The tuberculosis bacteria induce increased hydrogen sulfide production by human macrophages, which increases pathogenesis.
BIRMINGHAM, Ala. – A new culprit — hydrogen sulfide — has been found for the deadly infectious disease tuberculosis. Hydrogen sulfide gas is known for its rotten egg smell, yet it has normal physiological roles in the human body to communicate among cells.
When tuberculosis bacteria invade the lung, however, the amounts of hydrogen sulfide in the lung microenvironment appear to greatly increase, and this makes the microbe more virulent and better able to block the body’s protective immune response, according to research led by Andries “Adrie” Steyn, Ph.D., a University of Alabama at Birmingham professor of microbiology.
The source of this hydrogen sulfide? Mycobacterium tuberculosis bacteria, or Mtb, are able to induce human macrophage immune cells to produce more hydrogen sulfide. Thus, Mtb exploits macrophage metabolism to increase Mtb virulence. During the disease, Mtb grows and safely persists inside macrophages, the immune cells that normally should have protected the lungs by killing the engulfed bacteria. In a bacterial sense, the Mtb become wolves in sheep’s clothing.
“To the best of our knowledge,” Steyn said, “no study has yet reported a role for host hydrogen sulfide in the control of bacterial disease.”
Two research papers by Steyn and colleagues — the first descriptions of this unexpected role for host-generated hydrogen sulfide in bacterial pathogenesis — are published in Nature Communications and Proceedings of the National Academy of Sciences, or PNAS.
“Tuberculosis is responsible for about a million and a half deaths each year, and roughly 2 billion people are latently infected with Mtb worldwide,” Steyn said. “Our results indicate that Mtb exploits host-derived hydrogen sulfide to promote growth and disease and suggest that host-directed therapies targeting hydrogen sulfide production may be useful for the management of tuberculosis and other microbial infections.”
Steyn oversees labs at UAB and at the Africa Health Research Institute, or AHRI, in Durban, KwaZulu Natal, South Africa, an area that is the worldwide epicenter for tuberculosis infections. The experimenters used two different mouse models and also showed clinical relevance by examining the spatial distribution of human hydrogen sulfide-generating enzymes in excised lung samples from South African tuberculosis patients. The samples come from a Durban hospital whose surgeons often resect diseased portions of an infected lung; this surgery provides nearly immediate symptomatic relief for seriously ill patients.
The human tuberculosis lung tissue experiments, described in the PNAS paper, showed that hydrogen sulfide is produced at a spectrum of tuberculosis lesions that are the sites of Mtb infection.
Hydrogen sulfide has roles in normal physiology as one of three gasses — along with nitric oxide and carbon monoxide — that can diffuse from producer cells to send a signal to nearby cells. However, when Mtb invades macrophage cells, Steyn and colleagues found a 34-fold increase in the level of the macrophage enzyme cystathionine beta-synthase, or CBS, a major producer of hydrogen sulfide in mammalian cells.
So, in the Nature Communications paper, the researchers examined the roles of CBS and different levels of hydrogen sulfide using a variety of approaches.
One was mice that have one of their two genes for CBS inactivated, so they make only half as much CBS enzyme. When these mice were infected with Mtb, they survived a significantly longer time compared to wild-type mice. They also had fewer Mtb bacilli in their lungs and spleen, and their lungs showed less pathology.
In another approach, the researchers found that exposing Mtb cells to increasing concentrations of hydrogen sulfide significantly increased the rate of Mtb growth.
Mechanistically, hydrogen sulfide stimulates Mtb respiration and bioenergetics, acting at a protein called cytochrome bc oxidase. It also reverses one of the body’s immune defense mechanisms — the inhibition of Mtb respiration by increased amounts of nitric oxide produced by host cells. Furthermore, exposure of Mtb to hydrogen sulfide regulated bacterial genes involved in sulfur and copper metabolism and a 48-gene regulon involved in bacterial dormancy during latent infections.
“This suggested that Mtb infection of host cells upregulates CBS production, leading to increased hydrogen sulfide levels, which exacerbates disease as indicated by reduced host survival, and to a lesser extent by increased organ burden,” Steyn said. “These ?ndings identify a new phenotypic category of host genes that exacerbates tuberculosis disease, whereas their disruption prolongs survival during infection.”
Importantly, as seen in the PNAS paper, the increased hydrogen sulfide also alters host immunometabolism in a way that increases Mtb burden — and hence disease — in the lungs and other organs.
This was shown with mice that lacked a second major hydrogen sulfide producing enzyme, macrophage cystathionine gamma-synthase, or CSE.
Similar to what was shown for the CBS-deficient mice, the Mtb-infected CSE-knockout mice survived longer than wild-type mice and showed reduced pathology and lowered bacterial burdens in the lung, spleen and liver. Thus, they were more resistant to Mtb infection.
For CSE-knockout macrophages grown outside of mice, Mtb infection of macrophages resulted fewer live bacteria in the macrophages. Experiments with a chemical that slowly releases hydrogen sulfide or experiments with a CSE inhibitor showed that hydrogen sulfide was the effector molecule regulating Mtb survival in macrophages.
Comparison of the immune responses in wild-type mice or CSE-knockout mice showed that CSE promoted an excessive innate immune response and pathological inflammation, as measured by levels of various cytokines in the serum and numbers and types of immune cells in the lungs. This change exacerbated disease. The CSE-knockout mice also had a reduced adaptive immune response; a functional adaptive immune response is needed to control Mtb infection.
Mechanistically, hydrogen sulfide appears to induce these changes by reprogramming central metabolism in the macrophages, including decreasing flux through glycolysis and the pentose phosphate pathway, which causes dysfunctional immunity.
Steyn and colleagues note that their findings highlight the hydrogen sulfide-producing enzyme CSE as a potential therapeutic target to restrain tuberculosis disease; one current drug that is used to treat rheumatoid arthritis, D-penicillamine, targets CSE.
Steyn is the corresponding author for both tuberculosis papers.
Co-authors for the Nature Communications paper, “Hydrogen sul?de stimulates Mycobacterium tuberculosis respiration, growth and pathogenesis,” are Vikram Saini, Krishna C. Chinta, Vineel P. Reddy and Joel N. Glasgow, UAB Department of Microbiology; Asaf Stein and Shannon M. Bailey, Department of Environmental Health Science, UAB School of Public Health; Dirk A. Lamprecht, Md. Aejazur Rahman, Jared S. Mackenzie, Barry E. Truebody, John H. Adamson and Tafara T.R. Kunota, AHRI, Durban, KwaZulu Natal, South Africa; Douglas R. Moellering, UAB Center for Free Radical Biology and Department of Nutrition Sciences, UAB School of Health Professions; and Jack R. Lancaster Jr., University of Pittsburgh School of Medicine.
Co-authors for the PNAS paper, “Hydrogen sulfide dysregulates the immune response by suppressing central carbon metabolism to promote tuberculosis,” are Md. Aejazur Rahman, Bridgette M. Cumming, Kelvin Addicott, Shannon Russell, Kievershen Nargan and John H. Adamson, AHRI, Durban, KwaZulu Natal, South Africa; Hayden Pacl, UAB Department of Microbiology; Threnesan Naidoo and Pratistadevi K. Ramdial, Department of Anatomical Pathology, National Health Laboratory Service, University of KwaZulu-Natal, Inkosi Albert Luthuli Central Hospital, Durban, South Africa; and Rui Wang, Department of Biology, York University, Toronto, Canada.
Support came from National Institutes of Health grants Al111940, AI134810, AI137043, HL092857, A127182, AI138280, DK079626 and HL007918; Bill and Melinda Gates Foundation Award OPP1130017; the UAB Center for Aids Research; the UAB Center for Free Radical Biology; the UAB Infectious Diseases and Global Health and Vaccines Initiative; CRDF Global; Discovery Grant RGPIN-2017-04392 from the Natural Sciences and Engineering Research Council of Canada; the South African Medical Research Council; American Lung Association fellowship RT-232840-N; and the Innovative Young Biotechnologist Award BT/11/IYBA/2018/01 from the Department of Biotechnology, Government of India.
Steyn is a member of AHRI, and he is a senior scientist at the UAB Center for Free Radical Biology and the UAB Center for AIDS Research.
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