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Rv3091, An Extracellular Patatin-Like Phospholipase in , Prolongs Intracellular Survival of Recombinant by Mediating Phagosomal Escape

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2020 Oct 12
PMID 33042041
Citations 4
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Abstract

Patatin-like phospholipases (PLPs) are important virulence factors of many pathogens. However, there are no prevailing studies regarding PLPs as a virulence factor of (Mtb). Analysis of Rv3091, a putative protein of Mtb, shows that it belongs to the PLPs family. Here, we cloned and expressed the gene in and, subsequently, conducted protein purification and characterization. We show that it possesses phospholipase A, phospholipase A, and lipase activity. We confirm the putative active site residues, namely, Ser214 and Asp407, using site directed mutagenesis. The Rv3091 is an extracellular protein that alters the colony morphology of . The presence of Rv3091 enhances the intracellular survival capability of in murine peritoneal macrophages. Additionally, it promotes phagosomal escape from macrophages. Moreover, Rv3091 significantly increased the survival of and aggravated lesions in C57BL/6 J murine lungs . Taken together, our results indicate that Rv3091 as an extracellular PLP that is critical to the pathogenicity of mycobacterium as it allows mycobacterium to utilize phospholipids for its growth and provides resistance to phagosome killing, resulting in its enhanced intracellular survival.

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References
1.
Flores-Diaz M, Monturiol-Gross L, Naylor C, Alape-Giron A, Flieger A . Bacterial Sphingomyelinases and Phospholipases as Virulence Factors. Microbiol Mol Biol Rev. 2016; 80(3):597-628. PMC: 4981679. DOI: 10.1128/MMBR.00082-15. View

2.
Kaur J, Kaur J . Rv0518, a nutritive stress inducible GDSL lipase of Mycobacterium tuberculosis, enhanced intracellular survival of bacteria by cell wall modulation. Int J Biol Macromol. 2019; 135:180-195. DOI: 10.1016/j.ijbiomac.2019.05.121. View

3.
Dedieu L, Serveau-Avesque C, Kremer L, Canaan S . Mycobacterial lipolytic enzymes: a gold mine for tuberculosis research. Biochimie. 2012; 95(1):66-73. DOI: 10.1016/j.biochi.2012.07.008. View

4.
KUZE F, Uchihira F . Various colony-formers of Mycobacterium avium-intracellulare. Eur J Respir Dis. 1984; 65(6):402-10. View

5.
Kovacic F, Granzin J, Wilhelm S, Kojic-Prodic B, Batra-Safferling R, Jaeger K . Structural and functional characterisation of TesA - a novel lysophospholipase A from Pseudomonas aeruginosa. PLoS One. 2013; 8(7):e69125. PMC: 3715468. DOI: 10.1371/journal.pone.0069125. View