» Articles » PMID: 28082973

An Overview of Infections: An Intense Host-Parasite Interaction

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2017 Jan 14
PMID 28082973
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

and , the causative agents of Human African Trypanosomiasis, are transmitted by tsetse flies. Within the vector, the parasite undergoes through transformations that prepares it to infect the human host. Sequentially these developmental stages are the replicative procyclic (in which the parasite surface is covered by procyclins) and trypo-epimastigote forms, as well as the non-replicative, infective, metacyclic form that develops in the vector salivary glands. As a pre-adaptation to their life in humans, metacyclic parasites begin to express and be densely covered by the Variant Surface Glycoprotein (VSG). Once the metacyclic form invades the human host the parasite develops into the bloodstream form. Herein the VSG triggers a humoral immune response. To avoid this humoral response, and essential for survival while in the bloodstream, the parasite changes its cover periodically and sheds into the surroundings the expressed VSG, thus evading the consequences of the immune system activation. Additionally, tools comparable to quorum sensing are used by the parasite for the successful parasite transmission from human to insect. On the other hand, the human host promotes clearance of the parasite triggering innate and adaptive immune responses and stimulating cytokine and chemokine secretion. All in all, the host-parasite interaction is extremely active and leads to responses that need multiple control sites to develop appropriately.

Citing Articles

Benign-by-Design SAHA Analogues for Human and Animal Vector-Borne Parasitic Diseases.

Rossi M, Martinengo B, Diamanti E, Salerno A, Rizzardi N, Fato R ACS Med Chem Lett. 2024; 15(9):1506-1515.

PMID: 39291036 PMC: 11403742. DOI: 10.1021/acsmedchemlett.4c00242.


Cholesterol Efflux Decreases TLR4-Target Gene Expression in Cultured Macrophages Exposed to Ghosts.

Fernando L, Echesabal-Chen J, Miller M, Powell R, Bruce T, Paul A Microorganisms. 2024; 12(8).

PMID: 39203572 PMC: 11357207. DOI: 10.3390/microorganisms12081730.


Coinfection with Enhances Disease Severity in Human African Trypanosomiasis.

Mitalo N, Waiganjo N, Mokua Mose J, Bosire D, Oula J, Isaac A J Trop Med. 2023; 2023:1063169.

PMID: 37954132 PMC: 10637842. DOI: 10.1155/2023/1063169.


A structural classification of the variant surface glycoproteins of the African trypanosome.

dakovic S, Zeelen J, Gkeka A, Chandra M, van Straaten M, Foti K PLoS Negl Trop Dis. 2023; 17(9):e0011621.

PMID: 37656766 PMC: 10501684. DOI: 10.1371/journal.pntd.0011621.


Manipulative neuroparasites: uncovering the intricacies of neurological host control.

Gowda V, Dinesh S, Sharma S Arch Microbiol. 2023; 205(9):314.

PMID: 37603130 DOI: 10.1007/s00203-023-03637-2.


References
1.
Vaidya T, Bakhiet M, Hill K, Olsson T, Kristensson K, Donelson J . The gene for a T lymphocyte triggering factor from African trypanosomes. J Exp Med. 1997; 186(3):433-8. PMC: 2199003. DOI: 10.1084/jem.186.3.433. View

2.
Murray M, Clifford D, Gettinby G, Snow W, McINTYRE W . Susceptibility to African trypanosomiasis of N'Dama and Zebu cattle in an area of Glossina morsitans submorsitans challenge. Vet Rec. 1981; 109(23):503-10. View

3.
Morrison L, Tweedie A, Black A, Pinchbeck G, Christley R, Schoenefeld A . Discovery of mating in the major African livestock pathogen Trypanosoma congolense. PLoS One. 2009; 4(5):e5564. PMC: 2679202. DOI: 10.1371/journal.pone.0005564. View

4.
Sbicego S, Vassella E, Kurath U, Blum B, Roditi I . The use of transgenic Trypanosoma brucei to identify compounds inducing the differentiation of bloodstream forms to procyclic forms. Mol Biochem Parasitol. 1999; 104(2):311-22. DOI: 10.1016/s0166-6851(99)00157-7. View

5.
Vickerman K . Developmental cycles and biology of pathogenic trypanosomes. Br Med Bull. 1985; 41(2):105-14. DOI: 10.1093/oxfordjournals.bmb.a072036. View