» Articles » PMID: 32628666

Aquatic Macrophytes and Macroinvertebrate Predators Affect Densities of Snail Hosts and Local Production of Schistosome Cercariae That Cause Human Schistosomiasis

Abstract

Background: Schistosomiasis is responsible for the second highest burden of disease among neglected tropical diseases globally, with over 90 percent of cases occurring in African regions where drugs to treat the disease are only sporadically available. Additionally, human re-infection after treatment can be a problem where there are high numbers of infected snails in the environment. Recent experiments indicate that aquatic factors, including plants, nutrients, or predators, can influence snail abundance and parasite production within infected snails, both components of human risk. This study investigated how snail host abundance and release of cercariae (the free swimming stage infective to humans) varies at water access sites in an endemic region in Senegal, a setting where human schistosomiasis prevalence is among the highest globally.

Methods/principal Findings: We collected snail intermediate hosts at 15 random points stratified by three habitat types at 36 water access sites, and counted cercarial production by each snail after transfer to the laboratory on the same day. We found that aquatic vegetation was positively associated with per-capita cercarial release by snails, probably because macrophytes harbor periphyton resources that snails feed upon, and well-fed snails tend to produce more parasites. In contrast, the abundance of aquatic macroinvertebrate snail predators was negatively associated with per-capita cercarial release by snails, probably because of several potential sublethal effects on snails or snail infection, despite a positive association between snail predators and total snail numbers at a site, possibly due to shared habitat usage or prey tracking by the predators. Thus, complex bottom-up and top-down ecological effects in this region plausibly influence the snail shedding rate and thus, total local density of schistosome cercariae.

Conclusions/significance: Our study suggests that aquatic macrophytes and snail predators can influence per-capita cercarial production and total abundance of snails. Thus, snail control efforts might benefit by targeting specific snail habitats where parasite production is greatest. In conclusion, a better understanding of top-down and bottom-up ecological factors that regulate densities of cercarial release by snails, rather than solely snail densities or snail infection prevalence, might facilitate improved schistosomiasis control.

Citing Articles

Nutritional effects of invasive macrophyte detritus on infections in snail intermediate hosts.

Desautels D, Wang Y, Ripp A, Beaman A, Andea S, Hartman R Hydrobiologia. 2025; 849(16):3607-3616.

PMID: 39822186 PMC: 11737597. DOI: 10.1007/s10750-022-04974-x.


Modeling how and why aquatic vegetation removal can free rural households from poverty-disease traps.

Doruska M, Barrett C, Rohr J Proc Natl Acad Sci U S A. 2024; 121(52):e2411838121.

PMID: 39689171 PMC: 11670121. DOI: 10.1073/pnas.2411838121.


Swimmer's itch control: Timely waterfowl brood relocation significantly reduces an avian schistosome population and human cases on recreational lakes.

Blankespoor C, Blankespoor H, DeJong R PLoS One. 2024; 19(2):e0288948.

PMID: 38359003 PMC: 10868848. DOI: 10.1371/journal.pone.0288948.


A planetary health innovation for disease, food and water challenges in Africa.

Rohr J, Sack A, Bakhoum S, Barrett C, Lopez-Carr D, Chamberlin A Nature. 2023; 619(7971):782-787.

PMID: 37438520 DOI: 10.1038/s41586-023-06313-z.


Identification of Bulinus forskalii as a potential intermediate host of Schistosoma hæmatobium in Senegal.

Gaye P, Doucoure S, Sow D, Sokhna C, Ranque S PLoS Negl Trop Dis. 2023; 17(5):e0010584.

PMID: 37159452 PMC: 10198482. DOI: 10.1371/journal.pntd.0010584.


References
1.
Upatham E, Sturrock R . Field investigations on the effect of other aquatic animals on the infection of Biomphalaria glabrata by Schistosoma mansoni miracidia. J Parasitol. 1973; 59(3):448-53. View

2.
Frandsen F, CHRISTENSEN N . An introductory guide to the identification of cercariae from African freshwater snails with special reference to cercariae of trematode species of medical and veterinary importance. Acta Trop. 1984; 41(2):181-202. View

3.
Chu K . Trials of ecological and chemical measures for the control of Schistosoma haematobium transmission in a Volta Lake village. Bull World Health Organ. 1978; 56(2):313-22. PMC: 2395562. View

4.
Gryseels B, Nkulikyinka L . The distribution of Schistosoma mansoni in the Rusizi plain (Burundi). Ann Trop Med Parasitol. 1988; 82(6):581-90. DOI: 10.1080/00034983.1988.11812294. View

5.
Mouchet F, Theron A, Bremond P, Sellin E, Sellin B . Pattern of cercarial emergence of Schistosoma curassoni from Niger and comparison with three sympatric species of schistosomes. J Parasitol. 1992; 78(1):61-3. View