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Amoeba Predation of Cryptococcus neoformans Results in Pleiotropic Changes to Traits Associated with Virulence
Amoeboid predators, such as amoebae, are proposed to select for survival traits in soil microbes such as ; these traits can also function in animal virulence by defeating phagocytic immune cells, such as macrophages. Consistent with this notion, incubation of various fungal species with amoebae enha...
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description | Amoeboid predators, such as amoebae, are proposed to select for survival traits in soil microbes such as
; these traits can also function in animal virulence by defeating phagocytic immune cells, such as macrophages. Consistent with this notion, incubation of various fungal species with amoebae enhanced their virulence, but the mechanisms involved are unknown. In this study, we exposed three strains of
(1 clinical and 2 environmental) to predation by
for prolonged times and then analyzed surviving colonies phenotypically and genetically. Surviving colonies comprised cells that expressed either pseudohyphal or yeast phenotypes, which demonstrated variable expression of traits associated with virulence, such as capsule size, urease production, and melanization. Phenotypic changes were associated with aneuploidy and DNA sequence mutations in some amoeba-passaged isolates, but not in others. Mutations in the gene encoding the oligopeptide transporter (CNAG_03013;
) were observed among amoeba-passaged isolates from each of the three strains. Isolates derived from environmental strains gained the capacity for enhanced macrophage toxicity after amoeba selection and carried mutations on the CNAG_00570 gene encoding Pkr1 (AMP-dependent protein kinase regulator) but manifested reduced virulence in mice because they elicited more effective fungal-clearing immune responses. Our results indicate that
survival under constant amoeba predation involves the generation of strains expressing pleiotropic phenotypic and genetic changes. Given the myriad potential predators in soils, the diversity observed among amoeba-selected strains suggests a bet-hedging strategy whereby variant diversity increases the likelihood that some will survive predation.
is a ubiquitous environmental fungus that is also a leading cause of fatal fungal infection in humans, especially among immunocompromised patients. A major question in the field is how an environmental yeast such as
becomes a human pathogen when it has no need for an animal host in its life cycle. Previous studies showed that
increases its pathogenicity after interacting with its environmental predator amoebae. Amoebae, like macrophages, are phagocytic cells that are considered an environmental training ground for pathogens to resist macrophages, but the mechanism by which
changes its virulence through interactions with protozoa is unknown. Our study indicates that fungal survival in the face of amoeba predation is associated with |
doi_str_mv | 10.1128/mBio.00567-21 |
format | article |
fullrecord | <record><control><sourceid>pubmed_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_7d807b6732be42d59a6d6c9ece540127</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_7d807b6732be42d59a6d6c9ece540127</doaj_id><sourcerecordid>33906924</sourcerecordid><originalsourceid>FETCH-LOGICAL-a488t-506ab126fe26728bb9f7eb5a1f3912fd889d53abdd47a7c1fc2bf5d8ddc6d6e93</originalsourceid><addsrcrecordid>eNp1kctrHDEMxofS0oQkx16Lz4VJ_RiPPZfCdukjEEgoSa7GD3nXy4y92J6U_PedZNuQHKqLhPTph9DXNB8IPieEys_T15DOMea9aCl50xxTwnErOCFvX9RHzVkpO7wEY0Qy_L45YmzA_UC74yaupgRGo-sMTteQIkoerfPDviabrJ0LipB8ypOOBf2CMo-1oBDR9Qgh1Zz2waL1VscNFFQTusk6LIJVKckGXcGh36Fu0V3I8wjRwmnzzuuxwNnffNLcfv92s_7ZXl79uFivLlvdSVlbjnttCO090F5QaczgBRiuiWcDod5JOTjOtHGuE1pY4i01njvpnO1dDwM7aS4OXJf0Tu1zmHR-UEkH9dRIeaN0rsGOoISTWJheMGqgo44PekHYASzwDhMqFtaXA2s_mwmchVizHl9BX09i2KpNulcSD5RyugDaA8DmVEoG_7xLsHr0UT36qJ58VJQs-k8HvS4TVbs057j86r_ijy-ve0b_s5j9AXMNqgI</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Amoeba Predation of Cryptococcus neoformans Results in Pleiotropic Changes to Traits Associated with Virulence</title><source>American Society for Microbiology</source><source>PubMed Central</source><creator>Fu, Man Shun ; Liporagi-Lopes, Livia C ; Dos Santos, Júnior, Samuel R ; Tenor, Jennifer L ; Perfect, John R ; Cuomo, Christina A ; Casadevall, Arturo</creator><contributor>Wormley, Floyd L ; Olszewski, Michal A ; Olszewski, Michal A. ; Wormley, Floyd L.</contributor><creatorcontrib>Fu, Man Shun ; Liporagi-Lopes, Livia C ; Dos Santos, Júnior, Samuel R ; Tenor, Jennifer L ; Perfect, John R ; Cuomo, Christina A ; Casadevall, Arturo ; Wormley, Floyd L ; Olszewski, Michal A ; Olszewski, Michal A. ; Wormley, Floyd L.</creatorcontrib><description>Amoeboid predators, such as amoebae, are proposed to select for survival traits in soil microbes such as
; these traits can also function in animal virulence by defeating phagocytic immune cells, such as macrophages. Consistent with this notion, incubation of various fungal species with amoebae enhanced their virulence, but the mechanisms involved are unknown. In this study, we exposed three strains of
(1 clinical and 2 environmental) to predation by
for prolonged times and then analyzed surviving colonies phenotypically and genetically. Surviving colonies comprised cells that expressed either pseudohyphal or yeast phenotypes, which demonstrated variable expression of traits associated with virulence, such as capsule size, urease production, and melanization. Phenotypic changes were associated with aneuploidy and DNA sequence mutations in some amoeba-passaged isolates, but not in others. Mutations in the gene encoding the oligopeptide transporter (CNAG_03013;
) were observed among amoeba-passaged isolates from each of the three strains. Isolates derived from environmental strains gained the capacity for enhanced macrophage toxicity after amoeba selection and carried mutations on the CNAG_00570 gene encoding Pkr1 (AMP-dependent protein kinase regulator) but manifested reduced virulence in mice because they elicited more effective fungal-clearing immune responses. Our results indicate that
survival under constant amoeba predation involves the generation of strains expressing pleiotropic phenotypic and genetic changes. Given the myriad potential predators in soils, the diversity observed among amoeba-selected strains suggests a bet-hedging strategy whereby variant diversity increases the likelihood that some will survive predation.
is a ubiquitous environmental fungus that is also a leading cause of fatal fungal infection in humans, especially among immunocompromised patients. A major question in the field is how an environmental yeast such as
becomes a human pathogen when it has no need for an animal host in its life cycle. Previous studies showed that
increases its pathogenicity after interacting with its environmental predator amoebae. Amoebae, like macrophages, are phagocytic cells that are considered an environmental training ground for pathogens to resist macrophages, but the mechanism by which
changes its virulence through interactions with protozoa is unknown. Our study indicates that fungal survival in the face of amoeba predation is associated with the emergence of pleiotropic phenotypic and genomic changes that increase the chance of fungal survival, with this diversity suggesting a bet-hedging strategy to ensure that some forms survive.</description><identifier>ISSN: 2150-7511</identifier><identifier>EISSN: 2150-7511</identifier><identifier>DOI: 10.1128/mBio.00567-21</identifier><identifier>PMID: 33906924</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Acanthamoeba castellanii - microbiology ; Acanthamoeba castellanii - physiology ; Animals ; Cryptococcosis - immunology ; Cryptococcosis - microbiology ; Cryptococcus neoformans - classification ; Cryptococcus neoformans - genetics ; Cryptococcus neoformans - pathogenicity ; Cytokines - immunology ; Female ; Humans ; Larva - microbiology ; Macrophages - microbiology ; Mice ; Mice, Inbred C57BL ; Moths - microbiology ; Phagocytes - microbiology ; Phagocytosis ; Phenotype ; Research Article ; Virulence</subject><ispartof>mBio, 2021-04, Vol.12 (2)</ispartof><rights>Copyright © 2021 Fu et al.</rights><rights>Copyright © 2021 Fu et al. 2021 Fu et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a488t-506ab126fe26728bb9f7eb5a1f3912fd889d53abdd47a7c1fc2bf5d8ddc6d6e93</citedby><cites>FETCH-LOGICAL-a488t-506ab126fe26728bb9f7eb5a1f3912fd889d53abdd47a7c1fc2bf5d8ddc6d6e93</cites><orcidid>0000-0002-9402-9167 ; 0000-0002-5778-960X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/mBio.00567-21$$EPDF$$P50$$Gasm2$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/mBio.00567-21$$EHTML$$P50$$Gasm2$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,52751,52752,52753,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33906924$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Wormley, Floyd L</contributor><contributor>Olszewski, Michal A</contributor><contributor>Olszewski, Michal A.</contributor><contributor>Wormley, Floyd L.</contributor><creatorcontrib>Fu, Man Shun</creatorcontrib><creatorcontrib>Liporagi-Lopes, Livia C</creatorcontrib><creatorcontrib>Dos Santos, Júnior, Samuel R</creatorcontrib><creatorcontrib>Tenor, Jennifer L</creatorcontrib><creatorcontrib>Perfect, John R</creatorcontrib><creatorcontrib>Cuomo, Christina A</creatorcontrib><creatorcontrib>Casadevall, Arturo</creatorcontrib><title>Amoeba Predation of Cryptococcus neoformans Results in Pleiotropic Changes to Traits Associated with Virulence</title><title>mBio</title><addtitle>mBio</addtitle><addtitle>mBio</addtitle><description>Amoeboid predators, such as amoebae, are proposed to select for survival traits in soil microbes such as
; these traits can also function in animal virulence by defeating phagocytic immune cells, such as macrophages. Consistent with this notion, incubation of various fungal species with amoebae enhanced their virulence, but the mechanisms involved are unknown. In this study, we exposed three strains of
(1 clinical and 2 environmental) to predation by
for prolonged times and then analyzed surviving colonies phenotypically and genetically. Surviving colonies comprised cells that expressed either pseudohyphal or yeast phenotypes, which demonstrated variable expression of traits associated with virulence, such as capsule size, urease production, and melanization. Phenotypic changes were associated with aneuploidy and DNA sequence mutations in some amoeba-passaged isolates, but not in others. Mutations in the gene encoding the oligopeptide transporter (CNAG_03013;
) were observed among amoeba-passaged isolates from each of the three strains. Isolates derived from environmental strains gained the capacity for enhanced macrophage toxicity after amoeba selection and carried mutations on the CNAG_00570 gene encoding Pkr1 (AMP-dependent protein kinase regulator) but manifested reduced virulence in mice because they elicited more effective fungal-clearing immune responses. Our results indicate that
survival under constant amoeba predation involves the generation of strains expressing pleiotropic phenotypic and genetic changes. Given the myriad potential predators in soils, the diversity observed among amoeba-selected strains suggests a bet-hedging strategy whereby variant diversity increases the likelihood that some will survive predation.
is a ubiquitous environmental fungus that is also a leading cause of fatal fungal infection in humans, especially among immunocompromised patients. A major question in the field is how an environmental yeast such as
becomes a human pathogen when it has no need for an animal host in its life cycle. Previous studies showed that
increases its pathogenicity after interacting with its environmental predator amoebae. Amoebae, like macrophages, are phagocytic cells that are considered an environmental training ground for pathogens to resist macrophages, but the mechanism by which
changes its virulence through interactions with protozoa is unknown. Our study indicates that fungal survival in the face of amoeba predation is associated with the emergence of pleiotropic phenotypic and genomic changes that increase the chance of fungal survival, with this diversity suggesting a bet-hedging strategy to ensure that some forms survive.</description><subject>Acanthamoeba castellanii - microbiology</subject><subject>Acanthamoeba castellanii - physiology</subject><subject>Animals</subject><subject>Cryptococcosis - immunology</subject><subject>Cryptococcosis - microbiology</subject><subject>Cryptococcus neoformans - classification</subject><subject>Cryptococcus neoformans - genetics</subject><subject>Cryptococcus neoformans - pathogenicity</subject><subject>Cytokines - immunology</subject><subject>Female</subject><subject>Humans</subject><subject>Larva - microbiology</subject><subject>Macrophages - microbiology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Moths - microbiology</subject><subject>Phagocytes - microbiology</subject><subject>Phagocytosis</subject><subject>Phenotype</subject><subject>Research Article</subject><subject>Virulence</subject><issn>2150-7511</issn><issn>2150-7511</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp1kctrHDEMxofS0oQkx16Lz4VJ_RiPPZfCdukjEEgoSa7GD3nXy4y92J6U_PedZNuQHKqLhPTph9DXNB8IPieEys_T15DOMea9aCl50xxTwnErOCFvX9RHzVkpO7wEY0Qy_L45YmzA_UC74yaupgRGo-sMTteQIkoerfPDviabrJ0LipB8ypOOBf2CMo-1oBDR9Qgh1Zz2waL1VscNFFQTusk6LIJVKckGXcGh36Fu0V3I8wjRwmnzzuuxwNnffNLcfv92s_7ZXl79uFivLlvdSVlbjnttCO090F5QaczgBRiuiWcDod5JOTjOtHGuE1pY4i01njvpnO1dDwM7aS4OXJf0Tu1zmHR-UEkH9dRIeaN0rsGOoISTWJheMGqgo44PekHYASzwDhMqFtaXA2s_mwmchVizHl9BX09i2KpNulcSD5RyugDaA8DmVEoG_7xLsHr0UT36qJ58VJQs-k8HvS4TVbs057j86r_ijy-ve0b_s5j9AXMNqgI</recordid><startdate>20210427</startdate><enddate>20210427</enddate><creator>Fu, Man Shun</creator><creator>Liporagi-Lopes, Livia C</creator><creator>Dos Santos, Júnior, Samuel R</creator><creator>Tenor, Jennifer L</creator><creator>Perfect, John R</creator><creator>Cuomo, Christina A</creator><creator>Casadevall, Arturo</creator><general>American Society for Microbiology</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>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-9402-9167</orcidid><orcidid>https://orcid.org/0000-0002-5778-960X</orcidid></search><sort><creationdate>20210427</creationdate><title>Amoeba Predation of Cryptococcus neoformans Results in Pleiotropic Changes to Traits Associated with Virulence</title><author>Fu, Man Shun ; Liporagi-Lopes, Livia C ; Dos Santos, Júnior, Samuel R ; Tenor, Jennifer L ; Perfect, John R ; Cuomo, Christina A ; Casadevall, Arturo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a488t-506ab126fe26728bb9f7eb5a1f3912fd889d53abdd47a7c1fc2bf5d8ddc6d6e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acanthamoeba castellanii - microbiology</topic><topic>Acanthamoeba castellanii - physiology</topic><topic>Animals</topic><topic>Cryptococcosis - immunology</topic><topic>Cryptococcosis - microbiology</topic><topic>Cryptococcus neoformans - classification</topic><topic>Cryptococcus neoformans - genetics</topic><topic>Cryptococcus neoformans - pathogenicity</topic><topic>Cytokines - immunology</topic><topic>Female</topic><topic>Humans</topic><topic>Larva - microbiology</topic><topic>Macrophages - microbiology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Moths - microbiology</topic><topic>Phagocytes - microbiology</topic><topic>Phagocytosis</topic><topic>Phenotype</topic><topic>Research Article</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fu, Man Shun</creatorcontrib><creatorcontrib>Liporagi-Lopes, Livia C</creatorcontrib><creatorcontrib>Dos Santos, Júnior, Samuel R</creatorcontrib><creatorcontrib>Tenor, Jennifer L</creatorcontrib><creatorcontrib>Perfect, John R</creatorcontrib><creatorcontrib>Cuomo, Christina A</creatorcontrib><creatorcontrib>Casadevall, Arturo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>mBio</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fu, Man Shun</au><au>Liporagi-Lopes, Livia C</au><au>Dos Santos, Júnior, Samuel R</au><au>Tenor, Jennifer L</au><au>Perfect, John R</au><au>Cuomo, Christina A</au><au>Casadevall, Arturo</au><au>Wormley, Floyd L</au><au>Olszewski, Michal A</au><au>Olszewski, Michal A.</au><au>Wormley, Floyd L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amoeba Predation of Cryptococcus neoformans Results in Pleiotropic Changes to Traits Associated with Virulence</atitle><jtitle>mBio</jtitle><stitle>mBio</stitle><addtitle>mBio</addtitle><date>2021-04-27</date><risdate>2021</risdate><volume>12</volume><issue>2</issue><issn>2150-7511</issn><eissn>2150-7511</eissn><abstract>Amoeboid predators, such as amoebae, are proposed to select for survival traits in soil microbes such as
; these traits can also function in animal virulence by defeating phagocytic immune cells, such as macrophages. Consistent with this notion, incubation of various fungal species with amoebae enhanced their virulence, but the mechanisms involved are unknown. In this study, we exposed three strains of
(1 clinical and 2 environmental) to predation by
for prolonged times and then analyzed surviving colonies phenotypically and genetically. Surviving colonies comprised cells that expressed either pseudohyphal or yeast phenotypes, which demonstrated variable expression of traits associated with virulence, such as capsule size, urease production, and melanization. Phenotypic changes were associated with aneuploidy and DNA sequence mutations in some amoeba-passaged isolates, but not in others. Mutations in the gene encoding the oligopeptide transporter (CNAG_03013;
) were observed among amoeba-passaged isolates from each of the three strains. Isolates derived from environmental strains gained the capacity for enhanced macrophage toxicity after amoeba selection and carried mutations on the CNAG_00570 gene encoding Pkr1 (AMP-dependent protein kinase regulator) but manifested reduced virulence in mice because they elicited more effective fungal-clearing immune responses. Our results indicate that
survival under constant amoeba predation involves the generation of strains expressing pleiotropic phenotypic and genetic changes. Given the myriad potential predators in soils, the diversity observed among amoeba-selected strains suggests a bet-hedging strategy whereby variant diversity increases the likelihood that some will survive predation.
is a ubiquitous environmental fungus that is also a leading cause of fatal fungal infection in humans, especially among immunocompromised patients. A major question in the field is how an environmental yeast such as
becomes a human pathogen when it has no need for an animal host in its life cycle. Previous studies showed that
increases its pathogenicity after interacting with its environmental predator amoebae. Amoebae, like macrophages, are phagocytic cells that are considered an environmental training ground for pathogens to resist macrophages, but the mechanism by which
changes its virulence through interactions with protozoa is unknown. Our study indicates that fungal survival in the face of amoeba predation is associated with the emergence of pleiotropic phenotypic and genomic changes that increase the chance of fungal survival, with this diversity suggesting a bet-hedging strategy to ensure that some forms survive.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>33906924</pmid><doi>10.1128/mBio.00567-21</doi><tpages>25</tpages><orcidid>https://orcid.org/0000-0002-9402-9167</orcidid><orcidid>https://orcid.org/0000-0002-5778-960X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acanthamoeba castellanii - microbiology Acanthamoeba castellanii - physiology Animals Cryptococcosis - immunology Cryptococcosis - microbiology Cryptococcus neoformans - classification Cryptococcus neoformans - genetics Cryptococcus neoformans - pathogenicity Cytokines - immunology Female Humans Larva - microbiology Macrophages - microbiology Mice Mice, Inbred C57BL Moths - microbiology Phagocytes - microbiology Phagocytosis Phenotype Research Article Virulence |
title | Amoeba Predation of Cryptococcus neoformans Results in Pleiotropic Changes to Traits Associated with Virulence |
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