Key result
Serological testing of equal-volume milk samples using indirect ELISAs demonstrated a strong linear relationship (r = 0.946) with the proportion of seropositive samples up to 50% prevalence.
Why the study?
Variable milk volumes in bulk-tank milk weaken the relationship between ELISA results and within-herd prevalence, prompting evaluation of equal-volume milk samples to accurately estimate caprine arthritis-encephalitis seroprevalence.
Does serological testing of equal-volume milk samples accurately estimate the within-herd seroprevalence of caprine arthritis-encephalitis in goats?
Does serological testing of equal-volume milk samples accurately estimate the within-herd seroprevalence of caprine arthritis-encephalitis in goats?
Effect estimate: r = 0.946 (95% CI 0.905-0.970)
p-value: p=<0.001
Serological testing of equal-volume milk samples using indirect ELISAs can estimate the proportion of strongly seropositive goats in a herd when the prevalence is below 50%.
EVMS ELISA may estimate goat SRLV seroprevalence in controlled pools; leaves open field validation before herd surveillance use.
Background In cattle attempts to evaluate within-herd prevalence of various infectious and parasitic diseases by bulk-tank milk (BTM) testing with ELISA have been made with moderate success. The fact that BTM is composed of variable and unknown volumes of milk from individual lactating animals weakens the relationship between numerical result of the ELISA and the within-herd prevalence. We carried out a laboratory experimental study to evaluate if a pooled milk sample created by mixing an equal volume of individual milk samples from seropositive and seronegative goats, henceforth referred to as an equal-volume milk sample (EVMS), would allow for accurate estimation of within-herd seroprevalence of caprine arthritis-encephalitis (CAE) using 3 different commercial ELISAs. By mixing randomly selected milk samples from seronegative and seropositive goats, 193 EVMS were created – 93 made of seronegative samples and 100 with the proportion of seropositive individual milk samples (EVMS%POS) ranging from 1 to 100%. EVMS%POScould be considered as a proxy for the within-herd seroprevalence. Then, OD of EVMS (ODEVMS) of the 193 EVMS was measured using 3 commercial ELISAs for CAE – 2 indirect and 1 competitive. Results The cut-off values of ODEVMSindicating SRLV infection were determined. The regression functions were developed to link ODEVMSwith EVMS%POS. A significant monotonic relationship between ODEVMSmeasured with 2 commercial indirect ELISAs and EVMS%POSwas identified. Two regression models developed on this basis described approximately 90% of variability and allowed to estimate EVMS%POS, when it was below 50%. High ODEVMSindicated EVMS%POSof > 50%. Conclusion Our study introduces the concept of serological testing of EVMS as a method of detecting SRLV-infected herds and estimating the proportion of strongly seropositive goats. Further field studies are warranted to assess practical benefits of EVMS serological testing.
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Potărniche et al. (2023) studied Small ruminant lentivirus (SRLV) infection / Caprine arthritis-encephalitis (n=200). Equal-volume milk sample (EVMS) serological testing vs. Proportion of seropositive individual milk samples (EVMS%POS) was evaluated on Correlation between optical density of EVMS (ODEVMS) and the proportion of seropositive samples (EVMS%POS) up to 50% using sp-iELISA (r = 0.946, 95% CI 0.905-0.970, p=<0.001). Serological testing of equal-volume milk samples using indirect ELISAs demonstrated a strong linear relationship (r = 0.946) with the proportion of seropositive samples up to 50% prevalence.
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