Gene expression profiling of protease and non-protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysis

Abstract Trichophyton mentagrophytes secretes Metallocarboxypeptidase A and B of the M14 family as endoproteases and exoprotease. T. mentagrophytes produce Metalloprotease 3 and 4 which degrades the protein into the short peptides and amino acids. To understand the host fungal relationship and ident...

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Main Authors: Shyama Datt, Shukla Das, M. Ahmad Ansari, Rahul Sharma, Thakur Datt, S. N. Bhattacharya
Format: Article
Language:English
Published: Nature Publishing Group 2021-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-020-79839-1
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spelling doaj-47b5b61c09884f11959fa9f204a98c672021-01-17T12:33:17ZengNature Publishing GroupScientific Reports2045-23222021-01-0111111010.1038/s41598-020-79839-1Gene expression profiling of protease and non-protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysisShyama Datt0Shukla Das1M. Ahmad Ansari2Rahul Sharma3Thakur Datt4S. N. Bhattacharya5Department of Microbiology, University College of Medical Sciences and Guru Teg Bahadur HospitalDepartment of Microbiology, University College of Medical Sciences and Guru Teg Bahadur HospitalMolecular Oncology Laboratory, Delhi State Cancer Institute Dilshad GardenDepartment of Community Medicine, University College of Medical Sciences and Guru Teg Bahadur HospitalDepartment of Microbiology, University College of Medical Sciences and Guru Teg Bahadur HospitalDepartment of Dermatology, University College of Medical Sciences and Guru Teg Bahadur HospitalAbstract Trichophyton mentagrophytes secretes Metallocarboxypeptidase A and B of the M14 family as endoproteases and exoprotease. T. mentagrophytes produce Metalloprotease 3 and 4 which degrades the protein into the short peptides and amino acids. To understand the host fungal relationship and identification of such genes expressed during infection is utmost important. T. mentagrophytes encodes some proteins which are associated with the glyoxylate cycle. The glyoxylate cycle enzymes have been involving in virulence of dermatophytes and their up-regulation during dermatophytes growth on keratin. On comparing the expression level of virulence protease and non-protease genes, we observed, among exoprotease protease genes, Metallocarboxypeptidase B was strongly up regulated (134.6 fold high) followed by Metallocarboxypeptidase A (115.6 fold high) and Di-peptidyl-peptidases V (10.1 fold high), in dermatophytic patients as compared to ATCC strain. Furthermore, among endoprotease, Metalloprotease 4 was strongly up regulated (131.6 fold high) followed by Metalloprotease 3 (16.7 fold high), in clinical strains as compared to T. mentagrophytes ATCC strain. While among non-protease genes, Citrate Synthase was highly expressed (118 fold high), followed by Isocitrate Lyase (101.6 fold high) and Malate Synthase (52.9 fold high). All the studied virulence genes were considered the best suitable ones by geNorm, Best keeper, Norm Finder and Ref finder.https://doi.org/10.1038/s41598-020-79839-1
collection DOAJ
language English
format Article
sources DOAJ
author Shyama Datt
Shukla Das
M. Ahmad Ansari
Rahul Sharma
Thakur Datt
S. N. Bhattacharya
spellingShingle Shyama Datt
Shukla Das
M. Ahmad Ansari
Rahul Sharma
Thakur Datt
S. N. Bhattacharya
Gene expression profiling of protease and non-protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysis
Scientific Reports
author_facet Shyama Datt
Shukla Das
M. Ahmad Ansari
Rahul Sharma
Thakur Datt
S. N. Bhattacharya
author_sort Shyama Datt
title Gene expression profiling of protease and non-protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysis
title_short Gene expression profiling of protease and non-protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysis
title_full Gene expression profiling of protease and non-protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysis
title_fullStr Gene expression profiling of protease and non-protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysis
title_full_unstemmed Gene expression profiling of protease and non-protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysis
title_sort gene expression profiling of protease and non-protease genes in trichophyton mentagrophytes isolates from dermatophytosis patients by qrt-pcr analysis
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-01-01
description Abstract Trichophyton mentagrophytes secretes Metallocarboxypeptidase A and B of the M14 family as endoproteases and exoprotease. T. mentagrophytes produce Metalloprotease 3 and 4 which degrades the protein into the short peptides and amino acids. To understand the host fungal relationship and identification of such genes expressed during infection is utmost important. T. mentagrophytes encodes some proteins which are associated with the glyoxylate cycle. The glyoxylate cycle enzymes have been involving in virulence of dermatophytes and their up-regulation during dermatophytes growth on keratin. On comparing the expression level of virulence protease and non-protease genes, we observed, among exoprotease protease genes, Metallocarboxypeptidase B was strongly up regulated (134.6 fold high) followed by Metallocarboxypeptidase A (115.6 fold high) and Di-peptidyl-peptidases V (10.1 fold high), in dermatophytic patients as compared to ATCC strain. Furthermore, among endoprotease, Metalloprotease 4 was strongly up regulated (131.6 fold high) followed by Metalloprotease 3 (16.7 fold high), in clinical strains as compared to T. mentagrophytes ATCC strain. While among non-protease genes, Citrate Synthase was highly expressed (118 fold high), followed by Isocitrate Lyase (101.6 fold high) and Malate Synthase (52.9 fold high). All the studied virulence genes were considered the best suitable ones by geNorm, Best keeper, Norm Finder and Ref finder.
url https://doi.org/10.1038/s41598-020-79839-1
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