2005
DOI: 10.1645/ge-3310
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Molecular Characterization of Isosporoid Coccidia (Isospora and Atoxoplasma Spp.) in Passerine Birds

Abstract: Prevalence and disease caused by isosporoid coccidia in passerine birds are well recognized, but confusion about the life cycles of the parasites has led to taxonomic inconsistencies. In this study, we characterized segments of the chromosomal small and large-subunit ribosomal RNA (rRNA) genes of coccidial parasites from 23 species of passerine birds, as well as heat shock protein 70, apicoplast rRNA, and chromosomal 5.8s rRNA genes from a subgroup of these animals, and we correlated genetic data with morpholo… Show more

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Cited by 90 publications
(87 citation statements)
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“…Later, this species and more than 18 others, all with extra-intestinal life-cycles, were redescribed and allocated to Atoxoplasma Garnham, 1950by Levine (1982c. However, the validity of this genus was questioned by Boulard et al (1987) and, more recently, by Carreno & Barta (1999), Schrenzel et al (2005), Barta et al (2005) and Gill & Paperna (2008).…”
Section: Discussionmentioning
confidence: 99%
“…Later, this species and more than 18 others, all with extra-intestinal life-cycles, were redescribed and allocated to Atoxoplasma Garnham, 1950by Levine (1982c. However, the validity of this genus was questioned by Boulard et al (1987) and, more recently, by Carreno & Barta (1999), Schrenzel et al (2005), Barta et al (2005) and Gill & Paperna (2008).…”
Section: Discussionmentioning
confidence: 99%
“…The particular species of coccida used in this study, Isospora lacazei (family Eimeriidae; E. Greiner, personal communication), has a relatively broad geographical and host range within passerines (Levine 1982), though local adaption of haplotypes is likely common (Schrenzel et al 2005;Dolnik et al 2009). In infected chickens, oocysts are released in the feces 4-5 d postinfection, with peak shedding 6-9 d postinfection, followed by chronic shedding (Allen and Fetterer 2002).…”
Section: Parasitesmentioning
confidence: 99%
“…The PCR for the 28S rRNA locus was carried out using a nested PCR with the external primers: 28SExF: 5′-TAC CCG CTG AAC TTA AGC-3′ and 28SExR: 5′-CMA CCA AGA TCT GCA CTA G-3′ as previously described (Schrenzel et al, 2005), which produced a PCR product size of~1495 bp. The internal primers (28InF: 5′-ACT ATG TTC CCT AGT AAC G-3′ and 28SInR 5′-AAC GCT TCG CCA CGA TCC-3′) were as previously reported (Yang et al, 2014) and produced an amplicon size of 1420 bp.…”
Section: Pcr Amplification and Sequencingmentioning
confidence: 99%