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Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death
PLoS ONE, Volume: 8, Issue: 12, Start page: e81686
Swansea University Authors:
Tariq Butt , Carolyn Greig, Thierry Maffeis
, Ed Dudley, Dan Eastwood
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C 2013 Butt et al. 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.
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DOI (Published version): 10.1371/journal.pone.0081686
Abstract
Metarhizium anisopliae, a fungal pathogen of terrestrial arthropods, kills the aquatic larvae of Aedes aegypti, the vector of dengue and yellow fever. The fungus kills without adhering to the host cuticle. Ingested conidia also fail to germinate and are expelled in fecal pellets. This study investig...
Published in: | PLoS ONE |
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ISSN: | 1932-6203 |
Published: |
2013
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URI: | https://cronfa.swan.ac.uk/Record/cronfa30740 |
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The fungus kills without adhering to the host cuticle. Ingested conidia also fail to germinate and are expelled in fecal pellets. This study investigates the mechanism by which this fungus adapted to terrestrial hosts kills aquatic mosquito larvae. Genes associated with the M. anisopliae early pathogenic response (proteinases Pr1 and Pr2, and adhesins, Mad1 and Mad2) are upregulated in the presence of larvae, but the established infection process observed in terrestrial hosts does not progress and insecticidal destruxins were not detected. Protease inhibitors reduce larval mortality indicating the importance of proteases in the host interaction. The Ae. aegypti immune response to M. anisopliae appears limited, whilst the oxidative stress response gene encoding for thiol peroxidase is upregulated. Cecropin and Hsp70 genes are downregulated as larval death occurs, and insect mortality appears to be linked to autolysis through caspase activity regulated by Hsp70 and inhibited, in infected larvae, by protease inhibitors. Evidence is presented that a traditional host-pathogen response does not occur as the species have not evolved to interact. M. anisopliae retains pre-formed pathogenic determinants which mediate host mortality, but unlike true aquatic fungal pathogens, does not recognise and colonise the larval host.</abstract><type>Journal Article</type><journal>PLoS ONE</journal><volume>8</volume><journalNumber>12</journalNumber><paginationStart>e81686</paginationStart><publisher/><issnElectronic>1932-6203</issnElectronic><keywords/><publishedDay>13</publishedDay><publishedMonth>12</publishedMonth><publishedYear>2013</publishedYear><publishedDate>2013-12-13</publishedDate><doi>10.1371/journal.pone.0081686</doi><url/><notes/><college>COLLEGE NANME</college><department>Biosciences Geography and Physics School</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>BGPS</DepartmentCode><institution>Swansea University</institution><apcterm/><lastEdited>2017-12-29T17:55:35.4248205</lastEdited><Created>2016-10-20T17:55:06.1877158</Created><path><level id="1">Faculty of Science and Engineering</level><level id="2">School of Biosciences, Geography and Physics - Biosciences</level></path><authors><author><firstname>Jorge Luis</firstname><surname>Folch-Mallol</surname><order>1</order></author><author><firstname>Tariq</firstname><surname>Butt</surname><orcid>0000-0002-8789-9543</orcid><order>2</order></author><author><firstname>Bethany P. 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2017-12-29T17:55:35.4248205 v2 30740 2016-10-20 Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death 85d1c2ddde272a1176e74978e25ebece 0000-0002-8789-9543 Tariq Butt Tariq Butt true false 7f95061328bd6726f7472ced9cb8d937 Carolyn Greig Carolyn Greig true false 992eb4cb18b61c0cd3da6e0215ac787c 0000-0003-2357-0092 Thierry Maffeis Thierry Maffeis true false c7d05f992a817cd3b9a5f946bd909b71 Ed Dudley Ed Dudley true false 4982f3fa83886c0362e2bb43ce1c027f 0000-0002-7015-0739 Dan Eastwood Dan Eastwood true false 2016-10-20 BGPS Metarhizium anisopliae, a fungal pathogen of terrestrial arthropods, kills the aquatic larvae of Aedes aegypti, the vector of dengue and yellow fever. The fungus kills without adhering to the host cuticle. Ingested conidia also fail to germinate and are expelled in fecal pellets. This study investigates the mechanism by which this fungus adapted to terrestrial hosts kills aquatic mosquito larvae. Genes associated with the M. anisopliae early pathogenic response (proteinases Pr1 and Pr2, and adhesins, Mad1 and Mad2) are upregulated in the presence of larvae, but the established infection process observed in terrestrial hosts does not progress and insecticidal destruxins were not detected. Protease inhibitors reduce larval mortality indicating the importance of proteases in the host interaction. The Ae. aegypti immune response to M. anisopliae appears limited, whilst the oxidative stress response gene encoding for thiol peroxidase is upregulated. Cecropin and Hsp70 genes are downregulated as larval death occurs, and insect mortality appears to be linked to autolysis through caspase activity regulated by Hsp70 and inhibited, in infected larvae, by protease inhibitors. Evidence is presented that a traditional host-pathogen response does not occur as the species have not evolved to interact. M. anisopliae retains pre-formed pathogenic determinants which mediate host mortality, but unlike true aquatic fungal pathogens, does not recognise and colonise the larval host. Journal Article PLoS ONE 8 12 e81686 1932-6203 13 12 2013 2013-12-13 10.1371/journal.pone.0081686 COLLEGE NANME Biosciences Geography and Physics School COLLEGE CODE BGPS Swansea University 2017-12-29T17:55:35.4248205 2016-10-20T17:55:06.1877158 Faculty of Science and Engineering School of Biosciences, Geography and Physics - Biosciences Jorge Luis Folch-Mallol 1 Tariq Butt 0000-0002-8789-9543 2 Bethany P. J. Greenfield 3 Carolyn Greig 4 Thierry Maffeis 0000-0003-2357-0092 5 James W. D. Taylor 6 Justyna Piasecka 7 Ed Dudley 8 Ahmed Abdulla 9 Ivan M. Dubovskiy 10 Inmaculada Garrido-Jurado 11 Enrique Quesada-Moraga 12 Mark W. Penny 13 Daniel C. Eastwood 14 Dan Eastwood 0000-0002-7015-0739 15 0030740-02112017151812.pdf Buttetal2013MetarhiziumpathogenesisofAedeslarvae.pdf 2017-11-02T15:18:12.9600000 Output 2686262 application/pdf Version of Record true 2017-11-02T00:00:00.0000000 C 2013 Butt et al. 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. true eng |
title |
Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death |
spellingShingle |
Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death Tariq Butt Carolyn Greig Thierry Maffeis Ed Dudley Dan Eastwood |
title_short |
Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death |
title_full |
Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death |
title_fullStr |
Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death |
title_full_unstemmed |
Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death |
title_sort |
Metarhizium anisopliae Pathogenesis of Mosquito Larvae: A Verdict of Accidental Death |
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85d1c2ddde272a1176e74978e25ebece 7f95061328bd6726f7472ced9cb8d937 992eb4cb18b61c0cd3da6e0215ac787c c7d05f992a817cd3b9a5f946bd909b71 4982f3fa83886c0362e2bb43ce1c027f |
author_id_fullname_str_mv |
85d1c2ddde272a1176e74978e25ebece_***_Tariq Butt 7f95061328bd6726f7472ced9cb8d937_***_Carolyn Greig 992eb4cb18b61c0cd3da6e0215ac787c_***_Thierry Maffeis c7d05f992a817cd3b9a5f946bd909b71_***_Ed Dudley 4982f3fa83886c0362e2bb43ce1c027f_***_Dan Eastwood |
author |
Tariq Butt Carolyn Greig Thierry Maffeis Ed Dudley Dan Eastwood |
author2 |
Jorge Luis Folch-Mallol Tariq Butt Bethany P. J. Greenfield Carolyn Greig Thierry Maffeis James W. D. Taylor Justyna Piasecka Ed Dudley Ahmed Abdulla Ivan M. Dubovskiy Inmaculada Garrido-Jurado Enrique Quesada-Moraga Mark W. Penny Daniel C. Eastwood Dan Eastwood |
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Metarhizium anisopliae, a fungal pathogen of terrestrial arthropods, kills the aquatic larvae of Aedes aegypti, the vector of dengue and yellow fever. The fungus kills without adhering to the host cuticle. Ingested conidia also fail to germinate and are expelled in fecal pellets. This study investigates the mechanism by which this fungus adapted to terrestrial hosts kills aquatic mosquito larvae. Genes associated with the M. anisopliae early pathogenic response (proteinases Pr1 and Pr2, and adhesins, Mad1 and Mad2) are upregulated in the presence of larvae, but the established infection process observed in terrestrial hosts does not progress and insecticidal destruxins were not detected. Protease inhibitors reduce larval mortality indicating the importance of proteases in the host interaction. The Ae. aegypti immune response to M. anisopliae appears limited, whilst the oxidative stress response gene encoding for thiol peroxidase is upregulated. Cecropin and Hsp70 genes are downregulated as larval death occurs, and insect mortality appears to be linked to autolysis through caspase activity regulated by Hsp70 and inhibited, in infected larvae, by protease inhibitors. Evidence is presented that a traditional host-pathogen response does not occur as the species have not evolved to interact. M. anisopliae retains pre-formed pathogenic determinants which mediate host mortality, but unlike true aquatic fungal pathogens, does not recognise and colonise the larval host. |
published_date |
2013-12-13T06:55:36Z |
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11.055135 |