The effect of temperature upon Tipula iridescent virus infection in Tipula oleracea

The mean incubation period (time from inoculation with virus to first appearance of iridescence) was used as an indication of the rate of replication of Tipula iridescent virus (TIV) in Tipula oleracea larvae. The mean incubation period and survival time (time from inoculation with virus to death) were compared with the mean instar duration at a series of temperatures. In most stages of the insect the optimum temperature for the replication of TIV and the temperature for the shortest mean survival time coincided with the peak temperature (the temperature for the fastest development of the insect stage). The peak temperature for T. oleracea does not appear to be the same for each stage, and the optimum temperature for TIV replication appears to be closely linked to the peak temperature of the infected stage. The optimum temperature (the temperature at which most individuals survived from hatching to the adult stage) of the insect was 20°C. Tipula iridescent virus replicated in T. oleracea larvae and pupae at 3° and 27°C, which are near the temperature limits for the insect. Incubation periods and survival times in TIV-inoculated larvae incubated in the field were much longer in winter than in summer.     

Per os transmission of iridescent virus of Heliothis zea (Lepidoptera: Noctuidae)

In per os transmission of iridescent virus (IV), the first signs of infection are small iridescent patches in the prolegs, clypeus, labrum, and intersegmental membranes. Per os exposure of neonatal larvae to IV produced 18–40% infection. Per os exposure of 5- and 9-day-old larvae produced 11–47% and 10–30% infection, respectively. A few larvae with a patent infection pupated; however, none reached the adult stage. Infected larvae remained in the larval stage up to 89 days, compared to 12–21 days for normal larvae. Transovum or transovarian transmission was not detected. Examination of fat body, silk glands, and muscles of infected larvae by electron microscopy confirmed the presence of numerous intracytoplasmic virus particles. The mean particle diameter of hexagonal profiles within viral paracrystals was 118±3.5 nm.     

Restriction endonuclease patterns of three baculoviruses isolated from species of Heliothis

The DNA of three baculoviruses propagated in larvae of a common host species (Heliothis zea) were easily distinguished from each other by their restriction endonuclease patterns. Molecular weights of 79.7 ± 7.3, 119.6 ± 5.1, and 86.6 ± 6.3 × 10⁶ daltons were estimated for the viral genome of a single-embedded nucleopolyhedrosis virus isolated from Heliothis zea, a multiple-embedded nucleopolyhedrosis virus isolated from Heliothis armigera, and a granulosis virus isolated from Heliothis armigera, respectively.     

The mode of transmission of Tipula iridescent virus: I. Source of infection

A virus was isolated from a diseased tipulid larva and identified as Tipula iridescent virus (TIV) on the basis of the size and morphology of the virion, the production of iridescence in vitro and in infected tipulid larvae, and a serological reaction between antiserum against the virus and an isolate of TIV.A stock of Tipula oleracea was bred in the laboratory. Subjection of larvae to several stress factors did not result in any evidence for activation of a latent virus. Healthy T. oleracea larvae did not develop iridescence when confined in petri dishes with either live TIV-infected larvae or with large amounts of their feces, although these feces were found to contain infective virus by injecting extracts into healthy larvae. It appears that the concentration of virus in the feces of infected larvae is not high enough for them to serve as a source of infection. It was shown that the cadavers of TIV-infected larvae can serve as a source of infection for healthy first- and fourth-instar larvae.     

The mode of transmission of Tipula iridescent virus: II. Route of infection

Tipula iridescent virus (TIV) was inoculated into Tipula oleracea larvae via different routes. It was found to be much more infective when it was injected into the hemocoel than when it was ingested by the larvae.T. oleracea embryos did not become infected when eggs were laid in agar containing TIV, and there was no evidence that larvae can become infected via the spiracles or that transovum transmission occurs. It is suggested that TIV is transmitted principally by cannibalism, including killing and ingesting infected larvae, and finding dead infected larvae and ingesting them. It is proposed that a new generation becomes infected by first-instar larvae feeding upon infected fourth-instar larvae which have survived from the previous generation.     

An iridescent virus and a rickettsia from the grass grub Costelytra zealandica (Coleoptera: Scarabaeidae)

Natural iridescent virus and rickettsia infections of Costelytra zealandica (White) and Odontria sp. indet. larvae were studied at a site in the upper Pareora Gorge scenic reserve, S. Canterbury. By sequentially sampling the site, it was found that neither the iridescent virus nor the rickettsiae appear to give rise to host mortalities that significantly alter the population density. Many larvae were found that appeared healthy, but carried inapparent iridescent virus infections. These diseases are not suitable for biological control of the grass grub.     

Bioassay of mosquito iridescent virus of Aedes taeniorhynchus in cell cultures of Aedes aegypti.

A bioassay of mosquito iridescent virus (MIV) of Aedes taeniorhynchus was developed using cell cultures of Aedes aegypti. The dilution end point technique was based on the occurrence of cytopathic effects which were optimum at 31°C. Peleg's A. aegypti cell line was more sensitive and reliable than Singh's A. aegypti cell line for infectivity titration of the “R” and “T” strains of MIV. The highest tissue culture infectivity dose 50s (TCID₅₀) were elicited by virion:cell ratios of approximately 10. TCID₅₀ titers were significantly reduced by virus neutralization with either homologous or heterologous antiserum to either RMIV or TMIV. The virus propagated in either cell line was not infectious to A. taeniorhynchus larvae, or to the respective cells from which the virus was produced. All plaque assay attempts were unsuccessful.     

Field trials withTipula iridescent virus againstTipula spp. larvae in grassland

Field trials withTipula iridescent virus (TIV) were carried out to determine whether the infection can be introduced into populations ofTipula spp. in grassland. The virus was introduced into plots in live and deadTipula oleracea L. larvae, in a bran bait and in sprayed aqueous suspensions. Trials were conducted at 1 site in 3 successive years and at 5 further sites in the 3rd year. Tipulid larval populations in the plots were sampled at intervals of approximately 2 months. The majority of sampled larvae were not iridescent and did not become iridescent when they were incubated at 20°C for 30 days. In plots where iridescent larvae were found they generally comprised between 1 and 17% of the tipulid population. The identity of the virus infecting these insects was confirmed by the latex agglutination test. The results suggest that all the treatments introduced the virus infection into one or more of the tipulid populations; they all did so, however, with low efficiencies.

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Résumé Des essais en parcelles avec le virus irisant deTipula (TIV) ont été effectués pour déterminer si l'on peut introduire l'infection dans des populations deTipula spp. en prairie. Le virus a été utilisé sous forme de larves vivantes ou mortes deTipula oleracea L., d'appat de son, et en suspensions aqueuses. L'expérimentation a été réalisée dans un emplacement pendant 3 ans successifs et dans 5 sites complémentaires pendant la 3^e année. L'échantillonnage des populations de larves de tipules a eu lieu tous les 2 mois. La majorité des larves récoltées n'etaient pas irisantes et elles ne le sont pas devenues après un élevage à 20°C pendant 30 jours. Dans les parcelles où l'on a trouvé des larves irisantes, celles-ci représentaient 1 à 17% de la population de tipules. L'identité du virus dans ces insectes a été confirmée par agglutination au latex. Les résultats suggèrent que tous les traitements ont introduit l'infection virale dans les populations de tipules mais avec une faible efficacité.

     

Tipula iridescent virus infection in the developmental stages of Tipula oleracea

Tipula iridescent virus (TIV) is infective to all four larval instars, pupae, and adults of both sexes of Tipula oleracea, and iridescence has been observed in infected insects at all these stages. Third- and fourth-instar larvae were more resistant to ingested TIV than first and second instars. When TIV was injected into the hemocoel, the results suggested a possible decrease in resistance from the third larval instar to the pupa. Incubation periods (times from injection of TIV to appearance of iridescence) were significantly shorter in older fourth-instar larvae than in younger fourth-instar or thirdinstar larvae, but variability in incubation period was significantly greater in younger fourth-instar larvae than in the other two stages. Many insects which were inoculated with TIV in one stage developed iridescence and died in later stages. The amounts of infective TIV in two infected adults were estimated.     

A newly isolated densonucleosis virus from Pseudoplusia includens (Lepidoptera: Noctuidae)

An icosahedral DNA virus isolated from the soybean looper, Pseudoplusia includens, was characterized. Purified virus had a diameter of 20 ± 1 nm and negatively stained preparations showed a trend to form linear to three-dimensional crystals. The virus had a sedimentation coefficient of 120 ± 3 S and a buoyant density of 1.40 ± 0.01 g/cm³. The DNA content of the virus was 37.8 ± 0.1% and the absorption spectrum showed it to be a typical nucleoprotein. Viral DNA in situ was shown to be single-stranded by staining the virus with acridine orange as well as by reaction to formaldehyde. Evidence of inverted terminal repetition of the DNA was observed by electron microscopy. The terminal repetition comprises ca. 6–7% of the genome. The molecular weight of the ssDNA was 2.0 ± 0.1 × 10⁶ as determined by agarose gel electrophoresis or 2.1 ± 0.1 × 10⁶ as determined by electron microscopy. Four virion proteins with molecular weights of 46.5 ± 0.1, 54.0 ± 0.1, 64.0 ± 0.2, and 87.0 ± 0.1 × 10³ were detected by 9% SDS-polyacrylamide gel electrophoresis. Double-diffusion tests showed the virus to be serologically related but not identical to DNV-1. Ultrathin sections showed that the nucleus of the hemocyte, muscle, hypodermal, and fat body cells contained virus-like particles. The chromatin of an infected nucleus always underwent a margination and the nucleoplasm was often replaced largely by virions.Data indicate that the virus belongs to the Densovirus of the family Parvoviridae.     

The use of enzyme-linked immunosorbent assay to detect, and discriminate between, small iridescent viruses

The enzyme-linked immunosorbent assay (ELISA) double antibody method provided an efficient method for detecting iridescent virus (type 22) in purified preparations and extracts of Galleria mellonella larvae; 10 ng of purified virus/ml were detected with confidence. The ELISA method discriminated between the five iridescent viruses tested.     

An iridescent virus fromPopillia japonica (Col.: Scarabaeidae)

A very low incidence (<0.01%) of a blue iridovirus (IV) was found in larvae of the Japanese beetle,Popillia japonica Newman, that were sampled over a two year period on Terceira Island (Azores, Portugal). In the most heavily infected larvae, a deep blue iridescence was observed, particularly in the fat body. Transmission electron microscopy revealed the characteristic crystalline arrays of the hexagonal virus particles in the cytoplasm of fat body cells, tracheal matrix, muscle, hypodermis and blood cells. Crystals of the virus particles were also observed freely circulating in the hemolymph. The average diameter of negatively stained purified virus particles was 157 nm. Similarities and differences with other IVs found in the Scarabaeidae are discussed. Considering the broad host range of some of the iridescent viruses, the relatively recent invasion of Terceira byP. japonica, and the rarity of the virus in the beetle, it is probable that the infection was the result of transmission from another species of soil-inhabiting arthropod. Its value as a potential biological control agent ofP. japonica is negligible.     

A Tipula paludosa population with a high incidence of two pathogens

The incidence of lethal parasites in the larvae of a Tipula paludosa population was monitored for two seasons. The proportions of larvae infected with Tipula iridescent virus (TIV) and a tachinid insect were similar to those in previously studied populations, whereas the proportions of larvae infected with Tipula nuclear polyhedrosis virus (NPV) and a spore-forming bacterium (SFB) were higher. Conservative estimates of mortality due to these four agents were 10.7% in 1977–1978 and 7.7% in 1978–1979. The mean population density and the proportion of SFB-infected larvae were lower in 1978–1979 than in 1977–1978, while the proportion of NPV-infected larvae was higher. In 1979 the proportion of NPV-infected larvae was positively correlated with population density, which was highest in the wettest part of the study area. In both seasons the proportion of SFB-infected larvae was negatively correlated with population density. Larvae infected with the NPV or the SFB became pallid at an advanced stage of infection, but, although infected larvae were found throughout the larval period, pallid larvae were only found in the later part. It is suggested that larvae become infected in an early instar, then the infections slowly develop throughout the remainder of the larval period. Five larvae were found with mixed infections; four were infected with the SFB and NPV, while the fifth was infected with the SFB and TIV.     

Comparison of in vivo infectivity of tissue-cultured nonoccluded virus and alkali-liberated occluded virus of Baculovirus heliothis

Feeding and intrahemocelic injection studies using tissue-culture-derived-nonoccluded virus (TCNOV) and occluded virus liberated by alkaline solution (ALOV) from polyhedral inclusion bodies were conducted with the single-embedded Heliothis nuclear polyhedrosis virus, Baculo-virus heliothis (H_zSEV). Comparisons of infectivity between ALOV and NOV were based upon the number of adminstered plaque-forming-units (PFU). There was little, if any, difference in infectivity between ALOV and TCNOV of H_zSEV when injected into 4th-instar larvae of Heliothis virescens. The LD₅₀, from the multiple dose injection studies, for ALOV and TCNOV was 6.5 ± 1.2 PFU per larva and 3.4 ± 0.9 PFU per larva, respectively. Injection of a single dose (5 PFU per larva) resulted in a larval mortality of 83.2 ± 3.4 and 62.6 ± 5.7% for ALOV and TCNOV of the H_zSEV, respectively. The LC₅₀ of ALOV and TCNOV, from the multiple-dose feeding tests, was 3.1 ± 0.4 PFU/cm² and 4.5 ± 0.9 PFU/cm², respectively. Feeding 24-hr-old larvae on virus-treated diets at a single dose (50.0 PFU/cm²) resulted in a 1.5-fold difference in percentage larval mortality between ALOV (91.0 ± 4.0%) and TCNOV (61.2 ± 3.0%). Counts of viral particles (VP), based upon electron microscopy, were 14.3 ± 2.6 × 10¹⁰ and 5.2 ± 1.1 × 10⁷ VP/ml for the ALOV and TCNOV, respectively. Thus, each larva ingesting or injected with one PFU received ca. 3500 × more VP of ALOV than in did of TCNOV.     

Infectivity of an iridescent virus for larvae of Anticarsia gemmatalis (Lepidoptera: Noctuidae)

Laboratory tests were conducted with an iridescent virus (IV) of Anticarsia gemmatalis from Argentina to determine its infectivity for all six larval instars. For first, second, and third instars, the LC₅₀ values were 5.93, 6.14, and 11.30 mg/ml, respectively. The LD₅₀ values for fourth, fifth, and sixth instars were 1.21, 3.12, and 1.31μg/mg, respectively. The time until death was greater for early instars than for late instars; first instars averaged 23.1 days, second instars 19.6 days, third instars 19.5 days, fourth instars 14.3 days, fifth instars 8.2 days and sixth instars 6.5 days until death. High levels of iridescent virus inoculum appeared to activate a latent nuclear polyhedrosis virus in an average of less than 10% of larvae succumbing to a viral infection. Variable mortality rates were caused with low levels of IV inoculum; high dosages produced a high percentage of mortality, but it was virtually impossible to raise levels of inoculum to concentrations sufficient to produce 100% mortality.     

Properties of flacherie virus of the silkworm, Bombyx mori

The flacherie virus of the silkworm, Bombyx mori, was isolated from infected larvae reared under aseptic conditions. Two types of infectious particles, tentatively designated FVS I and FVS II, were separated by density gradient centrifugation. Some properties of the separated particles were investigated. Electron micrographs showed that FVS I and FVS II were spherical particles with diameters of 27 ± 2 nm and 22 ± 2 nm, respectively. The sedimentation coefficients of FVS I and FVS II were 180 S and 134 S, respectively. It was concluded from experiments of incorporation of ³H-uracil inoculated into diseased larvae at late stage of flacherie disease that the nucleic acid of FVS II was RNA. The two types of particles were present in Sakaki and Wadayama strains of flacherie virus.     

Culex pipiens affected by joint infection of a mosquito iridescent virus and Strelkovimermis spiculatus

Dual infections with a mosquito iridescent virus (MIV) and the mermithid nematode, Strelkovimermis spiculatus were recorded in natural Culex pipiens populations around La Plata city, Argentina. S. spiculatus was detected in 82% of samples that were positive for MIV infection. Dissected larvae of Cx. pipiens with patent MIV infection presented 42% infection with S. spiculatus. Larvae of Cx. pipiens exposed to MIV and S. spiculatus under laboratory conditions produced a high joint infection rate (82.5%) while no infection was recorded on larvae exposed to virus suspension only. Field and laboratory results suggest a strong association between S. spiculatus and MIV in natural populations of Cx. pipiens, in which S. spiculatus could be a mode of entry for the virus into the mosquito hemocele.     

Physicochemical properties of tipula iridescent virus

The molecular weight of Tipula iridescent virus, based on sedimentation and diffusion coefficients, was 5.51 × 10⁸, with hydration of 0.57 g of water per g of virus. Deoxyribonucleic acid content, based on total inorganic phosphorus liberated, was 19 ± 0.2%. At 260 mμ, the virus gave an uncorrected absorbance of 18.2 cm²/mg of virus and a light-scattering corrected absorbance of 9.8 cm²/mg of virus. Amino acid analyses of the virus protein revealed a remarkable similarity to Sericesthis iridescent virus. The possibility is discussed that the four iridescent insect viruses reported to date bear a strain relationship.     

Infection of the boll weevil by Chilo iridescent virus

When infections with Chilo iridescent virus (CIV) were induced in larvae of boll weevils, Anthonomus grandis, by intrahemocoelic injection or by feeding, and in adults by feeding, the typical blue coloration of adipose tissue developed at 3–7 days postinfection, and mortality occurred after 3 days. The symptomatology and the pathological expressions depended on the initial infectious titer. The virus remained viable when it was added to the feeding stimulant bait used to infect weevils with protozoan pathogens in the field, and weevils feeding on the formulation became infected when it had been exposed 1–3 days in nature.     

Iridescent virus replication: patterns of nucleic acid synthesis in insect cells infected with iridescent virus types 2 and 6

The patterns of nucleic acid synthesis in insect cells infected with iridescent virus types 2 and 6 has been examined using nucleic acid hybridization techniques. Virus-specific RNA synthesis was detected 24 hr after infection. Virus-specific DNA synthesis was detected 96 hr after infection. Host-specific nucleic acid synthesis declined throughout infection, and host-specific nucleic acid synthesis was detected only in the first 48 hr of infection. The synthesis of iridescent virus progeny DNA molecules precedes the appearance of mature iridescent virus particles.