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Cricket paralysis virus

Cricket paralysis virus
Virus classification
Group: Group IV ((+)ssRNA)
Order: Picornavirales
Family: Dicistroviridae
Genus: Cripavirus
Species: Cricket paralysis virus

Cricket Paralysis Virus (CrPV) was initially discovered in Australian field crickets (Teleogryllus commodus and Teleogryllus oceanicus) by Carl Reinganum and his colleagues at the Victorian Plant Research Institute (Burnley, Melbourne, Australia). The paralytic disease spread rapidly through a breeding colony as well as through a laboratory population causing about 95% mortality. This was the first recorded isolate of the virus and is generally referred to as CrPVvic to distinguish it from subsequent isolates.

The spheroidal, non-enveloped virus particles of CrPV are about 27 nm diameter in negatively stained electron micrographs and contain a single piece of positive-sense ssRNA. The virion is composed of 4 capsid proteins with molecular masses generally reported to be 33, 31 and 30 with a minor VP4 protein of about 8 kDa. The particles resemble those of the mammalian picornaviruses but CrPV virions sediment at a faster rate (167 s) than poliovirus particles (158 s) in sucrose rate-zonal gradients and, in isopycnic neutral cesium chloride gradients, CrPV particles are denser than those of poliovirus (1.368 g/cm3 vs 1.340 g/cm3 respectively).

CrPV has been detected in a number of insect species from at least five different orders of the class Insecta, in both natural and laboratory populations, and is usually identified by standard serological methods. The infections include not only the Australian cricket species but the New Zealand cricket, Pteronemobius nigrovus, as well as the European house cricket, Acheta domesticus. CrPV does not appear to infect locusts. It is a commonly detected virus in honeybees as an inapparent infection. The strain CrPVbrk was isolated from the cricket A. domesticus ca.1980 following a major population collapse at a cricket rearing farm in Georgia. A related virus from Arkansas, initially called Pseudoplusia includens virus and redesignated CrPVark, was recorded in the mid-1980s. The brk and ark strains are closely related serologically but appear to be very distantly related to the other CrPV isolates so, despite their physical and chemical similarities, it remains speculative that these two American isolates are actually strains of CrPV. Reported detections and/or isolations of CrPV have been made in Australia, New Zealand, the United States of America, the United Kingdom and Indonesia. CrPV has one of the widest host-ranges, if not the widest, of any virus, insect or not. The potential for the use of CrPV as a biological control agent for insects has been suggested. In laboratory experiments CrPVbrk proved to be extremely infectious and pathogenic for adult Ceratitis capitata (Mediterranean fruit fly). Detailed studies have also been made on the use of a CrPV strain to control the European olive fruit fly (Dacus oleae)


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