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Pilot Malacology Surveys for the Intermediate Hosts of Schistosomiasis in Rural and Semi-Urban Areas of the Moyen-Ogooué Province, Gabon

by
Jean Claude Dejon Agobé
1,2,
Henry Curtis Kariuki
3,
Jeannot Fréjus Zinsou
1,4,
Yabo Josiane Honkpehedji
1,4,
Martin Peter Grobusch
1,2,5 and
Ayola Akim Adegnika
1,4,5,6,7,*
1
Centre de Recherches Médicales de Lambaréné (CERMEL), Lambaréné P.O. Box 242, Gabon
2
Center of Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Division of Internal Medicine, Amsterdam University Medical Centers, Location AMC, University of Amsterdam, P.O. Box 22660, 1100 DD Amsterdam, The Netherlands
3
School of Medicine and Health Sciences, Kenya Methodist University (KeMU), P.O. Box 267, Meru 60200, Kenya
4
Leiden Medical University Centre, University of Leiden, Albinusdreef 2, 2333 ZA Leiden, The Netherlands
5
Institut für Tropenmedizin, Eberhad Karls Universität Tübingen, Wilhelmstraße 27, 72074 Tübingen, Germany
6
German Centre for Infection Research (DZIF), Partner Site Tübingen, Wilhelmstraße 27, 72074 Tübingen, Germany
7
German Centre for Infection Research (DZIF), African Partner Institution, CERMEL, Lambaréné P.O. Box 242, Gabon
*
Author to whom correspondence should be addressed.
Trop. Med. Infect. Dis. 2022, 7(1), 1; https://doi.org/10.3390/tropicalmed7010001
Submission received: 11 November 2021 / Revised: 16 December 2021 / Accepted: 17 December 2021 / Published: 22 December 2021

Abstract

:
The objective of this pilot malacological survey was to identify the snail intermediate hosts for Schistosoma haematobium in endemic rural and semi-urban areas of Gabon. Snails were collected, morphologically identified, and tested for infection by cercarial shedding. Released cercariae were morphologically identified using low-power light microscopy. A total of six species of snails were collected throughout the study area, with Bulinus truncatus, B. forskalii, and Potadoma spp. being the most predominant species collected. Only the Bulinus species were tested for infection by cercarial shedding, of which only B. truncatus shed cercariae. Some B. truncatus shed mammalian schistosome cercariae, while others shed Gymnocephalus cercariae. Our results indicate that B. truncatus appears to be a potential intermediate host of schistosomiasis in Gabon, where cases of S. haematobium, S. guineensis, and S. intercalatum infection are reported. However, it will be important to further understand the species diversity and transmission dynamics of schistosomes.

1. Introduction

Schistosomiasis, a water-borne helminthic disease, is the second most important parasitic infection after malaria in terms of public health and economic impact [1]. Human infections are caused by three main species of flukes, namely, Schistosoma haematobium causing urogenital schistosomiasis, and S. japonicum and S. mansoni, which both cause intestinal schistosomiasis. There are other species that cause intestinal schistosomiasis, although their distribution is restricted to specific foci, including S. guineensis and its variant S. intercalatum in Central Africa, and S. mekongi in South East Asia [2]. The worldwide geographical distribution of the different Schistosoma species depends on the presence and distribution of their freshwater snail intermediate hosts; the snail genus is specific to the species of the parasite, with some variations across countries. In Africa, for instance, predominantly snails of the genus Biomphalaria serve as intermediate hosts of S. mansoni, while snails of the genus Bulinus serve as intermediate hosts of S. haematobium, as well as of S. intercalatum and S. guineensis [3]. Bulinus spp. are also known as the intermediate hosts of S. bovis [4], a schistosome parasite of ruminants such as cattle, goats, sheep, and pigs. The geographical distribution and density of the snail population and their dynamics over time relate to the epidemiological situation of the disease in a particular human population, rendering schistosomiasis a focal disease.
Freshwater snail control is part of the WHO’s recommendation for the control of schistosomiasis [2]. Malacological data is therefore essential for a better understanding of the disease transmission, but also for the implementation of a proper and adequate schistosomiasis control program. Gabon is a central African country located on the equator. Although the region is known to be endemic for schistosomiasis, very few malacological data are available for the country, and most of it is historic. More recent data by Mintsa et al. (2009) reported the presence of B. globosus and B. forskalii in two different sites in the Estuaire province; Libreville and Ekouk [5]. We conducted a pilot survey in rural and semi-urban areas located central to the country, known to be endemic for urogenital schistosomiasis, with the aim to provide basic information on the snails as intermediate hosts for schistosomiasis and on molluscan diversity in the Moyen-Ogooué, one of the nine provinces of Gabon.

2. Materials and Methods

The surveys were carried out at CERMEL [6] and were conducted from 15–19 November 2013 on three different locations: Lambaréné, the provincial capital of the Moyen-Ogooué; the Zilé-PK area, which is a string of villages along the national road (RN1) south of Lambaréné from PK8 to PK33, including Tsouka and Massika I and II villages; and in Mbolani, namely the Bindo-Makouké villages, which is a remote area 65 km from Lambaréné by road (Figure 1). All these locations are either close to the Ogooué river, or are irrigated by its tributaries, with many lakes and swamps. In the region, the vegetation is made up of rainforests, and the weather is characterized by four seasons, long rainy (February to May) and dry (June to September) seasons, followed by short rainy (October to mid-December) and dry (mid-December and January) seasons. These areas are known to be schistosomiasis-endemic, with S. haematobium being the predominant species [7,8,9]. Indeed, we reported, in 2020, a 26% schistosomiasis prevalence in Lambaréné [9], while a prevalence of around 45% and 15% were reported earlier in 2014 and 2018 for the Nzilé-PK area and Bindo village, respectively [7,8].
For each of the three study areas, human-water contact sites, known as potential schistosomiasis foci, were identified. All sites had on average up to 50% vegetation cover, with the watercourse bed being either muddy, sandy, or both. At the selected sites, snails were collected systematically by three collectors for about ten minutes between 8 a.m. and 11 a.m. from aquatic plants and other objects in the habitats. Specifically, vegetation and any materials such as discarded pieces of clothing and tires were thoroughly searched for possibly attached mollusks. During the snail collections, the geographic coordinates of the site were taken using a hand-held GPS, and human-water contact behaviors were observed. All collected snails were placed in a perforated container with wet cotton wool or wet vegetation before being transported back to the CERMEL laboratory.
At the laboratory, snails were separated and identified mostly to the genus level based on the shell morphological characteristics using the standardized taxonomic keys proposed by the WHO identification center [10]. On the day of collection, snails were individually placed in a well plate for cercariae shedding, and dechlorinated clean commercial drinking water was added. The plate was covered to prevent snails from escaping but opened and closed regularly for air circulation. The plate was placed in indirect daylight and left for about three hours from noon to 3 p.m., and then it was examined. The wells were examined under a low-powered microscope for evidence of any emitted cercariae, which were then morphologically differentiated using standardized taxonomic keys [11].

3. Results

3.1. Snail Collection and Species Distribution

A number of snail collection points were selected over the study area (Figure 1). In the Zilé-PK area, the first area visited was Tsouka village, where six water contact sites that appeared as potential transmission hotspots were selected along a tributary of the Ogoouée River, namely, Mikoli River. Other sites that were visited included various sites in Massika I and Massika II villages. Within Lambaréné, snails were collected in small streams of some neighborhoods; Château, Fanguy, and Moussamoukougou, respectively. In Mbolani, Bindo, and Makouké villages, a total of four collection sites were targeted, as these were known as the main human-water contact points.
In total, six snail species were collected from a number of collection points. The overall freshwater snails that were found were: Potadoma species (most likely P. freethi), Bulinus truncatus, Bulinus forskalii, Melanoides species (most likely M. tuberculata), Lanistes (most likely L. nsedweensis), and Gabiella species. Table 1 presents the distribution of snail species collected in each study site. With regard to the Bulinus species, a total of 44 snails were collected over the study area, including four B. forskalii and 40 B. truncatus.

3.2. Cercarial Shedding

When testing for cercarial shedding, none of the four B. forskalii snails examined were infected, while 12 (30%) of the 40 B. truncatus (Figure 2a) examined shed mammalian Schistosoma cercariae (Figure 2b), whilst others shed Gymnocephalus cercariae. Bulinus snails that shed schistosome cercariae were collected only in the Mikoli River of Tsouka village (Zilé-PK area).

4. Discussion

The present survey adds malacological information to the scarce data available from the schistosomiasis-endemic region. Our results establish the first evidence of cercarial shedding in the Moyen-Ogooué province. Indeed, we found that B. truncatus appears to be an intermediate host of schistosomiasis in the region. It is known that some Bulinus snails may act as intermediate hosts of Schistosoma bovis [4,12] which cannot be separated from S. haematobium by cercariae morphology. However, no domestic animals were observed at the study sites, nor any evidence of bovine game. Moreover, no data are available on the potential presence of S. bovis in Gabon, and particularly in the study area. Since the study area is known to be endemic for S. haematobium [7,8,9], we therefore strongly suspect that the mammalian cercariae were actually S. haematobium cercariae, shed by B. truncatus. However, the use of molecular tools to accurately identify B. truncatus as a snail host for S. haematobium cercariae in the area remains. As some cases of Schistosome eggs in stool have been reported in the region [9], and cases of S. guineensis have been reported in the country, the role of B. truncatus in the transmission of S. intercalatum and S. guineensis [13] in the country has to be further investigated.
The study was conducted in November, corresponding with the beginning of the rainy season. During the surveys, we observed a low density of snails in the study areas, particularly in the Bindo-Makouké villages. Since seasonal rainfall affects snail density [14], we hypothesize that this reflects the snail population density usually observed during the rainy season. Despite the low density of snails observed, the genus Bulinus was present in all three study areas, while B. truncatus was found in Lambaréné and in the Zilé-PK areas, known as areas with a moderate or high prevalence of urogenital schistosomiasis [7,8,9], compared to Bindo-Makouké, where the prevalence of the disease is low [7,8]. This suggests that the distribution of B. truncatus could sustain the prevalence of schistosomiasis in the region, and probably in the country.
When exposed to daylight illumination, only B. truncatus shed cercariae. Similar to what was reported earlier by Mintsa et al. [5], no B. forskalii we collected shed cercariae. However, we found that a high proportion of B. truncatus shed cercariae (around 30%), particularly those from the Zilé-PK rural area. This is in contrast to what was reported from southern Mauritania and western Kenya where no to few (1.8%) snails sampled shed cercariae [15,16], respectively. Similarly, the number of cercariae shed by most of the snails was considerably higher than what is usually reported from other naturally infected snails. These results suggest that the B. truncatus intermediate hosts we identified are a very efficient vector of schistosomiasis in our study area, which contrasts with the observation of a similar snail species in Kenya, which is refractive to the local S. haematobium [17].
In addition to the Bulinus snails involved in schistosomiasis transmission, we found other snail intermediate hosts that are capable of transmitting other parasitic diseases. Potadoma spp. was one of the snail genera found, particularly in the Zilé-PK area. It has been suspected that Potadoma snails may be the intermediate hosts of the lung flukes of the human Paragonimus species (most likely P. africanus or P. uterobilateralis), which are reported to occur in parts of Central (Zaire and Cameroon) and West (Nigeria) Africa, respectively [18]. It would be of interest to clarify the role of this snail in Gabon, and particularly in Lambaréné and its surroundings, where some cases of paragonimiasis have already been reported [19,20].

5. Conclusions

Bulinus spp., a potential intermediate host of schistosomiasis, appears to be present in Gabon, particularly B. globosus, B forskalii, and, as we reported, B. truncatus, which appears to be an efficient intermediate host of schistosomiasis. However, it remains necessary to properly identify the species in Lambaréné and the surrounding areas using molecular analyses to understand the seasonality of snail transmission and population dynamics to guide an appropriate strategy for schistosomiasis control.

Author Contributions

Conceptualization: A.A.A. and H.C.K.; Methodology: A.A.A. and H.C.K.; Investigation: J.C.D.A. and H.C.K.; Writing—Original Draft Preparation, J.C.D.A., Writing—Review & Editing, J.C.D.A., H.C.K., J.F.Z., Y.J.H., M.P.G. and A.A.A.; Supervision: A.A.A.; Funding Acquisition: A.A.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding and was conducted with the financial support of CERMEL through the funding granted to AAA by EDCTP through a Senior Fellowship training award TA_11_40200 (www.edctp.org (accessed on 25 May 2021)) and by the European Union’s seventh Framework Program 7 for research, technological development and demonstration under grant agreement N° 242107.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We want to thank the local population for their collaboration during the surveys. A special thanks to M. Guy Gaspard Nzadi for the assistance during the field activities and for his commitment during the surveys. Thanks to M. Ance Manganboula for his contribution and elaboration of the map used for this report. We are grateful to CERMEL for the all support and facilities we were granted during the surveys. AAA, MPG are members of CANTAM (EDCTP-RegNet2015-1045) and AAA is PANDORA-ID-Net (EDCTP Grant Agreement RIA2016E-1609) network member.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Distribution of the human-freshwater contact points selected for snail collection over the study area.
Figure 1. Distribution of the human-freshwater contact points selected for snail collection over the study area.
Tropicalmed 07 00001 g001
Figure 2. (a) Some Bulinus truncatus snails collected at Tsouka village; (b) Microscopic view of shedding of some mammalian (forked tail) and Gymnocephalus (single tail) cercariae.
Figure 2. (a) Some Bulinus truncatus snails collected at Tsouka village; (b) Microscopic view of shedding of some mammalian (forked tail) and Gymnocephalus (single tail) cercariae.
Tropicalmed 07 00001 g002
Table 1. Distribution of snail species collected by study area.
Table 1. Distribution of snail species collected by study area.
Study AreaSnail GenusSnail Species
Zilé-PK area; Tsouka, Massika I and Massika II villagesBulinusB. truncatus
PotadomaP. freethi1
MelanoidesM. tuberculate1
LanistesL. nsedweensis1
Lambaréné townBulinusB. truncatus
B. forskalii
Mbolani, Bindo, and Makouké villagesBulinusB. forskalii
GabiellaGabiella spp.
1 Most likely.
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MDPI and ACS Style

Dejon Agobé, J.C.; Kariuki, H.C.; Zinsou, J.F.; Honkpehedji, Y.J.; Grobusch, M.P.; Adegnika, A.A. Pilot Malacology Surveys for the Intermediate Hosts of Schistosomiasis in Rural and Semi-Urban Areas of the Moyen-Ogooué Province, Gabon. Trop. Med. Infect. Dis. 2022, 7, 1. https://doi.org/10.3390/tropicalmed7010001

AMA Style

Dejon Agobé JC, Kariuki HC, Zinsou JF, Honkpehedji YJ, Grobusch MP, Adegnika AA. Pilot Malacology Surveys for the Intermediate Hosts of Schistosomiasis in Rural and Semi-Urban Areas of the Moyen-Ogooué Province, Gabon. Tropical Medicine and Infectious Disease. 2022; 7(1):1. https://doi.org/10.3390/tropicalmed7010001

Chicago/Turabian Style

Dejon Agobé, Jean Claude, Henry Curtis Kariuki, Jeannot Fréjus Zinsou, Yabo Josiane Honkpehedji, Martin Peter Grobusch, and Ayola Akim Adegnika. 2022. "Pilot Malacology Surveys for the Intermediate Hosts of Schistosomiasis in Rural and Semi-Urban Areas of the Moyen-Ogooué Province, Gabon" Tropical Medicine and Infectious Disease 7, no. 1: 1. https://doi.org/10.3390/tropicalmed7010001

APA Style

Dejon Agobé, J. C., Kariuki, H. C., Zinsou, J. F., Honkpehedji, Y. J., Grobusch, M. P., & Adegnika, A. A. (2022). Pilot Malacology Surveys for the Intermediate Hosts of Schistosomiasis in Rural and Semi-Urban Areas of the Moyen-Ogooué Province, Gabon. Tropical Medicine and Infectious Disease, 7(1), 1. https://doi.org/10.3390/tropicalmed7010001

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