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Next-generation sequencing amplicon analysis of the genetic diversity of Eimeria populations in livestock and wildlife samples from Australia.
Zahedi, Alireza; Liu, Dandan; Yang, Rongchang; Austen, Jill M; Potter, Abbey; Ryan, Una.
Afiliação
  • Zahedi A; Harry Butler Institute, Murdoch University, Perth, WA, 6150, Australia. a.zahediabdi@murdoch.edu.au.
  • Liu D; Jiangsu Co-Innovation Centre for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, Jiangsu, 225009, People's Republic of China.
  • Yang R; Australian National Phenome Centre, Health Futures Institute, Murdoch University, Harry Perkins Building, Perth, WA, 6150, Australia.
  • Austen JM; Harry Butler Institute, Murdoch University, Perth, WA, 6150, Australia.
  • Potter A; Environmental Health Directorate, Public and Aboriginal Health Division, Department of Health, Biological and Applied Environmental Health Hazards, Perth, WA, 6849, Australia.
  • Ryan U; Harry Butler Institute, Murdoch University, Perth, WA, 6150, Australia.
Parasitol Res ; 122(2): 615-624, 2023 Feb.
Article em En | MEDLINE | ID: mdl-36544013
ABSTRACT
Eimeria is an important coccidian enteric parasite that infects a wide range of hosts and can cause substantial economic losses in the poultry and livestock industries. It is common for multiple Eimeria species to infect individual hosts, and this can make species identification difficult due to morphological similarities between species and mixed chromatograms when using Sanger sequencing. Relatively few studies have applied next-generation amplicon sequencing (NGS) to determining the genetic diversity of Eimeria species in different hosts. The present study screened 408 faecal samples from a range of hosts including livestock and wildlife using a previously developed quantitative polymerase chain reaction (qPCR) at the 18S locus and conducted amplicon NGS on the positives using a ~ 455-bp fragment of the 18S locus. A total of 41 positives (10.1%) were identified by qPCR from various hosts and NGS was successful for 38 of these positives. Fifteen Eimeria species and three genotypes were detected by NGS E. ferrisi, E. kanyana, E. potoroi, E. quokka, E. setonicis, E. trichosuri, E. reichenowi, E. angustus, E. ahsata, E. auburnensis, E. bovis, E. brasiliensis, E. christenseni, E. crandallis, E. ovinoidalis, Eimeria sp. (JF419345), Eimeria sp. (JF419349) and Eimeria sp. (JF419351). Mixed infections were detected in 55.3% (21/38) of positive samples. The most striking finding was the identification of the same species in different hosts. This could be due to contamination and/or mechanical transmission or may provide support for previous studies suggesting that Eimeria species can infect not just closely related hosts but different genera and further research is required. This is also the first study to audit Eimeria populations in livestock (sheep and cattle) by NGS and could be applied in the future to determine the extent of pathogenic species and outcomes of Eimeria control strategies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coccidiose / Eimeria Tipo de estudo: Prognostic_studies Limite: Animals País/Região como assunto: Oceania Idioma: En Revista: Parasitol Res Assunto da revista: PARASITOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coccidiose / Eimeria Tipo de estudo: Prognostic_studies Limite: Animals País/Região como assunto: Oceania Idioma: En Revista: Parasitol Res Assunto da revista: PARASITOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália