PLoS Neglected Tropical Diseases (Jul 2019)

Development and validation of an Onchocerca ochengi adult male worm gerbil model for macrofilaricidal drug screening.

  • Fidelis Cho-Ngwa,
  • Glory Enjong Mbah,
  • Rene Bilingwe Ayiseh,
  • Emmanuel Menang Ndi,
  • Elvis Monya,
  • Irene Memeh Tumanjong,
  • Evans Ngandung Mainsah,
  • Judy Sakanari,
  • Sara Lustigman

DOI
https://doi.org/10.1371/journal.pntd.0007556
Journal volume & issue
Vol. 13, no. 7
p. e0007556

Abstract

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BackgroundOnchocerciasis currently afflicts an estimated 15 million people and is the second leading infectious cause of blindness world-wide. The development of a macrofilaricide to cure the disease has been hindered by the lack of appropriate small laboratory animal models. This study therefore, was aimed at developing and validating the Mongolian gerbil, as an Onchocerca ochengi (the closest in phylogeny to O. volvulus) adult male worm model.Methodology/principal findingsMongolian gerbils (Meriones unguiculatus) were each implanted with 20 O. ochengi male worms (collected from infected cattle), in the peritoneum. Following drug or placebo treatments, the implanted worms were recovered from the animals and analyzed for burden, motility and viability. Worm recovery in control gerbils was on average 35%, with 89% of the worms being 100% motile. Treatment of the gerbils implanted with male worms with flubendazole (FBZ) resulted in a significant reduction (p = 0.0021) in worm burden (6.0% versus 27.8% in the control animals); all recovered worms from the treated group had 0% worm motility versus 91.1% motility in control animals. FBZ treatment had similar results even after four different experiments. Using this model, we tested a related drug, oxfendazole (OFZ), and found it to also significantly (p = 0.0097) affect worm motility (22.7% versus 95.0% in the control group).Conclusions/significanceWe have developed and validated a novel gerbil O. ochengi adult male worm model for testing new macrofilaricidal drugs in vivo. It was also used to determine the efficacy of oxfendazole in vivo.