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Protein methyltransferase 7 deficiency in Leishmania major increases neutrophil associated pathology in murine model
J. Alcoforado Diniz, MM. Chaves, S. Vaselek, RD. Miserani Magalhães, R. Ricci-Azevedo, RVH. de Carvalho, LB. Lorenzon, TR. Ferreira, D. Zamboni, PB. Walrad, P. Volf, DL. Sacks, AK. Cruz
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, Research Support, N.I.H., Intramural, práce podpořená grantem
Grantová podpora
MR/M02640X/1
Medical Research Council - United Kingdom
MR/N017633/1
Medical Research Council - United Kingdom
NLK
Directory of Open Access Journals
od 2007
Free Medical Journals
od 2007
Public Library of Science (PLoS)
od 2007
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2007-10-01
Open Access Digital Library
od 2007-08-30
Open Access Digital Library
od 2007-01-01
Open Access Digital Library
od 2007-01-01
Medline Complete (EBSCOhost)
od 2009-04-01
Health & Medicine (ProQuest)
od 2007-10-01
Public Health Database (ProQuest)
od 2007-10-01
ROAD: Directory of Open Access Scholarly Resources
od 2007
- MeSH
- delece genu MeSH
- Leishmania major enzymologie genetika metabolismus MeSH
- leishmanióza kožní parazitologie patologie MeSH
- myši MeSH
- neutrofily fyziologie MeSH
- proteinmethyltransferasy genetika metabolismus MeSH
- protozoální proteiny metabolismus MeSH
- regulace genové exprese enzymů MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Intramural MeSH
Leishmania major is the main causative agent of cutaneous leishmaniasis in the Old World. In Leishmania parasites, the lack of transcriptional control is mostly compensated by post-transcriptional mechanisms. Methylation of arginine is a conserved post-translational modification executed by Protein Arginine Methyltransferase (PRMTs). The genome from L. major encodes five PRMT homologs, including the cytosolic protein associated with several RNA-binding proteins, LmjPRMT7. It has been previously reported that LmjPRMT7 could impact parasite infectivity. In addition, a more recent work has clearly shown the importance of LmjPRMT7 in RNA-binding capacity and protein stability of methylation targets, demonstrating the role of this enzyme as an important epigenetic regulator of mRNA metabolism. In this study, we unveil the impact of PRMT7-mediated methylation on parasite development and virulence. Our data reveals that higher levels of LmjPRMT7 can impair parasite pathogenicity, and that deletion of this enzyme rescues the pathogenic phenotype of an attenuated strain of L. major. Interestingly, lesion formation caused by LmjPRMT7 knockout parasites is associated with an exacerbated inflammatory reaction in the tissue correlated with an excessive neutrophil recruitment. Moreover, the absence of LmjPRMT7 also impairs parasite development within the sand fly vector Phlebotomus duboscqi. Finally, a transcriptome analysis shed light onto possible genes affected by depletion of this enzyme. Taken together, this study highlights how post-transcriptional regulation can affect different aspects of the parasite biology.
Department of Biology University of York York United Kingdom
Department of Parasitology Charles University Prague Czech Republic
Citace poskytuje Crossref.org
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- $a Leishmania major is the main causative agent of cutaneous leishmaniasis in the Old World. In Leishmania parasites, the lack of transcriptional control is mostly compensated by post-transcriptional mechanisms. Methylation of arginine is a conserved post-translational modification executed by Protein Arginine Methyltransferase (PRMTs). The genome from L. major encodes five PRMT homologs, including the cytosolic protein associated with several RNA-binding proteins, LmjPRMT7. It has been previously reported that LmjPRMT7 could impact parasite infectivity. In addition, a more recent work has clearly shown the importance of LmjPRMT7 in RNA-binding capacity and protein stability of methylation targets, demonstrating the role of this enzyme as an important epigenetic regulator of mRNA metabolism. In this study, we unveil the impact of PRMT7-mediated methylation on parasite development and virulence. Our data reveals that higher levels of LmjPRMT7 can impair parasite pathogenicity, and that deletion of this enzyme rescues the pathogenic phenotype of an attenuated strain of L. major. Interestingly, lesion formation caused by LmjPRMT7 knockout parasites is associated with an exacerbated inflammatory reaction in the tissue correlated with an excessive neutrophil recruitment. Moreover, the absence of LmjPRMT7 also impairs parasite development within the sand fly vector Phlebotomus duboscqi. Finally, a transcriptome analysis shed light onto possible genes affected by depletion of this enzyme. Taken together, this study highlights how post-transcriptional regulation can affect different aspects of the parasite biology.
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