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The Upregulation of Cathepsin G Is Associated with Resistance to Bovine Paratuberculosis

SIMPLE SUMMARY: Cathepsin G (CTSG) is a serine protease that participates in the killing of pathogens and tissue remodeling at sites of inflammation. We previously found that the presence of the minor allele in the cis-eQTLs-rs41976219 (AC) was associated with increased CTSG mRNA levels in blood sam...

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Autores principales: Canive, Maria, Badia-Bringué, Gerard, Alonso-Hearn, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655680/
https://www.ncbi.nlm.nih.gov/pubmed/36359162
http://dx.doi.org/10.3390/ani12213038
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author Canive, Maria
Badia-Bringué, Gerard
Alonso-Hearn, Marta
author_facet Canive, Maria
Badia-Bringué, Gerard
Alonso-Hearn, Marta
author_sort Canive, Maria
collection PubMed
description SIMPLE SUMMARY: Cathepsin G (CTSG) is a serine protease that participates in the killing of pathogens and tissue remodeling at sites of inflammation. We previously found that the presence of the minor allele in the cis-eQTLs-rs41976219 (AC) was associated with increased CTSG mRNA levels in blood samples from Holstein cows. In this study, we test whether genetic variation in the cis-eQTL-rs41976219 is associated with changes in CTSG protein expression and control of Mycobacterium avium subsp. paratuberculosis (MAP) infection. We demonstrate that the heterozygous genotype for the rs41976219 (AC) results in higher CTSG protein levels in the supernatants of infected CD14+-monocyte-derived macrophages (MDMs) after 2 h of infection and a significantly lower intracellular MAP load at 7 d p.i. than in MDMs from cattle with the AA genotype. Furthermore, the rs41976219 genotype CC is more frequent in healthy cows than in cows with PTB-associated lesions in gut tissues. Higher CTSG levels are detected in plasmas from cows with the CC genotype when compared with cows with the AA + AC genotypes for the rs41976219. We conclude that the presence of the minor allele in the rs41976219 increases the CTSG expression in plasma samples and MAP-infected macrophages, and can influence PTB pathogenesis by modulating MAP load within infected macrophages. ABSTRACT: An in silico genomic–transcriptomic combined approach allowed the identification of a polymorphism (cis-eQTL-rs41976219) in the Bos taurus genome associated with the CTSG mRNA expression in bovine blood samples, which suggests that individual genetic variation might modulate the CTSG transcriptional response. In the current study, a sandwich ELISA is used to measure the CTSG protein levels in supernatants of monocyte-derived macrophages (MDMs) isolated from cows with the AA (n = 5) and AC (n = 11) genotypes for the rs41976219 and infected ex vivo with MAP. Cows with the AC genotype have significantly higher CTSG protein levels (1.85 ng/mL) in the supernatants of enriched CD14+-MDMs after 2 h of infection when compared with infected CD14+-MDMs from cows with the AA genotype (1.68 ng/mL). Statistically significant differences in the intracellular MAP load at 7 d p.i. are observed between animals with the AA (2.16 log CFUs) and AC (1.44 log CFUs) genotypes. Finally, the association between the rs41976219 allelic variants and resistance to PTB is tested in a larger cattle population (n = 943) classified according to the presence (n = 442) or absence (n = 501) of PTB-associated lesions. The presence of the two minor alleles in the rs41976219 (CC) is more frequent among healthy cows than in cows with PTB-associated lesions in gut tissues (2.2% vs. 1.4%, OR = 0.61). In agreement with this, the CTSG levels in plasma samples of cows without lesions in gut tissues and with the CC (n = 8) genotype are significantly higher than in the plasmas of cows with the AA + AC (n = 36) genotypes.
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spelling pubmed-96556802022-11-15 The Upregulation of Cathepsin G Is Associated with Resistance to Bovine Paratuberculosis Canive, Maria Badia-Bringué, Gerard Alonso-Hearn, Marta Animals (Basel) Article SIMPLE SUMMARY: Cathepsin G (CTSG) is a serine protease that participates in the killing of pathogens and tissue remodeling at sites of inflammation. We previously found that the presence of the minor allele in the cis-eQTLs-rs41976219 (AC) was associated with increased CTSG mRNA levels in blood samples from Holstein cows. In this study, we test whether genetic variation in the cis-eQTL-rs41976219 is associated with changes in CTSG protein expression and control of Mycobacterium avium subsp. paratuberculosis (MAP) infection. We demonstrate that the heterozygous genotype for the rs41976219 (AC) results in higher CTSG protein levels in the supernatants of infected CD14+-monocyte-derived macrophages (MDMs) after 2 h of infection and a significantly lower intracellular MAP load at 7 d p.i. than in MDMs from cattle with the AA genotype. Furthermore, the rs41976219 genotype CC is more frequent in healthy cows than in cows with PTB-associated lesions in gut tissues. Higher CTSG levels are detected in plasmas from cows with the CC genotype when compared with cows with the AA + AC genotypes for the rs41976219. We conclude that the presence of the minor allele in the rs41976219 increases the CTSG expression in plasma samples and MAP-infected macrophages, and can influence PTB pathogenesis by modulating MAP load within infected macrophages. ABSTRACT: An in silico genomic–transcriptomic combined approach allowed the identification of a polymorphism (cis-eQTL-rs41976219) in the Bos taurus genome associated with the CTSG mRNA expression in bovine blood samples, which suggests that individual genetic variation might modulate the CTSG transcriptional response. In the current study, a sandwich ELISA is used to measure the CTSG protein levels in supernatants of monocyte-derived macrophages (MDMs) isolated from cows with the AA (n = 5) and AC (n = 11) genotypes for the rs41976219 and infected ex vivo with MAP. Cows with the AC genotype have significantly higher CTSG protein levels (1.85 ng/mL) in the supernatants of enriched CD14+-MDMs after 2 h of infection when compared with infected CD14+-MDMs from cows with the AA genotype (1.68 ng/mL). Statistically significant differences in the intracellular MAP load at 7 d p.i. are observed between animals with the AA (2.16 log CFUs) and AC (1.44 log CFUs) genotypes. Finally, the association between the rs41976219 allelic variants and resistance to PTB is tested in a larger cattle population (n = 943) classified according to the presence (n = 442) or absence (n = 501) of PTB-associated lesions. The presence of the two minor alleles in the rs41976219 (CC) is more frequent among healthy cows than in cows with PTB-associated lesions in gut tissues (2.2% vs. 1.4%, OR = 0.61). In agreement with this, the CTSG levels in plasma samples of cows without lesions in gut tissues and with the CC (n = 8) genotype are significantly higher than in the plasmas of cows with the AA + AC (n = 36) genotypes. MDPI 2022-11-04 /pmc/articles/PMC9655680/ /pubmed/36359162 http://dx.doi.org/10.3390/ani12213038 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
Canive, Maria
Badia-Bringué, Gerard
Alonso-Hearn, Marta
The Upregulation of Cathepsin G Is Associated with Resistance to Bovine Paratuberculosis
title The Upregulation of Cathepsin G Is Associated with Resistance to Bovine Paratuberculosis
title_full The Upregulation of Cathepsin G Is Associated with Resistance to Bovine Paratuberculosis
title_fullStr The Upregulation of Cathepsin G Is Associated with Resistance to Bovine Paratuberculosis
title_full_unstemmed The Upregulation of Cathepsin G Is Associated with Resistance to Bovine Paratuberculosis
title_short The Upregulation of Cathepsin G Is Associated with Resistance to Bovine Paratuberculosis
title_sort upregulation of cathepsin g is associated with resistance to bovine paratuberculosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655680/
https://www.ncbi.nlm.nih.gov/pubmed/36359162
http://dx.doi.org/10.3390/ani12213038
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