A Novel Secreted Cysteine-Rich Anionic (Sca) Protein from the Citrus Postharvest Pathogen <i>Penicillium digitatum</i> Enhances Virulence and Modulates the Activity of the Antifungal Protein B (AfpB)

Antifungal proteins (AFPs) from ascomycete fungi could help the development of antimycotics. However, little is known about their biological role or functional interactions with other fungal biomolecules. We previously reported that AfpB from the postharvest pathogen <i>Penicillium digitatum&l...

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Main Authors: Sandra Garrigues, Jose F. Marcos, Paloma Manzanares, Mónica Gandía
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:Journal of Fungi
Subjects:
Online Access:https://www.mdpi.com/2309-608X/6/4/203
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spelling doaj-ceec12a480714766bca20e72e3bf390b2020-11-25T03:37:06ZengMDPI AGJournal of Fungi2309-608X2020-10-01620320310.3390/jof6040203A Novel Secreted Cysteine-Rich Anionic (Sca) Protein from the Citrus Postharvest Pathogen <i>Penicillium digitatum</i> Enhances Virulence and Modulates the Activity of the Antifungal Protein B (AfpB)Sandra GarriguesJose F. Marcos0Paloma Manzanares1Mónica Gandía2Food Biotechnology Department, Instituto de Agroquímica y Tecnología de Alimentos (IATA), Consejo Superior de Investigaciones Científicas (CSIC), 46980 Paterna, Valencia, SpainFood Biotechnology Department, Instituto de Agroquímica y Tecnología de Alimentos (IATA), Consejo Superior de Investigaciones Científicas (CSIC), 46980 Paterna, Valencia, SpainFood Biotechnology Department, Instituto de Agroquímica y Tecnología de Alimentos (IATA), Consejo Superior de Investigaciones Científicas (CSIC), 46980 Paterna, Valencia, SpainAntifungal proteins (AFPs) from ascomycete fungi could help the development of antimycotics. However, little is known about their biological role or functional interactions with other fungal biomolecules. We previously reported that AfpB from the postharvest pathogen <i>Penicillium digitatum</i> cannot be detected in the parental fungus yet is abundantly produced biotechnologically. While aiming to detect AfpB, we identified a conserved and novel small Secreted Cysteine-rich Anionic (Sca) protein, encoded by the gene PDIG_23520 from <i>P. digitatum</i> CECT 20796. The <i>sca</i> gene is expressed during culture and early during citrus fruit infection. Both null mutant (Δ<i>sca</i>) and Sca overproducer (Sca<sup>op</sup>) strains show no phenotypic differences from the wild type. Sca is not antimicrobial but potentiates <i>P. digitatum</i> growth when added in high amounts and enhances the in vitro antifungal activity of AfpB. The Sca<sup>op</sup> strain shows increased incidence of infection in citrus fruit, similar to the addition of purified Sca to the wild-type inoculum. Sca compensates and overcomes the protective effect of AfpB and the antifungal protein PeAfpA from the apple pathogen <i>Penicillium expansum</i> in fruit inoculations. Our study shows that Sca is a novel protein that enhances the growth and virulence of its parental fungus and modulates the activity of AFPs.https://www.mdpi.com/2309-608X/6/4/203antifungal protein (AFP)<i>Penicillium digitatum</i>AfpBpostharvest decaycitrus fruitvirulence
collection DOAJ
language English
format Article
sources DOAJ
author Sandra Garrigues
Jose F. Marcos
Paloma Manzanares
Mónica Gandía
spellingShingle Sandra Garrigues
Jose F. Marcos
Paloma Manzanares
Mónica Gandía
A Novel Secreted Cysteine-Rich Anionic (Sca) Protein from the Citrus Postharvest Pathogen <i>Penicillium digitatum</i> Enhances Virulence and Modulates the Activity of the Antifungal Protein B (AfpB)
Journal of Fungi
antifungal protein (AFP)
<i>Penicillium digitatum</i>
AfpB
postharvest decay
citrus fruit
virulence
author_facet Sandra Garrigues
Jose F. Marcos
Paloma Manzanares
Mónica Gandía
author_sort Sandra Garrigues
title A Novel Secreted Cysteine-Rich Anionic (Sca) Protein from the Citrus Postharvest Pathogen <i>Penicillium digitatum</i> Enhances Virulence and Modulates the Activity of the Antifungal Protein B (AfpB)
title_short A Novel Secreted Cysteine-Rich Anionic (Sca) Protein from the Citrus Postharvest Pathogen <i>Penicillium digitatum</i> Enhances Virulence and Modulates the Activity of the Antifungal Protein B (AfpB)
title_full A Novel Secreted Cysteine-Rich Anionic (Sca) Protein from the Citrus Postharvest Pathogen <i>Penicillium digitatum</i> Enhances Virulence and Modulates the Activity of the Antifungal Protein B (AfpB)
title_fullStr A Novel Secreted Cysteine-Rich Anionic (Sca) Protein from the Citrus Postharvest Pathogen <i>Penicillium digitatum</i> Enhances Virulence and Modulates the Activity of the Antifungal Protein B (AfpB)
title_full_unstemmed A Novel Secreted Cysteine-Rich Anionic (Sca) Protein from the Citrus Postharvest Pathogen <i>Penicillium digitatum</i> Enhances Virulence and Modulates the Activity of the Antifungal Protein B (AfpB)
title_sort novel secreted cysteine-rich anionic (sca) protein from the citrus postharvest pathogen <i>penicillium digitatum</i> enhances virulence and modulates the activity of the antifungal protein b (afpb)
publisher MDPI AG
series Journal of Fungi
issn 2309-608X
publishDate 2020-10-01
description Antifungal proteins (AFPs) from ascomycete fungi could help the development of antimycotics. However, little is known about their biological role or functional interactions with other fungal biomolecules. We previously reported that AfpB from the postharvest pathogen <i>Penicillium digitatum</i> cannot be detected in the parental fungus yet is abundantly produced biotechnologically. While aiming to detect AfpB, we identified a conserved and novel small Secreted Cysteine-rich Anionic (Sca) protein, encoded by the gene PDIG_23520 from <i>P. digitatum</i> CECT 20796. The <i>sca</i> gene is expressed during culture and early during citrus fruit infection. Both null mutant (Δ<i>sca</i>) and Sca overproducer (Sca<sup>op</sup>) strains show no phenotypic differences from the wild type. Sca is not antimicrobial but potentiates <i>P. digitatum</i> growth when added in high amounts and enhances the in vitro antifungal activity of AfpB. The Sca<sup>op</sup> strain shows increased incidence of infection in citrus fruit, similar to the addition of purified Sca to the wild-type inoculum. Sca compensates and overcomes the protective effect of AfpB and the antifungal protein PeAfpA from the apple pathogen <i>Penicillium expansum</i> in fruit inoculations. Our study shows that Sca is a novel protein that enhances the growth and virulence of its parental fungus and modulates the activity of AFPs.
topic antifungal protein (AFP)
<i>Penicillium digitatum</i>
AfpB
postharvest decay
citrus fruit
virulence
url https://www.mdpi.com/2309-608X/6/4/203
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