2019
DOI: 10.1016/j.meegid.2019.104021
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Molecular typing of Giardia duodenalis in cattle, sheep and goats in an arid area of central Iran

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Cited by 29 publications
(18 citation statements)
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References 26 publications
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“…The overall G. lamblia prevalence (9.2%) in cattle in this study was higher than that in cattle in Zhaoqing city, Guangdong Province (2.2%) [28], and Qinghai Province, China (5.2%) [29], an arid area of central Iran (4.2%) [30], Thailand (6.0%) [31], and Urmia, northwest Iran (9.34%) [32]; but lower than that in Guangdong Province (74.2%) [6], Hubei Province (22.6%) [33] and Sichuan Province, China (9.4%) [34]; Egypt (13.3%) [35], South Korea (10.0%) [36], Ethiopia (9.6%) [37] and Vietnam (13.8%) [38]. The difference in G. lamblia prevalence may be related to difference in study design, breed and age of cattle studied and sampling size.…”
contrasting
confidence: 57%
“…The overall G. lamblia prevalence (9.2%) in cattle in this study was higher than that in cattle in Zhaoqing city, Guangdong Province (2.2%) [28], and Qinghai Province, China (5.2%) [29], an arid area of central Iran (4.2%) [30], Thailand (6.0%) [31], and Urmia, northwest Iran (9.34%) [32]; but lower than that in Guangdong Province (74.2%) [6], Hubei Province (22.6%) [33] and Sichuan Province, China (9.4%) [34]; Egypt (13.3%) [35], South Korea (10.0%) [36], Ethiopia (9.6%) [37] and Vietnam (13.8%) [38]. The difference in G. lamblia prevalence may be related to difference in study design, breed and age of cattle studied and sampling size.…”
contrasting
confidence: 57%
“…In Iran, human giardiasis has been reported at infection rates ranging from 5% to 23% in different parts of the country [29]. Documented animal prevalences were 5-16% in goats, 6-20% in sheep, and 4% in cattle [30,31]; however, molecular [1,21,32,33]. These surveys coincide to identify assemblage A, sub-assemblage AII as the predominant G. duodenalis genetic variant circulating in Iranian human population.…”
Section: Discussionmentioning
confidence: 99%
“…The identification of G. intestinalis is usually based on molecular methods using the following five genes: glutamate dehydrogenase, beta-giardin, elongation factor-1 alpha, triose phosphate isomerase and small subunit rRNA ( SSU rRNA ) [1] . The current molecular methods of the identification of Giardia required scientist to extract DNA from homogenized faeces using commercial kit [2] , which may be expensive for developing regions. Furthermore, there are no methods to directly isolate living Giardia trophozoites from their host animals at present.…”
Section: Methods Detailsmentioning
confidence: 99%
“…3 Trophozoites of Giardia species. A Trophozoite of G. cricetidarum ; B Trophozoite of G. muris ; C Trophozoite of G. microti ; D Trophozoite of G. agilis [2] . Scale-bars: A, B, C 10 µm; D 20 µm.…”
Section: Methods Detailsmentioning
confidence: 99%