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The Search for Cryptic L-Rhamnosyltransferases on the Sporothrix schenckii Genome

The fungal cell wall is an attractive structure to look for new antifungal drug targets and for understanding the host-fungus interaction. Sporothrix schenckii is one of the main causative agents of both human and animal sporotrichosis and currently is the species most studied of the Sporothrix genu...

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Autores principales: Mora-Montes, Héctor M., García-Gutiérrez, Karina, García-Carnero, Laura C., Lozoya-Pérez, Nancy E., Ramirez-Prado, Jorge H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145935/
https://www.ncbi.nlm.nih.gov/pubmed/35628784
http://dx.doi.org/10.3390/jof8050529
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author Mora-Montes, Héctor M.
García-Gutiérrez, Karina
García-Carnero, Laura C.
Lozoya-Pérez, Nancy E.
Ramirez-Prado, Jorge H.
author_facet Mora-Montes, Héctor M.
García-Gutiérrez, Karina
García-Carnero, Laura C.
Lozoya-Pérez, Nancy E.
Ramirez-Prado, Jorge H.
author_sort Mora-Montes, Héctor M.
collection PubMed
description The fungal cell wall is an attractive structure to look for new antifungal drug targets and for understanding the host-fungus interaction. Sporothrix schenckii is one of the main causative agents of both human and animal sporotrichosis and currently is the species most studied of the Sporothrix genus. The cell wall of this organism has been previously analyzed, and rhamnoconjugates are signature molecules found on the surface of both mycelia and yeast-like cells. Similar to other reactions where sugars are covalently linked to other sugars, lipids, or proteins, the rhamnosylation process in this organism is expected to involve glycosyltransferases with the ability to transfer rhamnose from a sugar donor to the acceptor molecule, i.e., rhamnosyltransferases. However, no obvious rhamnosyltransferase has thus far been identified within the S. schenckii proteome or genome. Here, using a Hidden Markov Model profile strategy, we found within the S. schenckii genome five putative genes encoding for rhamnosyltransferases. Expression analyses indicated that only two of them, named RHT1 and RHT2, were significantly expressed in yeast-like cells and during interaction with the host. These two genes were heterologously expressed in Escherichia coli, and the purified recombinant proteins showed rhamnosyltransferase activity, dependent on the presence of UDP-rhamnose as a sugar donor. To the best of our knowledge, this is the first report about rhamnosyltransferases in S. schenckii.
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spelling pubmed-91459352022-05-29 The Search for Cryptic L-Rhamnosyltransferases on the Sporothrix schenckii Genome Mora-Montes, Héctor M. García-Gutiérrez, Karina García-Carnero, Laura C. Lozoya-Pérez, Nancy E. Ramirez-Prado, Jorge H. J Fungi (Basel) Article The fungal cell wall is an attractive structure to look for new antifungal drug targets and for understanding the host-fungus interaction. Sporothrix schenckii is one of the main causative agents of both human and animal sporotrichosis and currently is the species most studied of the Sporothrix genus. The cell wall of this organism has been previously analyzed, and rhamnoconjugates are signature molecules found on the surface of both mycelia and yeast-like cells. Similar to other reactions where sugars are covalently linked to other sugars, lipids, or proteins, the rhamnosylation process in this organism is expected to involve glycosyltransferases with the ability to transfer rhamnose from a sugar donor to the acceptor molecule, i.e., rhamnosyltransferases. However, no obvious rhamnosyltransferase has thus far been identified within the S. schenckii proteome or genome. Here, using a Hidden Markov Model profile strategy, we found within the S. schenckii genome five putative genes encoding for rhamnosyltransferases. Expression analyses indicated that only two of them, named RHT1 and RHT2, were significantly expressed in yeast-like cells and during interaction with the host. These two genes were heterologously expressed in Escherichia coli, and the purified recombinant proteins showed rhamnosyltransferase activity, dependent on the presence of UDP-rhamnose as a sugar donor. To the best of our knowledge, this is the first report about rhamnosyltransferases in S. schenckii. MDPI 2022-05-20 /pmc/articles/PMC9145935/ /pubmed/35628784 http://dx.doi.org/10.3390/jof8050529 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mora-Montes, Héctor M.
García-Gutiérrez, Karina
García-Carnero, Laura C.
Lozoya-Pérez, Nancy E.
Ramirez-Prado, Jorge H.
The Search for Cryptic L-Rhamnosyltransferases on the Sporothrix schenckii Genome
title The Search for Cryptic L-Rhamnosyltransferases on the Sporothrix schenckii Genome
title_full The Search for Cryptic L-Rhamnosyltransferases on the Sporothrix schenckii Genome
title_fullStr The Search for Cryptic L-Rhamnosyltransferases on the Sporothrix schenckii Genome
title_full_unstemmed The Search for Cryptic L-Rhamnosyltransferases on the Sporothrix schenckii Genome
title_short The Search for Cryptic L-Rhamnosyltransferases on the Sporothrix schenckii Genome
title_sort search for cryptic l-rhamnosyltransferases on the sporothrix schenckii genome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145935/
https://www.ncbi.nlm.nih.gov/pubmed/35628784
http://dx.doi.org/10.3390/jof8050529
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