Next Article in Journal
Modeling the Effects of Indoor Passive Smoking at Home, Work, or Other Households on Adult Cardiovascular and Mental Health: The Scottish Health Survey, 2008–2011
Previous Article in Journal
Time-Dependent Propensity Score for Assessing the Effect of Vaccine Exposure on Pregnancy Outcomes through Pregnancy Exposure Cohort Studies
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJERPH
Volume 11
Issue 3
10.3390/ijerph110303086
ijerph-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Sensitivity of Oncomelania hupensis to Niclosamide: A Nation-Wide Survey in China

by
Jianrong Dai
1,2,3,
Youzi Li
1,2,3,
Wei Wang
1,2,3,*,
Yuntian Xing
1,2,3,
Guoli Qu
1,2,3 and
Yousheng Liang
1,2,3,*
1
Jiangsu Institute of Parasitic Diseases, 117 Yangxiang, Meiyuan, Wuxi 214064, Jiangsu, China
2
Jiangsu Provincial Key Laboratory of Molecular Biology of Parasites, 117 Yangxiang, Meiyuan, Wuxi 214064, Jiangsu, China
3
Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, 117 Yangxiang, Meiyuan, Wuxi 214064, Jiangsu, China
*
Authors to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2014, 11(3), 3086-3095; https://doi.org/10.3390/ijerph110303086
Submission received: 24 January 2014 / Revised: 27 February 2014 / Accepted: 4 March 2014 / Published: 12 March 2014
Browse Figures
Versions Notes

Abstract

:
Schistosomiasis japonica, transmitted by the intermediate host snail Oncomelania hupensis of the causative agent Schistosoma japonicum, remains a major public-health concern in China, and control of this snail is one of the major approaches used in attempts to interrupt the transmission of this neglected tropical disease. Niclosamide is currently the only commercial molluscicide available for the control of O. hupensis snails in China. The purpose of this study was to evaluate the current sensitivity of O. hupensis to niclosamide in China. O. hupensis snails derived from 17 sampling sites from eight schistosomiasis-endemic provinces of China were used for the molluscicidal tests. Active adult snails (10 for each drug concentration), were immersed in solutions of 1, 0.5, 0.25, 0.125, 0.063, 0.032, 0.016 and 0.008 mg/L of 50% wettable powder of niclosamide ethanolamine salt (WPN) for 24 and 48 h at 25°C, and then the snail mortality was estimated and LC50 values were calculated. All field-derived O. hupensis snails were dead following immersion in 0.5 and 1 mg/L WPN for 24 h, whereas no death was observed after immersion in 0.008 mg/L WPN for 24 h. Immersion in 0.5, 0.25, 0.125, 0.063, 0.032 and 0.016 mg/L WPN for 24 h resulted in 80%–100%, 63.33%–100%, 0%–85%, 0%–50%, 0%–15%, and 0%–5% snail mortalities, respectively. The 24 h WPN LC50 values for the O. hupensis snails derived from the 17 sampling sites in China ranged from 0.0743 to 0.2285 mg/L, and no significant difference was detected by the Kolmogorov-Smirnov test (p = 0.2). The results indicate that there is no regional variation in the current susceptibility to niclosamide in O. hupensis populations in China. It is suggested that the current sensitivity of niclosamide against O. hupensis remains high and has not changed after more than two decades of repeated, extensive application for snail control in the main endemic areas of China.

Graphical Abstract

1. Introduction

Schistosomiasis, a snail-transmitted parasitic disease, is a major neglected tropical disease affecting more than 207 million people in the tropical and subtropical regions around the world [1]. Although great success has been achieved in its control in China, schistosomiasis japonica is still one of the four communicable diseases that have been given high priority by the central government [2,3,4]. It is estimated that over 0.7 million people are infected with the parasite in China, and the snail host Oncomelania hupensis is detected in habitats with an area of 3.73 billion m2 [5,6,7]. It has been proved that the transmission of S. japonicum is governed by the geographical distribution of its snail host; therefore, control of the O. hupensis snails, as a major part of the National Schistosomiasis Control Program, is currently one of the major approaches used for schistosomiasis control and elimination in China [8,9,10].
In China, many approaches have been used for the control of O. hupensis; however, snail control with chemicals remains the most widely used method to kill the snail intermediate host till now [11,12,13]. Niclosamide is recommended by the WHO as the only molluscicide for snail control in the endemic foci [14]; however, the agent is difficult to dissolve in both water and organic solvents. Therefore, many novel niclosamide formulations have been developed attempting to improve its water solubility. Of these a 50% wettable powder of niclosamide ethanolamine salt (WPN) has been recommended as the only market-available molluscicide since the initiation of the World Bank Loan Project for Schistosomiasis Control in China, due to its high efficacy and easy use [15]. Currently, WPN is recommended by the Ministry of Health, P. R. China at a dose of 1 mg/L for snail control in the field [15]. Following extensive, long-term, repeated use for more than two decades, the possible emergence of resistance to niclosamide in the intermediate host snails has received much attention [16]. Therefore, a systematic survey of the molluscicidal activity of niclosamide against O. hupensis would be of great significance for understanding the current sensitivity of niclosamide in China, and the prevention and rapid management of niclosamide resistance in snail populations. Here, a nationwide determination was carried out in regions where O. hupensis snails are present in China to assess the current efficacy of O. hupensis to niclosamide.

2. Materials and Methods

2.1. Snails

Adult O. hupensis snails were collected by individual picking with forceps [17], from 17 sampling sites from eight schistosomiasis-endemic provinces of China (Table 1, Figure 1). After feeding in the laboratory for 24 h, active adult snails with 7–8 spirals were randomly divided into groups for the molluscicidal test.
Table
Table 1. Location and environmental types of the snail sampling sites in China
Table 1. Location and environmental types of the snail sampling sites in China
Snail Sampling SiteEnvironmental TypeCodeEast LongitudeNorth Latitude
Weishan County, Yunnan ProvinceHillA100.33°25.23°
Shimen County, Hunan ProvinceHillB110.47°29.51°
Linli County, Hunan ProvinceHillC111.64°29.44°
Yuanjiang County, Hunan ProvinceLake and marshlandD112.20°28.52°
Nanxian County, Hunan ProvinceLake and marshlandE112.39°29.37°
Gong’an County, Hubei ProvinceLake and marshlandF112.00°30.05°
Jingshan County, Hubei ProvinceHillG113.11°31.03°
Wucheng County, Jiangxi ProvinceLake and marshlandH115.54°28.05°
Pengze County, Jiangxi ProvinceLake and marshlandI116.32°29.58°
Duchang County, Jiangxi ProvinceLake and marshlandJ116.24°29.25°
Yongxiu County, Jiangxi ProvinceLake and marshlandK115.82°29.04°
Nanchang County, Jiangxi ProvinceLake and marshlandL115.89°28.68°
Xuancheng County, Anhui ProvinceHillM118.77°30.74°
Dongtai County, Jiangsu ProvincePlain with waterway networksN120.31°32.84°
Zhenjiang County, Jiangsu ProvincePlain with waterway networksO119.44°32.20°
Pinghu County, Zhejiang ProvincePlain with waterway networksP121.02°30.70°
Yinxi County, Fujian ProvinceHillQ119.35°25.72°
Ijerph 11 03086 g001 1024
Figure 1. The sampling sites of Oncomelania hupensis snails in China.
Figure 1. The sampling sites of Oncomelania hupensis snails in China.
Ijerph 11 03086 g001

2.2. Niclosamide Formulation

WPN was provided by the Nanjing Essence Fine Chemical Co., Ltd. (Nanjing, China; lot: 1012031). WPN was weighed and solutions of 1, 0.5, 0.25, 0.125, 0.063, 0.032, 0.016 and 0.008 mg/L of niclosamide were prepared in dechlorinated tap water for the subsequent experiments.

2.3. Molluscicidal Test

One hundred milliliter flasks were filled with the solutions, then 10 active adult snails were added and the flasks covered with gauze to prevent their escape. Snails in flasks of dechlorinated water served as controls. After being immersed for 24 and 48 h at 25°C, the snails were washed with dechlorinated water and fed for a further 48 h. Those suspected of being dead were tested by the knocking method [18,19], and the snail mortality was estimated. All tests were performed in triplicate, and LC50 values were calculated.

2.4. Statistical Analysis

All data were double entered into Microsoft Excel 2003 (Microsoft Corporation; Redmond, WA, USA) and all statistical analyses were performed using the statistical software SPSS version 16.0 (SPSS Inc.; Chicago, IL, USA). Differences of LC50 values were tested for statistical significance with Kolmogorov-Smirnov test. A p value < 0.05 was considered statistically significant.

3. Results

All field-derived O. hupensis snails were dead following immersion in 1 mg/L WPN for 24 h, whereas no death was observed after immersion in 0.008 mg/L WPN for 24 h. Immersion with WPN at concentrations of 0.5, 0.25, 0.125, 0.063, 0.032 and 0.016 mg/L for 24 h resulted in 80%–100%, 63.33%–100%, 0%–85%, 0%–50%, 0%–15%, and 0%–5% mortalities of snails, respectively (Table 2). The 24 h WPN LC50 values for the O. hupensis snails derived from the 17 sampling sites in China ranged from 0.0743 to 0.2285 mg/L, and no significant difference was detected by the Kolmogorov-Smirnov test (p = 0.2).
Table
Table 2. Comparison of mortality rates and LC50 values of Oncomelania hupensis snails sampled from different regions of China following immersion in various concentrations of WPN for 24 h.
Table 2. Comparison of mortality rates and LC50 values of Oncomelania hupensis snails sampled from different regions of China following immersion in various concentrations of WPN for 24 h.
Snail PopulationMortality of Snails in Different Concentrations of WPNLC50 (mg/L)
1 mg/L0.5 mg/L0.25 mg/L0.125 mg/L0.063 mg/L0.032 mg/L0.016 mg/L0.008 mg/L
Weishan1001009020155000.1436
Shimen10010080805010000.0770
Linli100957515105500.1708
Ruanjiang100959570250000.0981
Nanxian10080652050000.2177
Gong’an10010063.333.3300000.2222
Jingshan10010093.336.676.670000.1684
Wucheng10010010083.3326.676.673.3300.0770
Pengze10096.6776.672000000.1856
Duchang10010010046.67200000.1115
Yongxiu100100100803015000.0743
Nanchang10010010085155000.0854
Xuancheng10096.6766.67000000.2285
Dongtai10010090500000.1830
Zhenjiang1001007727200000.1497
Pinghu10010086.6723.333.333.33000.1575
Yinxi1001001001000000.1649
The O. hupensis snails derived from 16 sampling sites (the number of snails sampled from Shimen county of Hunan province was not enough, due to death, to be used for assessing the mortality following immersion in WPN for 48 h) were employed to test the efficacy of WPN following immersion for 48 h. No snails survived the treatment with WPN at concentrations of 0.5 and 1 mg/L for 48 h, whereas all snails were alive by immersion in WPN at a concentration of 0.008 mg/L for 48 h. Immersion in WPN at concentrations of 0.25, 0.125, 0.063, 0.032 and 0.016 mg/L for 48 h resulted in 95%–100%, 10%–100%, 0%–55%, 0%–10%, and 0%–5% mortalities of snails, respectively (Table 3).
Table
Table 3. Comparison of mortality rates and LC50 values of Oncomelania hupensis snails sampled from different regions of China following immersion in various concentrations of WPN for 48 h.
Table 3. Comparison of mortality rates and LC50 values of Oncomelania hupensis snails sampled from different regions of China following immersion in various concentrations of WPN for 48 h.
Snail PopulationMortality of Snails in Different Concentrations of WPNLC50 (mg/L)
1 mg/L0.5 mg/L0.25 mg/L0.125 mg/L0.063 mg/L0.032 mg/L0.016 mg/L0.008 mg/L
Weishan10010010070105000.1015
Shimen a–––––––––
Linli10010010025205500.1208
Ruanjiang10010010075350000.0825
Nanxian1001009575150000.0981
Gong’an10010010060100000.1088
Jingshan100100100403.333.33000.1309
Wucheng1001001009013.333.33000.0864
Pengze10010010063.33100000.1063
Duchang1001001008033.330000.0806
Yongxiu1001001001005530000.0490
Nanchang100100100100300000.0718
Xuancheng10010096.6716.6703.33000.1575
Dongtai1001001002500000.1487
Zhenjiang10010097571310000.1037
Pinghu10010096.6723.3300000.1539
Yinxi1001001001050000.1593
Note: a The number of O. hupensis snails sampled from Shimen county of Hunan province is not enough to be used for assessing the mortality following immersion in WPN for 48 h.
The 48 h WPN LC50 values for the O. hupensis snails derived from 16 sampling sites in China ranged from 0.049 to 0.1593 mg/L, and no significant difference was detected by the Kolmogorov-Smirnov test (p = 0.197).

4. Discussion

In China, the description of schistosomiasis japonica dates back more than two millennia [2]. Since the control efforts initiated in the 1950s, snail control has been a key part of the National Schistosomiasis Control Program of China [8,12], and many approaches have been used for the control of the intermediate host snails, including environmental improvement, physical methods, building trees, molluscicide treatment and biological control [11]. Among all these strategies, molluscicide treatment is the most widely used method for snail control due to the wide application coverage, easy procedure and fast action [20]. A recent meta-analysis revealed that it is necessary to continuously apply molluscicidal treatments more than twice a year in the field to consolidate the schistosomiasis control achievements gained [21], and different molluscicidal treatment strategies should be utilized at different stages of the control programme to maximize cost-effectiveness [20].
Since 1950s, many chemicals have been tested for molluscicidal activity and several agents have been used for snail control in the schistosomiasis-endemic fields of China, including sodium pentachlorophenate, bromoacetamide, nicotinanilide, calcium cyanamide, niclosamide, META-Li, and so on [22,23,24,25]. In addition, some plants have been screened and tested for molluscicidal activity against O. hupensis in laboratories [26,27,28,29,30]. Since 1992 when the World Bank Loan Project for Schistosomiasis Control was initiated in China, WPN was introduced and has replaced other molluscicides to become the only molluscicide now used for snail control in the endemic areas of China [15]. Following the repeated, long-term, extensive use for more than two decades, there is a concern about the potential development of resistance to niclosamide in O. hupensis snails [16]. It is therefore of great importance to monitor the molluscicidal activity of niclosamide against the O. hupensis snails in regions where this is currently the only available chemical that is widely used in China.
WPN at a dose of 1 mg/L is recommended for snail control in the field [15]. Therefore, drug solutions at concentrations of 1, 0.5, 0.25, 0.125, 0.063, 0.032, 0.016 and 0.008 mg/L were designed for the molluscicidal tests in the laboratory. Our findings showed that all O. hupensis snails were dead following immersion in 1 mg/L WPN for 24 and 48 h or in 0.5 mg/L WPN for 48 h, and only 0%–20% survived the treatment with WPN at a concentration of 0.5 mg/L for 24 h. In addition, the 24 h WPN LC50 values for the O. hupensis snails derived from 17 sampling sites in China ranged from 0.0743 to 0.2285 mg/L, with no significant differences were detected (p = 0.2), and the 48-h WPN LC50 values for the O. hupensis snails derived from 16 sampling sites in China ranged from 0.049 to 0.1593 mg/L, with no significant differences detected (p = 0.197). The results from this study demonstrate that the molluscicidal activity of niclosamide against O. hupensis is still high in the main endemic areas of China after more than two decades of repeated, extensive use. This is important information for both the public health workers and health policy makers in the field of schistosomiasis control, considering that niclosamide, the currently only chemical of choice for snail control, plays an essential role in the current Chinese National Schistosomiasis Control Program of China.
It has been found that the environmental factors including temperature, vegetation, sunlight, soil and rainfall, the quality and concentration of the chemicals, as well as the technical skills may affect the molluscicidal actions in the endemic foci [11], whereas in the laboratory, the volume of drug solution [31], and the quantity, laboratorial breeding duration and the sampling time of snails used for molluscicidal test [32,33,34] are reported to affect the evaluation of the molluscicidal actions in the laboratory. Currently, a single WPN dose (1 mg/L) is employed for the field snail control in China [15], however, the variations in snail habitats, climate, temperature and rainfall may affect the concentration and duration of snail contact with niclosamide, thereby resulting in various molluscicidal efficacies. It is suggested that the dose of molluscicides should be appropriately adjusted based on the actual field settings, and temperature, climate and rainfall should be taken into account during the snail control in the field, so as to achieve the optimal molluscicidal efficacy.

5. Conclusions

The results indicate that there is no regional variation in the current susceptibility to niclosamide in O. hupensis populations, and the current activity of niclosamide against O. hupensis snails in China appears satisfactory; however, it does not mean that resistance cannot occur nor that in different geographical regions the response of O. hupensis snails will be the same. We, therefore, should not reduce our vigilance to the possible development of resistance to niclosamide in the intermediate host snails. Further periodical studies monitoring both the sensitivity of O. hupensis to the chemical and the development and epidemiology of niclosamide resistance of different geographical isolates of O. hupensis in China are still required, which would be of great significance for the elimination of schistosomiasis japonica in China.

Acknowledgements

Many thanks are due to the staff from Yunnan Provincial Institute of Endemic Diseases Control, Sichuan Provincial Center for Disease Control and Prevention, Hunan Institute of Parasitic Diseases, Hubei Provincial Center for Disease Control and Prevention, Jiangxi Institute of Parasitic Diseases, Anhui Institute of Schistosomiasis Control, Zhejiang Academy of Medical Sciences, Shanghai Center for Disease Control and Prevention and Fujian Provincial Center for Disease Control and Prevention, for their kind help to collect the snails. Thanks are also given to Jianying Wei and Na Guo for their work in breeding snails in laboratory. This work was supported by National Science and Technology Pillar Program of China (2009BAI78B06), the National Important Sci-Tech Special Projects (2012ZX10004-220), the Natural Science Foundation of China (81071379), the Jiangsu Province’s Outstanding Medical Academic Leader Programme (LJ201132), and Jiangsu Department of Health (X201103). The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.

Author Contributions

Jianrong Dai, Wei Wang and Yousheng Liang conceived and designed the study; Jianrong Dai, Youzi Li, Wei Wang, Yuntian Xing and Guoli Qu conducted the study. Jianrong Dai and Youzi Li collected the data and performed analysis of data. Jianrong Dai and Wei Wang prepared the first draft of the manuscript; Wei Wang and Yousheng Liang provided strategic advice and assisted with editing of the manuscript. All authors read and approved the final version of the manuscript.

Conflicts of Interests

The authors declare no conflicts of interest.

References

  1. 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]
  2. Wang, L.D.; Utzinger, J.; Zhou, X.N. Schistosomiasis control: Experiences and lessons from China. Lancet 2008, 372, 1793–1795. [Google Scholar] [CrossRef]
  3. Manus, D.P.; Li, Y.; Gray, D.J.; Ross, A.G. Conquering “snail fever”: Schistosomiasis and its control in China. Expert Rev. Anti Infect. Ther. 2009, 7, 473–485. [Google Scholar] [CrossRef]
  4. Utzinger, J.; Zhou, X.N.; Chen, M.G.; Bergquist, R. Conquering Schistosomiasis in China: The long march. Acta Trop. 2005, 96, 69–96. [Google Scholar] [CrossRef]
  5. Zhou, X.N.; Guo, J.G.; Wu, X.H.; Jiang, Q.W.; Zheng, J.; Dang, H.; Wang, X.H.; Xu, J.; Zhu, H.Q.; Wu, G.L.; et al. Epidemiology of Schistosomiasis in the People’s Republic of China, 2004. Emerg. Infect. Dis. 2007, 13, 1470–1476. [Google Scholar] [CrossRef]
  6. Li, S.Z.; Luz, A.; Wang, X.H.; Xu, L.L.; Wang, Q.; Qian, Y.J.; Wu, X.H.; Guo, J.G.; Xia, G.; Wang, L.Y.; Zhou, X.N. Schistosomiasis in China: Acute infections during 2005–2008. Chin. Med. J. 2009, 122, 1009–1014. [Google Scholar]
  7. Zheng, H.; Zhang, L.J.; Zhu, R.; Xu, J.; Li, S.Z.; Guo, J.G.; Xiao, N.; Zhou, X.N. Schistosomiasis situation in People’s Republic of China in 2011. Chin. J. Schisto. Control 2012, 24, 621–626. (in Chinese). [Google Scholar]
  8. Zhou, X.N.; Wang, L.Y.; Chen, M.G.; Wu, X.H.; Jiang, Q.W.; Chen, X.Y.; Zheng, J.; Utzinger, J. The public health significance and control of Schistosomiasis in China—Then and now. Acta Trop. 2005, 96, 97–105. [Google Scholar] [CrossRef]
  9. Zhou, X.N.; Bergquist, R.; Leonardo, L.; Yang, G.J.; Yang, K.; Sudomo, M.; Olveda, R. Schistosomiasis japonica control and research needs. Adv. Parasitol. 2010, 72, 145–178. [Google Scholar] [CrossRef]
  10. Wang, L.D.; Guo, J.G.; Wu, X.H.; Chen, H.G.; Wang, T.P.; Zhu, S.P.; Zhang, Z.H.; Steinmann, P.; Yang, G.J.; Wang, S.P.; Wu, Z.D.; Wang, L.Y.; Hao, Y.; Bergquist, R.; Utzinger, J.; Zhou, X.N. China’s new strategy to block Schistosoma. japonicu transmission: Experiences and impact beyond schistosomiasis. Trop. Med. Int. Health 2009, 14, 1475–1483. [Google Scholar] [CrossRef]
  11. Zhou, X.N. Science of Oncomelania Snail; (in Chinese). Science Press: Beijing, China, 2005; pp. 97–108, 317–318. [Google Scholar]
  12. Yuan, Y.; Xu, X.J.; Dong, H.F.; Jiang, M.S.; Zhu, H.G. Transmission control of Schistosomiasis japonica: Implementation and evaluation of different snail control interventions. Acta Trop. 2005, 96, 191–197. [Google Scholar] [CrossRef]
  13. Lin, D.D.; Hu, G.H.; Zhang, S.J. Optimal combined approaches of field intervention for Schistosomiasis control in China. Acta Trop. 2005, 96, 242–247. [Google Scholar] [CrossRef]
  14. WHO. The Role of Mollusciciding in Schistosomiasis Control; Division of Control of Tropical Diseases: Geneva, Switzerland, 1992; pp. 1–10. [Google Scholar]
  15. Xianyi, C.; Liying, W.; Jiming, C.; Xiaonong, Z.; Jiang, Z.; Jiagang, G.; Xiaohua, W.; Engels, D.; Minggang, C. Schistosomiasis control in China: The impact of a 10-year World Bank Loan Project (1992–2001). Bull WHO 2005, 83, 43–48. [Google Scholar]
  16. Cao, Z.G.; Wang, T.P.; Zhang, S.Q.; Tian, X.G.; Zhu, L.; Zhang, L.S.; Yao, G.X.; Jin, W.; Yang, W.P. Experimental study on the resistance of Oncomelania snails to niclosamide. Chin. J. Pathogen Biol. 2012, 7, 352–353, 376. (in Chinese). [Google Scholar]
  17. Mao, C.P. Biology of Schistosome and Control of Schistosomiasis; (in Chinese). People’s Medical Publishing House: Beijing, China, 1990. [Google Scholar]
  18. Webbe, G. Laboratory and field trials of a new molluscicide, Bayer 73, in Tanganyika. Bull WHO 1961, 25, 525–531. [Google Scholar]
  19. Gönnert, R. Results of laboratory and field trials with the molluscicide Bayer 73. Bull WHO 1961, 25, 483–501. [Google Scholar]
  20. Yang, G.J.; Sun, L.P.; Hong, Q.B.; Zhu, H.R.; Yang, K.; Gao, Q.; Zhou, X.N. Optimizing molluscicide treatment strategies in different control stages of Schistosomiasis in the People’s Republic of China. Parasit. Vector. 2012, 5. [Google Scholar] [CrossRef]
  21. Yang, G.J.; Li, W.; Sun, L.P.; Wu, F.; Yang, K.; Huang, Y.X.; Zhou, X.N. Molluscicidal efficacies of different formulations of niclosamide: Result of meta-analysis of Chinese literature. Parasit. Vectors 2010, 3. [Google Scholar] [CrossRef]
  22. Zhou, P.S.; Ma, L.; Huang, J.L. Research progress on molluscicides and their application. Chin. J. Vector Biol. Control 2002, 13, 231–233. (in Chinese). [Google Scholar]
  23. Wu, X.Y.; Yang, L.Q.; Zhang, L.H.; Ge, Q.J. Progress of research on molluscicides. Chin. J. Schistosomiasis Control 2006, 18, 474–476. (in Chinese). [Google Scholar]
  24. Zhu, D.; Yao, P.; Bao, Z. Mollusciciding action and toxicity of bromoacetamide. Chin. J. Parasitol. Parasit. Dis. 1999, 17, 244–246. (in Chinese). [Google Scholar]
  25. Zhu, D.; Zhou, X.N.; Zhang, S.Q.; Zhang, G.; Liu, H.X.; Lu, D.B.; Cai, G.Y.; Ni, Q.Z.; Cao, Z.G.; Wu, W.D. Study on the molluscicidal effect of META-Li against Oncomelania hupensis. Chin. J. Parasitol. Parasit. Dis. 2006, 17, 244–246. (in Chinese). [Google Scholar]
  26. Wei, F.H.; Xu, X.J.; Liu, J.B.; Dai, Y.H.; Dussart, G.; Trigwell, J. Toxicology of a potential molluscicide derived from the plant Solanum xanthocarpum: A preliminary study. Ann. Trop. Med. Parasitol. 2002, 96, 325–331. [Google Scholar] [CrossRef]
  27. Wang, H.; Cai, W.M.; Wang, W.X.; Yang, J.M. Molluscicidal activity of Nerium indicum Mill, Pterocarya stenoptera DC, and Rumex japonicum houtt on Oncomelania hupensis. Biomed. Environ. Sci. 2006, 19, 245–248. [Google Scholar]
  28. Yang, X.M.; Chen, S.X.; Xia, L.; Chen, J. Molluscicidal activity against Oncomelania hupensis of Ginkgo biloba. Fitoterapia 2008, 89, 250–254. [Google Scholar] [CrossRef]
  29. Zou, F.C.; Duan, G.; Xie, Y.J.; Zhou, Y.; Dong, G.D.; Lin, R.Q.; Zhu, X.Q. Molluscicidal activity of the plant Eupatorium adenophorum against Oncomelania hupensis, the intermediate host snail of Schistosoma japonicum. Ann. Trop. Med. Parasitol. 2009, 103, 549–553. [Google Scholar] [CrossRef]
  30. Peng, F.; Liu, M.; Huang, Q.; Liu, N.; Yang, H.; Sun, H.; Hu, Q.; Feng, F.; Jiang, C. Molluscicidal effect of Eomecon chionantha alkaloids against Oncomelania hupensis snails. Southeast Asian J. Trop. Med. Public Health 2011, 42, 289–296. [Google Scholar]
  31. Dai, J.R.; Zhang, Y.P.; Jiang, Y.J.; Xi, W.P.; Yang, G.J.; Liang, Y.S. Studies on standardization of methods for screening molluscicides in laboratory I Volume of molluscicidal solution to influence the efficacy. Chin. J. Schisto. Control 2002, 14, 122–124. (in Chinese). [Google Scholar]
  32. Dai, J.R.; Xi, W.P.; Zhang, Y.P.; Liang, Y.S. Studies on standardization of methods for screening molluscicides in laboratory II Quantity of snails used to influence the efficacy. Chin. J. Schisto. Control. 2002, 14, 263–265. (in Chinese). [Google Scholar]
  33. Dai, J.R.; Liang, Y.S.; Zhang, Y.P.; Xu, M.; Li, H.J.; Zhu, Y.C. Studies on standardization of methods for screening molluscicides in laboratory III Breeding time of snails to influence the efficacy. Chin. J. Schisto. Control. 2003, 14, 346–348. (in Chinese). [Google Scholar]
  34. Li, Y.Z.; Xing, Y.T.; Li, H.J.; Qu, G.L.; Wang, W.; Wei, J.Y.; Liang, Y.S.; Dai, J.R. Studies on standardization of methods for screening molluscicides in laboratory IV breeding time of snails to influence the efficacy. Chin. J. Schisto. Control. 2012, 24, 35–39. (in Chinese). [Google Scholar]

Share and Cite

MDPI and ACS Style

Dai, J.; Li, Y.; Wang, W.; Xing, Y.; Qu, G.; Liang, Y. Sensitivity of Oncomelania hupensis to Niclosamide: A Nation-Wide Survey in China. Int. J. Environ. Res. Public Health 2014, 11, 3086-3095. https://doi.org/10.3390/ijerph110303086

AMA Style

Dai J, Li Y, Wang W, Xing Y, Qu G, Liang Y. Sensitivity of Oncomelania hupensis to Niclosamide: A Nation-Wide Survey in China. International Journal of Environmental Research and Public Health. 2014; 11(3):3086-3095. https://doi.org/10.3390/ijerph110303086

Chicago/Turabian Style

Dai, Jianrong, Youzi Li, Wei Wang, Yuntian Xing, Guoli Qu, and Yousheng Liang. 2014. "Sensitivity of Oncomelania hupensis to Niclosamide: A Nation-Wide Survey in China" International Journal of Environmental Research and Public Health 11, no. 3: 3086-3095. https://doi.org/10.3390/ijerph110303086

APA Style

Dai, J., Li, Y., Wang, W., Xing, Y., Qu, G., & Liang, Y. (2014). Sensitivity of Oncomelania hupensis to Niclosamide: A Nation-Wide Survey in China. International Journal of Environmental Research and Public Health, 11(3), 3086-3095. https://doi.org/10.3390/ijerph110303086

Article Metrics

Back to TopTop