2000
DOI: 10.1016/s0020-7519(00)00084-9
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Single-strand restriction fragment length polymorphism analysis of the second internal transcribed spacer (ribosomal DNA) for six species of Eimeria from chickens in Australia

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Cited by 43 publications
(23 citation statements)
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“…A two-step PCR technique was used for differentiation of eight coccidian species. A PCR RFLP technique was used for characterisation of six species of coccidia in Australia (Woods et al 2000). However, conventional PCR has limitations in quantifying the number of Eimeria oocysts present in samples as well as detection of mixed-species infections which can be overcome by applications of realtime PCR.…”
Section: Diagnosis and Identification At Species Levelmentioning
confidence: 99%
“…A two-step PCR technique was used for differentiation of eight coccidian species. A PCR RFLP technique was used for characterisation of six species of coccidia in Australia (Woods et al 2000). However, conventional PCR has limitations in quantifying the number of Eimeria oocysts present in samples as well as detection of mixed-species infections which can be overcome by applications of realtime PCR.…”
Section: Diagnosis and Identification At Species Levelmentioning
confidence: 99%
“…by using ITS-1 or ITS-2 sequences (Woods et al, 2000;Gasser et al, 2001;Lew et al, 2003;Haug et al, 2007) or sequence characterized amplification regions (SCARs) (Fernandez et al, 2003). Woods et al, (2000) described a polymerase chain reaction-linked restriction fragment length polymor-phism (PCR-RFLP) approach targeting the second internal transcribed spacer (ITS-2) to characterize six Eimeria spp. However, the ITS sequences show some variability both within a genome as well as between species and strains (Cantacessi et al, 2008).…”
Section: Coccidian Infectionsmentioning
confidence: 99%
“…Additionally, because this approach gave limited information about strain variation, further work was carried out to develop a test based on the use of the second ITS region. 25,27,[43][44][45] Universal probes for family (Eimeriidae) and genus (Eimeria) 28S rRNA (at the 3′ end) and 5.8S rRNA (at the 5′ end) sequences respectively flanking the second ITS region enabled identification of and discrimination between all seven species. It also made it possible to detect variation within a single Eimeria species.…”
Section: Targeted Pcr On Individual Speciesmentioning
confidence: 99%
“…It also made it possible to detect variation within a single Eimeria species. 44,45 Therefore, in addition to abolishing the need for isotopes, electrophoretic gels, and monospecific reference controls, the major advantage of this novel test was the ability to detect all seven Eimeria species and their genetic variants in a single PCR reaction. These universal primers were validated in testing two Eimeria species concurrently as well as field samples, and it was concluded by the authors that these tests are accurate, less laborious than previous tests, and cheap enough to be used for testing field samples in routine diagnostic laboratories.…”
Section: Targeted Pcr On Individual Speciesmentioning
confidence: 99%