Prevalence and genotype distribution of TT virus in various specimen types from thalassaemic patients

被引:18
作者
Chan, PKS [1 ]
Chik, KW
Li, CK
Tang, NLS
Ming, MSK
Cheung, JLK
Ng, KC
Yuen, PMP
Cheng, AF
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Paediat, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Chem Pathol, Shatin, Hong Kong, Peoples R China
关键词
epidemiology; genotype; thalassaemia; TT virus; transmission; tropism;
D O I
10.1046/j.1365-2893.2001.00276.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Peripheral blood mononuclear cells (PBMC), plasma, saliva and urine samples were collected from 50 thalassaemic patients for TT virus (TTV) detection by two sets of PCR. The set B nested PCR was more sensitive than the widely used NG hemi-nested PCR with TTV positive rates approximate to PBMC: 98% vs. 70%; plasma: 92% vs. 66%; saliva: 62% vs. 22%; urine: 22% vs. 6%. All 50 patients had TTV detected in one or more specimens, with 16% of patients being positive in all four specimen types: 40% positive in PBMC, plasma and saliva; 30% positive in PBMC and plasma. In 82 NG hemi-nested PCR-positive samples TTV genotype was identified, 68.3% had a single genotype, 25.6% had multiple genotypes and 6.1% were uncharacterized. The positive rates for genotypes by specimen were: G1 (36/82), G2 (49/82), G3 (2/82), G4 (7/82), G5 (1/82) and G6 (3/82). Among the 42 patients for whom the genotype was examined, 42.9% had single-type infection, 45.2% had co-infections and 11.9% had uncharacterized genotypes. Sixteen of them had TTV detected both in PBMC and plasma with seven having identical genotypes in both samples. Eight patients had TTV detected in PBMC, plasma and saliva; two of them harboured identical genotypes in all three samples. The results indicate that, apart from hepatocytes, PBMC is a major cell type for TTV infection occurs. Shedding of TTV in urine and saliva is common and may have a significant role in nonblood-borne transmission among the general population. TTV-infected patients often harbour multiple genotypes suggesting infection with one genotype does not necessarily confer protection against the others. No correlation between TTV infection and liver dysfunction was observed.
引用
收藏
页码:304 / 309
页数:6
相关论文
共 34 条
[1]   TT virus infection is widespread in the general populations from different geographic regions [J].
Abe, K ;
Inami, T ;
Asano, K ;
Miyoshi, C ;
Masaki, N ;
Hayashi, S ;
Ishikawa, KI ;
Takebe, Y ;
Win, KM ;
El-Zayadi, AR ;
Han, KH ;
Zhang, DY .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (08) :2703-2705
[2]  
Chan PKS, 1997, J MED VIROL, V53, P295, DOI 10.1002/(SICI)1096-9071(199711)53:3&lt
[3]  
295::AID-JMV20&gt
[4]  
3.0.CO
[5]  
2-F
[6]   Prevalence of TT virus infection in US blood donors and populations at risk for acquiring parenterally transmitted viruses [J].
Desai, SM ;
Muerhoff, AS ;
Leary, TP ;
Erker, JC ;
Simons, JN ;
Chalmers, ML ;
Birkenmeyer, LG ;
Pilot-Matias, TJ ;
Mushahwar, IK .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (05) :1242-1244
[7]   Analyses of TT virus full-length genomic sequences [J].
Erker, JC ;
Leary, TP ;
Desai, SM ;
Chalmers, ML ;
Mushahwar, IK .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :1743-1750
[8]   Infection with a novel human DNA virus (TTV) has no pathogenic significance in patients with liver diseases [J].
Giménez-Barcons, M ;
Forns, X ;
Ampurdanés, S ;
Guilera, M ;
Soler, M ;
Soguero, C ;
Sánchez-Fueyo, A ;
Mas, A ;
Bruix, J ;
Sánchez-Tapias, JM ;
Rodés, J ;
Saiz, JC .
JOURNAL OF HEPATOLOGY, 1999, 30 (06) :1028-1034
[9]   Infection with an unenveloped DNA virus (TTV) in patients with acute or chronic liver disease of unknown etiology and in those positive for hepatitis C virus RNA [J].
Ikeda, H ;
Takasu, M ;
Inoue, K ;
Okamoto, H ;
Miyakawa, Y ;
Mayumi, M .
JOURNAL OF HEPATOLOGY, 1999, 30 (02) :205-212
[10]   TT virus in bone marrow transplant recipients [J].
Kanda, Y ;
Tanaka, Y ;
Kami, M ;
Saito, T ;
Asai, T ;
Izutsu, K ;
Yuji, K ;
Ogawa, S ;
Honda, H ;
Mitani, K ;
Chiba, S ;
Yazaki, Y ;
Hirai, H .
BLOOD, 1999, 93 (08) :2485-2490