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Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins

Ancestral sequence reconstruction has been widely used to test evolution-based hypotheses. The genome of the European tick vector, Ixodes ricinus, encodes for defensin peptides with diverse antimicrobial activities against distantly related pathogens. These pathogens include fungi, Gram-negative, an...

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Autores principales: Cabezas-Cruz, Alejandro, Tonk, Miray, Bouchut, Anne, Pierrot, Christine, Pierce, Raymond J., Kotsyfakis, Michalis, Rahnamaeian, Mohammad, Vilcinskas, Andreas, Khalife, Jamal, Valdés, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075766/
https://www.ncbi.nlm.nih.gov/pubmed/27822206
http://dx.doi.org/10.3389/fmicb.2016.01682
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author Cabezas-Cruz, Alejandro
Tonk, Miray
Bouchut, Anne
Pierrot, Christine
Pierce, Raymond J.
Kotsyfakis, Michalis
Rahnamaeian, Mohammad
Vilcinskas, Andreas
Khalife, Jamal
Valdés, James J.
author_facet Cabezas-Cruz, Alejandro
Tonk, Miray
Bouchut, Anne
Pierrot, Christine
Pierce, Raymond J.
Kotsyfakis, Michalis
Rahnamaeian, Mohammad
Vilcinskas, Andreas
Khalife, Jamal
Valdés, James J.
author_sort Cabezas-Cruz, Alejandro
collection PubMed
description Ancestral sequence reconstruction has been widely used to test evolution-based hypotheses. The genome of the European tick vector, Ixodes ricinus, encodes for defensin peptides with diverse antimicrobial activities against distantly related pathogens. These pathogens include fungi, Gram-negative, and Gram-positive bacteria, i.e., a wide antimicrobial spectrum. Ticks do not transmit these pathogens, suggesting that these defensins may act against a wide range of microbes encountered by ticks during blood feeding or off-host periods. As demonstrated here, these I. ricinus defensins are also effective against the apicomplexan parasite Plasmodium falciparum. To study the general evolution of antimicrobial activity in tick defensins, the ancestral amino acid sequence of chelicerate defensins, which existed approximately 444 million years ago, was reconstructed using publicly available scorpion and tick defensin sequences (named Scorpions-Ticks Defensins Ancestor, STiDA). The activity of STiDA was tested against P. falciparum and the same Gram-negative and Gram-positive bacteria that were used for the I. ricinus defensins. While some extant tick defensins exhibit a wide antimicrobial spectrum, the ancestral defensin showed moderate activity against one of the tested microbes, P. falciparum. This study suggests that amino acid variability and defensin family expansion increased the antimicrobial spectrum of ancestral tick defensins.
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spelling pubmed-50757662016-11-07 Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins Cabezas-Cruz, Alejandro Tonk, Miray Bouchut, Anne Pierrot, Christine Pierce, Raymond J. Kotsyfakis, Michalis Rahnamaeian, Mohammad Vilcinskas, Andreas Khalife, Jamal Valdés, James J. Front Microbiol Microbiology Ancestral sequence reconstruction has been widely used to test evolution-based hypotheses. The genome of the European tick vector, Ixodes ricinus, encodes for defensin peptides with diverse antimicrobial activities against distantly related pathogens. These pathogens include fungi, Gram-negative, and Gram-positive bacteria, i.e., a wide antimicrobial spectrum. Ticks do not transmit these pathogens, suggesting that these defensins may act against a wide range of microbes encountered by ticks during blood feeding or off-host periods. As demonstrated here, these I. ricinus defensins are also effective against the apicomplexan parasite Plasmodium falciparum. To study the general evolution of antimicrobial activity in tick defensins, the ancestral amino acid sequence of chelicerate defensins, which existed approximately 444 million years ago, was reconstructed using publicly available scorpion and tick defensin sequences (named Scorpions-Ticks Defensins Ancestor, STiDA). The activity of STiDA was tested against P. falciparum and the same Gram-negative and Gram-positive bacteria that were used for the I. ricinus defensins. While some extant tick defensins exhibit a wide antimicrobial spectrum, the ancestral defensin showed moderate activity against one of the tested microbes, P. falciparum. This study suggests that amino acid variability and defensin family expansion increased the antimicrobial spectrum of ancestral tick defensins. Frontiers Media S.A. 2016-10-24 /pmc/articles/PMC5075766/ /pubmed/27822206 http://dx.doi.org/10.3389/fmicb.2016.01682 Text en Copyright © 2016 Cabezas-Cruz, Tonk, Bouchut, Pierrot, Pierce, Kotsyfakis, Rahnamaeian, Vilcinskas, Khalife and Valdés. http://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) or licensor 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 Microbiology
Cabezas-Cruz, Alejandro
Tonk, Miray
Bouchut, Anne
Pierrot, Christine
Pierce, Raymond J.
Kotsyfakis, Michalis
Rahnamaeian, Mohammad
Vilcinskas, Andreas
Khalife, Jamal
Valdés, James J.
Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins
title Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins
title_full Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins
title_fullStr Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins
title_full_unstemmed Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins
title_short Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins
title_sort antiplasmodial activity is an ancient and conserved feature of tick defensins
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075766/
https://www.ncbi.nlm.nih.gov/pubmed/27822206
http://dx.doi.org/10.3389/fmicb.2016.01682
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