2021
DOI: 10.1016/j.cimid.2020.101607
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The first survey and molecular identification of Entamoeba spp. in farm animals on Qinghai-Tibetan Plateau of China

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Cited by 10 publications
(13 citation statements)
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“…The predominant Entamoeba species identified in the wild deer and cattle samples collected and analysed in this study was Entamoeba bovis, a species recognised to infect ruminants, including livestock animals (Stensvold et al, 2010;Matsubayashi et al, 2018;Ai et al, 2021). The prevalence of Entamoeba infections previously reported in cattle are relatively low [2.5% in Costa Rica (Jimenez et al, 2007), 4.8% in Korea (Ismail et al, 2010)] when detected by microscopic analysis; while higher prevalences have been reported following PCR analysis [72% in Japan (Matsubayashi et al, 2018), 80% in Uganda (Nolan et al, 2017), 100% in China (Ai et al, 2021)]. Similar to these last reports, the present study detected a prevalence of 100% for E. bovis in cattle samples (n=23) using a PCR-based analysis.…”
Section: Discussionmentioning
confidence: 92%
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“…The predominant Entamoeba species identified in the wild deer and cattle samples collected and analysed in this study was Entamoeba bovis, a species recognised to infect ruminants, including livestock animals (Stensvold et al, 2010;Matsubayashi et al, 2018;Ai et al, 2021). The prevalence of Entamoeba infections previously reported in cattle are relatively low [2.5% in Costa Rica (Jimenez et al, 2007), 4.8% in Korea (Ismail et al, 2010)] when detected by microscopic analysis; while higher prevalences have been reported following PCR analysis [72% in Japan (Matsubayashi et al, 2018), 80% in Uganda (Nolan et al, 2017), 100% in China (Ai et al, 2021)]. Similar to these last reports, the present study detected a prevalence of 100% for E. bovis in cattle samples (n=23) using a PCR-based analysis.…”
Section: Discussionmentioning
confidence: 92%
“…Genomic DNA was extracted using a DNeasy ® PowerSoil ® Kit (Qiagen, Valencia, CA, USA) following the manufacturer's instructions. PCR was performed with primers EntboF2 and EntboR3 (Matsubayashi et al, 2018;Ai et al, 2021) to amplify an internal fragment of 850 bp of the 18S rRNA Entamoeba gene. In addition, the methodology published by Ali et al (2005) was employed to detect tRNA-linked short tandem repeats (STRs).…”
Section: Dna Extraction and Pcr Amplificationmentioning
confidence: 99%
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