Satoru Arai

Dr. Satoru Arai

Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo 162-8640, Japan
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Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

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

Representative Publications

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1 July 2014 in Virus Research
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Journal Article
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Richard YanagiharaRichard Yanagihara
Richard Yanagihara
SGSe Hun Gu
Se Hun Gu
SASatoru Arai
Satoru Arai
HKHae Ji Kang
Hae Ji Kang
JSJin-Won Song
Jin-Won Song

29 September 2008 in Japanese Journal of Infectious Diseases
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Journal Article
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SASatoru Arai
Satoru Arai
YMYasuko Matsunaga
Yasuko Matsunaga
TTTomohiko Takasaki
Tomohiko Takasaki
KTKeiko Tanaka-Taya
Keiko Tanaka-Taya
KTKiyosu Taniguchi
Kiyosu Taniguchi
VJVaccine Preventable Diseases Surveillance Program Of Japan
Vaccine Preventable Diseases Surveillance Program Of Japan
Japanese encephalitis (JE) surveillance has been conducted since 1965 as a part of the National Epidemiological Surveillance of Vaccine Preventable Diseases in Japan. Over 1,000 JE cases were reported annually in the late 1960s. The number of JE cases has since markedly decreased, with less than 10 cases reported annually from 1992 to 2004. A total of 361 JE cases were reported between 1982 and 2004. Prognosis was available for 320 cases; 58 (18%) died, 160 (50%) recovered with neuropsychiatric sequelae, and 102 (32%) completely recovered. Seventy-eight percent of these cases were 40 years old or over with a peak age group of 60-69 years old. JE predominantly occurred in unvaccinated populations. A high seroconversion rate among sentinel pigs was recorded every year. This suggests the presence of JE virus-infected mosquitoes during the summer in most areas of Japan, including the northern districts where no JE cases were reported from 1982 to 2004. Although JE cases have been reported in single figures since 1992, the risk of JE virus infection is still present. Thus, high immunization rates of JE vaccine should be maintained in Japan.

7 July 2009 in PLOS ONE
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HKHae Ji Kang
Hae Ji Kang
SBShannon N. Bennett
Shannon N. Bennett
LSLaarni Sumibcay
Laarni Sumibcay
SASatoru Arai
Satoru Arai
AHAndrew G. Hope
Andrew G. Hope
RYRichard Yanagihara
Richard Yanagihara
The discovery of genetically distinct hantaviruses in shrews (Order Soricomorpha, Family Soricidae) from widely separated geographic regions challenges the hypothesis that rodents (Order Rodentia, Family Muridae and Cricetidae) are the primordial reservoir hosts of hantaviruses and also predicts that other soricomorphs harbor hantaviruses. Recently, novel hantavirus genomes have been detected in moles of the Family Talpidae, including the Japanese shrew mole (Urotrichus talpoides) and American shrew mole (Neurotrichus gibbsii). We present new insights into the evolutionary history of hantaviruses gained from a highly divergent hantavirus, designated Nova virus (NVAV), identified in the European common mole (Talpa europaea) captured in Hungary. Pair-wise alignment and comparison of the full-length S- and L-genomic segments indicated moderately low sequence similarity of 54–65% and 46–63% at the nucleotide and amino acid levels, respectively, between NVAV and representative rodent- and soricid-borne hantaviruses. Despite the high degree of sequence divergence, the predicted secondary structure of the NVAV nucleocapsid protein exhibited the characteristic coiled-coil domains at the amino-terminal end, and the L-segment motifs, typically found in hantaviruses, were well conserved. Phylogenetic analyses, using maximum-likelihood and Bayesian methods, showed that NVAV formed a distinct clade that was evolutionarily distant from all other hantaviruses. Newly identified hantaviruses harbored by shrews and moles support long-standing virus-host relationships and suggest that ancestral soricomorphs, rather than rodents, may have been the early or original mammalian hosts.

21 October 2008 in Proceedings of the National Academy of Sciences
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Journal Article
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SASatoru Arai
Satoru Arai
SOSatoshi D. Ohdachi
Satoshi D. Ohdachi
MAMitsuhiko Asakawa
Mitsuhiko Asakawa
HKHae Ji Kang
Hae Ji Kang
GMGabor Mocz
Gabor Mocz
RYRichard Yanagihara
Richard Yanagihara
Recent molecular evidence of genetically distinct hantaviruses in shrews, captured in widely separated geographical regions, corroborates decades-old reports of hantavirus antigens in shrew tissues. Apart from challenging the conventional view that rodents are the principal reservoir hosts, the recently identified soricid-borne hantaviruses raise the possibility that other soricomorphs, notably talpids, similarly harbor hantaviruses. In analyzing RNA extracts from lung tissues of the Japanese shrew mole ( Urotrichus talpoides ), captured in Japan between February and April 2008, a hantavirus genome, designated Asama virus (ASAV), was detected by RT-PCR. Pairwise alignment and comparison of the S-, M-, and L-segment nucleotide and amino acid sequences indicated that ASAV was genetically more similar to hantaviruses harbored by shrews than by rodents. However, the predicted secondary structure of the ASAV nucleocapsid protein was similar to that of rodent- and shrew-borne hantaviruses, exhibiting the same coiled-coil helix at the amino terminus. Phylogenetic analyses, using the maximum-likelihood method and other algorithms, consistently placed ASAV with recently identified soricine shrew-borne hantaviruses, suggesting a possible host-switching event in the distant past. The discovery of a mole-borne hantavirus enlarges our concepts about the complex evolutionary history of hantaviruses.

1 April 2007 in Microbiology and Immunology
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KTKenji Tabara
Kenji Tabara
SASatoru Arai
Satoru Arai
TKTakako Kawabuchi
Takako Kawabuchi
AIAsao Itagaki
Asao Itagaki
CIChiaki Ishihara
Chiaki Ishihara
MTMasayoshi Tsuji
Masayoshi Tsuji
A significant number of patients are diagnosed with “fevers of unknown origin” (FUO) in Shimane Prefecture in Japan where tick‐borne diseases are endemic. We conducted molecular surveys forBabesia microti, Ehrlichiaspecies, andCandidatusNeoehrlichia mikurensis in 62 FUO cases and 62 wild rodents from Shimane Prefecture, Japan. PCR using primers specific for theBabesia18S small‐subunit rRNA (rDNA) gene andAnaplasmataceae groESLamplified products from 45% (28/62) and 25.8% (16/62) of captured mice, respectively. Of the 28 18S rDNA PCR positives, 23 and five samples were positive for Hobetsu‐ and Kobe‐typeB. microti, respectively. In contrast, of the 16groESLPCR positives, eight, one and seven samples were positive forEhrlichia muris, Ehrlichiasp. HF565 andCandidatusN. mikurensis, respectively. Inoculation of selected blood samples into Golden Syrian hamsters indicated the presence of Hobetsu‐ and Kobe‐typeB. microtiin four and one sample, respectively. Isolation of the latter strain was considered important as previous studies suggested that the distribution of this type was so far confined to Awaji Island in Hyogo Prefecture, where the first case of transfusion‐associated human babesiosis originated. DNA samples from 62 FUO human cases tested negative forB. microti18S rDNA gene,Anaplasmataceae groESLgene,Rickettsia japonica17K genus‐common antigen gene andOrientia tsutsugamushi56K antigen gene by PCRs. We also conducted seroepidemiological surveys on 62 human sera collected in Shimane Prefecture from the FUO patients who were suspected of carrying tick‐borne diseases. However, indirect immunofluorescent antibody tests usingB. microti‐ andE. muris‐infected cells detected IgG againstE. murisin only a single positive sample. This study demonstrates the presence of several potentially important tick‐borne pathogens in Shimane Prefecture and suggests the need for further study on the causative agents of FUOs.

24 June 2020 in BioScience
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Journal Article
Open access
JCJoseph A Cook
Joseph A Cook
SASatoru Arai
Satoru Arai
BABlas Armién
Blas Armién
JBJohn Bates
John Bates
CBCarlos A Carrion Bonilla
Carlos A Carrion Bonilla
PSPamela S Soltis
Pamela S Soltis