Next Article in Journal
Unraveling the Contact Network Patterns between Commercial Turkey Operation in North Carolina and the Distribution of Salmonella Species
Next Article in Special Issue
Distinct Schistosoma mansoni-Specific Immunoglobulin Subclasses Are Induced by Different Schistosoma mansoni Stages—A Tool to Decipher Schistosoma mansoni Infection Stages
Previous Article in Journal
Safety and Seroconversion of Immunotherapies against SARS-CoV-2 Infection: A Systematic Review and Meta-Analysis of Clinical Trials
Previous Article in Special Issue
The Dynamics of Hepatic Fibrosis Related to Schistosomiasis and Its Risk Factors in a Cohort of China
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

From the One Health Perspective: Schistosomiasis Japonica and Flooding

National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention (Chinese Center for Tropical Diseases Research), NHC Key Laboratory of Parasite and Vector Biology, WHO Collaborating Centre for Tropical Diseases, National Center for International Research on Tropical Diseases, Shanghai 200025, China
*
Author to whom correspondence should be addressed.
Pathogens 2021, 10(12), 1538; https://doi.org/10.3390/pathogens10121538
Submission received: 26 August 2021 / Revised: 16 November 2021 / Accepted: 23 November 2021 / Published: 25 November 2021
(This article belongs to the Special Issue Schistosomiasis: Host-Pathogen Biology)

Abstract

:
Schistosomiasis is a water-borne parasitic disease distributed worldwide, while schistosomiasis japonica localizes in the People’s Republic of China, the Philippines, and a few regions of Indonesia. Although significant achievements have been obtained in these endemic countries, great challenges still exist to reach the elimination of schistosomiasis japonica, as the occurrence of flooding can lead to several adverse consequences on the prevalence of schistosomiasis. This review summarizes the influence of flooding on the transmission of schistosomiasis japonica and interventions responding to the adverse impacts from the One Health perspective in human beings, animals, and the environment. For human and animals, behavioral changes and the damage of water conservancy and sanitary facilities will increase the intensity of water contact. For the environment, the density of Oncomelania snails significantly increases from the third year after flooding, and the snail habitats can be enlarged due to active and passive diffusion. With more water contact of human and other reservoir hosts, and larger snail habitats with higher density of living snails, the transmission risk of schistosomiasis increases under the influence of flooding. With the agenda set for global schistosomiasis elimination, interventions from the One Health perspective are put forward to respond to the impacts of increased flooding. For human beings, conducting health education to increase the consciousness of self-protection, preventive chemotherapy for high-risk populations, supply of safe water, early case finding, timely reporting, and treating cases will protect people from infection and prevent the outbreak of schistosomiasis. For animals, culling susceptible domestic animals, herding livestock in snail-free areas, treating livestock with infection or at high risk of infection, harmless treatment of animal feces to avoid water contamination, and monitoring the infection status of wild animals in flooding areas are important to cut off the transmission chain from the resources. For the environment, early warning of flooding, setting up warning signs and killing cercaria in risk areas during and post flooding, reconstructing damaged water conservancy facilities, developing hygiene and sanitary facilities, conducting snail surveys, using molluscicide, and predicting areas with high risk of schistosomiasis transmission after flooding all contribute to reducing the transmission risk of schistosomiasis. These strategies need the cooperation of the ministry of health, meteorological administration, water resources, agriculture, and forestry to achieve the goal of minimizing the impact of flooding on the transmission of schistosomiasis. In conclusion, flooding is one of the important factors affecting the transmission of schistosomiasis japonica. Multi-sectoral cooperation is needed to effectively prevent and control the adverse impacts of flooding on human beings, animals, and the environment.

1. Introduction

Schistosomiasis is a widespread water-borne parasitic disease at a global level, caused by six species of the parasite Schistosoma: S. mansoni, S. japonicum, S. haematobium, S. mekongi, S. intercalatum and S. guineensis. It affects more than 240 million people worldwide and more than 700 million people live in endemic areas [1]. The adult schistosome worm resides in the portal system of the liver, mesenteric arteries, the vessels of the bladder, and the genital tract of its definitive hosts [2]. Partial eggs retain in the host tissues to cause damage, whereas other eggs are discharged into the environment with feces or urine. The discharged eggs hatch and release free-swimming miracidia to penetrate specific snail hosts. The miracidia then develop in the snails, including two generations of sporocysts through asexual propagation, and shed abundant cercariae into fresh water. People become infected when they make contact with fresh water infested with cercariae. The cercariae penetrate the skin of the hosts and become schistosomulae, migrate through the circulation systems, and mature into adults in hosts’ specific organ and tissue [3,4].
Being a parasitic zoonosis, schistosomiasis japonica is prevalent in the Peoples’ Republic of China, the Philippines, and a few regions of Indonesia [1], which is transmitted through a wide spectrum of mammalian hosts but a strict intermediate host of Oncomelania spp. The life cycle reveals its dependence on the existence of the hosts and a decent environment. Thus, the prevention and control of schistosomiasis, which aims to disrupt its complex life cycle, should focus on all of the influencing factors in the transmission chain, including the hosts and the environment.
One Health is a global strategy combining the health of people, animals, and the environment and employs a holistic approach encouraging and expanding multidisciplinary collaborations, integrative research, capacity building, clinical practice, policy, and communication among many stakeholders [5,6]. This strategy is suitable for the prevention and control of schistosomiasis. The ecological distribution of schistosome during its growth and development depends on the geographic distribution of snails [7,8]. The distribution of the snails is related to several environmental factors, such as temperature, surface humidity, vegetation index, seasonality, and extreme events [9]. Flooding is an extreme event which has considerable impacts on the distribution of the snails and the transmission risks of schistosomiasis. In this review, we take a One Health perspective on flooding and its impacts on the transmission of schistosomiasis and summarize the One Health approaches to address the adverse impacts of flooding.

2. The Impact of Flooding on the Transmission of Schistosomiasis

Flooding is one of the major natural disasters that has brought tremendous losses to mankind in the last century by disrupting social growth and economic development [10,11,12]. The World Meteorological Organization reported that floods have caused 58,700 deaths and economic losses of nearly USD 115 billion over the past 50 years [13]. In recent decades, flooding occurred more frequently than before due to climate change and urbanization [12]. A study developed an integrated multivariate trend-frequency analysis (IMTFA) approach to assess climate extremes under global warming. A significant wetting and warming trend was found in Central Asia during the period of 1881–2018, and the warming trend significantly affected the intensities and frequencies of extreme precipitations in most regions of Central Asia [14]. In addition, several studies reported increasing trends in flood discharges in western Europe in the past five decades [15], including a 44% increase in the occurrence of extreme flood discharges [16]. Similar trends in the magnitude and frequency of flooding were also found in Brazil [17]. During 1903–2015, a significant fivefold increase in flood frequency in Amazonia is observable, from roughly one flood every 20 years during the first half of the 20th century to one flood every four years from the 2000s onward [18]. A review analyzed the floods in East China during 1984–2010 and reported a statistically significant increase of 77.4% in the flood cases per decade [19]. Although infrastructures have been strengthened in recent years to decrease the impacts of flooding, two catastrophic floods occurred along the Yangtze River basin in China in 2016 and 2020 [20,21]. The flood in 2020 resulted in 142 deaths/missing cases and a direct economic loss of around 116 billion RMB (~16.5 billion USD), though this is much better than the similarly destructive flood in 1998 due to the development construction of large-scale water conservancy projects on the Yangtze River’s mainstream and its tributaries [20].
Except deaths and economic losses, flooding can also increase the transmission risk of infectious diseases [22]. After flooding, traumatic injury, exposure to contaminated environment, poor hygiene, inadequate sanitation, and the lack of access to clean water would increase host vulnerability to various communicable diseases, such as bacterial diarrheal illnesses, cholera, hepatitis A virus infections, cryptosporidiosis, vector-borne diseases, and water-borne diseases [11,23,24,25,26,27,28]. Being a water-borne disease, the transmission of schistosomiasis japonica is also affected by flooding from the aspects of human beings, animal hosts, and environmental health [29].

2.1. The Impact of Flooding on Schistosomiasis Japonica in Human Beings

The occurrence of flooding will change the behavior of human beings and increase the intensity of water contact. Residents in rural areas could suffer from worse consequences because mostly they are nearer to the rivers than residents in the cities. Currently, most published studies of the flood-impact on water contact are carried out in China. Therefore, taking evidence from China for example, there are three reasons for the increase in water contact. First, flooding damages the embankments and people who previously live inside the embankments are directly exposed to the large amount of water that may contain schistosome cercariae. In the past 30 years, several catastrophic floods occurred along the Yangtze River basin in China. During the destructive flood in 1991, 14 endemic counties of schistosomiasis japonica in Hubei province were inundated, with more than 200 embankments collapsed and more than nine million of the population exposed to the contaminated waterbody [30]. Second, risk of water contact comes with various specific flood-related activities, such as flood rescue and self-relieved measures [31]. These activities could provide an extra chance of water contact and lead to an extra risk of infection, because people will not take these actions in usual years without flooding. During the flood in 1998 in China, over eight million people were exposed to the flood water [32], and nearly 150,000 soldiers and civilians participated in the flood fighting and rescue [33]. These soldiers and civilians were not supposed to be exposed to the fecal contaminated water in normal and dry years. Third, other human behaviors also change as a result of flooding and the frequency and duration of water contact alter. Evidence revealed that the major pattern of water contact during flooding was daily life contact in adult females, and swimming and paddling in adult males and children under 18 years old [34]. Certain individuals may attend some water-related recreational activities during flooding because the water body is enlarged by flooding. It should be noted that some amusement activities, such as swimming and fishing in the unknown wild open water, will increase infection risk, since flooding could even carry infected snails or cercariae to previous non-endemic areas of schistosomiasis. Thus, under the condition of higher intensity of water contact, the incidence risk of schistosomiasis will rise. Research reported that, compared with the control group, people in the case group of schistosomiasis had a higher frequency, longer accumulating time, and larger body contact surface area of the water contact [34].
In addition to the higher level of water contact, the dwelling environment and sanitation conditions of the local residents in the flood plains can be greatly influenced by flooding, which is also associated with increased infection risk. The damage to water and sanitation infrastructures during flooding may lead to the disruption of sewage disposal, poor standards of hygiene, poor nutrition, and negligible sanitation, which provide suitable conditions for the transmission of infectious diseases [11,35]. The lack of basic hygiene and sanitation and population displacement will also carry out the outbreak of water-borne and vector-borne diseases, such as schistosomiasis [36,37]. Inadequate feces management will lead to the discharge of feces containing schistosome eggs into the environment. Due to the lack of access to clean water, the victims of flooding are more likely to contact the contaminated water with cercariae.
More water contact leads to the increase in the prevalence of schistosomiasis. A study explored that the average number of acute cases in flood years was 2.8 folds higher than in other non-flood years [38]. The acute cases in Anhui [39] and Hubei [40] provinces increased by 61.73% and 43.90%, from 81 and 246 cases in 1997 to 131 and 354 cases in 1998, respectively, after the catastrophic flood in 1998. In addition, increases in the prevalence of schistosomiasis were also observed in Anhui, Hubei, Jiangxi, and Hunan provinces in 1999 after the 1998 flood [39,40,41,42,43,44,45]. Along with the development of the sanitation and health facilities and the improvement of the natural disaster emergency responses, there was no research reporting acute infection cases or cases with positive stool test results after the similar catastrophic flood in China in 2016, but an increasing trend was detected in the positive rate of indirect hemagglutination assay (IHA). The positive IHA rate of local residents in 26 national surveillance sites in Jiangxi province rose from 4.72% in 2016 to 5.58% in 2017 [46]. Similar positive association between rainfall and higher prevalence is also observed in the Visayas, the Philippines, whereas the relationship is negative in Mindanao with different topography [47]. This is a hint that the impact of flooding on the prevalence can be inverse when adjusting the topography factor. Future studies should explore the reasons of association between lower rainfall and higher prevalence in certain areas, which may provide critical evidence for policy makers targeting world-wide elimination of schistosomiasis. Besides, more evidence is needed to fill up the gap to identify the current status of threats of schistosomiasis transmission caused by flooding in the past 20 years.

2.2. The Impact of Flooding on Schistosomiasis Japonica in Animals

Similar to humans, the risk of schistosome infection in animals is on the rise with the occurrence of flooding. There are over 40 mammalian species serving as the reservoir hosts of S. japonicum, with bovines being the most important [48]. In flood plains, vegetation may change in terms of community structure, population size and phenology [49]. For domestic animals, they can be attracted by the vegetation on marshlands and riverbanks, because the grass is lush under the effect of flooding. Moreover, flood water can be contaminated by feces carrying eggs, and then the potentially contaminated flood water will invade grazing areas alongside the embankments due to the damage to barns. In the meantime, feces are also more likely to be excreted into flood water in grazing areas. These two factors will together lead to the increase in exposure risk for the animals. Consistent with the trend in human prevalence of schistosomiasis, the prevalence among the cattle in four counties in Hubei province increased about 1.68 folds in 1999 after the catastrophic flood in 1998 [40]. For wild animals, heavy rainfall encourages wild grass production which supports the growing of outdoor wild animal populations, such as rodents, and the flooding forces the animals from their burrows into closer areas with human beings due to the growing population and the losses of previous natural habitats [50]. The potentially infected wild animals will carry the worm to areas where schistosomiasis had been under control or even to previously non-endemic areas, and further expand the scope of the distribution of reservoir hosts. Few studies have focused on the infection of S. japonicum in wild animals. Future research could investigate the infection status among wild animals and explore the impacts of flooding on them to fill this gap and provide evidence for developing emergency responses to control schistosomiasis after flooding, although the investigation is fairly tough to carry out. Besides, it is hard to identify the time frame for zoonotic transmission during flooding. More specifically, previously infected animals, especially wild animals which are difficult to manage, could excrete feces into the flood water and the water will become contaminated. Furthermore, the fecal contaminated water will carry the parasite to infect snails and shed cercariae to infect healthy animals which contact the water during flooding. Thus, in response to this reciprocal causation of animal infection and fecal contamination, interventions should focus both on the management of animals and the treatment of the water.

2.3. The Impact of Flooding on Environmental Health Specifically for Oncomelania hupensis

Flooding will change the ecological environment. Water conservancy (dams, river embankments, channels, levees, etc.) and sanitary facilities can be damaged by severe floods. The damage of sanitary facilities may lead to a higher risk of fecal contamination. The main impact of flooding on the environment is the change in the density and distribution of O. hupensis since the snail is the crucial link in the life cycle of S. japonicum [51]. Without the existence of O. hupensis, the transmission of schistosomiasis will be interrupted successfully. This is the reason why snail control is crucial for schistosomiasis elimination [52].
The density of O. hupensis could be influenced by flooding, through the impact on development, reproduction, and ability to survive under the condition of submergence [53]. On the short-term individual level, continuous rainfall and the subsequent flooding facilitate the establishment of snail colonies on vegetation [47]. During rainfall and flooding, the egg production of the snails significantly increases, with one female producing on average two eggs in five days [54]. Yang et al. reviewed the data between 1995–2002 in Hunan province of China, and claimed that the annual rainfall, days of daily rainfall greater than 0.1 mm, and the days inundated with water (favorable for 2 to 7 months) were significantly associated with the reproduction of O. hupensis [55]. On the long-term population level, there is a trend of the pattern of snail density in certain local snail habitats [56]. Several studies reported that the rate of the frames with living snails fell in the first two years after flooding and then rose quickly from the third year [38,57]. The decrease in the first two years can be explained as due to the considerable deaths of adult snails [58] and the limited capacity of developing and hatching for snail eggs [59] under the condition of submergence. However, some adult snails can survive through a period of natural drowning and young snails developed well under the drowning condition [58]. This may be the reason for the subsequent increasing trend from the third year after flooding. A study reviewed the annual snail survey in Jiangsu province in China from 1998 to 2003 and reported similar trends in the rate of the frames with infected snails, the snail infection rate, and the density of infected snails [57]. This provides an explanation for the higher risk of schistosomiasis transmission with a higher density of total living snails.
The influence is also demonstrated in the active and passive diffusion of the snails for the following expanded snail habitats. When flooding occurs, the snails drown, climb trees, and passively float down rivers [60]. Along with the side-weir flow after the flood discharge, the snails stay in the places where flow velocity is small, such as the vortex areas [61]. New decent potential habitats develop with the mud deposition due to the flood flow and the snails can actively and slowly move to neighboring new habitats. These active and passive dispersals can result in the enlargement of previous snail habitats, the emergence of new snail habitats, and the rebound in previously snail eliminated areas [52]. During the period from 1979 to 2000, the re-emerging and newly discovered snail habitats in the flooding years accounted for up to 5.8% and 10.1% of the total snail habitats in the Yangtze River valley and were 2.6 and 2.7 times larger than the areas in years with normal hydrologic conditions, respectively [38]. After the 2016 catastrophic flood in China, the re-emerging and the newly discovered snail habitat areas in Anhui province were 1375 hm2 and 1288 hm2, respectively [62]. It should be noted that snail dispersal often presents as a retardation effect of flooding, since snails in the new habitats may not reproduce to a large amount that could be easily found by snail surveys and surveillance in one or two years after flooding.

3. The Strategies to Control and Prevent the Impacts of Flooding on the Transmission of Schistosomiasis from the One Health Perspective

Flooding will increase the risk of S. japonicum infection. For human and animals, behavior changes increase the intensity of water contact. For the environment, the occurrence of flooding always occurs along with the change of the previous aquatic environment and the climate. These changes will be reflected in the breeding, development, and distribution of the intermediate host snails, and then have an influence on the prevalence of schistosomiasis. Meanwhile, flooding will damage the dams and reservoirs in non-endemic areas which should have protected the residents from infection, and further cause the spread of snails, leading to larger snail habitats and higher risk of transmission probability. Therefore, specific intervention should be developed and implemented comprehensively to prevent the outbreak of schistosomiasis when flooding occurs.

3.1. For the Human Beings

School-based and community-based health education projects using various education models should be continuously implemented in the endemic areas of schistosomiasis [63]. People should be educated about the modes of transmission and risk behaviors [64,65]. Through education, residents are more likely to avoid unnecessary water contact as well as apply self-protection when they have to make contact with the flood water. Towards the major pattern of water contact, specific health education strategies should be applied to each age or sex group. Evidence has proven the effectiveness of interpersonal communication approaches to improve knowledge about schistosomiasis prevention and correct previous high-risk behaviors [66,67]. Effective health education should continue to the period even after flooding.
During flooding, unsafe water contact should be minimized. Safe and clean water are necessary for victims to make them stay away from the contaminated water. Proper feces management should be implemented to avoid water contamination. For people who participate in flood rescue and necessary production activities, adequate self-protection measures should be equipped before inevitable water contact. The measures include smearing anti-miracidia drugs and wearing rubber clothes, gloves, and shoes, which will keep people safe from the cercariae in the water. Moreover, all individuals potentially exposed to the contaminated water should be registered and followed up with early screening, early reporting, and early treatment.
After flooding, chemotherapy should be available to the affected population. Praziquantel (PZQ) is the only choice of chemotherapy for schistosomiasis, recommended by the World Health Organization and has been widely used for over 40 years. People who have water contact in high-risk areas during flooding should take early preventive chemotherapy with PZQ within four to five weeks to prevent acute infection [68]. The anti-schistosome effect could remain over time [69]. For people who participate in flood recuses and repeatedly contact the water, the combinations of PZQ and artemisinin derivatives provide higher protection than PZQ monotherapy [68].

3.2. For Animals

For domestic animals, the interventions before, during, and after flooding are consistent. First, risk monitoring systems should be continuously operated, especially after flooding. With the analysis of long-term data of routine surveillance, the risk factors and emergent cases can be easily detected and managed followed by a quick response. Then the transmission will be limited at the initial stage. Second, the number of domestic animals that serve as major reservoir hosts should be reduced significantly in endemic areas. Excessive animals represent more potential infection sources and higher transmission risk. Third, contact with unknown open water and potential endemic water should be reduced, and better, be avoided. Especially, the pasturing of livestock in marshland infested with Oncomelania should be prohibited, although grass production in the plains is greatly supported by flooding. Instead, herding in snail-free areas can be allowed. Fourth, feces hazard-free treatment should be issued to reduce the risk of water pollution caused by the excreted feces with eggs, to cut off the transmission chain. Finally, the same as human beings, preventive chemotherapy towards domestic animals after flooding should be especially carried out to reduce the disease burden of livestock.
For wild animals, currently there are no proper approaches for control and management [70]. This remains one of the challenges for transmission control during flooding and future goals of schistosomiasis elimination. Conducting surveillance on wild animals continuously, especially after flooding, is crucial to explore the hotspot and transmission tendency of schistosomiasis in the environment, thus providing references for policymaking. In China, the current strategy towards schistosomiasis control in wild animals is to indirectly monitor the infection status of wild feces by the ministry of health. From the One Health perspective, cross-sectoral cooperation between the ministry of health, agriculture, and forestry is needed to routinely capture sentinel mice or other wild animals for monitoring of the infection situation.

3.3. For the Environment

Before flooding, better levee, enlarged reservoirs, improved early warning systems, and accurate hazard risk evaluations are needed to control the severe health and economic losses of flooding [71]. The earliest warning of flooding can be offered via communication and cooperation with the ministry of the meteorological administration, which will offer sufficient time for disease control departments to respond to the coming flooding in preparation for dealing with schistosomiasis transmission. The implementation of integrated water resource management is a sustainable approach to protect local residents and animals from the effects of flooding and prevent the breeding and dispersal of snails [72]. For instance, creation and improvement of dam reservoirs can decrease the risk of embankment collapse and ameliorate water supply and sanitation. The Three Gorges Dam significantly reduced the frequency of high-water levels that were beyond the warning level [73]. The dam reservoirs together with the irrigation systems can break the transmission cycle of schistosomiasis by reducing human-water contact, diminishing environmental contamination with excreta, and decreasing the density of the living snails [73,74]. However, it should be noted that the construction of the water conservancy project may also expand the snail habitats and result in the emergence of new transmission sites without appropriate anti-schistosomiasis measures. A meta-analysis reviewed studies about the association between the prevalence of schistosomiasis and the dam construction in Africa and reported a pooled risk ratio of 2.4 (95%CI 1.4–3.9) and 2.6 (95%CI 1.4–5.0) for the infection of S. haematobium and S. mansoni, respectively [74]. To date, these has been no similar report regarding S. japonicum prevalence. Thus, when considering a strategy from the One Health perspective, the water conservancy program for schistosomiasis control should combine with snail control approaches [75] and other interventions towards human and animals, such as health education and the control for all species of infection sources, to ensure effective measures for a comprehensive strategy. This intervention calls for cooperation between the ministry of health and water resources.
During flooding, temporary hygiene and sanitary facilities should be built in time. The toilets in crowd gathering areas where displaced people live should be constructed in a timely manner. The supply of safe and clean water could effectively prevent water-borne diseases, including schistosomiasis. Besides, human and livestock feces should be put through hazard-free treatment to avoid contamination. In addition, warning signs should be displayed in the most visible places to warn people to stay away from the risky areas.
After flooding, the damage of banks, water supply and sanitation facilities should be assessed. Priorities should be given to repairing damaged embankments and other water infrastructures. Then, drugs for killing cercaria should be discharged into the waterbody to preventively control the existence of schistosomes. Most importantly, snail control should be carried out to interrupt the transmission after flooding [76]. Repeated use of molluscicide is an effective strategy to reduce the density of Oncomelania and plays a key role in the elimination of schistosomiasis. Although niclosamide is reported to be toxic to fish and damaging to the environment and biodiversity, it is still the only molluscicide recommended by WHO, which is highly active against all stages of the snail life cycle, as well as schistosome larvae [77]. To advance precise snail control, remote sensing and geographic information system (GIS) technologies could be utilized as potentially powerful methods to simulate flood inundation, map flood dynamics, predict water levels, and forecast the spatial distribution of snails and the risk areas of schistosomiasis before and post flooding [78,79,80,81,82]. Using the data from Sentinel-1A and 1B, and Landsat 8 SAR remote sensing images, the accuracy of the model to predict the snail distribution during and after flooding is estimated to be around 85% [83,84]. By accurately predicting the snail distribution, the model could be a strong approach to timely identify the areas with higher transmission risk of schistosomiasis and provide a hint for targeted responses after flooding.
The strategies for the environment before, during, and after flooding may be applied in Africa for S. mansoni and S. haematobium control since all human- hosting Schistosoma spp. have a similar life cycle, although their intermediate hosts and major definitive hosts are diverse. The early warning of flooding, setting up warning signs and killing cercaria in risky areas during or post flooding, reconstructing water conservancy, developing hygiene and sanitary facilities, conducting snail surveillance, using molluscicide, and predicting the risky transmission areas after flooding can also be effective.

4. Conclusions and Next Steps

In this article, we reviewed the impact of flooding on the transmission of schistosomiasis japonica in human beings, animals, and the environment. Flooding damages water conservancy and sanitary facilities and increases the intensity of water contact for both humans and animals, which further increases the infection risk of S. japonicum. In addition to the impact of inundated conditions on the development and reproduction of Oncomelania, flooding may carry snails to previously snail-free areas and lead to the active and passive diffusion of the snails. As a result, the density of snails will significantly increase from the third year after flooding [38,57], and snail habitats can be enlarged due to the diffusion. With more water contact from human and other reservoir hosts, and larger snail habitats with higher density of living snails, the transmission risk of schistosomiasis increases under the influence of flooding, especially catastrophic flooding.
With the agenda set for the global schistosomiasis elimination by 2030, considering the life cycle of schistosomes and transmission features of schistosomiasis japonica, strategies for intervention must be developed and implemented with the context of One Health, responding to the impacts of flooding effectively. For humans, health education, adequate self-protection equipment, preventive chemotherapy, safe water supplements, and early case screening, reporting, and treatment will protect people from infection and prevent the rebound of schistosomiasis. For animals, culling susceptible domestic animals, herding in snail-free areas, proper feces treatment, and continuous surveillance, including of wild animals, should be carried out to block the transmission chain. For the environment, early warnings of flooding, setting up warning signs and killing cercaria in risky areas during or post flooding, reconstructing water conservancy, developing hygiene and sanitary facilities, conducting snail surveillance, using molluscicide, and predicting the risky transmission areas after flooding all contribute to reducing schistosomiasis transmission risk. The implementation of these strategies needs multi-sectoral cooperation to achieve the goal of minimizing the adverse impacts of flooding. In addition, there are still topics in need of discussion, such as wild animal management and the long-term impact of flooding on the spread of snails. Further research could provide more evidence for better control of flooding impacts on schistosomiasis.

Author Contributions

S.-Y.G. and J.X. conceived and designed the review. S.-Y.G. and L.L. collected the references and wrote the first draft manuscript. L.-J.Z., Y.-L.L., S.-Z.L. and J.X. revised the paper. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Science and Technology Major Project of China (No. 2018ZX10101002-002) and the National Natural Science Foundation of China (No. 82073619). The funding sources have no role in any aspect of this study.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. World Health Organization. Schistosomiasis (Bilharzia). Available online: https://www.who.int/health-topics/schistosomiasis#tab=tab_1 (accessed on 26 August 2021).
  2. Sah, V.K.; Wang, L.; Min, X.; Rizal, R.; Feng, Z.; Ke, Z.; Deng, M.; Li, L.; Li, H. Human schistosomiasis: A diagnostic imaging focused review of a neglected disease. Radiol. Infect. Dis. 2015, 2, 150–157. [Google Scholar] [CrossRef] [Green Version]
  3. Graham, B.B.; Bandeira, A.P.; Morrell, N.W.; Butrous, G.; Tuder, R.M. Schistosomiasis-associated pulmonary hypertension: Pulmonary vascular disease: The global perspective. Chest 2010, 137, 20S–29S. [Google Scholar] [CrossRef]
  4. Centers for Disease Control and Prevention U.S.; Laboratory Identification of Parasites of Public Health Concern U.S. Parasites—Schistosomiasis. Available online: https://www.cdc.gov/parasites/schistosomiasis/ (accessed on 26 August 2021).
  5. Destoumieux-Garzon, D.; Mavingui, P.; Boetsch, G.; Boissier, J.; Darriet, F.; Duboz, P.; Fritsch, C.; Giraudoux, P.; Le Roux, F.; Morand, S.; et al. The One Health concept: 10 Years old and a long road ahead. Front. Vet. Sci. 2018, 5, 14. [Google Scholar] [CrossRef] [Green Version]
  6. Overgaauw, P.A.M.; Vinke, C.M.; Hagen, M.; Lipman, L.J.A. A One Health perspective on the human-companion animal relationship with emphasis on zoonotic aspects. Int. J. Environ. Res. Public Health 2020, 17, 3789. [Google Scholar] [CrossRef]
  7. King, C.H.; Bertsch, D. Historical perspective: Snail control to prevent schistosomiasis. PLoS Negl. Trop. Dis. 2015, 9, e0003657. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Sokolow, S.H.; Wood, C.L.; Jones, I.J.; Swartz, S.J.; Lopez, M.; Hsieh, M.H.; Lafferty, K.D.; Kuris, A.M.; Rickards, C.; De Leo, G.A. Global assessment of schistosomiasis control over the past century shows targeting the snail intermediate host works best. PLoS Negl. Trop. Dis. 2016, 10, e0004794. [Google Scholar] [CrossRef]
  9. McCreesh, N.; Booth, M. Challenges in predicting the effects of climate change on Schistosoma mansoni and Schistosoma haematobium transmission potential. Trends Parasitol. 2013, 29, 548–555. [Google Scholar] [CrossRef] [Green Version]
  10. Kumar, P.; Debele, S.E.; Sahani, J.; Aragao, L.; Barisani, F.; Basu, B.; Bucchignani, E.; Charizopoulos, N.; Di Sabatino, S.; Domeneghetti, A.; et al. Towards an operationalisation of nature-based solutions for natural hazards. Sci. Total Environ. 2020, 731, 138855. [Google Scholar] [CrossRef]
  11. Okaka, F.O.; Odhiambo, B.D.O. Relationship between flooding and out break of infectious diseasesin Kenya: A review of the literature. J. Environ. Public Health 2018, 2018, 5452938. [Google Scholar] [CrossRef] [Green Version]
  12. Tanoue, M.; Hirabayashi, Y.; Ikeuchi, H. Global-scale river flood vulnerability in the last 50 years. Sci. Rep. 2016, 6, 36021. [Google Scholar] [CrossRef]
  13. World Meteorological Organization. Water-Related Hazards Dominate Disasters in the Past 50 Years. Available online: https://public.wmo.int/en/media/press-release/water-related-hazards-dominate-disasters-past-50-years (accessed on 26 August 2021).
  14. Liu, Y.R.; Li, Y.P.; Yang, X.; Huang, G.H.; Li, Y.F. Development of an integrated multivariate trend-frequency analysis method: Spatial-temporal characteristics of climate extremes under global warming for Central Asia. Environ. Res. 2021, 195, 110859. [Google Scholar] [CrossRef]
  15. Bloschl, G.; Hall, J.; Viglione, A.; Perdigao, R.A.P.; Parajka, J.; Merz, B.; Lun, D.; Arheimer, B.; Aronica, G.T.; Bilibashi, A.; et al. Changing climate both increases and decreases European river floods. Nature 2019, 573, 108–111. [Google Scholar] [CrossRef]
  16. Berghuijs, W.R.; Aalbers, E.E.; Larsen, J.R.; Trancoso, R.; Woods, R.A. Recent changes in extreme floods across multiple continents. Environ. Res. Lett. 2017, 12, 114035. [Google Scholar] [CrossRef]
  17. Bartiko, D.; Oliveira, D.Y.; Bonumá, N.B.; Chaffe, P.L.B. Spatial and seasonal patterns of flood change across Brazil. Hydrol. Sci. J. 2019, 64, 1071–1079. [Google Scholar] [CrossRef]
  18. Barichivich, J.; Gloor, E.; Peylin, P.; Brienen, R.J.W.; Schöngart, J.; Espinoza, J.C.; Pattnayak, K.C. Recent intensification of Amazon flooding extremes driven by strengthened Walker circulation. Sci. Adv. 2018, 4, eaat8785. [Google Scholar] [CrossRef] [Green Version]
  19. Shi, J.; Cui, L.; Tian, Z. Spatial and temporal distribution and trend in flood and drought disasters in East China. Environ. Res. 2020, 185, 109406. [Google Scholar] [CrossRef]
  20. Wei, K.; Ouyang, C.; Duan, H.; Li, Y.; Chen, M.; Ma, J.; An, H.; Zhou, S. Reflections on the catastrophic 2020 Yangtze River basin flooding in southern China. Innovation 2020, 1, 100038. [Google Scholar] [CrossRef]
  21. Zhang, N.; Song, D.; Zhang, J.; Liao, W.; Miao, K.; Zhong, S.; Lin, S.; Hajat, S.; Yang, L.; Huang, C. The impact of the 2016 flood event in Anhui Province, China on infectious diarrhea disease: An interrupted time-series study. Environ. Int. 2019, 127, 801–809. [Google Scholar] [CrossRef]
  22. Rossati, A. Global warming and its health impact. Int. J. Occup. Environ. Med. 2017, 8, 7–20. [Google Scholar] [CrossRef] [Green Version]
  23. Zinsstag, J.; Crump, L.; Schelling, E.; Hattendorf, J.; Maidane, Y.O.; Ali, K.O.; Muhummed, A.; Umer, A.A.; Aliyi, F.; Nooh, F.; et al. Climate change and One Health. FEMS Microbiol. Lett. 2018, 365, fny085. [Google Scholar] [CrossRef] [Green Version]
  24. Liang, S.Y.; Messenger, N. Infectious diseases after hydrologic disasters. Emerg. Med. Clin. N. Am. 2018, 36, 835–851. [Google Scholar] [CrossRef]
  25. Soneja, S.; Jiang, C.; Romeo Upperman, C.; Murtugudde, R.; Mitchell, C.S.; Blythe, D.; Sapkota, A.R.; Sapkota, A. Extreme precipitation events and increased risk of campylobacteriosis in Maryland, U.S.A. Environ. Res. 2016, 149, 216–221. [Google Scholar] [CrossRef]
  26. Gertler, M.; Durr, M.; Renner, P.; Poppert, S.; Askar, M.; Breidenbach, J.; Frank, C.; Preussel, K.; Schielke, A.; Werber, D.; et al. Outbreak of Cryptosporidium hominis following river flooding in the city of Halle (Saale), Germany, August 2013. BMC Infect. Dis. 2015, 15, 88. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Brown, L.; Murray, V. Examining the relationship between infectious diseases and flooding in Europe: A systematic literature review and summary of possible public health interventions. Disaster Health 2013, 1, 117–127. [Google Scholar] [CrossRef] [Green Version]
  28. Ahern, M.; Kovats, R.S.; Wilkinson, P.; Few, R.; Matthies, F. Global health impacts of floods: Epidemiologic evidence. Epidemiol. Rev. 2005, 27, 36–46. [Google Scholar] [CrossRef] [Green Version]
  29. Zhang, S. Flood disasters and schistosomiasis control. Chin. J. Schistosomiasis Control 2020, 32, 522–525. (In Chinese) [Google Scholar] [CrossRef]
  30. Disaster Relief and Disease Prevention Investigation Team Of the Ministry of Health. The impact of the catastrophic flood on the prevalence of schistosomiasis in Hunan and Hubei provinces. Chin. J. Schistosomiasis Control 1991, 3, 253. (In Chinese) [Google Scholar]
  31. Cao, C.; Li, S.; Zhou, X. Impact of schistosomiasis transmission by catastrophic flood damage and emergency response in China. Chin. J. Schistosomiasis Control 2016, 28, 618–623. (In Chinese) [Google Scholar] [CrossRef]
  32. Guo, J. National progress of schistosomiasis control in 1998. Chin. J. Schistosomiasis Control 1999, 11, 129–131. (In Chinese) [Google Scholar] [CrossRef]
  33. Zhang, S.; Lin, D.; Hu, F. The current endemic status of schistosomiasis in Poyang Lake region in China: A review of achievement for the celebration of the 50th anniversary of the founding of PRC. Chin. J. Schistosomiasis Control 1999, 11, 196–198. (In Chinese) [Google Scholar] [CrossRef]
  34. Yang, M.; Tan, H.; Zhou, Y.; Tang, G.; Li, P.; Yun, C.; Xu, X. Quantitative study on human water contact during disaster year in endemic region of schistosomiasis japonica. Chin. J. Schistosomiasis Control 2002, 14, 109–114. (In Chinese) [Google Scholar]
  35. Shokri, A.; Sabzevari, S.; Hashemi, S.A. Impacts of flood on health of Iranian population: Infectious diseases with an emphasis on parasitic infections. Parasite Epidemiol. Control 2020, 9, e00144. [Google Scholar] [CrossRef]
  36. Gautam, O.P.; Paudel, Y.V.K.P.; Dhimal, M.; Curtis, V. Water, sanitation, and hygiene interventions: An urgent requirement in post-flood Nepal. Lancet Infect. Dis. 2017, 17, 1118–1119. [Google Scholar] [CrossRef] [Green Version]
  37. Cissé, G. Food-borne and water-borne diseases under climate change in low- and middle-income countries: Further efforts needed for reducing environmental health exposure risks. Acta Trop. 2019, 194, 181–188. [Google Scholar] [CrossRef]
  38. Wu, X.H.; Zhang, S.Q.; Xu, X.J.; Huang, Y.X.; Steinmann, P.; Utzinger, J.; Wang, T.P.; Xu, J.; Zheng, J.; Zhou, X.N. Effect of floods on the transmission of schistosomiasis in the Yangtze River valley, People’s Republic of China. Parasitol. Int. 2008, 57, 271–276. [Google Scholar] [CrossRef] [PubMed]
  39. Ge, J.; Zhang, S.; Wang, T.; Zhang, G.; Tao, C.; Lv, D.; Wang, Q.; Wu, W. Effects of flood on the prevalence of schistosomiasis in Anhui province in 1998. J. Trop. Dis. Parasitol. 2004, 2, 131–134. (In Chinese) [Google Scholar]
  40. Chen, W.; Yang, X.; Huang, X.; Zhang, Y.; Cai, S.; Liu, J.; Fu, Y.; Li, S. Influence of flood in 1998 on schistosomiasis epidemic. Chin. J. Schistosomiasis Control 2000, 12, 202–205. (In Chinese) [Google Scholar] [CrossRef]
  41. McManus, D.P.; Dunne, D.W.; Sacko, M.; Utzinger, J.; Vennervald, B.J.; Zhou, X.N. Schistosomiasis. Nat. Rev. Dis Primers 2018, 4, 13. [Google Scholar] [CrossRef] [PubMed]
  42. Chen, H.; Lin, D.; Zhang, S.; Hu, F.; Ning, A.; Zeng, X.; Hu, G.; Xie, Z. Studies on the influence of flood disaster on schistosomiasis transmission and on its control in Poyang Lake region I. Analysis of schistosomiasis prevalence in flood year and following year. Chin. J. Schistosomiasis Control 2001, 13, 141–146. (In Chinese) [Google Scholar]
  43. Yang, M.; Tan, H.; Zhou, Y. Trend of prevalence of schistosomiasis before and after embankment collapsed in Dongting Lake area. Chin. J. Epidemiol. 2002, 23, 324–325. (In Chinese) [Google Scholar]
  44. Cai, Y.; Xu, J.; Steinmann, P.; Chen, S.; Chu, Y.; Tian, L.; Chen, M.; Li, H.; Lu, Y.; Zhang, L.; et al. Field comparison of circulating antibody assays versus circulating antigen assays for the detection of schistosomiasis japonica in endemic areas of China. Parasites Vectors 2014, 7, 138. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Whitty, C.J.M.; Mabey, D.C.; Armstrong, M.; Wright, S.G.; Chiodini, P.L. Presentation and outcome of 1107 cases of schistosomiasis from Africa diagnosed in a non-endemic country. Trans. R. Soc. Trop. Med. Hyg. 2000, 95, 531–534. [Google Scholar] [CrossRef]
  46. Yuan, M.; Li, Y.; Lv, S.; Hu, F.; Hang, C.; Chen, Z.; Lin, D.; Dang, H.; Lv, S. Endemic status of schistosomiasis in national surveillance sites in Jiangxi Province from 2015 to 2018. Chin. J. Parasitol. Parasit. Dis. 2019, 37, 652–657. (In Chinese) [Google Scholar] [CrossRef]
  47. Soares Magalhaes, R.J.; Salamat, M.S.; Leonardo, L.; Gray, D.J.; Carabin, H.; Halton, K.; McManus, D.P.; Williams, G.M.; Rivera, P.; Saniel, O.; et al. Geographical distribution of human Schistosoma japonicum infection in The Philippines: Tools to support disease control and further elimination. Int. J. Parasitol. 2014, 44, 977–984. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Zhou, X.-N.; Bergquist, R.; Leonardo, L.; Yang, G.-J.; Yang, K.; Sudomo, M.; Olveda, R. Schistosomiasis japonica: Control and research needs. In Important Helminth Infections in Southeast Asia: Diversity and Potential for Control and Elimination, Part A; Advances in Parasitology; Elsevier: Amsterdam, The Netherlands, 2010; Volume 72, pp. 145–178. [Google Scholar] [CrossRef]
  49. Alho, C.J.; Silva, J.S. Effects of severe floods and droughts on wildlife of the Pantanal Wetland (Brazil)—A review. Animals 2012, 2, 591–610. [Google Scholar] [CrossRef] [Green Version]
  50. Diaz, J.H. Rodent-borne infectious disease outbreaks after flooding disasters: Epidemiology, management, and prevention. J. Emerg. Manag. 2015, 13, 459–467. [Google Scholar] [CrossRef]
  51. Wood, C.L.; Sokolow, S.H.; Jones, I.J.; Chamberlin, A.J.; Lafferty, K.D.; Kuris, A.M.; Jocque, M.; Hopkins, S.; Adams, G.; Buck, J.C.; et al. Precision mapping of snail habitat provides a powerful indicator of human schistosomiasis transmission. Proc. Natl. Acad. Sci. USA 2019, 116, 23182–23191. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Wang, L.; Utzinger, J.; Zhou, X. Schistosomiasis control: Experiences and lessons from China. Lancet 2008, 372, 1793–1795. [Google Scholar] [CrossRef]
  53. McMullen, D.B. The control of schistosomiasis japonica; observations on the habits, ecology and life cycle of Oncomelania quadrasi, the molluscan intermediate host of Schistosoma japonicum in the Philippine Islands. Am. J. Hyg. 1947, 45, 259–273. [Google Scholar]
  54. Leonardo, L.; Varona, G.; Fornillos, R.J.; Manalo, D.; Tabios, I.K.; Moendeg, K.; de Cadiz, A.; Kikuchi, M.; Chigusa, Y.; Mistica, M.; et al. Oncomelania hupensis quadrasi: Snail intermediate host of Schistosoma japonicum in the Philippines. Acta Trop. 2020, 210, 105547. [Google Scholar] [CrossRef]
  55. Yang, Y.; Zheng, S.B.; Yang, Y.; Cheng, W.T.; Pan, X.; Dai, Q.Q.; Chen, Y.; Zhu, L.; Jiang, Q.W.; Zhou, Y.B. The Three Gorges Dam: Does the flooding time determine the distribution of schistosome-transmitting snails in the middle and lower reaches of the Yangtze River, China? Int. J. Environ. Res. Public Health 2018, 15, 1304. [Google Scholar] [CrossRef] [Green Version]
  56. Yang, Y.; Gao, J.; Cheng, W.; Pan, X.; Yang, Y.; Chen, Y.; Dai, Q.; Zhu, L.; Zhou, Y.; Jiang, Q. Three Gorges Dam: Polynomial regression modeling of water level and the density of schistosome-transmitting snails Oncomelania hupensis. Parasites Vectors 2018, 11, 183. [Google Scholar] [CrossRef] [Green Version]
  57. Huang, Y.; Sun, L.; Hong, Q.; Gao, Y.; Zhang, L.; Gao, Y.; Song, H.; Guo, J.; Liang, Y.; Zhu, Y. Longitudinal observation on fluctuation trend of distribution and spread of Oncomelania snails after floodwater in marshland of lower reaches of Yangtze River. Chin. J. Schistosomiasis Control 2004, 16, 253–256. (In Chinese) [Google Scholar]
  58. Zheng, Y.; Zhong, J.; Chen, X.; Lin, D.; Zhao, G.; Zhang, S.; Jiang, Q. Influence of drowning on survival of Oncomelania. Chin. J. Schistosomiasis Control 2002, 14, 46–48. (In Chinese) [Google Scholar]
  59. Lv, D.; Jiang, Q.; Wang, T. Research progress on the effects of drowning on the survival and reproduction of Oncomelania hupensis. Chin. J. Parasit. Dis. Control 2004, 17, 61–62. (In Chinese) [Google Scholar]
  60. Ross, A.G.; Sleigh, A.C.; Li, Y.; Davis, G.M.; Williams, G.M.; Jiang, Z.; Feng, Z.; McManus, D.P. Schistosomiasis in the People’s Republic of China: Prospects and challenges for the 21st century. Clin. Microbiol. Rev. 2001, 14, 270–295. [Google Scholar] [CrossRef] [Green Version]
  61. Liu, A.M. Research on the diffusion law of Oncomelania along with the flow through a side-weir. Open Biomed. Eng. J. 2014, 8, 160–165. [Google Scholar] [CrossRef]
  62. Gao, F.; Zhang, S.; Wang, T.; He, J.; Xu, X.; Li, T.; Zhang, G.; Wang, H. Endemic status of schistosomiasis in Anhui Province in 2016. J. Trop. Dis. Parasitol. 2017, 15, 125–130. [Google Scholar] [CrossRef]
  63. Kloos, H. Human behavior, health education and schistosomiasis control: A review. Soc. Sci. Med. 1995, 40, 1497–1511. [Google Scholar] [CrossRef]
  64. Munisi, D.Z.; Buza, J.; Mpolya, E.A.; Angelo, T.; Kinung’hi, S.M. Knowledge, attitude, and practices on intestinal schistosomiasis among primary schoolchildren in the Lake Victoria basin, Rorya District, north-western Tanzania. BMC Public Health 2017, 17, 731. [Google Scholar] [CrossRef] [Green Version]
  65. Mwanga, J.R.; Kaatano, G.M.; Siza, J.E.; Chang, S.Y.; Ko, Y.; Kullaya, C.M.; Nsabo, J.; Eom, K.S.; Yong, T.S.; Chai, J.Y.; et al. Improved perceptions and practices related to schistosomiasis and intestinal worm infections following PHAST intervention on Kome Island, North-Western Tanzania. Korean J. Parasitol. 2015, 53, 561–569. [Google Scholar] [CrossRef] [Green Version]
  66. Sun, L.P.; Wang, W.; Hong, Q.B.; Li, S.Z.; Liang, Y.S.; Yang, H.T.; Zhou, X.N. Approaches being used in the national schistosomiasis elimination programme in China: A review. Infect. Dis. Poverty 2017, 6, 55. [Google Scholar] [CrossRef] [Green Version]
  67. Liu, X.; Ma, Y.; Wang, F. Effect of health education on schistosomiasis control in fishmen and boatmen. Chin. J. Schistosomiasis Control 2009, 21, 424–425. (In Chinese) [Google Scholar]
  68. Liu, R.; Dong, H.-F.; Guo, Y.; Zhao, Q.-P.; Jiang, M.-S. Efficacy of praziquantel and artemisinin derivatives for the treatment and prevention of human schistosomiasis: A systematic review and meta-analysis. Parasites Vectors 2011, 4, 201. [Google Scholar] [CrossRef] [Green Version]
  69. Yu, Q.F.; Zhang, J.Y.; Sun, M.T.; Gu, M.M.; Zou, H.Y.; Webster, J.P.; Lu, D.B. In vivo praziquantel efficacy of Schistosoma japonicum over time: A systematic review and meta-analysis. Acta Trop. 2021, 222, 106048. [Google Scholar] [CrossRef]
  70. Lv, S.; Lv, C.; Li, Y.L.; Xu, J.; Hong, Q.B.; Zhou, J.; Zhang, J.F.; Wen, L.Y.; Zhang, J.F.; Zhang, S.Q.; et al. Expert consensus on the strategy and measures to interrupt the transmission of schistosomiasis in China. Chin. J. Schistosomiasis Control 2021, 33, 10–14. (In Chinese) [Google Scholar] [CrossRef]
  71. Zhou, Y.; Liu, Y.; Wu, W. Strengthen China’s flood control. Nature 2016, 536, 396. [Google Scholar] [CrossRef] [Green Version]
  72. Utzinger, J.; Bergquist, R.; Shu-Hua, X.; Singer, B.H.; Tanner, M. Sustainable schistosomiasis control—The way forward. Lancet 2003, 362, 1932–1934. [Google Scholar] [CrossRef]
  73. Knight, M.; Wu, J.-Y.; Zhou, Y.-B.; Chen, Y.; Liang, S.; Li, L.-H.; Zheng, S.-B.; Zhu, S.-P.; Ren, G.-H.; Song, X.-X.; et al. Three Gorges Dam: Impact of water level changes on the density of schistosome-transmitting snail Oncomelania hupensis in Dongting Lake area, China. PLOS Negl. Trop. Dis. 2015, 9, e0003882. [Google Scholar] [CrossRef] [Green Version]
  74. Steinmann, P.; Keiser, J.; Bos, R.; Tanner, M.; Utzinger, J. Schistosomiasis and water resources development: Systematic review, meta-analysis, and estimates of people at risk. Lancet Infect. Dis. 2006, 6, 411–425. [Google Scholar] [CrossRef]
  75. Zhou, Q.; Wan, L.; Hang, D.; You, Q.; You, J.; Zhang, Y.; Zhu, Z.; Huang, Y. Effect of water conservancy schistosomiasis control projects combined with molluscicide to control Oncomelania hupensis snails in rivers connecting with Yangtze River in Pukou District, Nanjing City. Chin. J. Schistosomiasis Control 2017, 29, 695–699. (In Chinese) [Google Scholar] [CrossRef]
  76. King, C.H.; Sturrock, R.F.; Kariuki, H.C.; Hamburger, J. Transmission control for schistosomiasis—Why it matters now. Trends Parasitol. 2006, 22, 575–582. [Google Scholar] [CrossRef]
  77. Rollinson, D.; Knopp, S.; Levitz, S.; Stothard, J.R.; Tchuem Tchuente, L.A.; Garba, A.; Mohammed, K.A.; Schur, N.; Person, B.; Colley, D.G.; et al. Time to set the agenda for schistosomiasis elimination. Acta Trop. 2013, 128, 423–440. [Google Scholar] [CrossRef]
  78. Brooker, S.; Michael, E. The potential of geographical information systems and remote sensing in the epidemiology and control of human helminth infections. Adv. Parasitol. 2000, 47, 245–288. [Google Scholar]
  79. Yang, G.J.; Vounatsou, P.; Utzinger, M.T.X.Z.J. Remote sensing for predicting potential habitats of Oncomelania hupensis in Hongze, Baima and Gaoyou lakes in Jiangsu province, China. Geospat. Health 2006, 1, 85–92. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  80. Yang, G.J.; Vounatsou, P.; Zhou, X.N.; Utzinger, J.; Tanner, M. A review of geographic information system and remote sensing with applications to the epidemiology and control of schistosomiasis in China. Acta Trop. 2005, 96, 117–129. [Google Scholar] [CrossRef]
  81. Shi, Y.; Qiu, J.; Li, R.; Shen, Q.; Huang, D. Identification of Potential High-Risk Habitats within the Transmission Reach of Oncomelania hupensis after Floods Based on SAR Techniques in a Plane Region in China. Int. J. Environ. Res. Public Health 2017, 14, 986. [Google Scholar] [CrossRef] [Green Version]
  82. Zhang, L.; Zhu, H.; Wang, Q.; Lv, S.; Xu, J.; Li, S. Assessment of schistosomiasis transmission risk along the Yangtze River basin after the flood disaster in 2020. Chin. J. Schistosomiasis Control 2020, 32, 464–468. (In Chinese) [Google Scholar] [CrossRef]
  83. Xia, S.; Xue, J.; Gao, F.; Lv, S.; Xu, J.; Zhang, S.; Li, S. Sentinel-1A radar remote sensing-based modeling for quick identification of potential risk areas of schistosomiasis transmission after flood. Chin. J. Parasitol. Parasit. Dis. 2020, 38, 417–422. (In Chinese) [Google Scholar] [CrossRef]
  84. Xue, J.-B.; Wang, X.-Y.; Zhang, L.-J.; Hao, Y.-W.; Chen, Z.; Lin, D.-D.; Xu, J.; Xia, S.; Li, S.-Z. Potential impact of flooding on schistosomiasis in Poyang Lake regions based on multi-source remote sensing images. Parasites Vectors 2021, 14, 16. [Google Scholar] [CrossRef]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Guo, S.-Y.; Li, L.; Zhang, L.-J.; Li, Y.-L.; Li, S.-Z.; Xu, J. From the One Health Perspective: Schistosomiasis Japonica and Flooding. Pathogens 2021, 10, 1538. https://doi.org/10.3390/pathogens10121538

AMA Style

Guo S-Y, Li L, Zhang L-J, Li Y-L, Li S-Z, Xu J. From the One Health Perspective: Schistosomiasis Japonica and Flooding. Pathogens. 2021; 10(12):1538. https://doi.org/10.3390/pathogens10121538

Chicago/Turabian Style

Guo, Su-Ying, Lu Li, Li-Juan Zhang, Yin-Long Li, Shi-Zhu Li, and Jing Xu. 2021. "From the One Health Perspective: Schistosomiasis Japonica and Flooding" Pathogens 10, no. 12: 1538. https://doi.org/10.3390/pathogens10121538

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop