The Role of Nitric Oxide and Reactive Oxygen Species in the Killing of Leishmania braziliensis by Monocytes from Patients with Cutaneous Leishmaniasis

• Published in: PloS one Vol. 11; no. 2; p. e0148084
• Main Authors: Carneiro, Pedro Paulo, Conceição, Jacilara, Macedo, Michael, Magalhães, Viviane, Carvalho, Edgar M., Bacellar, Olivia
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 03.02.2016; Public Library of Science (PLoS)
• Subjects: Adult; Aged; Biology and Life Sciences; Cell culture; Cutaneous leishmaniasis; Cytokines; Enzymes; Female; Health aspects; Humans; Infections; Inhibition; Leishmania; Leishmania braziliensis; Leishmania braziliensis - metabolism; Leishmaniasis, Cutaneous - metabolism; Leishmaniasis, Cutaneous - pathology; Lymphocytes T; Macrophages; Male; Medicine and Health Sciences; Middle Aged; Monocytes; Monocytes - metabolism; Monocytes - parasitology; Monocytes - pathology; Nitric oxide; Nitric Oxide - biosynthesis; Oxygen; Parasites; Parasitic diseases; Pathology; Patients; Promastigotes; Reactive oxygen species; Reactive Oxygen Species - metabolism; Research and Analysis Methods; Vector-borne diseases; United States; Brazil
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0148084

Human cutaneous leishmaniasis (CL) caused by Leishmania braziliensis, presents an exaggerated Th1 response that is associated with ulcer development. Macrophages are the primary cells infected by Leishmania parasites and both reactive oxygen species (ROS) and nitric oxide (NO) are important in the control of Leishmania by these cells. The mechanism involved in the killing of L. braziliensis is not well established. In this study, we evaluate the role of ROS and NO in the control of L. braziliensis infection by monocytes from CL patients. After in vitro infection with L. braziliensis, the oxidative burst by monocytes from CL patients was higher when compared to monocytes from healthy subjects (HS). Inhibition of the ROS pathway caused a significant decrease in the oxidative burst in L. braziliensis infected monocytes from both groups. In addition, we evaluated the intracellular expression of ROS and NO in L. braziliensis-infected monocytes. Monocytes from CL patients presented high expression of ROS after infection with L. braziliensis. The expression of NO was higher in monocytes from CL patients as compared to expression in monocytes from HS. A strong positive correlation between NO production and lesion size of CL patients was observed. The inhibition of ROS production in leishmania-infected monocytes from CL patients allowed the growth of viable promastigotes in culture supernatants. Thus, we demonstrate that while production of ROS is involved in L. braziliensis killing, NO alone is not sufficient to control infection and may contribute to the tissue damage observed in human CL.