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Liquid Fungal Cocultivation as a Strategy to Access Bioactive Metabolites.

Identifieur interne : 000132 ( Main/Exploration ); précédent : 000131; suivant : 000133

Liquid Fungal Cocultivation as a Strategy to Access Bioactive Metabolites.

Auteurs : Airton Damasceno Silva [Brésil] ; Alessandra Regina Pepe Ambrozin [Brésil] ; Ana Flávia S. De Camargo [Brésil] ; Felipe De Paula Nogueira Cruz [Brésil] ; Leonardo Luiz Gomes Ferreira [Brésil] ; Renata Krogh [Brésil] ; Taynara Lopes Silva [Brésil] ; Ilana Lopes Baratella Da Cunha Camargo [Brésil] ; Adriano Defini Andricopulo [Brésil] ; Paulo Cezar Vieira [Brésil]

Source :

RBID : pubmed:32645738

Abstract

Fungi are a rich source of bioactive compounds. Fungal cocultivation is a method of potentiating chemical interactions and, consequently, increasing bioactive molecule production. In this study, we evaluated the bactericidal, antiprotozoal, and cathepsin V inhibition activities of extracts from axenic cultures of 6 fungi (Fusarium guttiforme, Pestalotiopsis diospyri, Phoma caricae-papayae, Colletotrichum horii, Phytophthora palmivora, and C. gloeosporioides) that infest tropical fruits and 57 extracts obtained by their cocultivation. Our results reveal that fungal cocultivation enhances the biological activity of the samples, since all extracts that were active on Gram-positive bacteria, Gram-negative bacteria, Trypanosoma cruzi, and Leishmania infantum were obtained from cocultivation. Bacterial growth is either totally or partially inhibited by 46% of the extracts. Two extracts containing mainly fusaric and 9,10-dehydrofusaric acids were particularly active. The presence of the fungus F. guttiforme in co-cultures that give rise to extracts with the highest activities against L. infantum. An axenic culture gave rise to the most active extract for the inhibition of cathepsin V; however, other coculture extracts also exhibited activity toward this biological target. Therefore, the results of the biological activities indicate that fungal cocultivation increased the biological potential of samples, likely due to the hostile and competitive environment that pushes microorganisms to produce substances important for defense and allows access to metabolic routes then silenced in milder cultivation conditions.

DOI: 10.1055/a-1200-2046
PubMed: 32645738


Affiliations:


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<div type="abstract" xml:lang="en">Fungi are a rich source of bioactive compounds. Fungal cocultivation is a method of potentiating chemical interactions and, consequently, increasing bioactive molecule production. In this study, we evaluated the bactericidal, antiprotozoal, and cathepsin V inhibition activities of extracts from axenic cultures of 6 fungi (
<i>Fusarium guttiforme, Pestalotiopsis diospyri, Phoma caricae-papayae, Colletotrichum horii, Phytophthora palmivora</i>
, and
<i>C. gloeosporioides</i>
) that infest tropical fruits and 57 extracts obtained by their cocultivation. Our results reveal that fungal cocultivation enhances the biological activity of the samples, since all extracts that were active on Gram-positive bacteria, Gram-negative bacteria,
<i>Trypanosoma cruzi</i>
, and
<i>Leishmania infantum</i>
were obtained from cocultivation. Bacterial growth is either totally or partially inhibited by 46% of the extracts. Two extracts containing mainly fusaric and 9,10-dehydrofusaric acids were particularly active. The presence of the fungus
<i>F. guttiforme</i>
in co-cultures that give rise to extracts with the highest activities against
<i>L. infantum</i>
. An axenic culture gave rise to the most active extract for the inhibition of cathepsin V; however, other coculture extracts also exhibited activity toward this biological target. Therefore, the results of the biological activities indicate that fungal cocultivation increased the biological potential of samples, likely due to the hostile and competitive environment that pushes microorganisms to produce substances important for defense and allows access to metabolic routes then silenced in milder cultivation conditions.</div>
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<AbstractText>Fungi are a rich source of bioactive compounds. Fungal cocultivation is a method of potentiating chemical interactions and, consequently, increasing bioactive molecule production. In this study, we evaluated the bactericidal, antiprotozoal, and cathepsin V inhibition activities of extracts from axenic cultures of 6 fungi (
<i>Fusarium guttiforme, Pestalotiopsis diospyri, Phoma caricae-papayae, Colletotrichum horii, Phytophthora palmivora</i>
, and
<i>C. gloeosporioides</i>
) that infest tropical fruits and 57 extracts obtained by their cocultivation. Our results reveal that fungal cocultivation enhances the biological activity of the samples, since all extracts that were active on Gram-positive bacteria, Gram-negative bacteria,
<i>Trypanosoma cruzi</i>
, and
<i>Leishmania infantum</i>
were obtained from cocultivation. Bacterial growth is either totally or partially inhibited by 46% of the extracts. Two extracts containing mainly fusaric and 9,10-dehydrofusaric acids were particularly active. The presence of the fungus
<i>F. guttiforme</i>
in co-cultures that give rise to extracts with the highest activities against
<i>L. infantum</i>
. An axenic culture gave rise to the most active extract for the inhibition of cathepsin V; however, other coculture extracts also exhibited activity toward this biological target. Therefore, the results of the biological activities indicate that fungal cocultivation increased the biological potential of samples, likely due to the hostile and competitive environment that pushes microorganisms to produce substances important for defense and allows access to metabolic routes then silenced in milder cultivation conditions.</AbstractText>
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<ForeName>Paulo Cezar</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Chemistry, Federal University of São Carlos (UFSCar), São Carlos, SP, Brazil.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of BioMolecular Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo (USP), Ribeirão Preto, SP, Brazil.</Affiliation>
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<Country></Country>
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<li>Brésil</li>
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<li>Minas Gerais</li>
<li>État de São Paulo</li>
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<name sortKey="Camargo, Ilana Lopes Baratella Da Cunha" sort="Camargo, Ilana Lopes Baratella Da Cunha" uniqKey="Camargo I" first="Ilana Lopes Baratella Da Cunha" last="Camargo">Ilana Lopes Baratella Da Cunha Camargo</name>
<name sortKey="Cruz, Felipe De Paula Nogueira" sort="Cruz, Felipe De Paula Nogueira" uniqKey="Cruz F" first="Felipe De Paula Nogueira" last="Cruz">Felipe De Paula Nogueira Cruz</name>
<name sortKey="De Camargo, Ana Flavia S" sort="De Camargo, Ana Flavia S" uniqKey="De Camargo A" first="Ana Flávia S" last="De Camargo">Ana Flávia S. De Camargo</name>
<name sortKey="Ferreira, Leonardo Luiz Gomes" sort="Ferreira, Leonardo Luiz Gomes" uniqKey="Ferreira L" first="Leonardo Luiz Gomes" last="Ferreira">Leonardo Luiz Gomes Ferreira</name>
<name sortKey="Krogh, Renata" sort="Krogh, Renata" uniqKey="Krogh R" first="Renata" last="Krogh">Renata Krogh</name>
<name sortKey="Silva, Taynara Lopes" sort="Silva, Taynara Lopes" uniqKey="Silva T" first="Taynara Lopes" last="Silva">Taynara Lopes Silva</name>
<name sortKey="Vieira, Paulo Cezar" sort="Vieira, Paulo Cezar" uniqKey="Vieira P" first="Paulo Cezar" last="Vieira">Paulo Cezar Vieira</name>
<name sortKey="Vieira, Paulo Cezar" sort="Vieira, Paulo Cezar" uniqKey="Vieira P" first="Paulo Cezar" last="Vieira">Paulo Cezar Vieira</name>
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