The evolution of resistance against good and bad infections

Opportunities for genetic exchange are abundant between bacteria and foreign genetic elements (FGEs) such as conjugative plasmids, transposable elements and bacteriophages. The genetic novelty that may arise from these forms of genetic exchange is potentially beneficial to bacterial hosts, but there...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of evolutionary biology 2014-02, Vol.27 (2), p.303-312
Hauptverfasser: Gandon, S., Vale, P. F.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 312
container_issue 2
container_start_page 303
container_title Journal of evolutionary biology
container_volume 27
creator Gandon, S.
Vale, P. F.
description Opportunities for genetic exchange are abundant between bacteria and foreign genetic elements (FGEs) such as conjugative plasmids, transposable elements and bacteriophages. The genetic novelty that may arise from these forms of genetic exchange is potentially beneficial to bacterial hosts, but there are also potential costs, which may be considerable in the case of phage infection. Some bacterial resistance mechanisms target both beneficial and deleterious forms of genetic exchange. Using a general epidemiological model, we explored under which conditions such resistance mechanisms may evolve. We considered a population of hosts that may be infected by FGEs that either confer a benefit or are deleterious to host fitness, and we analysed the epidemiological and evolutionary outcomes of resistance evolving under different cost/benefit scenarios. We show that the degree of co‐infection between these two types of infection is particularly important in determining the evolutionarily stable level of host resistance. We explore these results using the example of CRISPR‐Cas, a form of bacterial immunity that targets a variety of FGEs, and we show the potential role of bacteriophage infection in selecting for resistance mechanisms that in turn limit the acquisition of plasmid‐borne antibiotic resistance. Finally, beyond microbes, we discuss how endosymbiotic associations may have shaped the evolution of host immune responses to pathogens.
doi_str_mv 10.1111/jeb.12291
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1505346931</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1505346931</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4211-38f0c9d7658f5590e9424e92b576168de67c542d5a1a9468bd45818a0b07eefd3</originalsourceid><addsrcrecordid>eNqF0E9LwzAYx_EgipvTg29ACl700C1PmqQNnnTMfwy8TPBW0ubp7Oia2bTK3r2tnR4EMZfk8OEH-RJyCnQM7ZmsMBkDYwr2yBA4o74CCvvtmwL1qYSXATlybkUpSC7EIRkwHjAVCjEkV4tX9PDdFk2d29KzmVehy12tyxQ9vdR56Wpvaa3xdGm8RBsvLzNMO-yOyUGmC4cnu3tEnm9ni-m9P3-6e5hez_2UMwA_iDKaKhNKEWVCKIqKM46KJSKUICODMkwFZ0Zo0IrLKDFcRBBpmtAQMTPBiFz0u5vKvjXo6niduxSLQpdoGxeDoCLgUgXwP-WKhW2VgLX0_Bdd2aYq2490CoAJGXXqsldpZZ2rMIs3Vb7W1TYGGnfx4zZ-_BW_tWe7xSZZo_mR37VbMOnBR17g9u-l-HF2009-ArSMip4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1491125682</pqid></control><display><type>article</type><title>The evolution of resistance against good and bad infections</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Wiley Online Library All Journals</source><creator>Gandon, S. ; Vale, P. F.</creator><creatorcontrib>Gandon, S. ; Vale, P. F.</creatorcontrib><description>Opportunities for genetic exchange are abundant between bacteria and foreign genetic elements (FGEs) such as conjugative plasmids, transposable elements and bacteriophages. The genetic novelty that may arise from these forms of genetic exchange is potentially beneficial to bacterial hosts, but there are also potential costs, which may be considerable in the case of phage infection. Some bacterial resistance mechanisms target both beneficial and deleterious forms of genetic exchange. Using a general epidemiological model, we explored under which conditions such resistance mechanisms may evolve. We considered a population of hosts that may be infected by FGEs that either confer a benefit or are deleterious to host fitness, and we analysed the epidemiological and evolutionary outcomes of resistance evolving under different cost/benefit scenarios. We show that the degree of co‐infection between these two types of infection is particularly important in determining the evolutionarily stable level of host resistance. We explore these results using the example of CRISPR‐Cas, a form of bacterial immunity that targets a variety of FGEs, and we show the potential role of bacteriophage infection in selecting for resistance mechanisms that in turn limit the acquisition of plasmid‐borne antibiotic resistance. Finally, beyond microbes, we discuss how endosymbiotic associations may have shaped the evolution of host immune responses to pathogens.</description><identifier>ISSN: 1010-061X</identifier><identifier>EISSN: 1420-9101</identifier><identifier>DOI: 10.1111/jeb.12291</identifier><identifier>PMID: 24329755</identifier><language>eng</language><publisher>Switzerland: Blackwell Publishing Ltd</publisher><subject>Bacteria ; Bacteria - drug effects ; Bacteria - genetics ; bacteriophage ; Bacteriophages - genetics ; Biological Evolution ; co‐infection ; CRISPR ; Drug Resistance, Bacterial - genetics ; endosymbionts ; Evolution, Molecular ; Evolutionary biology ; horizontal gene transfer ; Immune system ; Infections ; Pathogens ; plasmid ; Plasmids ; resistance evolution</subject><ispartof>Journal of evolutionary biology, 2014-02, Vol.27 (2), p.303-312</ispartof><rights>2013 The Authors. Journal of Evolutionary Biology © 2013 European Society For Evolutionary Biology</rights><rights>2013 The Authors. Journal of Evolutionary Biology © 2013 European Society For Evolutionary Biology.</rights><rights>Journal of Evolutionary Biology © 2014 European Society For Evolutionary Biology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4211-38f0c9d7658f5590e9424e92b576168de67c542d5a1a9468bd45818a0b07eefd3</citedby><cites>FETCH-LOGICAL-c4211-38f0c9d7658f5590e9424e92b576168de67c542d5a1a9468bd45818a0b07eefd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjeb.12291$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjeb.12291$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24329755$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gandon, S.</creatorcontrib><creatorcontrib>Vale, P. F.</creatorcontrib><title>The evolution of resistance against good and bad infections</title><title>Journal of evolutionary biology</title><addtitle>J Evol Biol</addtitle><description>Opportunities for genetic exchange are abundant between bacteria and foreign genetic elements (FGEs) such as conjugative plasmids, transposable elements and bacteriophages. The genetic novelty that may arise from these forms of genetic exchange is potentially beneficial to bacterial hosts, but there are also potential costs, which may be considerable in the case of phage infection. Some bacterial resistance mechanisms target both beneficial and deleterious forms of genetic exchange. Using a general epidemiological model, we explored under which conditions such resistance mechanisms may evolve. We considered a population of hosts that may be infected by FGEs that either confer a benefit or are deleterious to host fitness, and we analysed the epidemiological and evolutionary outcomes of resistance evolving under different cost/benefit scenarios. We show that the degree of co‐infection between these two types of infection is particularly important in determining the evolutionarily stable level of host resistance. We explore these results using the example of CRISPR‐Cas, a form of bacterial immunity that targets a variety of FGEs, and we show the potential role of bacteriophage infection in selecting for resistance mechanisms that in turn limit the acquisition of plasmid‐borne antibiotic resistance. Finally, beyond microbes, we discuss how endosymbiotic associations may have shaped the evolution of host immune responses to pathogens.</description><subject>Bacteria</subject><subject>Bacteria - drug effects</subject><subject>Bacteria - genetics</subject><subject>bacteriophage</subject><subject>Bacteriophages - genetics</subject><subject>Biological Evolution</subject><subject>co‐infection</subject><subject>CRISPR</subject><subject>Drug Resistance, Bacterial - genetics</subject><subject>endosymbionts</subject><subject>Evolution, Molecular</subject><subject>Evolutionary biology</subject><subject>horizontal gene transfer</subject><subject>Immune system</subject><subject>Infections</subject><subject>Pathogens</subject><subject>plasmid</subject><subject>Plasmids</subject><subject>resistance evolution</subject><issn>1010-061X</issn><issn>1420-9101</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0E9LwzAYx_EgipvTg29ACl700C1PmqQNnnTMfwy8TPBW0ubp7Oia2bTK3r2tnR4EMZfk8OEH-RJyCnQM7ZmsMBkDYwr2yBA4o74CCvvtmwL1qYSXATlybkUpSC7EIRkwHjAVCjEkV4tX9PDdFk2d29KzmVehy12tyxQ9vdR56Wpvaa3xdGm8RBsvLzNMO-yOyUGmC4cnu3tEnm9ni-m9P3-6e5hez_2UMwA_iDKaKhNKEWVCKIqKM46KJSKUICODMkwFZ0Zo0IrLKDFcRBBpmtAQMTPBiFz0u5vKvjXo6niduxSLQpdoGxeDoCLgUgXwP-WKhW2VgLX0_Bdd2aYq2490CoAJGXXqsldpZZ2rMIs3Vb7W1TYGGnfx4zZ-_BW_tWe7xSZZo_mR37VbMOnBR17g9u-l-HF2009-ArSMip4</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Gandon, S.</creator><creator>Vale, P. F.</creator><general>Blackwell Publishing Ltd</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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7TK</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>201402</creationdate><title>The evolution of resistance against good and bad infections</title><author>Gandon, S. ; Vale, P. F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4211-38f0c9d7658f5590e9424e92b576168de67c542d5a1a9468bd45818a0b07eefd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Bacteria</topic><topic>Bacteria - drug effects</topic><topic>Bacteria - genetics</topic><topic>bacteriophage</topic><topic>Bacteriophages - genetics</topic><topic>Biological Evolution</topic><topic>co‐infection</topic><topic>CRISPR</topic><topic>Drug Resistance, Bacterial - genetics</topic><topic>endosymbionts</topic><topic>Evolution, Molecular</topic><topic>Evolutionary biology</topic><topic>horizontal gene transfer</topic><topic>Immune system</topic><topic>Infections</topic><topic>Pathogens</topic><topic>plasmid</topic><topic>Plasmids</topic><topic>resistance evolution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gandon, S.</creatorcontrib><creatorcontrib>Vale, P. F.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of evolutionary biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gandon, S.</au><au>Vale, P. F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The evolution of resistance against good and bad infections</atitle><jtitle>Journal of evolutionary biology</jtitle><addtitle>J Evol Biol</addtitle><date>2014-02</date><risdate>2014</risdate><volume>27</volume><issue>2</issue><spage>303</spage><epage>312</epage><pages>303-312</pages><issn>1010-061X</issn><eissn>1420-9101</eissn><abstract>Opportunities for genetic exchange are abundant between bacteria and foreign genetic elements (FGEs) such as conjugative plasmids, transposable elements and bacteriophages. The genetic novelty that may arise from these forms of genetic exchange is potentially beneficial to bacterial hosts, but there are also potential costs, which may be considerable in the case of phage infection. Some bacterial resistance mechanisms target both beneficial and deleterious forms of genetic exchange. Using a general epidemiological model, we explored under which conditions such resistance mechanisms may evolve. We considered a population of hosts that may be infected by FGEs that either confer a benefit or are deleterious to host fitness, and we analysed the epidemiological and evolutionary outcomes of resistance evolving under different cost/benefit scenarios. We show that the degree of co‐infection between these two types of infection is particularly important in determining the evolutionarily stable level of host resistance. We explore these results using the example of CRISPR‐Cas, a form of bacterial immunity that targets a variety of FGEs, and we show the potential role of bacteriophage infection in selecting for resistance mechanisms that in turn limit the acquisition of plasmid‐borne antibiotic resistance. Finally, beyond microbes, we discuss how endosymbiotic associations may have shaped the evolution of host immune responses to pathogens.</abstract><cop>Switzerland</cop><pub>Blackwell Publishing Ltd</pub><pmid>24329755</pmid><doi>10.1111/jeb.12291</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1010-061X
ispartof Journal of evolutionary biology, 2014-02, Vol.27 (2), p.303-312
issn 1010-061X
1420-9101
language eng
recordid cdi_proquest_miscellaneous_1505346931
source MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals
subjects Bacteria
Bacteria - drug effects
Bacteria - genetics
bacteriophage
Bacteriophages - genetics
Biological Evolution
co‐infection
CRISPR
Drug Resistance, Bacterial - genetics
endosymbionts
Evolution, Molecular
Evolutionary biology
horizontal gene transfer
Immune system
Infections
Pathogens
plasmid
Plasmids
resistance evolution
title The evolution of resistance against good and bad infections
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T03%3A03%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20evolution%20of%20resistance%20against%20good%20and%20bad%20infections&rft.jtitle=Journal%20of%20evolutionary%20biology&rft.au=Gandon,%20S.&rft.date=2014-02&rft.volume=27&rft.issue=2&rft.spage=303&rft.epage=312&rft.pages=303-312&rft.issn=1010-061X&rft.eissn=1420-9101&rft_id=info:doi/10.1111/jeb.12291&rft_dat=%3Cproquest_cross%3E1505346931%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1491125682&rft_id=info:pmid/24329755&rfr_iscdi=true