Open Access

An integrated environmental improvement of marshlands: impact on control and elimination of schistosomiasis in marshland regions along the Yangtze River, China

Contributed equally
Infectious Diseases of Poverty20176:72

https://doi.org/10.1186/s40249-017-0287-1

Received: 19 January 2017

Accepted: 15 March 2017

Published: 22 March 2017

Abstract

Background

Schistosomiasis is a global snail-transmitted infectious disease of poverty. Transmission control had been achieved in China in 2015 after the control efforts for over 60 years. Currently, the remaining core regions endemic for Schistosoma japonicum are mainly located in the marshland and lake regions along the Yangtze River basin.

Methods

During the period from 2001 through 2015, an integrated environmental improvement of the marshlands was carried out through the implementation of industrial, agricultural and resources development projects in Yizheng County along the Yangtze River. S. japonicum infection in humans, livestock and snails was estimated by serology, stool examination, hatching technique and microscopy during the 15-year study period to evaluate the effect of the integrated environmental improvement on control and elimination of schistosomiasis.

Results

A 0.05% overall rate of S. japonicum infection was observed in snails during the 15-year study period, and no infected snails were detected since 2012. The overall prevalence of S. japonicum infection was 0.09% in humans during the study period, and no human infection was found since 2012. In addition, only 13 bovines were identified with S. japonicum infection in 2003 during the 15-year study period, and since 2004, no infection was found in livestock.

Conclusion

The results of the present study demonstrate that the implementation of industrial, agricultural and water resources development projects, not only alters snail habitats in marshland regions, and promotes local economic development, which appears a win-to-win strategy to block the transmission of S. japonicum and accelerate socio-economic development along the Yangtze River.

Keywords

Schistosomiasis Oncomelania hupensis Environmental improvement Marshland regions Yangtze River basin China

Multilingual abstracts

Please see Additional file 1 for translations of the abstract into the six official working languages of the United Nations.

Background

Schistosomiasis, caused by the blood fluke of the genus Schistosoma, is a snail-transmitted infectious disease of poverty that ranks second only to malaria in terms of morbidity and mortality among tropical parasitic diseases [13]. In China, schistosomiasis was once endemic in 453 counties of 12 provinces south of the Yangtze River [46]. According to the environmental ecosystems and snail habitats, schistosomiasis-endemic regions are classified into three types in China, including marshland and lake regions, plain regions with waterway network, and hilly and mountainous regions [7], and a “infection control-transmission control-transmission interruption-elimination” four-stage roadmap has been developed [810]. Since the initiation of the national schistosomiasis control program at early 1950s [1113], schistosomiasis control has been given a high priority in China [14, 15], and multiple integrated strategies have been proposed according to the epidemiological profile and intensity of transmission, which have resulted in a great success in schistosomiasis control in the country [16]. Notably, an integrated strategy with emphasis on infectious source control was developed in 2004 [17], and the wide implementation of the strategy results in a huge reduction in S. japonicum infection in humans, livestock and snails in China [1832]. By 2015, transmission control of schistosomiasis has been achieved across the country [33], indicating less than 1% S. japonicum infection in both humans and livestock, no local acute infections, and no infected snails for successive 2 years throughout the country [3436].

Currently, the remaining core regions endemic for S. japonicum are mainly located in the marshland and lake regions along the Yangtze River basin [37]. Oncomelania hupensis, the intermediate host of S. japonicum, is widely distributed in the shores of rivers and lakes along the middle and lower reaches of the Yangtze River [38], and the marshland is characterized by “land in winter, water in summer” due to seasonal tide, which provides an ideal environment for snail growth and reproduction [3941]. In addition, there are a huge number of livestock [42, 43] and a variety of wild animals on the marshland [44], and plenty of boatmen and fishermen living along the marshlands frequently contact with S. japonicum-infested water [4547], which complicate the control efforts, and result in frequent resurgence of schistosomiasis in the marshland regions of China [40]. Completely blocking the transmission of S. japonicum in the marshland regions is therefore critical to and it has become the primary task for elimination of schistosomiasis in China [48].

In order to effectively control the transmission of S. japonicum in the marshland regions, multiple integrated interventions have been developed, which are based on inter-sectoral collaboration between governmental departments from agriculture, health, water resource development, forestry, and land and resources [49]. The optimization and combination of these integrated strategies has been proved to greatly facilitate the progress towards the elimination of schistosomiasis in China [5052]. Previous studies have demonstrated that a thorough and integrated modification of the snail habitats is required in order to completely block the transmission of S. japonicum in the marshland regions [5355].

Since 2001, industrial development was initiated in Yizheng County along the Yangtze River, and an integrated environmental improvement was simultaneously performed targeting the marshland outside the embankment. In the current study, we evaluated the effect of this integrated environmental improvement of the marshlands on control and elimination of schistosomiasis in marshland regions of Yizheng County along the Yangtze River, China, from 2001 to 2015.

Methods

Study site

Yizheng County is located on the north bank of the lower reaches of the Yangtze River basin, which covers an area of 901 km2, and has a population of 600 thousand. Currently, there are 5 out of 12 townships and 31 out of 149 villages endemic for S. japonicum, with 260 thousand people at risk of infection. There are 12.6 thousand accumulated schistosomiasis cases, 1.79 thousand accumulated infected bovines, and accumulated snail habitats of about 9.14 km2 detected in Yizheng County.

Integrated environmental improvements of marshlands

Based on the epidemiological profile of the marshland regions, an integrated environmental improvement of the marshlands were carried out in Yizheng County through the implementation of industrial development projects from 2001 to 2004, and agricultural and water resources development projects conducted between 2005 and 2011. Three projects were implemented for industrial development. (1) Building boat factories. Firstly, all wild trees and grasses were cleaned on the marshland, and the snail habitats were given molluscicide treatment. Then, the soil containing snails was deeply buried with river sand, and the marshland was made flat. Finally, boat factories were built on the marshland, and tap-water treatment systems and public latrines with three-cell septic tanks were constructed. (2) Building docks and harbors. The wild trees and grasses were cleaned on the marshland, and docks and harbors were built with concrete. (3) Building ecological parks. The marshland was subjected to environmental improvement, and ornamental plants were grown in high-elevation marshlands, while fish was raised in low-elevation marshlands to ensure no snail survival in the ecological parks.

Agricultural development projects consisted of land reclamation and planting, aquatic product breeding, and building trees. (1) Land reclamation and planting. Wild trees and reeds were cleaned from high-elevation marshlands, which were then subjected to mechanized plough and molluscicide treatment. Economic crops were planted each year during the non-flood period, such as wheat and rape. (2) Aquatic product breeding. Fish ponds were constructed in low-elevation marshlands to breed aquatic products, such as fish and shrimp. (3) Building trees. Populus nigra was grown in marshlands that were not suitable for land reclamation and planting, and aquatic product breeding after reeds were removed, to achieve environmental improvement of the snail habitats.

Water resources development projects consisted of hardening river banks with concrete, building sluices for prevention of snail spread and construction of snail-retention pools to allow no snail entry into ditches.

The gross national product (GNP) and output values due to industrial, agricultural and water resources development were collected in Yizheng County during the study period from 2001 through 2015, and the proportion of the output values of economic development in GNP was estimated each year.

Effect of the integrated environmental improvements on schistosomiasis elimination

During the period from 2001 to 2015, the study villages were selected from Yizheng County using the clustering sampling method [56]. Briefly, the 31 endemic villages were classified into three types (low, moderate and high) according to the endemicity, and two villages were randomly selected from each type. All residents living in the selected villages were identified for S. japonicum infection by using serological screening followed by stool examinations. The individuals were detected for specific IgG antibodies against S. japonicum with a dipstick dye immunoassay (DDIA) during the schistosomiasis non-transmission period [5759], and then all seropositives received a miracidium hatching test (3 individual hatches read blind, of 50 grams faces per hatching) [60]. The annual rate of human S. japonicum infection was estimated using the following formula: rate of human S. japonicum infection (%) = No. of egg-positives/No. of residents examined × 100%. Acute schistosomiasis was diagnosed based on the following criteria: (1) A history of contact with S. japonicum-infested water during the past 2 weeks to 3 months; (2) presence of fever, hepatomegaly and peripheral blood eosinophilia, complicated by splenomegaly, cough, liver tenderness, abdominal distension or diarrhea; and (3) detection of S. japonicum egg or miracidium [61].

At spring and autumn of each year, all livestock were detected for S. japonicum infection with a miracidium hatching test [62], and the prevalence of S. japonicum infection was calculated in livestock.

At spring each year, snail survey was performed in ditches inside the embankment and in marshlands outside the embankment using a systematic method [38]. A snail collection device, measuring 0.1 m2, was placed every 5 (in ditches) or 15 m (in marshlands) along the survey line. All snails within the device were captured, transferred to laboratory and identified for S. japonicum infection under a microscope. The area of snail habitats and infected snail habitats was recorded, and the rate of S. japonicum infection in snails was estimated.

Ethical consideration

This study was approved by the Ethical Review Committee of Jiangsu Institute of Parasitic Diseases (permission number: IRB00001037). Animal experiments were done following the Guidelines for the Care and Use of Laboratory Animals, and signed informed consent was obtained from all subjects participating in the study.

Data management and analysis

All data were processed and analyzed in Microsoft Excel version 2007 (Microsoft Corporation; Redmond, WA, USA).

Results

Implementation of integrated environmental improvements of marshlands

During the period from 2001 through 2015, integrated environmental improvements were implemented in marshlands outside the embankment of Yizheng County, with a total area of 4.95 km2. The rate of environmental improvement appeared a rise over the study period, and was 90% in 2015 (Table 1, Fig. 1). By 2015, there were only 6 marshlands covering an area of 0.55 km2 that remained to be improved, consisting of 10% of the total marshlands outside the embankment (Fig. 2).
Table 1

Integrated improvements of marshlands in Yizheng County along the Yangtze River during the period from 2001 through 2015

Year

Status of integrated control

Rate of marshlands with integrated improvements in all marshlands (%)

Interventions

Integrated improvements of marshlands at local year (km2)

Marshlands with integrated improvements (km2)

Marshlands without integrated improvements (km2)

2001

Building factory and trees

0.22

0.22

5.28

4

2002

Building factory and burying snails with river sand

0.67

0.89

4.61

16.18

2003

Building factory and burying snails with river sand

2

2.89

2.61

52.55

2004

Building factory and burying snails with river sand

1.33

4.22

1.28

76.73

2005

Building fish ponds

0.42

4.64

0.86

84.36

2006

None

0

4.64

0.86

8436

2007

Building docks

0.03

4.67

0.83

84.91

2008

Building ecological parks

0.19

4.86

0.64

88.36

2009

None

0

4.86

0.64

88.36

2010

Plough and planting

0.08

4.94

0.56

89.82

2011

Building docks

0.01

4.95

0.55

90

2012

None

0

4.95

0.55

90

2013

None

0

4.95

0.55

90

2014

None

0

4.95

0.55

90

2015

None

0

4.95

0.55

90

Fig. 1

Annual area of the marshlands with and without integrated environmental improvements in Yizheng County along the Yangtze River from 2001 to 2015

Fig. 2

Constitution of interventions implemented for the integrated environmental improvements of marshlands in Yizheng County along the Yangtze River from 2001 to 2015

During the period from 2001 to 2015, a total of 15 marshlands outside the embankment were subjected to industrial development, which covered an area of 4.12 km2 and consisted of 74.91% of the total marshlands, and there were 3.75 (68.18%), 0.03 (0.55%), 0.15 (2.73%) and 0.19 km2 marshlands (3.45%) used for building boat factories, docks, harbors and ecological parks, respectively (Fig. 2). Agricultural development was conducted in 4 marshlands, which covered an area of 0.84 km2 and consisted of 15.27% of the total marshlands, and there were 0.39 (7.09%), 0.26 (4.73%) and 0.19 km2 marshlands (3.45%) with land reclamation and planting, aquatic product breeding, and trees building, respectively (Table 1, Fig. 2). In addition, 6 river banks were hardened with concrete with 4.87 km in length, and 6 sluices/snail-retention pools were built.

During the 15-year study period, the total output values due to industrial, agricultural and water resources development consisted of 44.23% of the total GNP in Yizheng Country from 2001 through 2015, and the rate of the output values of economic development in the total GNP appeared a tendency towards a rise between 2001 and 2012 (Table 2).
Table 2

Proportion of the output values of economic development in GNP in Yizheng County from 2001 to 2015

Year

GNP in Yizheng County (Billion Yuan)

Output values of industrial, agricultural and water resources development (Billion Yuan)

Proportion of the output values of economic development in GNP (%)

2001

5.67

1.86

32.8

2002

6.11

2.2

36.01

2003

7.17

3.35

46.72

2004

8.81

4.73

53.69

2005

10.6

6.13

57.83

2006

13.01

7.52

57.8

2007

16.25

8.98

55.26

2008

20.06

9.12

45.46

2009

22.73

12.3

54.11

2010

27.82

16.7

60.03

2011

33.35

24.3

72.86

2012

37.02

25.5

68.88

2013

41.02

11.16

27.21

2014

45.45

10.15

22.33

2015

50.2

8.71

17.35

Total

345.27

152.71

44.23

S. japonicum infection in snails

During the period from 2001 to 2015, a total of 72 095 snails were captured and examined for S. japonicum infection, and 34 snails were identified with infection, with a 0.05% overall infection rate observed. Since 2007, no infected snails were detected (Fig. 3). In addition, a total of 11.09 km2 snail habitats were identified during the 15-year study period. During the first 7 years of the integrated control, snail habitats were rapidly shrunk, and the area of snail habitats reduced by 80.47% in 2007 relative to 2001, with an annual decline of 13.41%. Since 2012, no snails were found. A total of 0.52 km2 infected snail habitats were identified from 2001 to 2015, and 98.08% were detected between 2002 and 2005. Since 2007, no infected snail habitats were found (Table 3).
Fig. 3

Annual rate of S. japonicum infection in humans, livestock and snails in Yizheng County along the Yangtze River from 2001 to 2015

Table 3

Results of snail survey in Yizheng County along the Yangtze River during the period from 2001 through 2015

Year

Snail survey (km2)

Area of snail habitats (km2)

S. japonicum infection in snails

Area of infected snail habitats (km2)

Outside embankment

Inside embankment

No. snails examined

Infection in snails (%)

2001

16.8

1.87

0.05

9464

0

0

2002

16.8

1.89

0.06

11955

0.03

0.02

2003

16.8

1.79

0.1

14175

0.12

0.16

2004

16.82

1.59

0.13

12177

0.07

0.24

2005

16.82

1.59

0.13

11938

0.02

0.09

2006

16.82

0.72

0.14

2445

0.12

0.01

2007

16.82

0.37

0.005

4342

0

0

2008

16.82

0.17

0.005

849

0

0

2009

9.14

0.14

0.009

1111

0

0

2010

9.14

0.15

0.008

2287

0

0

2011

9.14

0.16

0.009

1352

0

0

2012

9.14

0

0

0

0

0

2013

9.14

0

0

0

0

0

2014

9.14

0

0

0

0

0

2015

9.14

0

0

0

0

0

S. japonicum infection in humans and livestock

From 2001 to 2015, a total of 316 290 residents were detected for S. japonicum infection, and 276 individuals were identified with infections, with a 0.09% overall prevalence of S. japonicum infection. Most of the human S. japonicum infection was detected in the first 4 years of the integrated control between 2001 and 2004, which consisted of 88.77% of the total infections. No human infection was found since 2012 (Fig. 3). In addition, there were 122 acute infections identified during the 15-year study period, and all cases were detected between 2001 and 2004. Since 2005, no acute infection was observed (Fig. 4).
Fig. 4

Annual number of acute human S. japonicum infection in Yizheng County along the Yangtze River from 2001 to 2015

During the 15-year study period, a total of 15583 livestock were detected for S. japonicum infection, and only 13 bovines were identified with infection in 2003. Since 2004, no S. japonicum infection was found in livestock (Fig. 3).

Following 5-year integrated environmental improvements of the marshlands, infection control was achieved in Yizheng County in 2005, and transmission control was achieved in 2007. In addition, the transmission of S. japonicum has been interrupted in the county since 2013.

Discussion

Previous studies have demonstrated that elimination of the source of S. japonicum infection or the intermediate host snail is the key intervention leading to interruption of schistosomiasis transmission [63]. However, the source of S. japonicum infection is difficult to be eliminated in marshland regions since (1) A variety of wild animals, which may serve as reservoir hosts for S. japonicum, are living in marshlands, which complicate the control efforts [44]; (2) The massive marshlands are ideal sites for the gathering of livestock [42]; and (3) A large number of mobile boatmen and fishermen are living and working along the Yangtze River, which increases the risk of importation of infectious sources [4547]. In addition, the extensive snail dispersal due to flooding, and the high reproduction rate of residual snails result in a low possibility for elimination of snails from the marshland regions [39].

In this study, the integrated environmental improvements of the marshland regions experienced a long period of time, which may be classified into early- (environmental modification), intermediate- (building factory), and late-stages (surveillance). At the early stage, a large number of workers lived and worked in the marshlands which had a high risk of S. japonicum, and acute infection easily occurred. Our data showed a total of 122 acute cases during the period between 2001 and 2004, suggesting that individual protection is required for workers on the marshlands. At the intermediate stage, workers were busy in building factories, and had a reduction in the frequency to contact with infested water, resulting in a decline in human S. japonicum infection. Therefore, management of human feces and provision of access to safe water is required at this stage. At the late stage, the monitoring of S. japonicum infection in newly recruited workers should be strengthened to consolidate the control achievements, since no local source of S. japonicum infection was detected. Following 15-year integrated control, there were 10% of the total marshland that remained to be developed, and reeds are predominant vegetations on these marshlands, which are potential snail habitats and potential threat to resurgence of schistosomiasis. The surveillance and control of snails on the remaining marshlands without integrated improvements is required to consolidate the control efforts. In addition, the monitoring of external sources of S. japonicum infection should be strengthened to prevent the importation of mobile sources of S. japonicum infection from the Yangtze River, so as to achieve the elimination of schistosomiasis.

During the 15-year study period from 2001 through 2015, the total output values due to economic development consisted of 44.23% of the total GNP in the study site, and the rate of the output values of economic development in the total GNP showed an increasing tendency between 2001 and 2012. Our data demonstrate that the industrial, agricultural and water resources development projects facilitate local economic development in Yizheng County, and achieve complete improvements of snail habitats on the marshlands. The integrated environmental improvements of marshlands resulted in a rapid transfer from a hyper-endemic region to transmission interruption of schistosomiasis, and elimination of this infectious disease of poverty as a public health concern in Yizheng County. This strategy may provide new insights into the elimination of schistosomiasis in developing countries.

Our study has a limitation that no parallel control was designed. During the study period, the National Mid- and Long-term Plan for the Prevention and Control of Schistosomiasis in China (2004–2015) was implemented in the study site [17], which increased the difficulty to assign a parallel control. However, our data indicated the integrated environmental improvements of marshlands played a leading role in the control and elimination of schistosomiasis in Yizheng County. In addition, the Three Gorges Dam was operated during the study period [64], which may positively or negatively affect the progress towards the elimination of schistosomiasis in the middle and lower reaches of the Yangtze River [65]. The changes of water levels caused by the Three Gorges Dam operation result in the extension of the duration of marshland exposure, which may increase the humans and livestock activities on marshlands. This may increase the risk of schistosomiasis transmission. However, the effective regulation of the water levels by the Dam may reduce the anti-flood pressure in the lower reaches of the Yangtze River, and previously non-utilized marshlands may be gradually developed. Our findings also showed that the integrated environmental improvements of marshlands achieved double benefits of promoting local economic development and eliminating schistosomiasis.

Conclusions

The results of the present study demonstrate that the integrated environmental improvement of marshlands through the implementation of industrial, agricultural and water resources development projects, not only alters snail habitats in marshland regions, and promotes local economic development, which appears a win-to-win strategy to block the transmission of S. japonicum and accelerate socio-economic development along the Yangtze River. Our findings provide new insights into the development of strategies for transmission interruption and elimination of schistosomiasis in developing countries.

Abbreviations

DDIA: 

Dipstick dye immunoassay

GNP: 

Gross national product

Declarations

Acknowledgements

We would like to express our sincere thanks to the staff working in the Department of Schistosomiasis, Parasitic Diseases and Endemic Diseases, Yizheng County Center for Disease Control and Prevention for their kind help in the field work.

Funding

This study was supported by the grants from the National Science & Technology Pillar Program of China (grant no. 2009BAI78B07), Jiangsu Provincial Department of Science and Technology (grant no. BL2014021), Jiangsu Provincial Young Talents in Medical Sciences (grant no. QNRC2016621) and Jiangsu Department of Health (grant nos. X201408 and X201410).

Availability of data and materials

All data presented in the study can be accessed in Yizheng County Center for Disease Control and Prevention, China.

Authors’ contributions

LPS, YSL and WW conceived and designed the study. HTY provided kind comments on the implementation of the study, and revision of the manuscript. LPS, YPZ, ZQZ, QBH, GJY and HRZ performed the field experiments. LPS collected and analyzed the data. LPS prepared the first version of the manuscript. WW revised and finalized the manuscript. All authors read and approved the final version of the manuscript.

Competing interests

The authors declare no competing interests.

Consent for publication

All authors provided consent for publication.

Ethics approval and consent to participate

This study was approved by the Ethical Review Committee of Jiangsu Institute of Parasitic Diseases (permission number: IRB00001037). Animal experiments were done following the Guidelines for the Care and Use of Laboratory Animals, and signed informed consent was obtained from all subjects participating in the study.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Key Laboratory of National Health and Family Planning Commission on Parasitic Disease Control and Prevention
(2)
Jiangsu Provincial Key Laboratory on Parasites and Vector Control Technology
(3)
Jiangsu Institute of Parasitic Diseases
(4)
Yangzhou Municipal Center for Disease Control and Prevention
(5)
Yizheng County Center for Disease Control and Prevention

References

  1. Colley DG, Bustinduy AL, Secor WE, King CH. Human schistosomiasis. Lancet. 2014;383:2253–64.View ArticlePubMedPubMed CentralGoogle Scholar
  2. Bhutta ZA, Sommerfeld J, Lassi ZS, Salam RA, Das JK. Global burden, distribution, and interventions for infectious diseases of poverty. Infect Dis Poverty. 2014;3:21.View ArticlePubMedPubMed CentralGoogle Scholar
  3. Ross AG, Bartley PB, Sleigh AC, Olds GR, Li Y, Williams GM, McManus DP. Schistosomiasis. N Engl J Med. 2002;346:1212–20.View ArticlePubMedGoogle Scholar
  4. Chen MG. Assessment of morbidity due to Schistosoma japonicum infection in China. Infect Dis Poverty. 2014;3:6.View ArticlePubMedPubMed CentralGoogle Scholar
  5. Zhou XN, Wang LY, Chen MG, Wu XH, Jiang QW, Chen XY, Zheng J, Utzinger J. The public health significance and control of schistosomiasis in China--then and now. Acta Trop. 2005;96:97–105.View ArticlePubMedGoogle Scholar
  6. Utzinger J, Zhou XN, Chen MG, Bergquist R. Conquering schistosomiasis in China: the long march. Acta Trop. 2005;96:69–96.View ArticlePubMedGoogle Scholar
  7. Zhou XN, Guo JG, Wu XH, Jiang QW, Zheng J, Dang H, Wang XH, Xu J, Zhu HQ, Wu GL, Li YS, Xu XJ, Chen HG, Wang TP, Zhu YC, Qiu DC, Dong XQ, Zhao GM, Zhang SJ, Zhao NQ, Xia G, Wang LY, Zhang SQ, Lin DD, Chen MG, Hao Y. Epidemiology of schistosomiasis in the People’s Republic of China, 2004. Emerg Infect Dis. 2007;13:1470–6.View ArticlePubMedPubMed CentralGoogle Scholar
  8. Yan J, Hu Tao, Lei ZL. The endemic situation and challenges of major parasitic diseases in China. Chin J Parasitol Parasit Dis. 2015;33:412-7. (in Chinese).Google Scholar
  9. Spear RC, Seto EY, Carlton EJ, Liang S, Remais JV, Zhong B, Qiu D. The challenge of effective surveillance in moving from low transmission to elimination of schistosomiasis in China. Int J Parasitol. 2011;41:1243–7.View ArticlePubMedPubMed CentralGoogle Scholar
  10. Gray DJ, Li YS, Williams GM, Zhao ZY, Harn DA, Li SM, Ren MY, Feng Z, Guo FY, Guo JG, Zhou J, Dong YL, Li Y, Ross AG, McManus DP. A multi-component integrated approach for the elimination of schistosomiasis in the People’s Republic of China: design and baseline results of a 4-year cluster-randomised intervention trial. Int J Parasitol. 2014;44:659–68.View ArticlePubMedGoogle Scholar
  11. Xu J, Steinman P, Maybe D, Zhou XN, Lv S, Li SZ, Peeling R. Evolution of the national schistosomiasis control programmes in the People’s Republic of China. Adv Parasitol. 2016;92:1–38.View ArticlePubMedGoogle Scholar
  12. Collins C, Xu J, Tang S. Schistosomiasis control and the health system in P.R. China. Infect Dis Poverty. 2012;1:8.View ArticlePubMedPubMed CentralGoogle Scholar
  13. Wang W, Dai JR, Liang YS. Apropos: factors impacting on progress towards elimination of transmission of schistosomiasis japonica in China. Parasit Vectors. 2014;7:408.View ArticlePubMedPubMed CentralGoogle Scholar
  14. McManus DP, Gray DJ, Li Y, Feng Z, Williams GM, Stewart D, Rey-Ladino J, Ross AG. Schistosomiasis in the People’s Republic of China: the era of the Three Gorges Dam. Clin Microbiol Rev. 2010;23:442–66.View ArticlePubMedPubMed CentralGoogle Scholar
  15. Zhu H, Yap P, Utzinger J, Jia TW, Li SZ, Huang XB, Cai SX. Policy support and resources mobilization for the national schistosomiasis control programme in the People’s Republic of China. Adv Parasitol. 2016;92:341–83.View ArticlePubMedGoogle Scholar
  16. Xu J, Xu JF, Li SZ, Zhang LJ, Wang Q, Zhu HH, Zhou XN. Integrated control programmes for schistosomiasis and other helminth infections in P.R. China. Acta Trop. 2015;141:332–41.View ArticlePubMedGoogle Scholar
  17. Wang LD, Chen HG, Guo JG, Zeng XJ, Hong XL, Xiong JJ, Wu XH, Wang XH, Wang LY, Xia G, Hao Y, Chin DP, Zhou XN. A strategy to control transmission of Schistosoma japonicum in China. N Engl J Med. 2009;360:121–8.View ArticlePubMedGoogle Scholar
  18. Wang LD, Guo JG, Wu XH, Chen HG, Wang TP, Zhu SP, Zhang ZH, Steinmann P, Yang GJ, Wang SP, Wu ZD, Wang LY, Hao Y, Bergquist R, Utzinger J, Zhou XN. China’s new strategy to block Schistosoma japonicum transmission: experiences and impact beyond schistosomiasis. Trop Med Int Health. 2009;14:1475–83.View ArticlePubMedGoogle Scholar
  19. Wang X, Wang W, Wang P. Long-term effectiveness of the integrated schistosomiasis control strategy with emphasis on infectious source control in China: a 10-year evaluation from 2005 to 2014. Parasitol Res. 2016; in press.Google Scholar
  20. Liu R, Dong HF, Jiang MS. The new national integrated strategy emphasizing infection sources control for schistosomiasis control in China has made remarkable achievements. Parasitol Res. 2013;112:1483–91.View ArticlePubMedGoogle Scholar
  21. Qian YL, Wang W, Hong QB, Liang YS. Bibliometric analysis of literature regarding integrated schistosomiasis control strategy with emphasis on infectious source control. Chin J Schisto Control. 2014;26:626–31 (in Chinese).Google Scholar
  22. Chen HG, Zeng XJ, Xiong JJ, Jiang WS, Hong XL, Hu SZ, Guo JG. Study on comprehensive schistosomiasis control strategy with emphasis on infectious source control in Poyang Lake areas. Chin J Schisto Control. 2009;21:243–9 (in Chinese).Google Scholar
  23. Yi DH, Yi P, Liu ZC, Li YS, Quan MZ, Xiao SY. Practice and thought of schistosomiasis contorl with emphasis on control sources of infection in Dongting Lake area. Chin J Schisto Control. 2009;21:161–4 (in Chinese).Google Scholar
  24. Zhu SP, Li SM, Wei CJ, Yang QY, Lu BK, Liao YZ, Chen JA, Jia TW. Evaluation of schistosomiasis control effect of buffalo removal in Anxiang County. Chin J Schisto Control. 2011;23:546–50 (in Chinese).Google Scholar
  25. Hong XC, Xu XJ, Chen X, Li YS, Yu CH, Yuan Y, Chen YY, Li RD, Qiu J, Liu ZC, Yi P, Ren GH, He HB. Assessing the effect of an integrated control strategy for schistosomiasis japonica emphasizing bovines in a marshland area of Hubei Province, China: a cluster randomized trial. PLoS Negl Trop Dis. 2013;7:e2122.View ArticlePubMedPubMed CentralGoogle Scholar
  26. Chen YY, Liu JB, Huang XB, Cai SX, Su ZM, Zhong R, Zou L, Miao XP. New integrated strategy emphasizing infection source control to curb Schistosomiasis japonica in a marshland area of Hubei Province, China: findings from an 8-year longitudinal survey. PLoS ONE. 2014;9:e89779.View ArticlePubMedPubMed CentralGoogle Scholar
  27. Yang K, Li HJ, Yang WC, Shi XW, Qi YL. Effect of comprehensive schistosomiasis control measures with emphasis on infectious source control in dam areas of mountainous region, Yunnan Province. Chin J Schisto Control. 2009;21:272–75. in Chinese.Google Scholar
  28. Chen SR, Li BG, Luo JJ, Li WB, Mu LX, Tian SH, Li P, Liu YH, Yang H, Wang SW, Chen F, Luo BR, Li KR, Duan YC. Effect of comprehensive schistosomiasis control measures based on infection source control in mountainous areas of Yunnan Province. Chin J Schisto Control. 2015;27:11–6 (in Chinese).Google Scholar
  29. Yihuo WL, Zhou YB, Liu GM, Wu ZS, Wang SA, Xu L, Liu HB, Jiang QW. Effect of 4-year comprehensive schistosomiasis control in Puge County, Sichuan Province. Chin J Schisto Control. 2009;21:276–9.Google Scholar
  30. Chen Z, Rao XL, Li YF, Gu XN, Xu MX, Lin DD. Effect of schistosomiasis control strategy based on infection source control of Poyang Lake region in Yongxiu County promotion zone. Chin J Schisto Control. 2015;27:579–82. in Chinese.Google Scholar
  31. Zeng XJ, Chen HG, Hong XL, Hu ZH, Jiang WS, Hu SZ, Fan YL, Ge J. Evaluation on medium-term effect of schistosomiasis comprehensive control strategy based on infectious source control in Poyang Lake area. Chin J Schisto Control. 2012;24:382–6 (in Chinese).Google Scholar
  32. He LC, Wang JS, Rong XB, Peng XW, Fu ZY, He ZW, Huang WJ, Zhang HM, Liu J, Peng YX. Effect of comprehensive schistosomiasis control strategies with emphasis on infection source control in marshland and lake regions. Chin J Schisto Control. 2010;22:278–80 (in Chinese).Google Scholar
  33. Zhang LJ, Xu ZM, Qian YJ, Dang H, Lu S, Xu J, Li SZ, Zhou XN. Endemic situation of schistosomiasis in People’s Republic of China. Chin J Schisto Control. 2016;28:611–7 (in Chinese).Google Scholar
  34. Zhou XN, Xu J, Lin DD, Wang TP, Liang YS, Zhong B, Li SZ, Yang GJ, Jiang QW. Role of the new version of the Control and Elimination Criteria for Schistosomiasis in acceleration of the schistosomiasis elimination program in China. Chin J Schisto Control. 2013;25:1–4 (in Chinese).Google Scholar
  35. Zhou XN, Wang TP, Lin DD, Wen LY, Zhou B, Xu J, Li SZ. The evidences for formulation of schistosomiasis control and elimination criteria: results from a large scale of retrospective investigations. Chin J Schisto Control. 2014;26:479–81 (in Chinese).Google Scholar
  36. MOH. Control and elimination of schistosomiasis (GB 19976–2015). Beijing: People’s Medical Publishing House; 2015. p. 1–7. in Chinese.Google Scholar
  37. Zhang SQ, Sun CS, Wang M, Lin DD, Zhou XN, Wang TP. Epidemiological features and effectiveness of schistosomiasis control programme in lake and marshland region in the People’s Republic of China. Adv Parasitol. 2016;92:39–71.View ArticlePubMedGoogle Scholar
  38. Li ZJ, Ge J, Dai JR, Wen LY, Lin DD, Madsen H, Zhou XN, Lv S. Biology and control of snail intermediate host of Schistosoma japonicum in the People’s Republic of China. Adv Parasitol. 2016;92:197–236.View ArticlePubMedGoogle Scholar
  39. Gray DJ, Williams GM, Li Y, McManus DP. Transmission dynamics of Schistosoma japonicum in the lakes and marshlands of China. PLoS ONE. 2008;3, e4058.View ArticlePubMedPubMed CentralGoogle Scholar
  40. Hu Y, Zhang Z, Chen Y, Wang Z, Gao J, Tao B, Jiang Q, Jiang Q. Spatial pattern of schistosomiasis in Xingzi, Jiangxi Province, China: the effects of environmental factors. Parasit Vectors. 2013;6:214.View ArticlePubMedPubMed CentralGoogle Scholar
  41. Zhang ZJ, Carpenter TE, Lynn HS, Chen Y, Bivand R, Clark AB, Hui FM, Peng WX, Zhou YB, Zhao GM, Jiang QW. Location of active transmission sites of Schistosoma japonicum in lake and marshland regions in China. Parasitology. 2009;136:737–46.View ArticlePubMedGoogle Scholar
  42. Chen H, Lin D. The prevalence and control of schistosomiasis in Poyang Lake region, China. Parasitol Int. 2004;53:115–25.View ArticlePubMedGoogle Scholar
  43. McManus DP, Gray DJ, Ross AG, Williams GM, He HB, Li YS. Schistosomiasis research in the dongting lake region and its impact on local and national treatment and control in China. PLoS Negl Trop Dis. 2011;5, e1053.View ArticlePubMedPubMed CentralGoogle Scholar
  44. Zhou YB, Liang S, Jiang QW. Factors impacting on progress towards elimination of transmission of schistosomiasis japonica in China. Parasit Vectors. 2012;5:275.View ArticlePubMedPubMed CentralGoogle Scholar
  45. Ross AG, Yuesheng L, Sleigh AS, Yi L, Williams GM, Wu WZ, Xinsong L, Yongkang H, McManus DP. Epidemiologic features of Schistosoma japonicum among fishermen and other occupational groups in the Dongting Lake region (Hunan Province) of China. Am J Trop Med Hyg. 1997;57:302–8.PubMedGoogle Scholar
  46. Li YS, He YK, Zeng QR, McManus DP. Epidemiological and morbidity assessment of Schistosoma japonicum infection in a migrant fisherman community, the Dongting Lake region, China. Trans R Soc Trop Med Hyg. 2003;97:177–81.View ArticlePubMedGoogle Scholar
  47. Ding GS. Surveillance on schistosomiasis of boat fishermen along Yangtze River in Nantong City from 2006 to 2010. Chin J Schisto Control. 2012;24:214–6 (in Chinese).Google Scholar
  48. Lei ZL, Zhou XN. Eradication of schistosomiasis: a new target and a new task for the National Schistosomiasis Control Porgramme in the People’s Republic of China. Chin J Schisto Control. 2015;27:1–4 (in Chinese).Google Scholar
  49. Yang Y, Zhou YB, Song XX, Li SZ, Zhong B, Wang TP, Bergquist R, Zhou XN, Jiang QW. Integrated control strategy of schistosomiasis in the People’s Republic of China: projects involving agriculture, water conservancy, forestry, sanitation and environmental modification. Adv Parasitol. 2016;92:237–68.View ArticlePubMedGoogle Scholar
  50. Sun LP, Wang W, Liang YS, Tian ZX, Hong QB, Yang K, Yang GJ, Dai JR, Gao Y. Effect of an integrated control strategy for schistosomiasis japonica in the lower reaches of the Yangtze River, China: an evaluation from 2005 to 2008. Parasit Vectors. 2011;4:243.View ArticlePubMedPubMed CentralGoogle Scholar
  51. Hong QB, Yang K, Huang YX, Sun LP, Yang GJ, Gao Y, Gao Y, Zhang LH, Zhou M, Steinmann P, Liang YS. Effectiveness of a comprehensive schistosomiasis japonica control program in Jiangsu province, China, from 2005 to 2008. Acta Trop. 2011;120:S151–7.View ArticlePubMedGoogle Scholar
  52. Zhou YB, Liang S, Chen GX, Rea C, Han SM, He ZG, Li YP, Wei JG, Zhao GM, Jiang QW. Spatial-temporal variations of Schistosoma japonicum distribution after an integrated national control strategy: a cohort in a marshland area of China. BMC Public Health. 2013;13:297.View ArticlePubMedPubMed CentralGoogle Scholar
  53. Huang YX, Cai G. Survey on present situation of marshland and snail habitat areas and study on control strategy of marshland and Oncomelania hupensis in 5 cities along the Yangtze River in Jiangsu Province. Chin J Schisto Control. 2000;12:86–90 (in Chinese).Google Scholar
  54. Tao HY, Xia A, Zhao YM, Jiang J. Effect and cost-benefit of Oncomelania snail control by plowing and planting in Jiaobei Beach of Zhenjiang City. Chin J Schisto Control. 2012;24:576–8 (in Chinese).Google Scholar
  55. Song HT, Zhang JK, Li LG, Man HC, Shi M, Jiang H. Study on comprehensive development to control schistosomaisis transmission in marshland. Chin J Schisto Control. 1994;6:203–6 (in Chinese).Google Scholar
  56. Shen XH, Sun LP, Li YF, Wang L, Chen XP, Wang HS, Dai JR. Effect of mid- and long-term schistosomiasis control plan and discussion of consolidation strategy in marshland endemic regions. Chin J Schisto Control. 2015;27:457–62 (in Chinese).Google Scholar
  57. Zhu Y, He W, Liang Y, Xu M, Yu C, Hua W, Chao G. Development of a rapid, simple dipstick dye immunoassay for schistosomiasis diagnosis. J Immunol Methods. 2002;266:1–5.View ArticlePubMedGoogle Scholar
  58. Li YF, Wang HS, Chen XP, Shen XH, Hou HG, Wu FX, Zhang MH, Liu L. Investigation on infection of schistosomiasis japonica in school children by dipstick dye immunoassay. Chin J Schisto Control. 2005;17:60–1 (in Chinese).Google Scholar
  59. Wang XY, Yang K. Serological diagnosis methods of schistosomiasis japonica at different prevalence: a meta-analysis. Chin J Schisto Control. 2016;28:18–25. 29, (in Chinese).Google Scholar
  60. Zhu HQ, Xu J, Zhu R, Cao CL, Bao ZP, Yu Q, Zhang LJ, Xu XL, Feng Z, Guo JG. Comparison of the miracidium hatching test and modified Kato-Katz method for detecting Schistosoma japonicum in low prevalence areas of China. Southeast Asian J Trop Med Public Health. 2014;45:20–5.PubMedGoogle Scholar
  61. Li SZ, Zheng H, Abe EM, Yang K, Bergquist R, Qian YJ, Zhang LJ, Xu ZM, Xu J, Guo JG, Xiao N, Zhou XN. Reduction patterns of acute schistosomiasis in the People’s Republic of China. PLoS Negl Trop Dis. 2014;8, e2849.View ArticlePubMedPubMed CentralGoogle Scholar
  62. Li H, Dong GD, Liu JM, Gao JX, Shi YJ, Zhang YG, Jin YM, Lu K, Cheng GF, Lin JJ. Elimination of schistosomiasis japonica from formerly endemic areas in mountainous regions of southern China using a praziquantel regimen. Vet Parasitol. 2015;208:254–8.View ArticlePubMedGoogle Scholar
  63. Zhou XN, Jiang QW, Guo JG, Lin DD, Zhu R, Yang GJ, Yang K, Li SZ, Xu J. Road map for transmission interruption of schistosomiasis in China. Chin J Schisto Control. 2012;24:1–4 (in Chinese).Google Scholar
  64. Wu JY, Zhou YB, Chen Y, Liang S, Li LH, Zheng SB, Zhu SP, Ren GH, Song XX, Jiang QW. 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.View ArticlePubMedPubMed CentralGoogle Scholar
  65. Zhou YB, Liang S, Chen Y, Jiang QW. The Three Gorges Dam: Does it accelerate or delay the progress towards eliminating transmission of schistosomiasis in China? Infect Dis Poverty. 2016;5:63.View ArticlePubMedPubMed CentralGoogle Scholar

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