1988•Journal of Invertebrate PathologyOpen access

The number of nucleocapsids of enveloped Autographa californica nuclear polyhedrosis virus particles affects the survival time of neonate Trichoplusia ni larvae

Nikolai A.M. van Beek, H. Alan Wood, Patrick Hughes

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Abstract

The ability of the viral enhancing factor (VEF) from Trichoplusia ni granulosis virus to enhance the infectivity of Autographa californica multiply enveloped nuclear polyhedrosis virus (AcMNPV) was measured in mid-fourth instar T. ni bioassays. In dose-response bioassays with a constant AcMNPV dose and VEF concentrations varying from 1 to 40 ng/larva, mortality increased linearly with the log dose of VEF from 20.8 to 93.1%. Reciprocal bioassays in which the dose of VEF was constant while that of the virus was varied yielded parallel dose response lines with a calculated potency ratio (LD50 for virus alone/LD50 for virus + VEF) of 3. In addition to increasing mortality, 40 ng of VEF significantly reduced median survival times of LD20 and LD90 doses of AcMNPV by 9.5 and 10.7 hr, respectively. VEF also enhanced AcMNPV in neonates of T. ni. Increased susceptibility of T. ni larvae to T. ni singly enveloped nuclear polyhedrosis virus (a potency ratio of 16 with 40 ng of VEF), and Anticarsia gemmatalis multiply enveloped nuclear polyhedrosis virus (a potency ratio of ca. 10.0 with 40 ng of VEF) was also demonstrated.

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What this paper is about

The ability of the viral enhancing factor (VEF) from Trichoplusia ni granulosis virus to enhance the infectivity of Autographa californica multiply enveloped nuclear polyhedrosis virus (AcMNPV) was measured in mid-fourth instar T. ni bioassays. In dose-response bioassays with a constant AcMNPV dose and VEF concentrations varying from 1 to 40 ng/larva, mortality increased linearly with the log dose of VEF from 20.8 to 93.1%. Reciprocal bioassays in which the dose of VEF was constant while that of the virus was varied yielded parallel dose response lines with a calculated potency ratio (LD50 for virus alone/LD50 for virus + VEF) of 3. In addition to increasing mortality, 40 ng of VEF significantly reduced median survival times of LD20 and LD90 doses of AcMNPV by 9.5 and 10.7 hr, respectively. VEF also enhanced AcMNPV in neonates of T. ni. Increased susceptibility of T. ni larvae to T. ni singly enveloped nuclear polyhedrosis virus (a potency ratio of 16 with 40 ng of VEF), and Anticarsia gemmatalis multiply enveloped nuclear polyhedrosis virus (a potency ratio of ca. 10.0 with 40 ng of VEF) was also demonstrated.

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Available abstract

The ability of the viral enhancing factor (VEF) from Trichoplusia ni granulosis virus to enhance the infectivity of Autographa californica multiply enveloped nuclear polyhedrosis virus (AcMNPV) was measured in mid-fourth instar T. ni bioassays. In dose-response bioassays with a constant AcMNPV dose and VEF concentrations varying from 1 to 40 ng/larva, mortality increased linearly with the log dose of VEF from 20.8 to 93.1%. Reciprocal bioassays in which the dose of VEF was constant while that of the virus was varied yielded parallel dose response lines with a calculated potency ratio (LD50 for virus alone/LD50 for virus + VEF) of 3. In addition to increasing mortality, 40 ng of VEF significantly reduced median survival times of LD20 and LD90 doses of AcMNPV by 9.5 and 10.7 hr, respectively. VEF also enhanced AcMNPV in neonates of T. ni. Increased susceptibility of T. ni larvae to T. ni singly enveloped nuclear polyhedrosis virus (a potency ratio of 16 with 40 ng of VEF), and Anticarsia gemmatalis multiply enveloped nuclear polyhedrosis virus (a potency ratio of ca. 10.0 with 40 ng of VEF) was also demonstrated.

Key concepts: Autographa californica, Trichoplusia, Nuclear Polyhedrosis Virus, Biology, Virology, Infectivity, Virus, Potency

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The number of nucleocapsids of enveloped Autographa californica nuclear polyhedrosis virus particles affects the survival time of neonate Trichoplusia ni larvae — Research Paper | ScholarLens