Canonical pathways, networks and transcriptional factor regulation by clinical strains of Mycobacterium tuberculosis in pulmonary alveolar epithelial cells

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• 作者：Nontobeko E. Mvubu^a ; ^{207500550@stu.ukzn.ac.za" class="auth_mail" title="E-mail the corresponding author} ; Balakrishna Pillay^a ; ^{pillayb1@ukzn.ac.za" class="auth_mail" title="E-mail the corresponding author} ; Junaid Gamieldien^b ; ^{junaid@sanbi.ac.za" class="auth_mail" title="E-mail the corresponding author} ; William Bishai^c ; ^{wbishai1@jhmi.edu" class="auth_mail" title="E-mail the corresponding author} ; Manormoney Pillay^d ; ^{pillayc@ukzn.ac.za" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Mycobacterium tuberculosis ; Epithelial cells ; RNA sequencing ; Canonical pathways ; Networks ; Transcriptional factors
• 刊名：Tuberculosis
• 出版年：2016
• 出版时间：March 2016
• 年：2016
• 卷：97
• 期：Complete
• 页码：73-85
• 全文大小：3532 K

文摘

Limited knowledge exists on pathways, networks and transcriptional factors regulated within epithelial cells by diverse Mycobacterium tuberculosis genotypes. This study aimed to elucidate these mechanisms induced in A549 epithelial cells by dominant clinical strains in KwaZulu-Natal, South Africa. RNA for sequencing was extracted from epithelial cells at 48 h post-infection with 5 strains at a multiplicity of infection of approximately 10:1. Bioinformatics analysis performed with the RNA-Seq Tuxedo pipeline identified differentially expressed genes. Changes in pathways, networks and transcriptional factors were identified using Ingenuity Pathway Analysis (IPA). The interferon signalling and hepatic fibrosis/hepatic stellate cell activation pathways were among the top 5 canonical pathways in all strains. Hierarchical clustering for enrichment of cholesterol biosynthesis and immune associated pathways revealed similar patterns for Beijing and Unique; F15/LAM4/KZN and F11; and, F28 and H37Rv strains, respectively. However, the induction of top scoring networks varied among the strains. Among the transcriptional factors, only EHL, IRF7, PML, STAT1, STAT2 and VDR were induced by all clinical strains. Activation of the different pathways, networks and transcriptional factors revealed in the current study may be an underlying mechanism that results in the differential host response by clinical strains of M. tuberculosis.