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ISSN 313-4836 (Online)
UDC 636.2/3:619:578:57.083 doi: 10.15389/agrobiology.2014.6.67rus
doi: 10.15389/agrobiology.2014.6.67eng
DETECTION OF AKABANE VIRUS GENOME IN ORGANS AND BLOOD OF EXPERIMENTALLY INFECTED CAVIES
E.G. NIKITINA, N.I. SALNIKOV, S.A. KATORKIN, E.A. BALASHOVA,
S.ZH. TSYBANOV, D.V. KOLBASOV, A.V. LUNITSIN
All-Russian Institute of Veterinary Virology and Microbiology, Russian Academy of Agricultural Sciences, Pokrov, Petushinskii Region, Vladimir Province, 601120 Russia, e-mail [email protected], [email protected]
Received March 31, 2014
Abstract
Akabane disease, a transmissible pathology of cattle, sheep and goats, is caused by Simbu serotype virus (Bunyaviridae) and results in significant economical losses due to abortions, unviable and abnormal calves, or dead embryos and calves born. The Akabane disease epizooties, characterized by geographic locations and the coincidence with definite seasons, are widely registered. For preparative accumulation of Akabane virus the 1-2 day mice are used as the most sensitive system for Bunyaviridae isolation. Earlier we reported the development of a test system for Aka-bane virus RNA indication by real time reverse transcription PCR. Its efficacy was approved using infected mice and cell cultures. Furthermore, it was of interest to estimate this test system with respect to more wide range of model animals to be involved in the study and reproduction of Akabane virus. In this investigation, healthy cavies (n = 20, the animal weight of 400 g) were infected with a concentrated viral culture (B8935 strain) of 7.0 lg TCID50/cm3. In blood the Aka-bane virus RNA was detected in four animals only 4 days after inoculation, but not shown in the rest probes, which were sampled from 2 to 6 days, and one cavy died a day after infection, probably due to nonspecific reaction as the Akabane virus genome was not detected in the post mortem tissue samples of all the organs of the animal tested. After 4 days the Akabane virus RNA was also indicated in brain, lung, kidney, hart and lymphatic gland. Thus, the developed test-system is effective for Akabane disease diagnosis, and the experimentally infected cavies can be the model animals used to study and produce Akabane virus preparations.
Keywords: Akabane disease, Akabane virus, cavies, Culicoides, reverse transcription polymerase chain reaction, RT-PCR, test-system.
Akabane disease, a transmissible pathology of cattle, sheep and goats, is caused by Simbu serotype virus of Bunyaviridae family. When epizooties occur the infection results in significant economical losses in livestock due to abortions, unviable and abnormal calves, or dead embryos and calves born (1-3). The disease areal is not yet finally estimated. Since 1959 Akabane disease was registered in Japan, since 1972 in Australia and New South Wales, and since 1969-1970 in Israel, Korea and Kenya (4, 5). The Akabane disease epizooties are characterized by geographic locations and the coincidence with definite seasons, particularly from August to October and also in February, occurring periodically after a few years (1, 2, 6). The virus is transmitted by bloodsucking insects mostly from Culicoides genus, particularly C. milne and C. imicola in Africa, C. oxystoma in Japan, and C. brevitarsis and C. wadei in Australia. It also was isolated from Aedes vexans and Culex triaeniorhynchus in Japan (6, 7) and from Anopheles fenestus in Kenya (2-4, 8-10).
Recently there are a number of reports on Akabane virus detection worldwide (11-13). Its genetic characteristics and pathogenesis are under consideration (14) with serological and immunological research conducted (15, 16). Development of specific vaccines is also discussed (17, 18). Therefore, a special attention should be paid to diagnostics and indication of Akabane disease virus genome and to the test kits (19, 20), and also the model systems to
be used in investigations.
For Akabane disease diagnostics different approaches are commonly used such as fluorescent antibodies, virus neutralization test, delayed hemagglutination, complement binding assay, diffuse precipitation test and enzyme-linked immunosorbent assay. Organs and tissues of aborted animals such as brain, lymphatic gland, spleen, kidney, muscles, placenta and blood, and also the blood samples from sick animals are usually tested (2, 21).
The 1-2 day mice, as the most sensitive system for Bunyaviridae, are usually used for isolation preparative quantity of Akabane disease virus (21).
The test system based on real time RT-PCR that we have developed allows to detect the Akabane disease virus genome in the brain probes of experimentally infected mice and in infected cell cultures (22, 23).
Herein we report the results of studying whether it possible to use this system for the Akabane disease virus genome indication in blood of experimentally infected cavies and also estimate the different infectious biomaterial for further use in model experiments.
Technique. For virus production the CV-1 cells were infected with Akabane disease virus strain B8935 and cultivated at 37+0.5 °C for 2-3 days. For titration polystyrene plates with CV-1 cell monolayer in wells were used and the cytopathic effect estimated. The observations were continued for 7 days.
Healthy cavies (n = 20, the animal weight of 400 g; N = 3) were infected with a concentrated viral suspension (B8935 strain) of 7.0 lg TCID50/cm3. The animals were separated into two groups. The group I was infected using 50 pi of virus containing material while in the group II the dose was 500 pl.
From day 2 to day 6 after infecting the blood samples were obtained and analyzed using a developed Test system for Akabane virus RNA real time indication in RT-PCR (3, 22, 23). Additionally, to obtain biolmaterial for further investigation the brain, lung, kidney, lymphatic and hart tissues were sampled on day 4 from animals of the group II.
Viral RNA was extracted by nucleosorption using a TRIzol LS Reagent kit (Invitrogen, Inc., USA) according to the manufacturer’s recommendations (23, 24).
For RT-PCR a RotorGene-6000 (Corbett Research, Australia) was used as described in the instruction to the test system (3, 22, 23).
Results. Akabane disease virus can be propagated in hen embryos and also in sucking mice as test animals in which the paralytic symptoms develop for 2-3 days as a result of brain infection. Different continues cell lines such as VNK-21 of newborn hamster kidney, VERO, HmLu-1 are also sensitive to Aka-bane disease virus with clear cytopathic effect 48 to 72 hours after inoculation.
As far as one of our goals was to find an appropriate model for further investigations, the cavies were chosen due to their size and weight compared to rats and mice, that allows to decrease the number of animals used for biomaterial.
The test developed and applied in this investigation is based on a real time reverse transcription PCR with designed AV d and AV u primers flanking 113 bp fragment complementary to the nucleocapsid N protein gene sequence, and the AV z probe complementary to its internal region according to TagMan technique. The test system is high sensitive at 1.5+0.5 lg MLD50/CM3 for tissue and organ assay and 1.0+0.5 lg TCID50/cm3 for cell culture.
In blood the Akabane disease virus genome was detected only 4 days after the cavies were infected (Table). One cavy died a day after infection, probably due to nonspecific reaction as the Akabane disease virus genome was not detected in the post mortem tissue samples of all the organs of the animal tested.
Detection of Akabane disease virus genome in blood of experimentally infected cav-ies using developed real time RT-PCR test system
Days Animals
group I (n = 12) | group II (n = 8)
2 - -
3 - -
4 + +
5 - -
6 Comments. «+» or «- -» means detected or undetected genome, respectively. -
Figure 1 shows the amplification of nucleic acids extracted from blood of cavies in one of three repeated experiments.
Fig. 1. Detection of Akabane disease virus in blood of experimentally infected cavies using developed real time RT-PCR test system: 1 — recombinant positive control of the amplification; 2-5 — blood of the infected animals №№ 1-4, respectively; 6 — negative extraction control; 7 — negative PCR control (4 days after experimental infection; typical results of amplification are shown).
Fig. 2. Detection of Akabane disease virus in organs and tissues of experimentally infected cavy № 4 using developed real time RT-PCR test system: 1 —
brain; 2 — lungs; 3 — kidneys; 4 — lymphatic glands; 5 — hart; 6 — negative extraction control; 7 — negative PCR control; 8 — positive control (4 days after experimental infection).
The Akabane disease virus genome was detected in brain, lungs, kidney, lymphatic glands and hart of the animals from the group II (Fig. 2).
Thus, the developed test system based on real time RT-PCR allows detecting the Akabane disease virus genome in blood and organs of experimentally infected cavies. Therefore, these animals may serve a model in validation and approbation of the tests suggested for Akabane disease virus identification.
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