Differential expression of groEL-1, incB, pyk-F, tal, hctA and omcB genes during Chlamydia trachomatis developmental cycle
Autor: | Willem A. Sturm, Sinaye Ngcapu, Gugulethu F. Mzobe, Bronwyn C. Joubert |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Keratinocytes Time Factors Cellular differentiation Cultured tumor cells Gene Expression Chlamydia trachomatis medicine.disease_cause Pathology and Laboratory Medicine Epithelium Chlamydia Infection Medical Conditions Animal Cells Gene expression Medicine and Health Sciences Chlamydia Regulation of gene expression Multidisciplinary Cell Differentiation Bacterial Pathogens DNA-Binding Proteins Infectious Diseases Medical Microbiology Cell lines Medicine Pathogens Cellular Types Anatomy Biological cultures Research Article Bacterial Outer Membrane Proteins Science 030106 microbiology Pyruvate Kinase Sexually Transmitted Diseases Biology Microbiology Cell Line 03 medical and health sciences Bacterial Proteins medicine Genetics Humans Gene Regulation HeLa cells Gene Microbial Pathogens Transcription Activator-Like Effectors Bacteria Organisms Biology and Life Sciences Epithelial Cells Cell Biology Chaperonin 60 Gene Expression Regulation Bacterial medicine.disease Cell cultures Phosphoproteins Molecular biology In vitro Research and analysis methods 030104 developmental biology Biological Tissue Cell culture Developmental Biology |
Zdroj: | PLoS ONE, Vol 16, Iss 4, p e0249358 (2021) PLoS ONE |
ISSN: | 1932-6203 |
Popis: | Chlamydia trachomatis infects squamous and columnar epithelia at the mucosal surface. Research on gene expression patterns of C. trachomatis has predominantly focused on non-native host cells, with limited data on growth kinetics and gene expression of chlamydia in keratinocytes. Here, we investigated whether early, mid, and late chlamydial genes observed in HeLa cell line studies were co-ordinately regulated at the transcriptional level even in the keratinized cell line model and whether the expression was stage-specific during the developmental cycle. HaCaT cell lines were infected with chlamydia clinical isolates (US151and serovar E) and reference strain (L2 434). Expression of groEL-1, incB, pyk-F, tal, hctA, and omcB genes was conducted with comparative real-time PCR and transcriptional events during the chlamydial developmental cycle using transmission electron microscopy. The relative expression level of each gene and fold difference were calculated using the 2-ΔΔCT method. The expression of groEL-1 and pyk-F genes was highest at 2 hours post-infection (hpi) in the L2 434 and serovar E. The expression of incB gene increased at 2 hpi in L2 434 and serovar E but peaked at 12 hpi in serovar E. L2 434 and US151 had similar tal expression profiles. Increased expression of hctA and omcB genes were found at 2 and 36 hpi in L2 434. Both clinical isolates and reference strains presented the normal chlamydial replication cycle comprising elementary bodies and reticulate bodies within 36 hpi. We show different gene expression patterns between clinical isolates and reference strain during in vitro infection of keratinocytes, with reference strain-inducing consistent expression of genes. These findings confirm that keratinocytes are appropriate cell lines to interrogate cell differentiation, growth kinetics, and gene expression of C. trachomatis infection. Furthermore, more studies with different clinical isolates and genes are needed to better understand the Chlamydial pathogenesis in keratinocytes. |
Databáze: | OpenAIRE |
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