Literature DB >> 31865671

Evaluation of Next-Generation Amplicon Sequencing to Identify Eimeria spp. of Chickens.

Rüdiger Hauck1,2, Miranda Carrisosa3, Brigid A McCrea4, Teresa Dormitorio3, Kenneth S Macklin3.   

Abstract

Identifying Eimeria spp. circulating in a poultry flock assists in designing vaccine preventive programs, as different species do not cross-protect. Because species differ in anticoccidial drug susceptibility, species identification can also be used to optimize anticoccidial medication. In the present study, we designed pan-Eimeria-specific primers for the 18S rDNA and the cytochrome oxidase I (COI) genes, and tested whether next-generation sequencing of their amplicons allowed reliable identification of Eimeria spp. in samples of isolated oocysts. For each gene, two sets of primers to be used in a nested PCR (nPCR) system were designed. In silico evaluation of the primers using published sequences showed that nucleotide sequence identities of the nested amplicons were less than 97% between most species, while only identities of 18S rDNA genes of Eimeria necatrix and Eimeria tenella and between the COI genes of Eimeria mitis and Eimeria mivati were higher than 97%. Three vaccines and five Eimeria samples from chickens in backyard flocks were investigated by nPCRs and by direct PCRs (dPCR) using the nested (inner) primers with genomic DNA as the template. Seventeen further Eimeria samples from chickens in backyard flocks and three Eimeria samples from commercial broiler flocks were investigated only by nPCR. Sequencing nPCR products tended to detect more species than sequencing dPCR products and sequencing 18S rDNA products tended to detect more species than sequencing COI products. Regarding the detected species, there was a clear difference between the commercial broiler flocks and the backyard flocks. Eimeria acervulina, Eimeria maxima, and E. tenella/E. necatrix were the only species detected in broiler flocks, while the population in the backyard flocks was more varied, with Eimeria brunetti and E. mitis/E. mivati and the previously described operational taxonomic unit Y being more prevalent. Several sequences having less than 97% identity with one of the sequences used for clustering were detected in samples from backyard flocks. In conclusion, next-generation amplicon sequencing can be a useful tool to determine which Eimeria spp. are circulating in chicken flocks.

Entities:  

Keywords:  Illumina sequencing; coccidia; diagnosis

Mesh:

Year:  2019        PMID: 31865671     DOI: 10.1637/aviandiseases-D-19-00104

Source DB:  PubMed          Journal:  Avian Dis        ISSN: 0005-2086            Impact factor:   1.577


  5 in total

1.  Restoration of anticoccidial sensitivity to a commercial broiler chicken facility in Canada.

Authors:  R P Snyder; M T Guerin; B M Hargis; P S Kruth; G Page; E Rejman; J L Rotolo; W Sears; E G Zeldenrust; J Whale; J R Barta
Journal:  Poult Sci       Date:  2020-11-06       Impact factor: 3.352

2.  Prevalence of Select Intestinal Parasites in Alabama Backyard Poultry Flocks.

Authors:  Miranda Carrisosa; Shanhao Jin; Brigid A McCrea; Kenneth S Macklin; Teresa Dormitorio; Rüdiger Hauck
Journal:  Animals (Basel)       Date:  2021-03-26       Impact factor: 2.752

Review 3.  Chicken Coccidiosis: From the Parasite Lifecycle to Control of the Disease.

Authors:  Carolina Mesa-Pineda; Jeffer L Navarro-Ruíz; Sara López-Osorio; Jenny J Chaparro-Gutiérrez; Luis M Gómez-Osorio
Journal:  Front Vet Sci       Date:  2021-12-21

4.  A multiepitope vaccine encoding four Eimeria epitopes with PLGA nanospheres: a novel vaccine candidate against coccidiosis in laying chickens.

Authors:  ZhengQing Yu; SiYing Chen; JianMei Huang; WenXi Ding; YuFeng Chen; JunZhi Su; RuoFeng Yan; LiXin Xu; XiaoKai Song; XiangRui Li
Journal:  Vet Res       Date:  2022-04-01       Impact factor: 3.829

Review 5.  Exploring Eimeria Genomes to Understand Population Biology: Recent Progress and Future Opportunities.

Authors:  Damer P Blake; Kate Worthing; Mark C Jenkins
Journal:  Genes (Basel)       Date:  2020-09-21       Impact factor: 4.096

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.