2015
DOI: 10.1186/s12917-015-0387-8
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Molecular characterization and phylogenetic analysis of transmissible gastroenteritis virus HX strain isolated from China

Abstract: BackgroundPorcine transmissible gastroenteritis virus (TGEV) is the major etiological agent of viral enteritis and severe diarrhea in suckling piglets. In China, TGEV has caused great economic losses, but its role in epidemic diarrhea is unclear. This study aims to reveal the etiological role of TGEV in piglet diarrhea via molecular characterization and phylogenetic analysis.ResultsA TGEV-HX strain was isolated from China, and its complete genome was amplified, cloned, and sequenced. Sequence analysis indicate… Show more

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Cited by 35 publications
(63 citation statements)
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“…Piglets were fed a mixture of skim milk powder (Inner Mongolia Yi Li Industrial Group Co., Ltd, China) with warm water. Prior to inoculation, piglets were confirmed negative for the major porcine enteric viruses (PDCoV, PEDV, TGEV, PRoV) by testing of rectal swabs using specific RT-PCR according to previously described method (Hu, Li et al, 2015;Jeong et al, 2009;Saeng-Chuto et al, 2017). After 1-day acclimation, piglets in group 1 were orally inoculated with 5 ml of maintenance medium and served as uninfected controls.…”
Section: Experimental Infection With the Peav Gds04 Strain In Newbomentioning
confidence: 99%
“…Piglets were fed a mixture of skim milk powder (Inner Mongolia Yi Li Industrial Group Co., Ltd, China) with warm water. Prior to inoculation, piglets were confirmed negative for the major porcine enteric viruses (PDCoV, PEDV, TGEV, PRoV) by testing of rectal swabs using specific RT-PCR according to previously described method (Hu, Li et al, 2015;Jeong et al, 2009;Saeng-Chuto et al, 2017). After 1-day acclimation, piglets in group 1 were orally inoculated with 5 ml of maintenance medium and served as uninfected controls.…”
Section: Experimental Infection With the Peav Gds04 Strain In Newbomentioning
confidence: 99%
“…To detect PDCoV genome in collected fecal samples, the previously reported RT-PCR primers (41 F: 5'-TTT CAGGTGCTCAAAGCTCA-3' and 735R: 5'-GCGAAA AGCATTTCCTGAAC-3') targeting the nucleocapsid (N) gene with reaction conditions (50°C for 30 min and 95°C for 15 min for the reverse transcription reaction, followed by 40 cycles of PCR amplification at 95°C for 15 s, 55°C for 45 s, and 72°C for 1 min, with a final extension at 72°C for 7 min) were used [15]. In addition, molecular detection of the three diarrhea-related enteric viruses (Porcine epidemic diarrhea virus, PEDV; Porcine transmissible gastroenteritis virus, TGEV; Porcine rotavirus group C, Rota C) was performed in accordance with previous methods [20][21][22] for further evaluation of the possible co-infection status with PDCoV in investigated pig samples.…”
Section: Reverse Transcription Polymerase Chain Reaction (Rt-pcr) Detmentioning
confidence: 99%
“…Fifteen primer pairs were designed based on the conserved regions of CCoV strain TN-449 (Table S1). The RT-PCR assay was performed as described previously [13].…”
Section: Isolation Identification and Purification Of The Virusmentioning
confidence: 99%