Castro M E, Souza M L, Araujo S, Bilimoria S L
Department of Biological Sciences, Texas Tech University, Lubbock, Texas, 79409-3131, USA.
J Invertebr Pathol. 1997 Jan;69(1):40-5. doi: 10.1006/jipa.1996.4624.
Anticarsia gemmatalis nuclear polyhedrosis virus (AgNPV; family Baculoviridae) is pathogenic for larvae of the velvetbean caterpillar, Anticarsia gemmatalis Hübner-an important pest of soybean. AgNPV is a viable alternative to chemical control of A. gemmatalis in Brazil, where its use as a pesticide has brought significant economic and environmental benefits. Although a significant amount of information is available on the ecological and biological control aspects of AgNPV, very little is known about the replication cycle and host specificity of this virus. We examined the susceptibility of four lepidopteran cell lines to AgNPV. Infections of the A. gemmatalis UFL-AG-286 cell line were highly productive. Ninety percent of infected cells had polyhedral inclusion bodies by 48 hr after infection, and the infectious virus titer was 10(8) IU/ml. Viral DNA replication was efficient, and the maximal rate of synthesis was between 6 and 12 hr after infection. Infections of the Spodoptera frugiperda IPLB-SF-21 cell line were productive but less efficient. Infections of Choristoneura fumiferana IPRI-CF-124T cells with this virus were poor, with only 5% of the cells forming polyhedra and an infectious virus titer of 10(6) IU/ml. The level of viral DNA replication was low, suggesting that this system was predominantly abortive. Infections of Bombyx mori BM-5 cell lines were abortive, and cells had apoptosis-like morphology. No polyhedra or increase in infectious levels were observed, and there was little or no replication of viral DNA. Our data suggest that restriction of AgNPV replication in abortive cell lines is due mainly to inability of viral DNA to replicate efficiently. The possible causes of low DNA replication are discussed. Our results suggest that the cell lines utilized in this study can provide an important model for studying mechanisms of AgNPV host specificity.
豆夜蛾核型多角体病毒(AgNPV;杆状病毒科)对豆夜蛾幼虫具有致病性,豆夜蛾是大豆的一种重要害虫。在巴西,AgNPV是化学防治豆夜蛾的一种可行替代方法,其作为杀虫剂的使用带来了显著的经济和环境效益。尽管已有大量关于AgNPV生态和生物防治方面的信息,但对于该病毒的复制周期和宿主特异性却知之甚少。我们检测了四种鳞翅目细胞系对AgNPV的敏感性。感染豆夜蛾UFL-AG-286细胞系的效率很高。感染后48小时,90%的感染细胞含有多面体包涵体,感染性病毒滴度为10⁸国际单位/毫升。病毒DNA复制高效,合成的最大速率在感染后6至12小时之间。感染草地贪夜蛾IPLB-SF-21细胞系也有病毒产生,但效率较低。用该病毒感染云杉卷叶蛾IPRI-CF-124T细胞的效果不佳,只有5%的细胞形成多面体,感染性病毒滴度为10⁶国际单位/毫升。病毒DNA复制水平较低,表明该系统主要是流产性感染。感染家蚕BM-5细胞系也是流产性感染,细胞具有凋亡样形态。未观察到多面体或感染水平增加,病毒DNA几乎没有复制。我们的数据表明,AgNPV在流产性细胞系中的复制受限主要是由于病毒DNA无法有效复制。讨论了DNA复制水平低的可能原因。我们的结果表明,本研究中使用的细胞系可为研究AgNPV宿主特异性机制提供重要模型。