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Molecular Characterization of Indian Species of Steinernema (Nematoda: Steinernematidae) Based on Restriction Fragment Length Polymorphism Profile of Internal Transcribed Spacer Region of Ribosomal DNA
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作者 S. Kumar A. Yadav S. Ganguly 《Journal of Agricultural Science and Technology(A)》 2011年第3X期368-374,共7页
Restriction fragment length polymorphism (RFLP) profiles of the amplified products of Internal Transcribed Spacer (ITS) region of rDNA using four restriction enzymes (Alul, Rsal, HinfI and HhaI) revealed distinc... Restriction fragment length polymorphism (RFLP) profiles of the amplified products of Internal Transcribed Spacer (ITS) region of rDNA using four restriction enzymes (Alul, Rsal, HinfI and HhaI) revealed distinctness of six Indian isolates of Steinernema one each from Maharashtra (IARI-EPN-mh), Himachal Pradesh (IARI-EPN-hp), Dehradun (IARI-EPN-dhdl), Jharkhand (IARI-EPN-jhl) and two from Madhya Pradesh (IARI-EPN-bpll & IARI-EPN-gwll), when compared with the only native species Steinernema thermophilum. One of the restriction enzyme, Rsal could differentiate all the six species/strains from one another. The three restriction enzymes yielded patterns which were of diagnostic value but Rsal appeared to be the best diagnostic marker for differentiating these isolates. A tree constructed based upon the band sharing amongst the isolates, produced trichotomy which placed strains from Madhya Pradesh and Jharkhand in one group showing 94% homology, one strain from Bhopal (M.P) formed separate clade along with S. thermophilum with 72% similarity. These isolates, from Maharashtra, Himachal Pradesh and Dehradun, showed only 51% similarity with the S. thermophilum by forming separate clade. 展开更多
关键词 Entomopathogenic nematode ITS region RFLP ribosomal DNA Steinernema thermophilum molecularcharacterization.
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口蹄疫病毒OT株的全基因组序列测定及比较分析
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作者 吕占禄 王光祥 +1 位作者 尚佑军 刘湘涛 《畜牧兽医学报》 CAS CSCD 北大核心 2012年第1期90-97,共8页
参考GenBank上已发表的口蹄疫病毒(FMDV)全长基因组序列,设计了覆盖基因组全长的数对引物,通过RT-PCR方法对口蹄疫病毒OT株进行分段克隆及序列测定。结果表明不含poly(C)序列的OT株基因组全序列长8 142nt,开放读码框(ORF)长6 969nt、编... 参考GenBank上已发表的口蹄疫病毒(FMDV)全长基因组序列,设计了覆盖基因组全长的数对引物,通过RT-PCR方法对口蹄疫病毒OT株进行分段克隆及序列测定。结果表明不含poly(C)序列的OT株基因组全序列长8 142nt,开放读码框(ORF)长6 969nt、编码2 322aa,5′UTR长1 004nt,3′UTR长93nt,3′UTR之后为23nt的poly(A)尾巴。应用分子生物学软件将OT株与FMDV其它参考毒株进行序列比对,并对其基因特征进行分析。结果显示,OT株的假结节(Pseudoknots)从第415—499位连续缺失85nt,但是其3A基因却未发生碱基的缺失。其VP1基因的核苷酸同源性与O/Akesu58、OMⅢ两株最高,但OT株在进化时间上要比O/Akesu58、OMIII早很多,其毒株起源和遗传衍化关系还需要进一步的关注。 展开更多
关键词 口蹄疫病毒 全基因组 编码区 分子生物学特性 序列比对
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Detection, isolation, and characterization of chikungunya viruses associated with the Pakistan outbreak of 2016–2017
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作者 Si-Qinq Liu Xiao Li +8 位作者 Ya-Nan Zhang Ai-Li Gao Cheng-Lin Deng Jun-Hua Li Shoukat Jehan Nadia Jamil Fei Deng Hongping Wei Bo Zhang 《Virologica Sinica》 SCIE CAS CSCD 2017年第6期511-519,共9页
The chikungunya virus(CHIKV) is a mosquito-transmitted alphavirus, which has infected millions of people in Africa, Asia, Americas, and Europe since it reemerged in India and Indian Ocean regions in 2005–2006. Starti... The chikungunya virus(CHIKV) is a mosquito-transmitted alphavirus, which has infected millions of people in Africa, Asia, Americas, and Europe since it reemerged in India and Indian Ocean regions in 2005–2006. Starting in the middle of November 2016, CHIKV has been widely spread, and more than 4,000 cases of infections in humans were confirmed in Pakistan. Here, we report the first isolation and characterization of CHIKV from the Pakistan outbreak. Eight CHIKV strains were newly isolated from human serum samples using a cell culture procedure. A full-length genome sequence and eight complete envelope(E1) sequences of CHIKV from Pakistan were obtained in this study. Alignment of the CHIKV E1 sequences revealed that the eight new CHIKV isolates were highly homogeneous, with only two nonsynonymous substitutions found at generally conserved sites(E99 and Q235). Based on the comparison of 342 E1 sequences, the two nonsynonymous mutations were located in well-recognized domains associated with viral functions such as the cell fusion and vector specificity, suggesting their potential functional importance. Phylogenetic analysis indicated that the CHIKV strains from Pakistan originated from CHIKV circulating in the Indian region. This study helps elucidate the epidemics of CHIKV in Pakistan and also provides a foundation for studies of evolution and expansion of CHIKV in South Asia. 展开更多
关键词 chikungunya virus(CHIKV) Pakistan virus isolation clinical serum molecular characterization
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