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Dynamics of interaction and internalisation of the antifungal protein PeAfpA into Penicillium digitatum morphotypes
Antifungal proteins (AFPs) as the highly active PeAfpA from Penicillium expansum or PdAfpB from Penicillium digitatum exert promising antifungal activity, but their mode of action is not fully understood. We characterised the interaction of PeAfpA against P. digitatum, comparing it to the less activ...
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Published in: | International journal of biological macromolecules 2024-12, Vol.282 (Pt 5), p.136980, Article 136980 |
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description | Antifungal proteins (AFPs) as the highly active PeAfpA from Penicillium expansum or PdAfpB from Penicillium digitatum exert promising antifungal activity, but their mode of action is not fully understood. We characterised the interaction of PeAfpA against P. digitatum, comparing it to the less active PdAfpB. Despite similar effect on conidia germination, PeAfpA did not induce a burst of reactive oxygen species as PdAfpB. Live-cell fluorescence microscopy revealed complex dynamics of interaction and internalisation of both proteins with distinct P. digitatum morphotypes (quiescent conidia, swollen conidia, germlings and hyphae). Labelled PeAfpA co-localised at the cell wall of quiescent conidia, where its localisation was punctate and not uniformly distributed. This pattern changed during germination to a uniform distribution with increased intensity. Conidia from mutants of genes involved in melanin biosynthesis (pksP/alb1 or arp2) showed an altered distribution of PeAfpA but later mimicked the wild type trend of changes during germination. In swollen conidia and germlings, PeAfpA remained attached to the cell wall. In hyphae, PeAfpA was internalised through the growing hyphal tip after binding to the cell wall, in a non-endocytic but energy-dependent process that caused vacuolisation, which preceded cell death. These results may help the development of biofungicides based on AFPs.
•The antifungal protein PeAfpA from P. expansum shows unique mechanistic properties.•PeAfpA does not induce a burst of reactive oxygen species.•PeAfpA binds conidia with a punctate pattern that depends on melanin biosynthesis.•PeAfpA internalises through the tip of growing hyphae, causes collapse and death.•PeAfpA internalisation is energy-dependent but does not follow the endocytic route. |
doi_str_mv | 10.1016/j.ijbiomac.2024.136980 |
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•The antifungal protein PeAfpA from P. expansum shows unique mechanistic properties.•PeAfpA does not induce a burst of reactive oxygen species.•PeAfpA binds conidia with a punctate pattern that depends on melanin biosynthesis.•PeAfpA internalises through the tip of growing hyphae, causes collapse and death.•PeAfpA internalisation is energy-dependent but does not follow the endocytic route.</description><identifier>ISSN: 0141-8130</identifier><identifier>ISSN: 1879-0003</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2024.136980</identifier><identifier>PMID: 39471922</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Antifungal action ; Antifungal Agents - chemistry ; Antifungal Agents - pharmacology ; antifungal properties ; biopesticides ; biosynthesis ; cell death ; Cell wall ; Cell Wall - drug effects ; Cell Wall - metabolism ; cell walls ; Confocal microscopy ; conidia ; fluorescence microscopy ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; germination ; hyphae ; Hyphae - drug effects ; Hyphae - metabolism ; mechanism of action ; melanin ; Melanin biosynthesis ; morphs ; Penicillium - drug effects ; Penicillium - metabolism ; Penicillium digitatum ; Penicillium expansum ; Protein Binding ; Protein internalisation ; reactive oxygen species ; Reactive oxygen species (ROS) ; Reactive Oxygen Species - metabolism ; Spores, Fungal - drug effects</subject><ispartof>International journal of biological macromolecules, 2024-12, Vol.282 (Pt 5), p.136980, Article 136980</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c326t-af52e30adeb3d96014c3751d6882dc573e36b00ad5343605e9004f0df4876cde3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27900,27901</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39471922$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Giner-Llorca, Moisés</creatorcontrib><creatorcontrib>Ropero-Pérez, Carolina</creatorcontrib><creatorcontrib>Garrigues, Sandra</creatorcontrib><creatorcontrib>Thomson, Darren D.</creatorcontrib><creatorcontrib>Bignell, Elaine M.</creatorcontrib><creatorcontrib>Manzanares, Paloma</creatorcontrib><creatorcontrib>Marcos, Jose F.</creatorcontrib><title>Dynamics of interaction and internalisation of the antifungal protein PeAfpA into Penicillium digitatum morphotypes</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>Antifungal proteins (AFPs) as the highly active PeAfpA from Penicillium expansum or PdAfpB from Penicillium digitatum exert promising antifungal activity, but their mode of action is not fully understood. We characterised the interaction of PeAfpA against P. digitatum, comparing it to the less active PdAfpB. Despite similar effect on conidia germination, PeAfpA did not induce a burst of reactive oxygen species as PdAfpB. Live-cell fluorescence microscopy revealed complex dynamics of interaction and internalisation of both proteins with distinct P. digitatum morphotypes (quiescent conidia, swollen conidia, germlings and hyphae). Labelled PeAfpA co-localised at the cell wall of quiescent conidia, where its localisation was punctate and not uniformly distributed. This pattern changed during germination to a uniform distribution with increased intensity. Conidia from mutants of genes involved in melanin biosynthesis (pksP/alb1 or arp2) showed an altered distribution of PeAfpA but later mimicked the wild type trend of changes during germination. In swollen conidia and germlings, PeAfpA remained attached to the cell wall. In hyphae, PeAfpA was internalised through the growing hyphal tip after binding to the cell wall, in a non-endocytic but energy-dependent process that caused vacuolisation, which preceded cell death. These results may help the development of biofungicides based on AFPs.
•The antifungal protein PeAfpA from P. expansum shows unique mechanistic properties.•PeAfpA does not induce a burst of reactive oxygen species.•PeAfpA binds conidia with a punctate pattern that depends on melanin biosynthesis.•PeAfpA internalises through the tip of growing hyphae, causes collapse and death.•PeAfpA internalisation is energy-dependent but does not follow the endocytic route.</description><subject>Antifungal action</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - pharmacology</subject><subject>antifungal properties</subject><subject>biopesticides</subject><subject>biosynthesis</subject><subject>cell death</subject><subject>Cell wall</subject><subject>Cell Wall - drug effects</subject><subject>Cell Wall - metabolism</subject><subject>cell walls</subject><subject>Confocal microscopy</subject><subject>conidia</subject><subject>fluorescence microscopy</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>germination</subject><subject>hyphae</subject><subject>Hyphae - drug effects</subject><subject>Hyphae - metabolism</subject><subject>mechanism of action</subject><subject>melanin</subject><subject>Melanin biosynthesis</subject><subject>morphs</subject><subject>Penicillium - drug effects</subject><subject>Penicillium - metabolism</subject><subject>Penicillium digitatum</subject><subject>Penicillium expansum</subject><subject>Protein Binding</subject><subject>Protein internalisation</subject><subject>reactive oxygen species</subject><subject>Reactive oxygen species (ROS)</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Spores, Fungal - drug effects</subject><issn>0141-8130</issn><issn>1879-0003</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqNkU1P3DAQhi1EBcvHX0A59pKtPxInubHiq0hI7aGcLa89gVkldrCdSvvv6yXQa3vyeOZ5Z-x5CblidM0ok992a9xt0Y_arDnl1ZoJ2bX0iKxY23QlpVQckxVlFStbJugpOYtxl7OyZu0JORVd1bCO8xWJt3unRzSx8H2BLkHQJqF3hXZ2uTs9YNTvuYykV8ilhP3sXvRQTMEnQFf8hE0_bQ4Cn2OHBocB57Gw-IJJpxyNPkyvPu0niBfkS6-HCJcf5zl5vr_7dfO9fPrx8HizeSqN4DKVuq85CKotbIXtZP6MEU3NrGxbbk3dCBByS3O9FpWQtIaO0qqntq_aRhoL4px8XfrmV77NEJMaMRoYBu3Az1EJVlc8L0Sw_0A5l6LikmdULqgJPsYAvZoCjjrsFaPq4I3aqU9v1MEbtXiThVcfM-btCPav7NOMDFwvAOSl_EYIKhoEZ8BiAJOU9fivGX8ATbekuQ</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Giner-Llorca, Moisés</creator><creator>Ropero-Pérez, Carolina</creator><creator>Garrigues, Sandra</creator><creator>Thomson, Darren D.</creator><creator>Bignell, Elaine M.</creator><creator>Manzanares, Paloma</creator><creator>Marcos, Jose F.</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>202412</creationdate><title>Dynamics of interaction and internalisation of the antifungal protein PeAfpA into Penicillium digitatum morphotypes</title><author>Giner-Llorca, Moisés ; Ropero-Pérez, Carolina ; Garrigues, Sandra ; Thomson, Darren D. ; Bignell, Elaine M. ; Manzanares, Paloma ; Marcos, Jose F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-af52e30adeb3d96014c3751d6882dc573e36b00ad5343605e9004f0df4876cde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antifungal action</topic><topic>Antifungal Agents - chemistry</topic><topic>Antifungal Agents - pharmacology</topic><topic>antifungal properties</topic><topic>biopesticides</topic><topic>biosynthesis</topic><topic>cell death</topic><topic>Cell wall</topic><topic>Cell Wall - drug effects</topic><topic>Cell Wall - metabolism</topic><topic>cell walls</topic><topic>Confocal microscopy</topic><topic>conidia</topic><topic>fluorescence microscopy</topic><topic>Fungal Proteins - genetics</topic><topic>Fungal Proteins - metabolism</topic><topic>germination</topic><topic>hyphae</topic><topic>Hyphae - drug effects</topic><topic>Hyphae - metabolism</topic><topic>mechanism of action</topic><topic>melanin</topic><topic>Melanin biosynthesis</topic><topic>morphs</topic><topic>Penicillium - drug effects</topic><topic>Penicillium - metabolism</topic><topic>Penicillium digitatum</topic><topic>Penicillium expansum</topic><topic>Protein Binding</topic><topic>Protein internalisation</topic><topic>reactive oxygen species</topic><topic>Reactive oxygen species (ROS)</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Spores, Fungal - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Giner-Llorca, Moisés</creatorcontrib><creatorcontrib>Ropero-Pérez, Carolina</creatorcontrib><creatorcontrib>Garrigues, Sandra</creatorcontrib><creatorcontrib>Thomson, Darren D.</creatorcontrib><creatorcontrib>Bignell, Elaine M.</creatorcontrib><creatorcontrib>Manzanares, Paloma</creatorcontrib><creatorcontrib>Marcos, Jose F.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Giner-Llorca, Moisés</au><au>Ropero-Pérez, Carolina</au><au>Garrigues, Sandra</au><au>Thomson, Darren D.</au><au>Bignell, Elaine M.</au><au>Manzanares, Paloma</au><au>Marcos, Jose F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamics of interaction and internalisation of the antifungal protein PeAfpA into Penicillium digitatum morphotypes</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2024-12</date><risdate>2024</risdate><volume>282</volume><issue>Pt 5</issue><spage>136980</spage><pages>136980-</pages><artnum>136980</artnum><issn>0141-8130</issn><issn>1879-0003</issn><eissn>1879-0003</eissn><abstract>Antifungal proteins (AFPs) as the highly active PeAfpA from Penicillium expansum or PdAfpB from Penicillium digitatum exert promising antifungal activity, but their mode of action is not fully understood. We characterised the interaction of PeAfpA against P. digitatum, comparing it to the less active PdAfpB. Despite similar effect on conidia germination, PeAfpA did not induce a burst of reactive oxygen species as PdAfpB. Live-cell fluorescence microscopy revealed complex dynamics of interaction and internalisation of both proteins with distinct P. digitatum morphotypes (quiescent conidia, swollen conidia, germlings and hyphae). Labelled PeAfpA co-localised at the cell wall of quiescent conidia, where its localisation was punctate and not uniformly distributed. This pattern changed during germination to a uniform distribution with increased intensity. Conidia from mutants of genes involved in melanin biosynthesis (pksP/alb1 or arp2) showed an altered distribution of PeAfpA but later mimicked the wild type trend of changes during germination. In swollen conidia and germlings, PeAfpA remained attached to the cell wall. In hyphae, PeAfpA was internalised through the growing hyphal tip after binding to the cell wall, in a non-endocytic but energy-dependent process that caused vacuolisation, which preceded cell death. These results may help the development of biofungicides based on AFPs.
•The antifungal protein PeAfpA from P. expansum shows unique mechanistic properties.•PeAfpA does not induce a burst of reactive oxygen species.•PeAfpA binds conidia with a punctate pattern that depends on melanin biosynthesis.•PeAfpA internalises through the tip of growing hyphae, causes collapse and death.•PeAfpA internalisation is energy-dependent but does not follow the endocytic route.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39471922</pmid><doi>10.1016/j.ijbiomac.2024.136980</doi><oa>free_for_read</oa></addata></record> |
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subjects | Antifungal action Antifungal Agents - chemistry Antifungal Agents - pharmacology antifungal properties biopesticides biosynthesis cell death Cell wall Cell Wall - drug effects Cell Wall - metabolism cell walls Confocal microscopy conidia fluorescence microscopy Fungal Proteins - genetics Fungal Proteins - metabolism germination hyphae Hyphae - drug effects Hyphae - metabolism mechanism of action melanin Melanin biosynthesis morphs Penicillium - drug effects Penicillium - metabolism Penicillium digitatum Penicillium expansum Protein Binding Protein internalisation reactive oxygen species Reactive oxygen species (ROS) Reactive Oxygen Species - metabolism Spores, Fungal - drug effects |
title | Dynamics of interaction and internalisation of the antifungal protein PeAfpA into Penicillium digitatum morphotypes |
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