</title><author>Toomey, Michelle E ; Frydman, Horacio M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c633t-541c0ef8fbf3745fd31435a2b4b5588fdc0a2d5301516261dcad3078d1dc6ab23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animal reproduction</topic><topic>Animals</topic><topic>Bacteria</topic><topic>Biology and Life Sciences</topic><topic>Competition</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - microbiology</topic><topic>Eggs</topic><topic>Female</topic><topic>Females</topic><topic>Health aspects</topic><topic>Infections</topic><topic>Insects</topic><topic>Male</topic><topic>Males</topic><topic>Microbiological research</topic><topic>Ovary - microbiology</topic><topic>Phenotype</topic><topic>Phylogeny</topic><topic>Research and Analysis Methods</topic><topic>Sex Factors</topic><topic>Sperm</topic><topic>Stem Cell Niche - physiology</topic><topic>Stem cell research</topic><topic>Stem cells</topic><topic>Testis - microbiology</topic><topic>Tropical diseases</topic><topic>Tropism - physiology</topic><topic>Tropisms</topic><topic>Wolbachia</topic><topic>Wolbachia - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Toomey, Michelle E</creatorcontrib><creatorcontrib>Frydman, Horacio M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Toomey, Michelle E</au><au>Frydman, Horacio M</au><au>Rasgon, Jason L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extreme divergence of Wolbachia tropism for the stem-cell-niche in the Drosophila testis</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>10</volume><issue>12</issue><spage>e1004577</spage><epage>e1004577</epage><pages>e1004577-e1004577</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>Microbial tropism, the infection of specific cells and tissues by a microorganism, is a fundamental aspect of host-microbe interactions. The intracellular bacteria Wolbachia have a peculiar tropism for the stem cell niches in the Drosophila ovary, the microenvironments that support the cells producing the eggs. The molecular underpinnings of Wolbachia stem cell niche tropism are unknown. We have previously shown that the patterns of tropism in the ovary show a high degree of conservation across the Wolbachia lineage, with closely related Wolbachia strains usually displaying the same pattern of stem cell niche tropism. It has also been shown that tropism to these structures in the ovary facilitates both vertical and horizontal transmission, providing a strong selective pressure towards evolutionary conservation of tropism. Here we show great disparity in the evolutionary conservation and underlying mechanisms of stem cell niche tropism between male and female gonads. In contrast to females, niche tropism in the male testis is not pervasive, present in only 45% of niches analyzed. The patterns of niche tropism in the testis are not evolutionarily maintained across the Wolbachia lineage, unlike what was shown in the females. Furthermore, hub tropism does not correlate with cytoplasmic incompatibility, a Wolbachia-driven phenotype imprinted during spermatogenesis. Towards identifying the molecular mechanism of hub tropism, we performed hybrid analyses of Wolbachia strains in non-native hosts. These results indicate that both Wolbachia and host derived factors play a role in the targeting of the stem cell niche in the testis. Surprisingly, even closely related Wolbachia strains in Drosophila melanogaster, derived from a single ancestor only 8,000 years ago, have significantly different tropisms to the hub, highlighting that stem cell niche tropism is rapidly diverging in males. These findings provide a powerful system to investigate the mechanisms and evolution of microbial tissue tropism.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25521619</pmid><doi>10.1371/journal.ppat.1004577</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animal reproduction Animals Bacteria Biology and Life Sciences Competition Drosophila Drosophila melanogaster - microbiology Eggs Female Females Health aspects Infections Insects Male Males Microbiological research Ovary - microbiology Phenotype Phylogeny Research and Analysis Methods Sex Factors Sperm Stem Cell Niche - physiology Stem cell research Stem cells Testis - microbiology Tropical diseases Tropism - physiology Tropisms Wolbachia Wolbachia - physiology |
title | Extreme divergence of Wolbachia tropism for the stem-cell-niche in the Drosophila testis |
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