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一种源自棉铃虫HBN胚胎组织的新细胞系。(鳞翅目:夜蛾科)

A new cell line from the embryonic tissue of Helicoverpa armigera HBN. (Lepidoptera: Noctuidae).

作者信息

Sudeep A B, Mourya D T, Shouche Y S, Pidiyar V, Pant U

机构信息

National Institute of Virology, 20-A, Dr. Ambedkar Road, Pune 411 001, Maharashtra, India.

出版信息

In Vitro Cell Dev Biol Anim. 2002 May;38(5):262-4. doi: 10.1290/1071-2690(2002)038<0262:ANCLFT>2.0.CO;2.

Abstract

A new cell line from the embryonic tissue of Helicoverpa armigera was established and designated as NIV-HA-197. It was maintained in TNM-FH medium supplemented with 10% fetal bovine serum. The cell line at passage 20 had a heterogeneous population of cells consisting of mainly epithelial-like cells (70%), followed by fibroblast-like (27%), and multinucleated giant (3%) cells. The chromosome number ranged from 45 to 185. The growth curve at passage 40 showed a fivefold increase in cell number with a population-doubling time of approximately 60 h. The cell line was found infected with the microsporidium Nosema heliothids at passage 9. Using the antiprotozoan drug Metrogyl 400 and simultaneous heat treatment, the parasite was removed from the culture. The cell line can be cryopreserved for 30 mo. The species specificity of the new cell line was determined by studying the isoenzyme profile of four enzymes, viz., lactate dehydrogenase, malate dehydrogenase, isocitrate dehydrogenase, and glucose 6-phosphate dehydrogenase, and by heteroduplex analysis. Heteroduplex analysis was used to analyze the mitochondrial 16S ribosomal ribonucleic acid gene sequences along with the host insect gene sequences, and 100% homology was obtained, confirming the conspecificity of the cell line. The cell line was found to be susceptible to the baculoviruses Autographa californica multiple nucleopolyhedrovirus, Spodoptera litura multiple nucleopolyhedrovirus, and H. armigera single nucleopolyhedrovirus (HaSNPV). More than 90% of the cells were infected by HaSNPV on the seventh post infection day (PID), and 28.8 x 10(6) NPV/ml was yielded on the 10th PID. The in vitro-grown HaSNPV caused 100% mortality, when fed to the second instar H. armigera larvae, in 6 d. Cessation of feeding was observed on the second PID.

摘要

建立了一种源自棉铃虫胚胎组织的新细胞系,命名为NIV-HA-197。该细胞系在添加10%胎牛血清的TNM-FH培养基中培养。第20代细胞系具有异质性细胞群体,主要由上皮样细胞(70%)、成纤维细胞样细胞(27%)和多核巨细胞(3%)组成。染色体数目在45到185之间。第40代的生长曲线显示细胞数量增加了五倍,群体倍增时间约为60小时。在第9代时发现该细胞系感染了微孢子虫棉铃虫微孢子虫。使用抗原生动物药物甲硝唑400并同时进行热处理,从培养物中清除了寄生虫。该细胞系可冷冻保存30个月。通过研究四种酶(即乳酸脱氢酶、苹果酸脱氢酶、异柠檬酸脱氢酶和葡萄糖6-磷酸脱氢酶)的同工酶谱以及异源双链分析,确定了新细胞系的物种特异性。异源双链分析用于分析线粒体16S核糖体核糖核酸基因序列以及宿主昆虫基因序列,获得了100%的同源性,证实了细胞系的同种特异性。发现该细胞系对苜蓿银纹夜蛾多粒包埋型核多角体病毒、斜纹夜蛾多粒包埋型核多角体病毒和棉铃虫单粒包埋型核多角体病毒(HaSNPV)敏感。在感染后第7天(PID),超过90%的细胞被HaSNPV感染,在第10天PID时产生了28.8×10⁶个NPV/ml。将体外培养的HaSNPV喂食给棉铃虫二龄幼虫时,在6天内导致100%死亡。在第二个PID时观察到停止进食。

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