| Literature DB >> 27789543 |
Emily A Williams1, Felix Mba Medie1, Rachel E Bosserman1, Benjamin K Johnson2, Cristal Reyna1, Micah J Ferrell1, Matthew M Champion3, Robert B Abramovitch2, Patricia A Champion4.
Abstract
Mycobacterial pathogens use the ESAT-6 system 1 (Esx-1) exporter to promote virulence. Previously, we used gene disruption and complementation to conclude that the MMAR_0039 gene in Mycobacterium marinum is required to promote Esx-1 export. Here we applied molecular genetics, proteomics, and whole-genome sequencing to demonstrate that the MMAR_0039 gene is not required for Esx-1 secretion or virulence. These findings suggest that we initially observed an indirect mechanism of genetic complementation. We identified a spontaneous nonsense mutation in a known Esx-1-associated gene which causes a loss of Esx-1 activity. We show that the Esx-1 function was restored by nonsense suppression. Moreover, we identified a polar mutation in the ppsC gene which reduced cellular impermeability but did not impact cytotoxicity in macrophages. Our studies reveal insight into Esx-1 export, nonsense suppression, and cell envelope lipid biogenesis.Entities:
Keywords: Esx-1; PDIM; complementation; mycobacteria; nonsense suppression; spontaneous mutation
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Year: 2017 PMID: 27789543 PMCID: PMC5278160 DOI: 10.1128/IAI.00653-16
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441