FISHing in fungi: Visualisation of mushroom virus X in the mycelium of Agaricus bisporus by fluorescence in situ hybridisation

Agaricus bisporus is a commercial mushroom crop susceptible to a disease caused by a complex of viruses known collectively as mushroom virus X (MVX). Symptoms of MVX include bare patches and mushroom cap discolouration (browning) in the fruiting bodies, phenotypes associated with the viruses AbV6 an...

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Veröffentlicht in:Journal of microbiological methods 2020-06, Vol.173, p.105913-105913, Article 105913
Hauptverfasser: O'Connor, Eoin, Coates, Christopher J., Eastwood, Dan C., Fitzpatrick, David A., Grogan, Helen
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Coates, Christopher J.
Eastwood, Dan C.
Fitzpatrick, David A.
Grogan, Helen
description Agaricus bisporus is a commercial mushroom crop susceptible to a disease caused by a complex of viruses known collectively as mushroom virus X (MVX). Symptoms of MVX include bare patches and mushroom cap discolouration (browning) in the fruiting bodies, phenotypes associated with the viruses AbV6 and AbV16, respectively. Limited understanding exists of the localisation and mobilisation of these viruses within the mycelium of A. bisporus. To this end, a non-destructive fluorescence in situ hybridisation (FISH) method was developed for in situ targeting of AbV6 and AbV16 in A. bisporus mycelium. An MVX strain associated with the bare patch disease phenotype revealed predominantly high signal towards the growing edges of cultures when probed for AbV6, with a ‘halo-effect’ of high signal intensity around putative vacuoles. An MVX strain associated with the browning disease phenotype showed high signal intensities within reticulating networks of hyphae in a highly compartmentalised manner when probed for AbV16. Localisation of the two viruses in MVX-infected cultures appears independent, as both viruses were found in completely discrete areas of the mycelium in differential patterns. FISH detected low level presence of the two viruses, AbV6 and AbV16 in a number of cultures which had tested negative for the viruses by RT-PCR. This suggests that FISH may be more sensitive at detecting viruses at low levels than molecular methods. This study demonstrates that FISH is a powerful tool in the field of mycovirology. •The technique FISH was used to target viruses within the mycelium of Agaricus bisporus.•Hyphae was cultured, permeabilised and hybridised with FISH probes on a single platform for fluorescence microscopy.•Two distinct viruses from the MVX complex were localised within different areas of the mycelium of A. bisporus strains.•Low levels of virus were detected within non-MVX strain hyphae and high levels were observed in MVX strain hyphae.
doi_str_mv 10.1016/j.mimet.2020.105913
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Symptoms of MVX include bare patches and mushroom cap discolouration (browning) in the fruiting bodies, phenotypes associated with the viruses AbV6 and AbV16, respectively. Limited understanding exists of the localisation and mobilisation of these viruses within the mycelium of A. bisporus. To this end, a non-destructive fluorescence in situ hybridisation (FISH) method was developed for in situ targeting of AbV6 and AbV16 in A. bisporus mycelium. An MVX strain associated with the bare patch disease phenotype revealed predominantly high signal towards the growing edges of cultures when probed for AbV6, with a ‘halo-effect’ of high signal intensity around putative vacuoles. An MVX strain associated with the browning disease phenotype showed high signal intensities within reticulating networks of hyphae in a highly compartmentalised manner when probed for AbV16. Localisation of the two viruses in MVX-infected cultures appears independent, as both viruses were found in completely discrete areas of the mycelium in differential patterns. FISH detected low level presence of the two viruses, AbV6 and AbV16 in a number of cultures which had tested negative for the viruses by RT-PCR. This suggests that FISH may be more sensitive at detecting viruses at low levels than molecular methods. 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Localisation of the two viruses in MVX-infected cultures appears independent, as both viruses were found in completely discrete areas of the mycelium in differential patterns. FISH detected low level presence of the two viruses, AbV6 and AbV16 in a number of cultures which had tested negative for the viruses by RT-PCR. This suggests that FISH may be more sensitive at detecting viruses at low levels than molecular methods. This study demonstrates that FISH is a powerful tool in the field of mycovirology. •The technique FISH was used to target viruses within the mycelium of Agaricus bisporus.•Hyphae was cultured, permeabilised and hybridised with FISH probes on a single platform for fluorescence microscopy.•Two distinct viruses from the MVX complex were localised within different areas of the mycelium of A. bisporus strains.•Low levels of virus were detected within non-MVX strain hyphae and high levels were observed in MVX strain hyphae.</description><subject>Agaricus bisporus</subject><subject>FISH</subject><subject>Fluorescence in situ hybridisation</subject><subject>Mushroom virus X</subject><subject>MVX</subject><subject>Mycovirology</subject><subject>Mycovirus</subject><issn>0167-7012</issn><issn>1872-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE1v1DAQhi0EokvhFyAhH7lk8UcSJ0gcqorSSpU4tCBuluNMdmcVx4sdV9pLfztxd8uxp5E8zzszfgj5yNmaM15_2a0dOpjXgon8UrVcviIr3ihRNLJqX5PVQqlCMS7OyLsYd4zxSpbNW3ImhVBVK8oVeby6ubvGaUNxokOaNviV_saYzIjRzOgn6gfqUtwG7x19wJAi_ZPZeQvUHSyMmFxmLjYmoF26Hca9z1h3oMOYfIBoYbKQQxHnRLeHLmB_Gv-evBnMGOHDqZ6TX1ff7y-vi9ufP24uL24LW7JyLrhkopE1dKoE2wpbtdJaJofOsM6q2pRmgKoaVCV6kH0pJKt5x22zBGquLJfn5PNx7j74vwnirB0ud42jmcCnqIVsmkYoUWZUHlEbfIwBBr0P6Ew4aM50Fq93-km8zuL1UfyS-nRakDoH_f_Ms-kF-HYEYPnmA0LQ0WIW02MAO-ve44sL_gERnZcN</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>O'Connor, Eoin</creator><creator>Coates, Christopher J.</creator><creator>Eastwood, Dan C.</creator><creator>Fitzpatrick, David A.</creator><creator>Grogan, Helen</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20200601</creationdate><title>FISHing in fungi: Visualisation of mushroom virus X in the mycelium of Agaricus bisporus by fluorescence in situ hybridisation</title><author>O'Connor, Eoin ; Coates, Christopher J. ; Eastwood, Dan C. ; Fitzpatrick, David A. ; Grogan, Helen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-1302836eb74ec92c593cc03fba0bc76a4afe55f752de3d423061b1c8eb7617c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Agaricus bisporus</topic><topic>FISH</topic><topic>Fluorescence in situ hybridisation</topic><topic>Mushroom virus X</topic><topic>MVX</topic><topic>Mycovirology</topic><topic>Mycovirus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Connor, Eoin</creatorcontrib><creatorcontrib>Coates, Christopher J.</creatorcontrib><creatorcontrib>Eastwood, Dan C.</creatorcontrib><creatorcontrib>Fitzpatrick, David A.</creatorcontrib><creatorcontrib>Grogan, Helen</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of microbiological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Connor, Eoin</au><au>Coates, Christopher J.</au><au>Eastwood, Dan C.</au><au>Fitzpatrick, David A.</au><au>Grogan, Helen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FISHing in fungi: Visualisation of mushroom virus X in the mycelium of Agaricus bisporus by fluorescence in situ hybridisation</atitle><jtitle>Journal of microbiological methods</jtitle><addtitle>J Microbiol Methods</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>173</volume><spage>105913</spage><epage>105913</epage><pages>105913-105913</pages><artnum>105913</artnum><issn>0167-7012</issn><eissn>1872-8359</eissn><abstract>Agaricus bisporus is a commercial mushroom crop susceptible to a disease caused by a complex of viruses known collectively as mushroom virus X (MVX). Symptoms of MVX include bare patches and mushroom cap discolouration (browning) in the fruiting bodies, phenotypes associated with the viruses AbV6 and AbV16, respectively. Limited understanding exists of the localisation and mobilisation of these viruses within the mycelium of A. bisporus. To this end, a non-destructive fluorescence in situ hybridisation (FISH) method was developed for in situ targeting of AbV6 and AbV16 in A. bisporus mycelium. An MVX strain associated with the bare patch disease phenotype revealed predominantly high signal towards the growing edges of cultures when probed for AbV6, with a ‘halo-effect’ of high signal intensity around putative vacuoles. An MVX strain associated with the browning disease phenotype showed high signal intensities within reticulating networks of hyphae in a highly compartmentalised manner when probed for AbV16. Localisation of the two viruses in MVX-infected cultures appears independent, as both viruses were found in completely discrete areas of the mycelium in differential patterns. FISH detected low level presence of the two viruses, AbV6 and AbV16 in a number of cultures which had tested negative for the viruses by RT-PCR. This suggests that FISH may be more sensitive at detecting viruses at low levels than molecular methods. This study demonstrates that FISH is a powerful tool in the field of mycovirology. •The technique FISH was used to target viruses within the mycelium of Agaricus bisporus.•Hyphae was cultured, permeabilised and hybridised with FISH probes on a single platform for fluorescence microscopy.•Two distinct viruses from the MVX complex were localised within different areas of the mycelium of A. bisporus strains.•Low levels of virus were detected within non-MVX strain hyphae and high levels were observed in MVX strain hyphae.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32275924</pmid><doi>10.1016/j.mimet.2020.105913</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Agaricus bisporus
FISH
Fluorescence in situ hybridisation
Mushroom virus X
MVX
Mycovirology
Mycovirus
title FISHing in fungi: Visualisation of mushroom virus X in the mycelium of Agaricus bisporus by fluorescence in situ hybridisation
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