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RNAi-mediated gene silencing of Phlebotomus papatasi defensins favors Leishmania major infection

Introduction: Production of different antimicrobial peptides (AMPs) is one of the insect’s prominent defense strategies, regulated mainly by Toll and immune deficiency (IMD) humoral pathways. Here we focused mainly on two AMPs of Phlebotomus papatasi, vector of Leishmania major parasites, their asso...

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Autores principales: Vomáčková Kykalová, Barbora, Sassù, Fabiana, Volf, Petr, Telleria, Erich Loza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230645/
https://www.ncbi.nlm.nih.gov/pubmed/37265840
http://dx.doi.org/10.3389/fphys.2023.1182141
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author Vomáčková Kykalová, Barbora
Sassù, Fabiana
Volf, Petr
Telleria, Erich Loza
author_facet Vomáčková Kykalová, Barbora
Sassù, Fabiana
Volf, Petr
Telleria, Erich Loza
author_sort Vomáčková Kykalová, Barbora
collection PubMed
description Introduction: Production of different antimicrobial peptides (AMPs) is one of the insect’s prominent defense strategies, regulated mainly by Toll and immune deficiency (IMD) humoral pathways. Here we focused mainly on two AMPs of Phlebotomus papatasi, vector of Leishmania major parasites, their association with the relish transcription factor and the effective participation on Leishmania infection. Methods and results: We further characterized the role of previously described gut-specific P. papatasi defensin (PpDef1) and identified the second defensin (PpDef2) expressed in various sand fly tissues. Using the RNAi-mediated gene silencing, we report that the silencing of PpDef1 gene or simultaneous silencing of both defensin genes (PpDef1 and PpDef2) resulted in increased parasite levels in the sand fly (detectable by PCR) and higher sand fly mortality. In addition, we knocked down relish, the sole transcription factor of the IMD pathway, to evaluate the association of the IMD pathway with AMPs expression in P. papatasi. We demonstrated that the relish gene knockdown reduced the expression of PpDef2 and attacin, another AMP abundantly expressed in the sand fly body. Conclusions: Altogether, our experiments show the importance of defensins in the sand fly response toward L. major and the role of the IMD pathway in regulating AMPs in P. papatasi.
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spelling pubmed-102306452023-06-01 RNAi-mediated gene silencing of Phlebotomus papatasi defensins favors Leishmania major infection Vomáčková Kykalová, Barbora Sassù, Fabiana Volf, Petr Telleria, Erich Loza Front Physiol Physiology Introduction: Production of different antimicrobial peptides (AMPs) is one of the insect’s prominent defense strategies, regulated mainly by Toll and immune deficiency (IMD) humoral pathways. Here we focused mainly on two AMPs of Phlebotomus papatasi, vector of Leishmania major parasites, their association with the relish transcription factor and the effective participation on Leishmania infection. Methods and results: We further characterized the role of previously described gut-specific P. papatasi defensin (PpDef1) and identified the second defensin (PpDef2) expressed in various sand fly tissues. Using the RNAi-mediated gene silencing, we report that the silencing of PpDef1 gene or simultaneous silencing of both defensin genes (PpDef1 and PpDef2) resulted in increased parasite levels in the sand fly (detectable by PCR) and higher sand fly mortality. In addition, we knocked down relish, the sole transcription factor of the IMD pathway, to evaluate the association of the IMD pathway with AMPs expression in P. papatasi. We demonstrated that the relish gene knockdown reduced the expression of PpDef2 and attacin, another AMP abundantly expressed in the sand fly body. Conclusions: Altogether, our experiments show the importance of defensins in the sand fly response toward L. major and the role of the IMD pathway in regulating AMPs in P. papatasi. Frontiers Media S.A. 2023-05-09 /pmc/articles/PMC10230645/ /pubmed/37265840 http://dx.doi.org/10.3389/fphys.2023.1182141 Text en Copyright © 2023 Vomáčková Kykalová, Sassù, Volf and Telleria. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Vomáčková Kykalová, Barbora
Sassù, Fabiana
Volf, Petr
Telleria, Erich Loza
RNAi-mediated gene silencing of Phlebotomus papatasi defensins favors Leishmania major infection
title RNAi-mediated gene silencing of Phlebotomus papatasi defensins favors Leishmania major infection
title_full RNAi-mediated gene silencing of Phlebotomus papatasi defensins favors Leishmania major infection
title_fullStr RNAi-mediated gene silencing of Phlebotomus papatasi defensins favors Leishmania major infection
title_full_unstemmed RNAi-mediated gene silencing of Phlebotomus papatasi defensins favors Leishmania major infection
title_short RNAi-mediated gene silencing of Phlebotomus papatasi defensins favors Leishmania major infection
title_sort rnai-mediated gene silencing of phlebotomus papatasi defensins favors leishmania major infection
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230645/
https://www.ncbi.nlm.nih.gov/pubmed/37265840
http://dx.doi.org/10.3389/fphys.2023.1182141
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