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Exploration of Factors Associated with Spatial-temporal Veterinary Surveillance Diagnoses of Rumen Fluke () Infections in Ruminants Using Zero-inflated Mixed Modelling

Overview
Journal Parasitology
Specialty Parasitology
Date 2021 Oct 18
PMID 34658327
Citations 3
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Abstract

Rumen fluke (Calicophoron daubneyi) has emerged as a prominent parasite of ruminants in Europe over the past decades. Epidemiological questions remain regarding this observed increase in prevalence as well as the prospect for future paramphistomosis risk. This study aimed to identify factors associated with the temporal−spatial prevalence of rumen fluke as measured by veterinary surveillance in a temperate region using zero-inflated negative binomial mixed modelling. Modelling revealed that summer rainfall, raindays and sunshine hours and mean winter temperature as significant positively associated climate variables for rumen fluke prevalence over space and time (P < 0.05). Rumen fluke prevalence was also higher in counties with higher cattle/sheep densities and was positively associated with rumen fluke case rates in the previous years (P < 0.05). Equivalent models for fasciolosis prevalence revealed no significant association with winter temperature and sunshine hours, (P > 0.05). These results confirm a strong association between rainfall and the prevalence of both fluke species in a temperate environment, likely due to the role of Galba truncatula as their intermediate snail host. It also highlights the potential added importance of winter temperature and sunshine hours in rumen fluke epidemiology when compared to liver fluke.

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References
1.
Titi A, Rondelaud D, Mekroud A, Vignoles P, Dreyfuss G . Natural light influences cercarial emergence of Calicophoron daubneyi but not that of Haplometra cylindracea from temperature-challenged Galba truncatula. Parasitol Res. 2014; 113(10):3557-63. DOI: 10.1007/s00436-014-4021-7. View

2.
Ross J . A study of the application of the Stormont "wet day" fluke forecasting system in Scotland. Br Vet J. 1975; 131(4):486-98. DOI: 10.1016/s0007-1935(17)35244-2. View

3.
Morley N . Thermodynamics of miracidial survival and metabolism. Parasitology. 2012; 139(12):1640-51. DOI: 10.1017/S0031182012000960. View

4.
Sargison N, Shahzad K, Mazeri S, Chaudhry U . A high throughput deep amplicon sequencing method to show the emergence and spread of Calicophoron daubneyi rumen fluke infection in United Kingdom cattle herds. Vet Parasitol. 2019; 268:9-15. DOI: 10.1016/j.vetpar.2019.02.007. View

5.
Fairweather I . Reducing the future threat from (liver) fluke: realistic prospect or quixotic fantasy?. Vet Parasitol. 2011; 180(1-2):133-43. DOI: 10.1016/j.vetpar.2011.05.034. View