Microplitis demolitor bracovirus genome segments vary in abundance and are individually packaged in virions

被引:66
作者
Beck, Markus H.
Inman, Ross B.
Strand, Michael R. [1 ]
机构
[1] Univ Georgia, Dept Entomol, Athens, GA 30602 USA
[2] Univ Georgia, Ctr Trop & Emerging Global Dis, Athens, GA 30602 USA
[3] Univ Wisconsin, Inst Mol Virol, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
关键词
polydnavirus; genome organization; gene expression; real-time PCR; parasitoid;
D O I
10.1016/j.virol.2006.09.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Polydnaviruses (PDVs) are distinguished by their unique association with parasitoid wasps and their segmented, double-stranded (ds) DNA genomes that are non-equimolar in abundance. Relatively little is actually known, however, about genome packaging or segment abundance of these viruses. Here, we conducted electron microscopy (EM) and real-time polymerase chain reaction (PCR) studies to characterize packaging and segment abundance of Microplitis demolitor bracovirus (MdBV). Like other PDVs, MdBV replicates in the ovaries of females where virions accumulate to form a suspension called calyx fluid. Wasps then inject a quantity of calyx fluid when ovipositing into hosts. The MdBV genome consists of 15 segments that range from 3.6 (segment A) to 34.3 kb (segment O). EM analysis indicated that MdBV virions contain a single nucleocapsid that encapsidates one circular DNA of variable size. We developed a semi-quantitative real-time PCR assay using SYBR Green 1. This assay indicated that five (J, O, H, N and B) segments of the MdBV genome accounted for more than 60% of the viral DNAs in calyx fluid. Estimates of relative segment abundance using our real-time PCR assay were also very similar to DNA size distributions determined from micrographs. Analysis of parasitized Pseudoplusia includens larvae indicated that copy number of MdBV segments C, B and J varied between hosts but their relative abundance within a host was virtually identical to their abundance in calyx fluid. Among-tissue assays indicated that each viral segment was most abundant in hemocytes and least abundant in salivary glands. However, the relative abundance of each segment to one another was similar in all tissues. We also found no clear relationship between MdBV segment and transcript abundance in hemocytes and fat body. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:179 / 189
页数:11
相关论文
共 44 条
[11]   DARSTELLUNG UND LANGENMESSUNGEN DES GESAMTEN DESOXYRIBONUCLEINSAURE-INHALTES VON T2-BAKTERIOPHAGEN [J].
KLEINSCHMIDT, A ;
ZAHN, RK ;
LANG, D ;
JACHERTS, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1962, 61 (06) :857-&
[12]   UNUSUAL BACULOVIRUS OF THE PARASITOID WASP APANTELES-MELANOSCELUS - ISOLATION AND PRELIMINARY CHARACTERIZATION [J].
KRELL, PJ ;
STOLTZ, DB .
JOURNAL OF VIROLOGY, 1979, 29 (03) :1118-1130
[13]   Iκβ-related vankytin genes in the Campoletis sonorensis Ichnovirus:: Temporal and tissue-specific patterns of expression in parasitized Heliothis virescens lepidopteran hosts [J].
Kroemer, JA ;
Webb, BA .
JOURNAL OF VIROLOGY, 2005, 79 (12) :7617-7628
[14]  
Kroemer JA, 2004, ANNU REV ENTOMOL, V49, P431, DOI 10.1146/annurev.ento.49.072103.120132
[15]   Persistence and expression of Cotesia congregata polydnavirus in host larvae of the tobacco hornworm, Manduca sexta [J].
Le, NT ;
Asgari, S ;
Amaya, K ;
Tan, FF ;
Beckage, NE .
JOURNAL OF INSECT PHYSIOLOGY, 2003, 49 (05) :533-543
[16]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408
[17]   Real-time PCR in virology [J].
Mackay, IM ;
Arden, KE ;
Nitsche, A .
NUCLEIC ACIDS RESEARCH, 2002, 30 (06) :1292-1305
[18]  
MAHY B, 1996, VIROLOGY METHODS MAN
[19]  
MUBARAK HS, 2005, J CLIN VIROL, V32, P313
[20]   Experimental validation of novel and conventional approaches to quantitative real-time PCR data analysis [J].
Peirson, SN ;
Butler, JN ;
Foster, RG .
NUCLEIC ACIDS RESEARCH, 2003, 31 (14) :e73