» Articles » PMID: 20889898

Genetic Consequences of Mass Human Chemotherapy for Schistosoma Mansoni: Population Structure Pre- and Post-praziquantel Treatment in Tanzania

Overview
Specialty Tropical Medicine
Date 2010 Oct 5
PMID 20889898
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

Recent shifts in global health policy have led to the implementation of mass drug administration (MDA) for neglected tropical diseases. Here we show how population genetic analyses can provide vital insights into the impact of such MDA on endemic parasite populations. We show that even a single round of MDA produced a genetic bottleneck with reductions in a range of measures of genetic diversity of Schistosoma mansoni. Phylogenetic analyses and indices of population differentiation indicated that schistosomes collected in the same schools in different years were more dissimilar than those from different schools collected within either of the study's 2 years, in addition to distinguishing re-infection from non-clearance (that might indicate putatively resistant parasites) from within those children infected at both baseline and follow-up. Such unique results illustrate the importance of genetic monitoring and examination of long lived multi-cellular parasites such as these under novel or increased chemotherapeutic selective pressures.

Citing Articles

Praziquantel resistance in schistosomes: a brief report.

Eastham G, Fausnacht D, Becker M, Gillen A, Moore W Front Parasitol. 2025; 3():1471451.

PMID: 39817170 PMC: 11732111. DOI: 10.3389/fpara.2024.1471451.


Integrating genomic and epidemiologic data to accelerate progress toward schistosomiasis elimination.

Lund A, Wade K, Nikolakis Z, Ivey K, Perry B, Pike H Elife. 2022; 11.

PMID: 36040013 PMC: 9427098. DOI: 10.7554/eLife.79320.


Genome-wide analysis of Schistosoma mansoni reveals limited population structure and possible praziquantel drug selection pressure within Ugandan hot-spot communities.

Vianney T, Berger D, Doyle S, Sankaranarayanan G, Serubanja J, Nakawungu P PLoS Negl Trop Dis. 2022; 16(8):e0010188.

PMID: 35981002 PMC: 9426917. DOI: 10.1371/journal.pntd.0010188.


Whole-genome sequencing of Schistosoma mansoni reveals extensive diversity with limited selection despite mass drug administration.

Berger D, Crellen T, Lamberton P, Allan F, Tracey A, Noonan J Nat Commun. 2021; 12(1):4776.

PMID: 34362894 PMC: 8346512. DOI: 10.1038/s41467-021-24958-0.


Revisiting density-dependent fecundity in schistosomes using sibship reconstruction.

Neves M, Gower C, Webster J, Walker M PLoS Negl Trop Dis. 2021; 15(5):e0009396.

PMID: 33983965 PMC: 8148369. DOI: 10.1371/journal.pntd.0009396.


References
1.
Liu K, Muse S . PowerMarker: an integrated analysis environment for genetic marker analysis. Bioinformatics. 2005; 21(9):2128-9. DOI: 10.1093/bioinformatics/bti282. View

2.
Wang T, Shrivastava J, Johansen M, Zhang S, Wang F, Webster J . Does multiple hosts mean multiple parasites? Population genetic structure of Schistosoma japonicum between definitive host species. Int J Parasitol. 2006; 36(12):1317-25. DOI: 10.1016/j.ijpara.2006.06.011. View

3.
Agola L, Mburu D, DeJong R, Mungai B, Muluvi G, Njagi E . Microsatellite typing reveals strong genetic structure of Schistosoma mansoni from localities in Kenya. Infect Genet Evol. 2006; 6(6):484-90. DOI: 10.1016/j.meegid.2006.03.002. View

4.
Curtis J, Minchella D . Schistosome population genetic structure: when clumping worms is not just splitting hairs. Parasitol Today. 2000; 16(2):68-71. DOI: 10.1016/s0169-4758(99)01553-7. View

5.
Ardelli B, Guerriero S, Prichard R . Ivermectin imposes selection pressure on P-glycoprotein from Onchocerca volvulus: linkage disequilibrium and genotype diversity. Parasitology. 2005; 132(Pt 3):375-86. DOI: 10.1017/S0031182005008991. View