Resistance to niclosamide in Oncomelania hupensis, the intermediate host of Schistosoma japonicum: should we be worried?

Parasitology ◽  
2014 ◽  
Vol 142 (2) ◽  
pp. 332-340 ◽  
Author(s):  
JIAN-RONG DAI ◽  
YOU-ZI LI ◽  
WEI WANG ◽  
YUN-TIAN XING ◽  
GUO-LI QU ◽  
...  

SUMMARYAs the currently only available molluscicide, niclosamide has been widely used for snail control for over 2 decades in China. There is therefore a concern about the emergence of niclosamide-resistant snail populations following repeated, extensive use of the chemical. The purpose of this study was to investigate the likelihood of niclosamide resistance in Oncomelania hupensis in China. Active adult O. hupensis snails derived from 20 counties of 10 schistosomiasis-endemic provinces of China, of 10 snails in 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−1 of a 50% wettable powder of niclosamide ethanolamine salt (WPN) for 24 and 48 h at 25 °C, and the median lethal concentration (LC50) was estimated. Then, the 24- and 48-h WPN LC50 values were compared with those determined in the same sampling sites in 2002. The results indicated that the 24- and 48-h WPN LC50 values for O. hupensis were not significantly different from those determined in 2002 (P = 0·202 and 0·796, respectively). It is concluded that the current sensitivity of O. hupensis to niclosamide has not changed after more than 2 decades of repeated, extensive application in the main endemic foci of China, and there is no evidence of resistance to niclosamide detected in O. hupensis.

Acta Tropica ◽  
2020 ◽  
Vol 210 ◽  
pp. 105547
Author(s):  
Lydia Leonardo ◽  
Gracia Varona ◽  
Raffy Jay Fornillos ◽  
Daria Manalo ◽  
Ian Kim Tabios ◽  
...  

2009 ◽  
Vol 123 (3) ◽  
pp. 277-281 ◽  
Author(s):  
Daoyi Guo ◽  
Yun Zhang ◽  
Dan Zeng ◽  
Hua Wang ◽  
Xun Li ◽  
...  

2020 ◽  
Vol 477 (12) ◽  
pp. 2133-2151
Author(s):  
Zhiming Su ◽  
Xuyang Tian ◽  
Huanjun Li ◽  
Zhiming Wei ◽  
Lifan Chen ◽  
...  

Oncomelania hupensis is the unique intermediate host of Schistosoma japonicum. As an irreplaceable prerequisite in the transmission and prevalence of schistosomiasis japonica, an in-depth study of this obligate host–parasite interaction can provide glimpse into the molecular events in the competition between schistosome infectivity and snail immune resistance. In previous studies, we identified a macrophage migration inhibitory factor (MIF) from O. hupensis (OhMIF), and showed that it was involved in the snail host immune response to the parasite S. japonicum. Here, we determined the crystal structure of OhMIF and revealed that there were distinct structural differences between the mammalian and O. hupensis MIFs. Noticeably, there was a projecting and structured C-terminus in OhMIF, which not only regulated the MIF's thermostability but was also critical in the activation of its tautomerase activity. Comparative studies between OhMIF and human MIF (hMIF) by analyzing the tautomerase activity, oxidoreductase activity, thermostability, interaction with the receptor CD74 and activation of the ERK signaling pathway demonstrated the functional differences between hMIF and OhMIF. Our data shed a species-specific light on structural, functional, and immunological characteristics of OhMIF and enrich the knowledge on the MIF family.


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