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Background Classical faecal egg counts (FEC) provide less reliable diagnostic information for nematode infections in chickens. We developed an ELISA based on Ascaridia galli antigens and tested two hypotheses, as follows: (i) IgY antibodies developed against A. galli will also be useful to identify Heterakis gallinarum infections, and (ii) circulating antibodies stored in egg yolks are as good as plasma samples, so a non-invasive diagnosis is possible. The aim of this study, therefore, was to compare the diagnostic accuracy of the ELISA system with FEC, using both plasma and egg yolks from experimentally infected hens. In addition, naturally infected animals were evaluated to validate the assay. Results The assay quantified large differences (P 0.90 for both nematodes using either plasma or egg yolks. Sensitivity of the assay was 94 and 93% with plasma and egg yolk samples, respectively, whereas FEC yielded in a sensitivity of 84% in A. galli experiment. Total test accuracy of the assay with plasma samples (AUC = 0.99) tended to be higher (P = 0.0630) than FEC (AUC = 0.92) for A. galli, while the assay with either sample matrix performed similar to FEC (AUC ≥ 0.91) for H. gallinarum. Among the three tests, the FECs correlated better with A. galli burden than the ELISA. Although 90% of naturally infected hens were correctly identified by the ELISA, 45% of the infected hens tested negative with FEC, indicating the validity of the higher test accuracy of the ELISA. Conclusions Antigens of A. galli can be used successfully to identify H. gallinarum-infected animals, indicating that chickens develop cross-reactive antibodies against the two closely related species. Egg yolks are as informative as plasma samples, so that animal welfare-friendly sampling is possible. Although the assay with plasma samples reveals qualitative information of higher quality than FECs on the infection status of naturally infected birds, the latter is still a better tool to assess the intensity of A. galli but not of H. gallinarum infections. Electronic supplementary material The online version of this article (doi:10.1186/s13071-017-2121-9) contains supplementary material, which is available to authorized users.

Background Density related effects, both inverse density- and density-dependent, contribute to regulating population dynamics of parasites. We investigated whether density related effects are directly controlling lifetime fecundity of Heterakis gallinarum. Methods Daily total numbers of H. gallinarum eggs in faeces samples (N = 1365) from chickens (N = 39) were quantified starting from 3 weeks (wk) post-infection (p.i.). The birds were necropsied 8 wk p.i., and intensity and demographic characteristics of infrapopulations were determined. Density related effects on cumulative egg excretion (CEE), lifetime fecundity and worm length were investigated with a segmented regression analysis. Results For CEE, lifetime fecundity and female worm length, we determined highly similar parasite intensity thresholds (52–54 worms), which separated infrapopulations for influences of inverse density- and density dependence. CEE increased as parasite intensity increased up to an intensity of 52 worms. After this threshold, the relationship followed more of a horizontal line indicating impaired worm fecundity at higher parasite intensities. Lifetime fecundity was enhanced linearly in infrapopulations with up to 54 worms, but thereafter decreased gradually with increasing infrapopulation size. Female worm length increased linearly with elevating parasite intensity up to a threshold of 54 worms and thereafter declined with a rate of -0.014 mm for each additional worm. Lifetime fecundity and female worm length did not significantly differ between infrapopulations below and above the thresholds (P > 0.05). Lifetime fecundity was positively associated with the percentage of male worms (r = 0.44; P 0.05). Conclusions Egg production of H. gallinarum is regulated by the effects of both inverse density- and density-dependent mechanisms, which result in similar average lifetime fecundity below or above intensity thresholds. In infrapopulations below the intensity thresholds, inverse density dependence effects on lifetime fecundity appear to result partly from sex-ratio fluctuations and impaired mating success of the nematode. peerReviewed