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1.
Vet Parasitol ; 275: 108925, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31605937

ABSTRACT

Modern chickens have been genetically developed to perform high under optimal conditions. We hypothesized that high-performance is associated with a higher sensitivity to environmental challenges in laying hens. By using nematode infections as an environmental stressor, we assessed performance-level associated host responses in a high (i.e. Lohmann Brown Plus, LB) and in a lower performing, a so-called dual-purpose chicken genotype (i.e. Lohmann Dual, LD). The hens were infected with 1000 eggs of Ascaridia galli and Heterakis gallinarum at 24 weeks of age. Hen performance parameters, humoral immune responses in plasma and egg yolks and worm burdens were assessed at several occasions over a period of 18 weeks post infection (wpi). While infections had no significant effect on feed intake (P = 0.130) and body weight in both genotypes (P = 0.392), feed conversion efficiency was negatively affected by infections (P = 0.017). Infections reduced both laying rate and egg weight and thereby per capita egg mass in both genotypes (P < 0.05). While laying rate in infected LB hens decreased significantly (P < 0.05) in the early infection period (i.e. by 3 wpi), the decrease in LD hens appeared much later (i.e. by 14 wpi). Worm burdens resulting from the experimental infection were not different between the genotypes for both worm species (P > 0.05), whereas LB hens were more susceptible (P < 0.05) to re-infections than LD hens. Changes in humoral immune responses (i.e. ascarid-specific IgY antibodies in plasma and egg yolks) of the two genotypes over time reflected closely the corresponding changes in larval counts of the hens, descending from both experimental and subsequent natural infections in both genotypes. Infections caused a shift in egg size classes, leading to smaller frequency of larger eggs in both genotypes. Infections reduced egg weight (P = 0.018) and led to a reduced fat content in the egg yolks (P = 0.045). The proportion of poly-unsaturated fatty acids (PUFA), especially n-6-PUFA, was also lower in egg yolks of the infected hens (P = 0.032). We conclude that tolerance to nematode infections in laying hens is dependent on host-performance level. The impairment in host tolerance was both genotype and time dependent, likely due to differences in genetic programming for production peak and persistency of the two genotypes. The two genotypes exhibited similar levels of resistance after a fully controlled experimental infection, but the high performing hens were more susceptible to subsequent natural infections. Infections negatively affected economically important egg-quality traits, including egg weight, fat content and fatty acid profiles in egg yolks.


Subject(s)
Chickens/parasitology , Egg Yolk/chemistry , Eggs/standards , Nematode Infections/veterinary , Poultry Diseases/parasitology , Animals , Antibodies, Helminth/blood , Ascaridida/growth & development , Ascaridida/immunology , Chickens/classification , Chickens/genetics , Chickens/physiology , Egg Yolk/immunology , Egg Yolk/parasitology , Enzyme-Linked Immunosorbent Assay/veterinary , Fatty Acids/analysis , Feces/parasitology , Female , Genotype , Immunoglobulins/analysis , Immunoglobulins/blood , Male , Nematode Infections/immunology , Nematode Infections/parasitology , Parasite Egg Count/veterinary , Poultry Diseases/immunology , Rhabditida/growth & development , Rhabditida/immunology
2.
Emerg Infect Dis ; 23(8): 1397-1399, 2017 08.
Article in English | MEDLINE | ID: mdl-28726612

ABSTRACT

Baylisascaris procyonis (raccoon roundworm) infection is common in raccoons and can cause devastating pathology in other animals, including humans. Limited information is available on the frequency of asymptomatic human infection. We tested 150 adults from California, USA, for B. procyonis antibodies; 11 were seropositive, suggesting that subclinical infection does occur.


Subject(s)
Ascaridida Infections/epidemiology , Ascaridida/immunology , Animals , Ascaridida Infections/history , Ascaridida Infections/immunology , California/epidemiology , Feces/parasitology , Female , History, 21st Century , Humans , Male , Prevalence , Raccoons , Seroepidemiologic Studies , Zoonoses
3.
Parasit Vectors ; 10(1): 187, 2017 Apr 18.
Article in English | MEDLINE | ID: mdl-28420423

ABSTRACT

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 < 0.001) in plasma or in egg-yolk IgY concentrations between infected and uninfected animals in two experiments, each performed with either of the nematode species. The assay performed with high accuracy as quantified with the area under the ROC curve (AUC) values of > 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.


Subject(s)
Antibodies, Helminth/blood , Ascaridiasis/veterinary , Ascaridida/immunology , Chickens , Egg Yolk/immunology , Enzyme-Linked Immunosorbent Assay/veterinary , Poultry Diseases/diagnosis , Animals , Antibodies, Helminth/immunology , Antigens, Helminth/immunology , Area Under Curve , Ascaridia/immunology , Ascaridia/isolation & purification , Ascaridiasis/diagnosis , Ascaridiasis/parasitology , Ascaridida/isolation & purification , Chickens/immunology , Chickens/parasitology , Cross Reactions , Feces/parasitology , Immunoglobulins/blood , Immunoglobulins/immunology , Parasite Egg Count , Poultry Diseases/parasitology , Sensitivity and Specificity
4.
W V Med J ; 112(6): 32-3, 2016.
Article in English | MEDLINE | ID: mdl-29368826

ABSTRACT

We report a case of exposure to raccoon feces found to be contaminated with baylisascaris procyonis. The exposure was recognized early enough by the family to allow prophylaxis with albendazole. Because of the potential fatal or neurologically catastrophic effects of this disease immediate treatment is indicated. This is started in advance of environmental studies that are done to determine if the feces is indeed contaminated.


Subject(s)
Albendazole , Anthelmintics , Ascaridida Infections/veterinary , Ascaridida , Raccoons/parasitology , Adult , Albendazole/therapeutic use , Animals , Anthelmintics/therapeutic use , Antibodies, Helminth/blood , Ascaridida/immunology , Ascaridida/isolation & purification , Ascaridida Infections/blood , Ascaridida Infections/diagnosis , Ascaridida Infections/drug therapy , Child , Feces/parasitology , Humans , Male , Risk Factors , Time Factors , Treatment Outcome
5.
Fish Shellfish Immunol ; 33(4): 780-7, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22820379

ABSTRACT

Congerin is a proto-type galectin distributed on the skin and mucosal epithelia of the upper digestive tract of the Japanese conger eel Conger myriaster. It has at least 2 isotypes, namely, congerin I and II, and plays a role in bio-defense at the body surface. In the current study, we identified both isotypes in the peritoneal fluid and peritoneal cells of C. myriaster by western blot and mass spectrometry (MS)/MS analysis. Cucullanus nematodes parasitize the abdominal cavity of C. myriaster, and immunohistochemical analyses demonstrated that congerins can bind to both the body surface of the encapsulated nematodes and the encapsulating cells. Furthermore, adhesion of the peritoneal cells to Sepharose particles was greatly accelerated when the microspheres were coated with congerin. Indeed, this effect was significantly hampered by the addition of lactose. These results indicate that congerin participates in the cellular encapsulation of the Cucullanus nematode via the induction of cellular adhesion to the parasites depending on lectin-glycoside recognition.


Subject(s)
Abdominal Cavity/parasitology , Ascaridida Infections/veterinary , Eels/immunology , Fish Diseases/immunology , Fish Proteins/metabolism , Galectins/metabolism , Animals , Ascaridida/immunology , Ascaridida/physiology , Ascaridida Infections/immunology , Ascaridida Infections/metabolism , Ascitic Fluid/immunology , Ascitic Fluid/parasitology , Blotting, Western/veterinary , Cell Adhesion , Eels/parasitology , Fish Diseases/metabolism , Fish Proteins/immunology , Galectins/immunology , Gene Expression Profiling , Immunohistochemistry/veterinary , Intestinal Mucosa/immunology , Intestinal Mucosa/parasitology , Lactose/metabolism , Tandem Mass Spectrometry/veterinary
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