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1.
Avian Dis ; 56(2): 306-9, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22856186

ABSTRACT

Vaccines composed of either virulent or attenuated Eimeria spp. oocysts have been developed as an alternative to medication of feed with ionophore drugs or synthetic chemicals. The purpose of this study was to evaluate the use of gel-beads containing a mixture of Eimeria acervulina, Eimeria maxima, and Eimeria tenella oocysts as a vaccine against coccidiosis. Newly hatched chicks (Gallus gallus domesticus) were either sprayed with an aqueous suspension of Eimeria oocysts or were allowed to ingest feed containing Eimeria oocysts-incorporated gel-beads. Control day-old chicks were given an equivalent number of Eimeria oocysts (10(4) total) by oral gavage. After 3 days, chicks were randomly assigned to individual cages, and feces were collected between days 5 and 8 postinfection. All samples were processed for total Eimeria oocysts. At 4 wk of age, all chickens and a control nonimmunized group received a high-dose E acervulina, E maxima, and E. tenella challenge infection. Oocyst excretion by chicks fed gel-beads or inoculated by oral gavage was 10- to 100-fold greater than that of chicks spray-vaccinated with the Eimeria oocysts mixture (log 6.3-6.6 vs. log 4.8). Subsequent protection against challenge as measured by weight gain and feed conversion efficiency was significantly greater (P < 0.05) in gel-bead and oral gavage groups compared with spray-vaccinated or nonimmunized groups. Also, gel-bead and oral gavage groups showed no significant difference (P > 0.05) in weight gain and feed conversion efficiency compared with nonchallenged controls. These findings indicate that incorporation of Eimeria spp. oocysts in gel-beads may represent an effective way to deliver live oocyst vaccines to day-old chicks for preventing subsequent outbreaks of coccidiosis in the field.


Subject(s)
Chickens , Coccidiosis/veterinary , Eimeria/physiology , Gelatin/therapeutic use , Poultry Diseases/prevention & control , Protozoan Vaccines/immunology , Animals , Coccidiosis/immunology , Coccidiosis/prevention & control , Eimeria tenella/immunology , Eimeria tenella/physiology , Gelatin/administration & dosage , Oocysts/physiology , Poultry Diseases/immunology , Protozoan Vaccines/administration & dosage , Species Specificity , Vaccination/veterinary , Vaccines, Attenuated/administration & dosage , Vaccines, Attenuated/immunology
2.
J Parasitol ; 95(4): 871-80, 2009 Aug.
Article in English | MEDLINE | ID: mdl-20049993

ABSTRACT

The impact of coccidiosis outbreaks on the productivity of broiler chicken farms can be substantial, depending on the severity of disease caused by particular species and strains of Eimeria. We examined the genetic diversity of Eimeria species present in commercial broiler farms in relation to their performance level. Four groups of broiler chicken farms in Arkansas (AR) and North Carolina (NC), having either high or low performance levels, were sampled for Eimeria spp. oocysts. We amplified gDNA from oocysts by using genus-specific primers targeting 18S ribosomal RNA, the first and second internal transcribed spacer regions, and cytochrome c oxidase subunit I as the established species-specific primers. Eimeria spp. diversity was not homogenous among the 4 farm groups, with less-pathogenic species (E. mitis and E. mivati-like) associated with AR and NC high-performance farms, respectively, and a pathogenic species (E. brunetti) associated with AR low-performance farms. Sequence analyses identified multiple E. maxima and E. mitis genetic variants, from which 2 E. maxima variants were unique to low-performance farms. Distinct populations of sequences at the NC high-performance farms were identified as E. mivati-like, based on homology searches. Our study demonstrated the utility of analyzing multiple genomic loci to assess composition and polymorphisms of Eimeria spp. populations.


Subject(s)
Chickens/parasitology , Coccidiosis/veterinary , Disease Outbreaks/veterinary , Eimeria/genetics , Genomics , Poultry Diseases/parasitology , Animal Husbandry/economics , Animals , Arkansas/epidemiology , Base Sequence , Cloning, Molecular , Coccidiosis/economics , Coccidiosis/epidemiology , Coccidiosis/parasitology , DNA Primers , DNA, Protozoan/chemistry , DNA, Protozoan/isolation & purification , Disease Outbreaks/economics , Eimeria/classification , Eimeria/pathogenicity , Feces/parasitology , Genetic Variation , Molecular Sequence Data , North Carolina/epidemiology , Parasite Egg Count/veterinary , Phylogeny , Polymerase Chain Reaction/veterinary , Poultry Diseases/economics , Poultry Diseases/epidemiology , RNA, Ribosomal, 18S/genetics , Sequence Alignment/veterinary , Sequence Analysis, DNA/veterinary , Species Specificity
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