Molecular basis of mycobacterial survival in macrophages.
Jane Atesoh AwuhTrude Helen FloPublished in: Cellular and molecular life sciences : CMLS (2016)
Macrophages play an essential role in the immune system by ingesting and degrading invading pathogens, initiating an inflammatory response and instructing adaptive immune cells, and resolving inflammation to restore homeostasis. More interesting is the fact that some bacteria have evolved to use macrophages as a natural habitat and tools of spread in the host, e.g., Mycobacterium tuberculosis (Mtb) and some non-tuberculous mycobacteria (NTM). Mtb is considered one of humanity's most successful pathogens and is the causal agent of tuberculosis, while NTMs cause opportunistic infections all of which are of significant public health concern. Here, we describe mechanisms by which intracellular pathogens, with an emphasis on mycobacteria, manipulate macrophage functions to circumvent killing and live inside these cells even under considerable immunological pressure. Such macrophage functions include the selective evasion or engagement of pattern recognition receptors, production of cytokines, reactive oxygen and nitrogen species, phagosome maturation, as well as other killing mechanisms like autophagy and cell death. A clear understanding of host responses elicited by a specific pathogen and strategies employed by the microbe to evade or exploit these is of significant importance for the development of effective vaccines and targeted immunotherapy against persistent intracellular infections like tuberculosis.
Keyphrases
- mycobacterium tuberculosis
- cell death
- pulmonary tuberculosis
- cell cycle arrest
- public health
- gram negative
- inflammatory response
- induced apoptosis
- oxidative stress
- antimicrobial resistance
- adipose tissue
- endoplasmic reticulum stress
- climate change
- reactive oxygen species
- emergency department
- social media
- cancer therapy
- lps induced
- immune response
- candida albicans
- drug delivery
- human immunodeficiency virus
- antiretroviral therapy
- hiv aids