Author/Authors :
Sarkandi, Mohammad Kamran Department of Microbiology- Science and Research Branch-, Islamic Azad University, Tehran , Behrouzi, Ava Department of Mycobacteriology and Pulmonary Research- Pasteur Institute of Iran, Tehran , Fateh, Aboulfazl Department of Mycobacteriology and Pulmonary Research- Pasteur Institute of Iran, Tehran , Vaziri, Farzam Department of Mycobacteriology and Pulmonary Research- Pasteur Institute of Iran, Tehran , Mirsaeidi, Mehdi Division of Pulmonary- Critical Care, Sleep and Allergy- Department of Medicine- University of Miami, Miller School of Medicine, Miami, USA , Siadat, Davar Department of Mycobacteriology and Pulmonary Research- Pasteur Institute of Iran, Tehran
Abstract :
Mycobacterium avium complex (MAC) is an ubiquitous acid-fast bacterium. MAC cell wall and membrane release
extracellular vesicles (EVs) into different media. The immunogenic effects of EVs isolated from MAC remain
unknown. The aim of this study was to determine the EVs effect on macrophage cytokine production. MAC EVs
were extracted and purified using differential centrifuges also known as Claassen’s method, with some
modifications. After protein analysis of EVs, and scanning electron microscopy (SEM), the EVs were injected into
BALB/c mice for in vivo experiments. The concentration of interferon gamma (IFN-γ) and interleukin 10 (IL-10) in
the spleen immune cell culture was measured by sandwich ELISA. We for the first time showed that MAC can
naturally produce EVs. The extraction method was technically-feasible, efficient and affordable. The SEM analysis
showed that EVs diameter was similar to other studies on mycobacteria, and EVs maintained their spatial
characterization. The results of the cytokine assays indicated that EV-treated cells secreted IL-10 (P = 0.034) but not
IFN-γ (P = 0.037). Our findings suggest that EVs of M. avium could have anti-inflammatory effects. They can be
used as a suppressor or regulator of inflammation via IL-10. The replication of the anti-inflammatory response of
MAC EVs in future studies may indicate a new therapeutic agent for inflammation.
Keywords :
Mycobacterium avium complex , extracellular vesicle , interferon gamma (IFN-γ) , interleukin 10 (IL-10)