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1999 Fiscal Year Final Research Report Summary

Wide spectrum of symptoms by parvovirus B19 infection and its relation to the virus strain

Research Project

Project/Area Number 09670823
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionSapporo Medical University

Principal Investigator

KUDOH Tooru  Sapporo Medical University, School of Medicine, Asso. Pro., 医学部, 助教授 (30117618)

Project Period (FY) 1997 – 1999
KeywordsParvovirus / B19
Research Abstract

The genetic diversity in the VP1 unique region, which is important for the neutralizing response to human parvovirus B19 was examined by the mismatch detection method using Non-isotopic RNase Cleavage Assay (NIRCAィイD1TMィエD1) and direct nucleotide sequencing. Twenty three B19 strains derived from various sources between 1986 and 1997 were examined. Three electrophoresis patterns were observed by NIRCAィイD1TMィエD1. The nucleotide sequence showed that there were 14 nucleotide changes and 4 amino acid substitutions in comparison with Au strains employed as a standard strain. The nucleotide variability of all samples ranged from 0.3% to 2.7% and the amino acid variability ranged from 1.0% to 3.0%. They were classified into three types according to NIRCAィイD1TMィエD1. Type 1 and 3 had similar sequences, but the type 2 sequence was quite different. Although there were some nucleotide variations in the same NIRCAィイD1TMィエD1 type, these were silent. However, there was no relationship between the clinical features and NIRCAィイD1TMィエD1 types or between clinical features and nucleotide sequence. All samples obtained before 1987 were NIRCAィイD1TMィエD1 type 2. On the other hand, 19 for 20 samples obtained after 1989 were NIRCAィイD1TMィエD1 type 1. The other sample obtained in 1992 was type 3. The results suggest that the B19 strain of type2 disappeared by 1988 and changed to other B19 strains such as type 1 and type 3 after 1988, indicating a correlation between genome type and prevalence. NIRCAィイD1TMィエD1 is a convenient method for screening mutations due to its simplicity and quickness.

  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] 関 公平 他: "活性化部分トロンボプラスチン時間の延長を伴ったパルボウイルスB19感染による健常児での血小板減少症"臨小医. 46. 161-164 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Haseyama K et al: "Analysis of genetic diversity in the VP1 unique region gene of human parvovirus B19 using the mismatch ditection method and direct nucleotide sequencing"J Med Virol. 56. 205-209 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Sato T et al: "Pancytopenia with hemophagocytosis secondary to parvovirus B19 in a family with hereditary spherocytosis"Pediatr Int. 41. 561-564 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] SEKI,K., HATAZAWA,T., TACHIBANA,N., ABO,W., HASEYAMA,K.,KUDOH,T., CHIBA,S.: "Patient with thrombocytopenia and prolonged thromboplastin time due to parvovirus B19 infection."Rinshou Shouni Igaku. 46(in Japanese). 161-164 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] HASEYAMA,K., KUDOH,T., YOTO,Y., SUZUKI,N.,CHIBA,S.: "Analysis of genetic diversity in the VP1 unique region gene of human parvovirus B19 using the mismatch detection method and direct nucleotide sequencing."J Med Virol. 56. 205-209 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] SATO,T., UEDA,D., SAKOTA,S., HASEYAMA,K., CHIBA,S., KUDOH,T.: "Pancytopenia with hemophagocytosis secondary to parvovirus B19 infection in a family with hereditary spherocytosis."Pediatr Int. 41. 561-564 (1999)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2001-10-23  

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