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Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice

Interferon-induced GTPases [guanylate-binding proteins (GBPs)] play an important role in inflammasome activation and mediate innate resistance to many intracellular pathogens, but little is known about their role in leishmaniasis. We therefore studied expression of Gbp2b/Gbp1 and Gbp5 mRNA in skin,...

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Autores principales: Sohrabi, Yahya, Volkova, Valeryia, Kobets, Tatyana, Havelková, Helena, Krayem, Imtissal, Slapničková, Martina, Demant, Peter, Lipoldová, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808352/
https://www.ncbi.nlm.nih.gov/pubmed/29467757
http://dx.doi.org/10.3389/fimmu.2018.00130
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author Sohrabi, Yahya
Volkova, Valeryia
Kobets, Tatyana
Havelková, Helena
Krayem, Imtissal
Slapničková, Martina
Demant, Peter
Lipoldová, Marie
author_facet Sohrabi, Yahya
Volkova, Valeryia
Kobets, Tatyana
Havelková, Helena
Krayem, Imtissal
Slapničková, Martina
Demant, Peter
Lipoldová, Marie
author_sort Sohrabi, Yahya
collection PubMed
description Interferon-induced GTPases [guanylate-binding proteins (GBPs)] play an important role in inflammasome activation and mediate innate resistance to many intracellular pathogens, but little is known about their role in leishmaniasis. We therefore studied expression of Gbp2b/Gbp1 and Gbp5 mRNA in skin, inguinal lymph nodes, spleen, and liver after Leishmania major infection and in uninfected controls. We used two different groups of related mouse strains: BALB/c, STS, and CcS-5, CcS-16, and CcS-20 that carry different combinations of BALB/c and STS genomes, and strains O20, C57BL/10 (B10) and B10.O20, OcB-9, and OcB-43 carrying different combinations of O20 and B10 genomes. The strains were classified on the basis of size and number of infection-induced skin lesions as highly susceptible (BALB/c, CcS-16), susceptible (B10.O20), intermediate (CcS-20), and resistant (STS, O20, B10, OcB-9, OcB-43). Some uninfected strains differed in expression of Gbp2b/Gbp1 and Gbp5, especially of Gbp2b/Gbp1 in skin. Uninfected BALB/c and STS did not differ in their expression, but in CcS-5, CcS-16, and CcS-20, which all carry BALB/c-derived Gbp gene-cluster, expression of Gbp2b/Gbp1 exceeds that of both parents. These data indicate trans-regulation of Gbps. Infection resulted in approximately 10× upregulation of Gbp2b/Gbp1 and Gbp5 mRNAs in organs of both susceptible and resistant strains, which was most pronounced in skin. CcS-20 expressed higher level of Gbp2b/Gbp1 than both parental strains in skin, whereas CcS-16 expressed higher level of Gbp2b/Gbp1 than both parental strains in skin and liver. This indicates a trans-regulation present in infected mice CcS-16 and CcS-20. Immunostaining of skin of five strains revealed in resistant and intermediate strains STS, CcS-5, O20, and CcS-20 tight co-localization of Gbp2b/Gbp1 protein with most L. major parasites, whereas in the highly susceptible strain, BALB/c most parasites did not associate with Gbp2b/Gbp1. In conclusion, expression of Gbp2b/Gbp1 and Gbp5 was increased even in organs of clinically asymptomatic resistant mice. It suggests a hidden inflammation, which might contribute to control of persisting parasites. This is supported by the co-localization of Gbpb2/Gbp1 protein and L. major parasites in skin of resistant and intermediate but not highly susceptible mice.
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spelling pubmed-58083522018-02-21 Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice Sohrabi, Yahya Volkova, Valeryia Kobets, Tatyana Havelková, Helena Krayem, Imtissal Slapničková, Martina Demant, Peter Lipoldová, Marie Front Immunol Immunology Interferon-induced GTPases [guanylate-binding proteins (GBPs)] play an important role in inflammasome activation and mediate innate resistance to many intracellular pathogens, but little is known about their role in leishmaniasis. We therefore studied expression of Gbp2b/Gbp1 and Gbp5 mRNA in skin, inguinal lymph nodes, spleen, and liver after Leishmania major infection and in uninfected controls. We used two different groups of related mouse strains: BALB/c, STS, and CcS-5, CcS-16, and CcS-20 that carry different combinations of BALB/c and STS genomes, and strains O20, C57BL/10 (B10) and B10.O20, OcB-9, and OcB-43 carrying different combinations of O20 and B10 genomes. The strains were classified on the basis of size and number of infection-induced skin lesions as highly susceptible (BALB/c, CcS-16), susceptible (B10.O20), intermediate (CcS-20), and resistant (STS, O20, B10, OcB-9, OcB-43). Some uninfected strains differed in expression of Gbp2b/Gbp1 and Gbp5, especially of Gbp2b/Gbp1 in skin. Uninfected BALB/c and STS did not differ in their expression, but in CcS-5, CcS-16, and CcS-20, which all carry BALB/c-derived Gbp gene-cluster, expression of Gbp2b/Gbp1 exceeds that of both parents. These data indicate trans-regulation of Gbps. Infection resulted in approximately 10× upregulation of Gbp2b/Gbp1 and Gbp5 mRNAs in organs of both susceptible and resistant strains, which was most pronounced in skin. CcS-20 expressed higher level of Gbp2b/Gbp1 than both parental strains in skin, whereas CcS-16 expressed higher level of Gbp2b/Gbp1 than both parental strains in skin and liver. This indicates a trans-regulation present in infected mice CcS-16 and CcS-20. Immunostaining of skin of five strains revealed in resistant and intermediate strains STS, CcS-5, O20, and CcS-20 tight co-localization of Gbp2b/Gbp1 protein with most L. major parasites, whereas in the highly susceptible strain, BALB/c most parasites did not associate with Gbp2b/Gbp1. In conclusion, expression of Gbp2b/Gbp1 and Gbp5 was increased even in organs of clinically asymptomatic resistant mice. It suggests a hidden inflammation, which might contribute to control of persisting parasites. This is supported by the co-localization of Gbpb2/Gbp1 protein and L. major parasites in skin of resistant and intermediate but not highly susceptible mice. Frontiers Media S.A. 2018-02-07 /pmc/articles/PMC5808352/ /pubmed/29467757 http://dx.doi.org/10.3389/fimmu.2018.00130 Text en Copyright © 2018 Sohrabi, Volkova, Kobets, Havelková, Krayem, Slapničková, Demant and Lipoldová. 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) and the copyright owner 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 Immunology
Sohrabi, Yahya
Volkova, Valeryia
Kobets, Tatyana
Havelková, Helena
Krayem, Imtissal
Slapničková, Martina
Demant, Peter
Lipoldová, Marie
Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice
title Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice
title_full Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice
title_fullStr Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice
title_full_unstemmed Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice
title_short Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice
title_sort genetic regulation of guanylate-binding proteins 2b and 5 during leishmaniasis in mice
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808352/
https://www.ncbi.nlm.nih.gov/pubmed/29467757
http://dx.doi.org/10.3389/fimmu.2018.00130
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