Browsing by Author "Yashiki,"

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    High Prevalence of HBV in Tibet, China.
    (2001-01-30) Zhao,; Li,; Lou,; Lu,; Yu,; Gao,; Hu,; Chiba,; Takezaki,; Takeshita,; Yashiki,; Fujiyoshi,; Sonoda,; Tajima,
    Hepatitis B virus (HBV), distributed throughout the world, is classified into seven geographically separated genotypes designated A to G. Since the prevalence of HBV infection in isolated ethnic Tibetan populations in China, and the HBV genotypes involved have been hither to remained unclear, we collected 262 blood samples from four isolated villages in the east and west regions of Tibet. The prevalence of HBV infection was estimated by EIA for HBV Ag and HBV Ab. The HBV genotypes were determined by a PCR-microwell plate hybridization method using plasma DNA. The prevalence of HBV Ag and HBV Ab positives was 19.1% (50/262 cases) and 29.0% (76/262 cases), respectively. We detected only the C genotype (20/20 cases), this being known as a predominant type of HBV among Mongoloid populations in Asia. The results revealed, for the first time, that Tibetan villagers have a high rate of infection with HBV of C genotype, in line with the available data for chronic hepatitis and liver cancer.
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    Human Papillomavirus Infection among Bolivian Amazonian Women.
    (2001-01-30) Lema,; Hurtado,; Segurondo,; Romero,; Dulon,; Asturizaga,; Panoso,; Garcia,; Fujiyoshi,; Yashiki,; Li,; Lou,; Cervantes,; Gomez,; Sonoda,
    Cervical cancer is the most common malignancy among women in Latin America. Human papilloma virus infection is known to be an important risk factor. However, HPV infection among Bolivian women has not yet been fully evaluated. The present study aimed to investigate HPV infection among women living in a rural region of the Bolivian Amazon. Cervical swab samples were collected from 151 healthy women in three Amazonian villages. From every woman, two samples were collected by cotton swab; one for cytological examination and the other for ethanol-preservation of cervical epithelial cells for HPV DNA testing. High molecular DNA was extracted from the ethanol-preserved cervical epithelial cells and tested for HPV DNA by a PCR-RFLP protocol. Ethanol-preserved cervical epithelial cells remained suitable for DNA isolation and PCR amplification of human b-globin and HPV E6/E7 genes, 25 days after sample collection in the field. HPV-31, HPV-58 and HPV-6 were detected in the studied population. The overall prevalence of HPV infection among Bolivian Amazonian women was 8.0%. Neither dual nor multiple HPV infections were found in any of the positive samples. This is the first report of HPV prevalence and type distribution among Bolivian Amazonian women. Our new method for preservation of cervical epithelial cells in ethanol may be useful for viro-epidemiological studies in rural areas.