2009
DOI: 10.1099/vir.0.006783-0
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Two viruses that cause salivary gland hypertrophy in Glossina pallidipes and Musca domestica are related and form a distinct phylogenetic clade

Abstract: Glossina pallidipes and Musca domestica salivary gland hypertrophy viruses (GpSGHV and MdSGHV) replicate in the nucleus of salivary gland cells causing distinct tissue hypertrophy and reduction of host fertility. They share general characteristics with the non-occluded insect nudiviruses, such as being insect-pathogenic, having enveloped, rod-shaped virions, and large circular double-stranded DNA genomes. MdSGHV measures 65¾550 nm and contains a 124 279 bp genome (~44 mol% G+C content) that codes for 108 putat… Show more

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Cited by 45 publications
(43 citation statements)
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“…GpSGHV and MdSGHV share 37 homologous ORFs and are phylogenetically closely related (Garcia-Maruniak et al 2009). Surprisingly, several core gene homologues of baculoviruses was identified in the marine WSSV as well (Wang et al 2011), suggesting that WSSV, as suspected since it was observed, is evolutionarily related, albeit distantly, to baculoviruses.…”
Section: Gene Content and Conserved Gene Functionsmentioning
confidence: 91%
“…GpSGHV and MdSGHV share 37 homologous ORFs and are phylogenetically closely related (Garcia-Maruniak et al 2009). Surprisingly, several core gene homologues of baculoviruses was identified in the marine WSSV as well (Wang et al 2011), suggesting that WSSV, as suspected since it was observed, is evolutionarily related, albeit distantly, to baculoviruses.…”
Section: Gene Content and Conserved Gene Functionsmentioning
confidence: 91%
“…MdSGHVspecific primer pairs were designed using Primer3 software, and a series of PCR assays was conducted to amplify five genes, including ORFs MdSGHV001 (forward primer 5Ј-ATTTCCGCCACACCATACAT-3Ј and reverse primer 3Ј-GTCACGCATAACATCCGTTG-5Ј; 630 bp), MdSGHV039 (forward primer 5Ј-CCGGATTCCATTATGTGGAC-3Ј and reverse primer 3ЈTTTGACGCGC TTGCATATAG-5Ј; 669 bp), MdSGHV029 (forward primer 5Ј-TCTTTCCGG TGTTCGTATCC-3Ј and reverse primer 3Ј-GCAAATTGGAACGGTTGACT-5Ј; 666 bp), MdSGHV089 (forward primer 5Ј-CCTTTTCCTGTTCGTTCAG C-3Ј and reverse primer 3Ј-CCGAATGAGGCAAATTGTTT-5Ј; 627 bp), and MdSGHV106 (forward primer 5Ј-CGGCAGCAACCTTATTCATT-3Ј and reverse primer 3Ј-CGTCGTCTCCTCCTCTTCAG-5Ј; 608 bp). These five genes were selected because of sequence homology to the DNA polymerase, p74, pif-1, pif-2, and pif-3 genes, respectively, found in other dsDNA insect viruses (5). The 25-l reaction mixtures used for PCR amplification consisted of 2.5 l of 10ϫ Taq buffer with 25 mM MgCl 2 , 0.5 l of 10 mM solutions of deoxynucleoside triphosphates, 1 l of a 10 M forward primer solution, 1 l of a 10 M reverse primer solution, 1 l of salivary gland DNA, and 0.25 l of Taq DNA polymerase.…”
Section: Methodsmentioning
confidence: 99%
“…Recent work further revealed that these proteins have homologues in other large invertebrate DNA viruses which replicate in the nucleus, such as salivary gland hypertrophy viruses (SGHVs) (9), nudiviruses (30) and white spot syndrome virus (WSSV) (Nimaviridae) (J. A. Jehle, personal communication).…”
mentioning
confidence: 99%