Defensive symbiosis in the real world – advancing ecological studies of heritable, protective bacteria in aphids and beyond
Symbiotic microbes have become increasingly recognized to mediate interactions between natural enemies and their hosts. The ecologies of these symbioses, however, are poorly understood in many systems, and a predictive framework is needed to guide future studies. To achieve this, we focus on heritab...
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description | Symbiotic microbes have become increasingly recognized to mediate interactions between natural enemies and their hosts. The ecologies of these symbioses, however, are poorly understood in many systems, and a predictive framework is needed to guide future studies. To achieve this, we focus on heritable, defensive microbes of insects. Our review of laboratory‐based studies identifies diverse bacterial species that have independently evolved to protect a range of insects against parasitoids, parasites, predators and pathogens. Although defensive mechanisms are typically unknown, some involve toxins or the upregulation of host immunity. Despite substantial benefits of infection in the presence of natural enemies, the protective symbionts of insects are often found at intermediate levels in natural populations. Using a host‐centred population genetics approach made possible by the host restriction and cytoplasmic inheritance of these microbes, we propose that balancing selection plays a major role in symbiont maintenance, with protective benefits in the presence of enemies and infection costs in their absence. Other mediating factors are likely to be important, including temperature, superinfections and transmission dynamics. While few studies have provided evidence for defence in the field, several studies have shown symbiont infection frequencies to be dynamic, varying across temporal and spatial gradients and food–plant associations. Newly presented data from our pea aphid research reveal that temporal shifts in defensive symbiont prevalence can be quite rapid, with Hamiltonella defensa showing 10–20% shifts around a seasonal average of c. 50%. Such findings contrast with more unidirectional changes seen in laboratory population cages, suggesting temporal changes in the costs and benefits of symbionts in the field. To frame future research on defensive symbiont ecology, we briefly consider a range of studies needed to test laboratory‐ and field‐derived predictions on defensive symbiosis. Included are investigations of defensive mechanisms, symbiont‐driven co‐evolution and community‐level effects. We also consider the need for more thorough and highly resolved molecular diagnostics of natural infections, laboratory studies on functional differences between symbiont strains and species and studies on the relative costs and benefits of defenders in nature. The emerging theme of symbiont‐mediated defence across eukaryotes suggests that knowledge of the functiona |
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The ecologies of these symbioses, however, are poorly understood in many systems, and a predictive framework is needed to guide future studies. To achieve this, we focus on heritable, defensive microbes of insects. Our review of laboratory‐based studies identifies diverse bacterial species that have independently evolved to protect a range of insects against parasitoids, parasites, predators and pathogens. Although defensive mechanisms are typically unknown, some involve toxins or the upregulation of host immunity. Despite substantial benefits of infection in the presence of natural enemies, the protective symbionts of insects are often found at intermediate levels in natural populations. Using a host‐centred population genetics approach made possible by the host restriction and cytoplasmic inheritance of these microbes, we propose that balancing selection plays a major role in symbiont maintenance, with protective benefits in the presence of enemies and infection costs in their absence. Other mediating factors are likely to be important, including temperature, superinfections and transmission dynamics. While few studies have provided evidence for defence in the field, several studies have shown symbiont infection frequencies to be dynamic, varying across temporal and spatial gradients and food–plant associations. Newly presented data from our pea aphid research reveal that temporal shifts in defensive symbiont prevalence can be quite rapid, with Hamiltonella defensa showing 10–20% shifts around a seasonal average of c. 50%. Such findings contrast with more unidirectional changes seen in laboratory population cages, suggesting temporal changes in the costs and benefits of symbionts in the field. To frame future research on defensive symbiont ecology, we briefly consider a range of studies needed to test laboratory‐ and field‐derived predictions on defensive symbiosis. Included are investigations of defensive mechanisms, symbiont‐driven co‐evolution and community‐level effects. We also consider the need for more thorough and highly resolved molecular diagnostics of natural infections, laboratory studies on functional differences between symbiont strains and species and studies on the relative costs and benefits of defenders in nature. The emerging theme of symbiont‐mediated defence across eukaryotes suggests that knowledge of the functional mechanisms behind protection and natural symbiont dynamics could be key to understanding many of the world's antagonistic species interactions. Thus, the development of insects as a model for such studies holds promise for these organisms and beyond.</description><identifier>ISSN: 0269-8463</identifier><identifier>EISSN: 1365-2435</identifier><identifier>DOI: 10.1111/1365-2435.12133</identifier><identifier>CODEN: FECOE5</identifier><language>eng</language><publisher>London: John Wiley & Sons Ltd</publisher><subject>Acyrthosiphon pisum ; aphid‐parasitoid ; Bacteria ; balancing selection ; cages ; cytoplasmic inheritance ; Ecological genetics ; ecological immunity ; endosymbiont ; eukaryotic cells ; Heritability ; hosts ; host‐parasite ; Human ecology ; immunity ; Infections ; Insect ecology ; insects ; Medical research ; microbial diversity ; microsymbionts ; mutualism ; natural enemies ; Parasite hosts ; parasites ; pathogens ; Population ecology ; population genetics ; predators ; SPECIAL FEATURE: DEFENSIVE SYMBIOSIS ; Symbionts ; Symbiosis ; temperature ; temporal variation ; toxins</subject><ispartof>Functional ecology, 2014-04, Vol.28 (2), p.341-355</ispartof><rights>2014 British Ecological Society</rights><rights>2013 The Authors. Functional Ecology © 2013 British Ecological Society</rights><rights>Functional Ecology © 2014 British Ecological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4683-8fdbfe33638b4a363010d08888f7291a02439195ff812e9542ebddd7448205313</citedby><cites>FETCH-LOGICAL-c4683-8fdbfe33638b4a363010d08888f7291a02439195ff812e9542ebddd7448205313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/24033669$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/24033669$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,1411,1427,27903,27904,45553,45554,46388,46812,57996,58229</link.rule.ids></links><search><contributor>Clay, Keith</contributor><creatorcontrib>Oliver, Kerry M</creatorcontrib><creatorcontrib>Smith, Andrew H</creatorcontrib><creatorcontrib>Russell, Jacob A</creatorcontrib><creatorcontrib>Clay, Keith</creatorcontrib><title>Defensive symbiosis in the real world – advancing ecological studies of heritable, protective bacteria in aphids and beyond</title><title>Functional ecology</title><description>Symbiotic microbes have become increasingly recognized to mediate interactions between natural enemies and their hosts. The ecologies of these symbioses, however, are poorly understood in many systems, and a predictive framework is needed to guide future studies. To achieve this, we focus on heritable, defensive microbes of insects. Our review of laboratory‐based studies identifies diverse bacterial species that have independently evolved to protect a range of insects against parasitoids, parasites, predators and pathogens. Although defensive mechanisms are typically unknown, some involve toxins or the upregulation of host immunity. Despite substantial benefits of infection in the presence of natural enemies, the protective symbionts of insects are often found at intermediate levels in natural populations. Using a host‐centred population genetics approach made possible by the host restriction and cytoplasmic inheritance of these microbes, we propose that balancing selection plays a major role in symbiont maintenance, with protective benefits in the presence of enemies and infection costs in their absence. Other mediating factors are likely to be important, including temperature, superinfections and transmission dynamics. While few studies have provided evidence for defence in the field, several studies have shown symbiont infection frequencies to be dynamic, varying across temporal and spatial gradients and food–plant associations. Newly presented data from our pea aphid research reveal that temporal shifts in defensive symbiont prevalence can be quite rapid, with Hamiltonella defensa showing 10–20% shifts around a seasonal average of c. 50%. Such findings contrast with more unidirectional changes seen in laboratory population cages, suggesting temporal changes in the costs and benefits of symbionts in the field. To frame future research on defensive symbiont ecology, we briefly consider a range of studies needed to test laboratory‐ and field‐derived predictions on defensive symbiosis. Included are investigations of defensive mechanisms, symbiont‐driven co‐evolution and community‐level effects. We also consider the need for more thorough and highly resolved molecular diagnostics of natural infections, laboratory studies on functional differences between symbiont strains and species and studies on the relative costs and benefits of defenders in nature. The emerging theme of symbiont‐mediated defence across eukaryotes suggests that knowledge of the functional mechanisms behind protection and natural symbiont dynamics could be key to understanding many of the world's antagonistic species interactions. Thus, the development of insects as a model for such studies holds promise for these organisms and beyond.</description><subject>Acyrthosiphon pisum</subject><subject>aphid‐parasitoid</subject><subject>Bacteria</subject><subject>balancing selection</subject><subject>cages</subject><subject>cytoplasmic inheritance</subject><subject>Ecological genetics</subject><subject>ecological immunity</subject><subject>endosymbiont</subject><subject>eukaryotic cells</subject><subject>Heritability</subject><subject>hosts</subject><subject>host‐parasite</subject><subject>Human ecology</subject><subject>immunity</subject><subject>Infections</subject><subject>Insect ecology</subject><subject>insects</subject><subject>Medical research</subject><subject>microbial diversity</subject><subject>microsymbionts</subject><subject>mutualism</subject><subject>natural enemies</subject><subject>Parasite hosts</subject><subject>parasites</subject><subject>pathogens</subject><subject>Population ecology</subject><subject>population genetics</subject><subject>predators</subject><subject>SPECIAL FEATURE: DEFENSIVE SYMBIOSIS</subject><subject>Symbionts</subject><subject>Symbiosis</subject><subject>temperature</subject><subject>temporal variation</subject><subject>toxins</subject><issn>0269-8463</issn><issn>1365-2435</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFUTtPwzAQthBIlMLMhLDESsDPNBlReUpIDMBsOfG5dRXiYqegDkj8B_4hvwSHACu3nOTvcb7vENqn5ISmOqU8lxkTXJ5QRjnfQKO_l000Iiwvs0LkfBvtxLgghJSSsRF6OwcLbXQvgOP6qXI-uohdi7s54AC6wa8-NAZ_vn9gbV50W7t2hqH2jZ-5OsGxWxkHEXuL5xBcp6sGjvEy-A7qrnetdN0lQPemejl3JmLdGlzB2rdmF21Z3UTY--lj9Hh58TC9zm7vrm6mZ7dZLfKCZ4U1lQXOc15UQqdGKDGkSGUnrKSapCVLWkprC8qglIJBZYyZCFEwIjnlY3Q0-KaPPa8gdmrhV6FNIxWVZJIoZeKN0enAqoOPMYBVy-CedFgrSlSfseoTVX2i6jvjpJCD4tU1sP6Pri4vpr-6g0G3iJ0PfzomSFoyLxN-OOBWe6VnwUX1eM8IFelu6Wxc8i-WSpE6</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Oliver, Kerry M</creator><creator>Smith, Andrew H</creator><creator>Russell, Jacob A</creator><creator>Clay, Keith</creator><general>John Wiley & Sons Ltd</general><general>Wiley Subscription Services, Inc</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201404</creationdate><title>Defensive symbiosis in the real world – advancing ecological studies of heritable, protective bacteria in aphids and beyond</title><author>Oliver, Kerry M ; Smith, Andrew H ; Russell, Jacob A ; Clay, Keith</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4683-8fdbfe33638b4a363010d08888f7291a02439195ff812e9542ebddd7448205313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acyrthosiphon pisum</topic><topic>aphid‐parasitoid</topic><topic>Bacteria</topic><topic>balancing selection</topic><topic>cages</topic><topic>cytoplasmic inheritance</topic><topic>Ecological genetics</topic><topic>ecological immunity</topic><topic>endosymbiont</topic><topic>eukaryotic cells</topic><topic>Heritability</topic><topic>hosts</topic><topic>host‐parasite</topic><topic>Human ecology</topic><topic>immunity</topic><topic>Infections</topic><topic>Insect ecology</topic><topic>insects</topic><topic>Medical research</topic><topic>microbial diversity</topic><topic>microsymbionts</topic><topic>mutualism</topic><topic>natural enemies</topic><topic>Parasite hosts</topic><topic>parasites</topic><topic>pathogens</topic><topic>Population ecology</topic><topic>population genetics</topic><topic>predators</topic><topic>SPECIAL FEATURE: DEFENSIVE SYMBIOSIS</topic><topic>Symbionts</topic><topic>Symbiosis</topic><topic>temperature</topic><topic>temporal variation</topic><topic>toxins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oliver, Kerry M</creatorcontrib><creatorcontrib>Smith, Andrew H</creatorcontrib><creatorcontrib>Russell, Jacob A</creatorcontrib><creatorcontrib>Clay, Keith</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Functional ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oliver, Kerry M</au><au>Smith, Andrew H</au><au>Russell, Jacob A</au><au>Clay, Keith</au><au>Clay, Keith</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Defensive symbiosis in the real world – advancing ecological studies of heritable, protective bacteria in aphids and beyond</atitle><jtitle>Functional ecology</jtitle><date>2014-04</date><risdate>2014</risdate><volume>28</volume><issue>2</issue><spage>341</spage><epage>355</epage><pages>341-355</pages><issn>0269-8463</issn><eissn>1365-2435</eissn><coden>FECOE5</coden><abstract>Symbiotic microbes have become increasingly recognized to mediate interactions between natural enemies and their hosts. The ecologies of these symbioses, however, are poorly understood in many systems, and a predictive framework is needed to guide future studies. To achieve this, we focus on heritable, defensive microbes of insects. Our review of laboratory‐based studies identifies diverse bacterial species that have independently evolved to protect a range of insects against parasitoids, parasites, predators and pathogens. Although defensive mechanisms are typically unknown, some involve toxins or the upregulation of host immunity. Despite substantial benefits of infection in the presence of natural enemies, the protective symbionts of insects are often found at intermediate levels in natural populations. Using a host‐centred population genetics approach made possible by the host restriction and cytoplasmic inheritance of these microbes, we propose that balancing selection plays a major role in symbiont maintenance, with protective benefits in the presence of enemies and infection costs in their absence. Other mediating factors are likely to be important, including temperature, superinfections and transmission dynamics. While few studies have provided evidence for defence in the field, several studies have shown symbiont infection frequencies to be dynamic, varying across temporal and spatial gradients and food–plant associations. Newly presented data from our pea aphid research reveal that temporal shifts in defensive symbiont prevalence can be quite rapid, with Hamiltonella defensa showing 10–20% shifts around a seasonal average of c. 50%. Such findings contrast with more unidirectional changes seen in laboratory population cages, suggesting temporal changes in the costs and benefits of symbionts in the field. To frame future research on defensive symbiont ecology, we briefly consider a range of studies needed to test laboratory‐ and field‐derived predictions on defensive symbiosis. Included are investigations of defensive mechanisms, symbiont‐driven co‐evolution and community‐level effects. We also consider the need for more thorough and highly resolved molecular diagnostics of natural infections, laboratory studies on functional differences between symbiont strains and species and studies on the relative costs and benefits of defenders in nature. The emerging theme of symbiont‐mediated defence across eukaryotes suggests that knowledge of the functional mechanisms behind protection and natural symbiont dynamics could be key to understanding many of the world's antagonistic species interactions. Thus, the development of insects as a model for such studies holds promise for these organisms and beyond.</abstract><cop>London</cop><pub>John Wiley & Sons Ltd</pub><doi>10.1111/1365-2435.12133</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acyrthosiphon pisum aphid‐parasitoid Bacteria balancing selection cages cytoplasmic inheritance Ecological genetics ecological immunity endosymbiont eukaryotic cells Heritability hosts host‐parasite Human ecology immunity Infections Insect ecology insects Medical research microbial diversity microsymbionts mutualism natural enemies Parasite hosts parasites pathogens Population ecology population genetics predators SPECIAL FEATURE: DEFENSIVE SYMBIOSIS Symbionts Symbiosis temperature temporal variation toxins |
title | Defensive symbiosis in the real world – advancing ecological studies of heritable, protective bacteria in aphids and beyond |
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