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. 2022 Mar 31;11(4):425.
doi: 10.3390/pathogens11040425.

Population Genetic Structure and Hybridization of Schistosoma haematobium in Nigeria

Amos Mathias Onyekwere  1   2 , Olivier Rey  2 , Jean-François Allienne  2 , Monday Chukwu Nwanchor  3 , Moses Alo  4 , Clementina Uwa  1 , Jerome Boissier  2
Affiliations

Population Genetic Structure and Hybridization of Schistosoma haematobium in Nigeria

Amos Mathias Onyekwere et al. Pathogens. .

Abstract

Background: Schistosomiasis is a major poverty-related disease caused by dioecious parasitic flatworms of the genus Schistosoma with a health impact on both humans and animals. Hybrids of human urogenital schistosome and bovine intestinal schistosome have been reported in humans in several of Nigeria’s neighboring West African countries. No empirical studies have been carried out on the genomic diversity of Schistosoma haematobium in Nigeria. Here, we present novel data on the presence and prevalence of hybrids and the population genetic structure of S. haematobium. Methods: 165 Schistosoma-positive urine samples were obtained from 12 sampling sites in Nigeria. Schistosoma haematobium eggs from each sample were hatched and each individual miracidium was picked and preserved in Whatman® FTA cards for genomic analysis. Approximately 1364 parasites were molecularly characterized by rapid diagnostic multiplex polymerase chain reaction (RD-PCR) for mitochondrial DNA gene (Cox1 mtDNA) and a subset of 1136 miracidia were genotyped using a panel of 18 microsatellite markers. Results: No significant difference was observed in the population genetic diversity (p > 0.05), though a significant difference was observed in the allelic richness of the sites except sites 7, 8, and 9 (p < 0.05). Moreover, we observed two clusters of populations: west (populations 1−4) and east (populations 7−12). Of the 1364 miracidia genotyped, 1212 (89%) showed an S. bovis Cox1 profile and 152 (11%) showed an S. haematobium cox1 profile. All parasites showed an S. bovis Cox1 profile except for some at sites 3 and 4. Schistosoma miracidia full genotyping showed 59.3% of the S. bovis ITS2 allele. Conclusions: This study provides novel insight into hybridization and population genetic structure of S. haematobium in Nigeria. Our findings suggest that S. haematobium x S. bovis hybrids are common in Nigeria. More genomic studies on both human- and animal-infecting parasites are needed to ascertain the role of animals in schistosome transmission.

Keywords: Nigeria; Schistosoma bovis; Schistosoma haematobium; hybrids; population genetic analysis.

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Conflict of interest statement

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of manuscript, or in the decision to publish the results.

Figures

Figure 1
Figure 1
Population genetic structure graph assessed by principal component analysis of 1136 S. haematobium parasites collected in Nigeria revealed by graph (PCA). Each sampling site is represented by a dot. The first and second axis of the PCA represent 43.8% and 22.9%, respectively, of the total variation in allele frequency.
Figure 2
Figure 2
Bar plot showing the population genetic structure using Structure software of 1136 S. haematobium miracidia collected in Nigeria. Each column represents one miracidium. The colors show the proportion of contribution of each cluster to each genotype. The cluster structure K = 2, produced by structure software for 10 sampling sites.
Figure 3
Figure 3
Map showing sampling sites 1–12 in the survey study carried out to determine the prevalence of S. haematobium infection among primary school-age pupils across Nigeria (Onyekwere, et al. Submitted). Sampling sites were represented according to infection status of the disease among the participants. Darker to lighter colors correspond to higher to lower infection status observed at the studied sites.
See this image and copyright information in PMC

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