Kunitoshi Imai

Dr. Kunitoshi Imai

orcid

Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2012 in Antiviral Research
Verified
Journal Article
Closed access
KIKunitoshi Imai
Kunitoshi Imai
HOHaruko Ogawa
Haruko Ogawa
VBVuong Nghia Bui
Vuong Nghia Bui
HIHiroshi Inoue
Hiroshi Inoue
JFJiro Fukuda
Jiro Fukuda
KNKikuyasu Nakamura
Kikuyasu Nakamura

1 January 2017 in Virus Research
Verified
Journal Article
Closed access
RTRapeewan Thampaisarn
Rapeewan Thampaisarn
VBVuong N. Bui
Vuong N. Bui
DTDai Q. Trinh
Dai Q. Trinh
MNMakoto Nagai
Makoto Nagai
TMTetsuya Mizutani
Tetsuya Mizutani
KIKunitoshi Imai
Kunitoshi Imai

1 January 2014 in Journal of Veterinary Medical Science
Verified
Journal Article
Open access
KNKikuyasu Nakamura
Kikuyasu Nakamura
MIMitsuru Ito
Mitsuru Ito
TNToshiki Nakamura
Toshiki Nakamura
YYYu Yamamoto
Yu Yamamoto
MYManabu Yamada
Manabu Yamada
KIKunitoshi Imai
Kunitoshi Imai
The pathogenicity of Newcastle disease (ND) virus, isolated from ND outbreak in vaccinated chickens, was evaluated through experiments. The pathogenicity indexes (mean death time (MDT); 58 hr, intracerebral pathogenicity index (ICPI); 1.7 and intravenous pathogenicity index (IVPI); 2.51) indicated that the ND virus was velogenic. The ND virus caused lymphocytic necrosis in the spleen with fibrinous exudation and proliferation of macrophages, sinusoidal fibrin exudation in the liver, proliferation of macrophages in the lung, lymphocytic necrosis and depletion in the bursa of Fabricius, cecal tonsils and thymus, necrosis of bone marrow, tracheitis, conjunctivitis and necrosis of feather epithelial cells in specific-pathogen-free chickens. Immunohistochemically, ND virus antigens were seen in the lesions mentioned above. The ND virus could not induce the encephalitis and pancreatitis that were observed in the natural case of ND in vaccinated chickens. There was no clinical disease in vaccinated chickens after the challenge of the ND virus. In diluted ND vaccine experiments, chickens vaccinated with a high dilution of vaccine and then challenged with the ND virus showed clinical sign and mortality with pancreatic focal necrosis. Vaccine diluted with fresh tap water had no effect on protection against the challenge of the ND virus. This study suggests that improper vaccination may be involved in outbreaks of ND in vaccinated chickens.

1 January 2016 in Journal of Veterinary Medical Science
Verified
Journal Article
Open access
TBTugsbaatar Baatartsogt
Tugsbaatar Baatartsogt
VBVuong N. Bui
Vuong N. Bui
DTDai Q. Trinh
Dai Q. Trinh
EYEmi Yamaguchi
Emi Yamaguchi
DGDulyatad Gronsang
Dulyatad Gronsang
KIKunitoshi Imai
Kunitoshi Imai
Viral neuraminidase inhibitors are widely used as synthetic anti-influenza drugs for the prevention and treatment of influenza. However, drug-resistant influenza A virus variants, including H5N1 highly pathogenic avian influenza viruses (HPAIVs), have been reported. Therefore, the discovery of novel and effective antiviral agents is warranted. We screened the antiviral effects of 11 herbal tea extracts (hibiscus, black tea, tencha, rosehip tea, burdock tea, green tea, jasmine tea, ginger tea, lavender tea, rose tea and oak tea) against the H5N1 HPAIV in vitro. Among the tested extracts, only the hibiscus extract and its fractionated extract (frHibis) highly and rapidly reduced the titers of all H5 HPAIVs and low pathogenic AIVs (LPAIVs) used in the pre-treatment tests of Madin-Darby canine kidney (MDCK) cells that were inoculated with a mixture of the virus and the extract. Immunogold electron microscopy showed that anti-H5 monoclonal antibodies could not bind to the deformed H5 virus particles pretreated with frHibis. In post-treatment tests of MDCK cells cultured in the presence of frHibis after infection with H5N1 HPAIV, the frHibis inhibited viral replication and the expression of viral antigens and genes. Among the plants tested, hibiscus showed the most prominent antiviral effects against both H5 HPAIV and LPAIV.

1 August 2014 in Virus Research
Verified
Journal Article
Closed access
EYEmi Yamaguchi
Emi Yamaguchi
MSMariko Sashika
Mariko Sashika
KFKei Fujii
Kei Fujii
KKKohei Kobayashi
Kohei Kobayashi
VBVuong Nghia Bui
Vuong Nghia Bui
KIKunitoshi Imai
Kunitoshi Imai

1 January 2008 in Journal of Veterinary Medical Science
Verified
Journal Article
Open access
PDF file
YUYoshihide Usami
Yoshihide Usami
KFKatsuhiko Fukai
Katsuhiko Fukai
YIYutaka Ichikawa
Yutaka Ichikawa
YOYo Okuda
Yo Okuda
ISIsao Shibata
Isao Shibata
RKRikio Kirisawa
Rikio Kirisawa
We detected transmissible gastroenteritis virus (TGEV) antibodies in pig farms in Tochigi prefecture, although the farms had no past record of TGEV vaccination or TGE. Among the farms, Farm A showed a high antibody incidence. We could not confirm if either TGEV or porcine respiratory coronavirus (PRCV) induced the antibodies, since conventional tests failed to discriminate PRCV from TGEV. Therefore, we conducted virological and serological examinations of this farm for 4 years to establish the etiology - TGEV or PRCV. Although no TGEV was detected, PRCVs were isolated from the nasal samples of pigs. Using a commercial ELISA kit, it was found that the antibodies detected in pigs of all the raising stages and sows were raised against PRCV but not TGEV. The phylogenetic analysis of the nucleotide sequences of the isolates showed that they were closely related to each other, and formed a separate cluster apart from the U.S.A. and European strains. In Cesarean-derived, colostrums-deprived piglets inoculated with a PRCV isolate, no clinical signs were seen, and the viruses were mainly isolated from the nasal samples. Moreover, viral genes were detected from the nasal sample of the contact pig. The result suggested that PRCV infection was located in the nasal cavity of pigs, and horizontal transmission easily occurs. From these results, PRCVs with different origins from the exotic PRCVs might be prevalent in pig farms in Japan.