Reduction of faecal worm egg count, worm numbers and worm fecundity in sheep selected for worm resistance following artificial infection with Teladorsagia circumcincta and Trichostrongylus colubriformis

Kemper, K. E., Palmer, D. G., Liu, S. M., Greeff, J. C., Bishop, S. C. and Karlsson, L. J. E. (2010) Reduction of faecal worm egg count, worm numbers and worm fecundity in sheep selected for worm resistance following artificial infection with Teladorsagia circumcincta and Trichostrongylus colubriformis. Veterinary Parasitology, 171 3-4: 238-246. doi:10.1016/j.vetpar.2010.04.005


Author Kemper, K. E.
Palmer, D. G.
Liu, S. M.
Greeff, J. C.
Bishop, S. C.
Karlsson, L. J. E.
Title Reduction of faecal worm egg count, worm numbers and worm fecundity in sheep selected for worm resistance following artificial infection with Teladorsagia circumcincta and Trichostrongylus colubriformis
Formatted title
Reduction of faecal worm egg count, worm numbers and worm fecundity in sheep selected for worm resistance following artificial infection with Teladorsagia circumcincta and Trichostrongylus colubriformis
Journal name Veterinary Parasitology   Check publisher's open access policy
ISSN 0304-4017
1873-2550
Publication date 2010-08-04
Year available 2010
Sub-type Article (original research)
DOI 10.1016/j.vetpar.2010.04.005
Open Access Status Not yet assessed
Volume 171
Issue 3-4
Start page 238
End page 246
Total pages 9
Place of publication Amsterdam, Netherlands
Publisher Elsevier BV
Language eng
Formatted abstract
We examined the changes to populations of Trichostrongylus colubriformis and Teledorsagia circumcincta in mature sheep selected for reduced faecal worm egg count (WEC). Worm resistant (n=19) and control (n=10) genotype sheep were penned and dosed with a total of 10,000 T. colubriformis and 10,000 T. circumcincta per week for 18-weeks. Sheep genotypes were from lines previously bred over 15 years for either low WEC (resistant) or non-selected (control). Weekly WEC and the proportion of larvae from each species in faecal culture were measured during weeks 3-17. Egg hatchability was assessed on a pooled faecal sample from worm resistant or control genotype sheep at weeks 7, 9, 10, 13, 14 and 17. At week 18 the number of adult and immature worms (early and late 4th, and 5th stage), and indicators of worm fecundity (female worm length and number of eggs in utero) were assessed at necropsy. Results show that resistant sheep had reduced mean WEC to only 18% of the control (P<0.05) and increased the proportion of T. circumcincta larvae in faecal culture during weeks 8-17 (P<0.10). Egg hatch assays indicated a slight reduction in the viability of eggs from worm resistant genotypes at weeks 14 (P<0.05) and 17 (P<0.10). At necropsy, resistant animals had 93% fewer adult T. colubriformis, 44% fewer adult T. circumcincta and had reduced indicators of fecundity in T. circumcincta by up to 40% (P<0.05). We observed no change in the number T. circumcincta worms but an 11% increase in the proportion of early 4th stage T. circumcincta larvae in resistant animals (P<0.05). There were different temporal patterns in WEC and different prediction equations for WEC from necropsy traits for the two sheep genotypes (P<0.05). Thus, our results suggest a changed host-parasite relationship in sheep selected for low WEC. We conclude that lower WEC is achieved through reduced number of adult worms for both species and reduced fecundity for T. circumcincta. These results support the hypotheses that worm resistant sheep with a strong immune function can regulate T. colubriformis by rejecting adult worms but that T. circumcincta is regulated through a combination of suppressed development and reduced female fecundity.
Keyword Faecal worm egg count
Genetic resistance
Host-parasite interaction
Nematode
Population regulation
Sheep
Teladorsagia circumcincta
Trichostrongylus colubriformis
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collection: Institute for Molecular Bioscience - Publications
 
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