Exponential spread of hepatitis C virus genotype 4a in Egypt

被引:69
作者
Tanaka, Y
Agha, S
Saudy, N
Kurbanov, F
Orito, E
Kato, T
Abo-Zeid, M
Khalaf, M
Miyakawa, Y
Mizokami, M [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Clin Mol Informat Med, Nagoya, Aichi 4678601, Japan
[2] Nagoya City Univ, Grad Sch Med Sci, Dept Internal Med & Mol Sci, Nagoya, Aichi, Japan
[3] Univ Mansoura, Fac Med, Dept Clin Pathol, Mansoura, Egypt
[4] Univ Mansoura, Fac Med, Dept Surg, Mansoura, Egypt
[5] Assiut Univ, Fac Med, Dept Clin Pathol, Assiut, Egypt
[6] Miyakawa Mem Res Fdn, Tokyo, Japan
关键词
hepatic C virus; genotype; 4a; Egypt; neutral theory; molecular evolutionary;
D O I
10.1007/s00239-003-2541-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis C virus (HCV) infects > 10% of the general population in Egypt, in which intravenous injection with an antimony compound for endemic schistosomiasis in the past has been implicated. To simulate the epidemic history of HCV in Egypt, sera were obtained from 3608 blood donors at 13 governorates in or surrounding the Nile valley during 1999. The prevalence of antibody to HCV (anti-HCV) and genotypes was determined in them, and the molecular evolutionary analysis based on the neutral theory was applied to HCV isolates of genotype 4a, which is outstandingly prevalent in Egypt and indigenous there. Of 3608 sera, 317 (8.8%) were positive for anti-HCV. The molecular evolutionary analysis on 47 HCV genotype 4a isolates of carriers from various districts in Egypt indicated that the spread of HCV-4a would have increased exponentially during the 1940s through 1980 when oral medications became available. In conclusion, the estimated spread time is consistent with the duration of intravenous antimony campaigns in Egypt.
引用
收藏
页码:191 / 195
页数:5
相关论文
共 18 条
[1]  
[Anonymous], 1993, WHO TECHN REP SER, V830
[2]   RISK-FACTORS ASSOCIATED WITH A HIGH SEROPREVALENCE OF HEPATITIS-C VIRUS-INFECTION IN EGYPTIAN BLOOD-DONORS [J].
DARWISH, MA ;
RAOUF, TA ;
RUSHDY, P ;
CONSTANTINE, NT ;
RAO, MR ;
EDELMAN, R .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1993, 49 (04) :440-447
[3]   HEPATITIS-C VIRUS GENOTYPES - AN INVESTIGATION OF TYPE-SPECIFIC DIFFERENCES IN GEOGRAPHIC ORIGIN AND DISEASE [J].
DUSHEIKO, G ;
SCHMILOVITZWEISS, H ;
BROWN, D ;
MCOMISH, F ;
YAP, PL ;
SHERLOCK, S ;
MCINTYRE, N ;
SIMMONDS, P .
HEPATOLOGY, 1994, 19 (01) :13-18
[4]   The role of parenteral antischistosomal therapy in the spread of hepatitis C virus in Egypt [J].
Frank, C ;
Mohamed, MK ;
Strickland, GT ;
Lavanchy, D ;
Arthur, RR ;
Magder, LS ;
El Khoby, T ;
Abdel-Wahab, Y ;
Ohn, EA ;
Anwar, W ;
Sallam, I .
LANCET, 2000, 355 (9207) :887-891
[5]   THE EPIDEMIOLOGY OF ANTIBODY TO HEPATITIS-C IN EGYPT [J].
HIBBS, RG ;
CORWIN, AL ;
HASSAN, NF ;
KAMEL, M ;
DARWISH, M ;
EDELMAN, R ;
CONSTANTINE, NT ;
RAO, MR ;
KHALIFA, AS ;
MOKHTAR, S ;
FAM, NS ;
EKLADIOUS, EM ;
BASSILY, SB .
JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (03) :789-790
[6]   HIGH HCV PREVALENCE IN EGYPTIAN BLOOD-DONORS [J].
KAMEL, MA ;
GHAFFAR, YA ;
WASEF, MA ;
WRIGHT, M ;
CLARK, LC ;
MILLER, FD .
LANCET, 1992, 340 (8816) :427-427
[7]   GEOGRAPHICAL-DISTRIBUTION OF HEPATITIS-C VIRUS GENOTYPES IN BLOOD-DONORS - AN INTERNATIONAL COLLABORATIVE SURVEY [J].
MCOMISH, F ;
YAP, PL ;
DOW, BC ;
FOLLETT, EAC ;
SEED, C ;
KELLER, AJ ;
COBAIN, TJ ;
KRUSIUS, T ;
KOLHO, E ;
NAUKKARINEN, R ;
LIN, C ;
LAI, C ;
LEONG, S ;
MEDGYESI, GA ;
HEJJAS, M ;
KIYOKAWA, H ;
FUKADA, K ;
CUYPERS, T ;
SAEED, AA ;
ALRASHEED, AM ;
LIN, M ;
SIMMONDS, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (04) :884-892
[8]   Hepatitis C in a community in Upper Egypt: I. Cross-sectional survey [J].
Nafeh, MA ;
Medhat, A ;
Shehata, M ;
Mikhail, NNH ;
Swifee, Y ;
Abdel-Hamid, M ;
Watts, S ;
Fix, AD ;
Strickland, GT ;
Anwar, W ;
Sallam, I .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2000, 63 (5-6) :236-241
[9]   New hepatitis C virus (HCV) genotyping system that allows for identification of HCV genotypes 1a, 1b, 2a, 2b, 3a, 3b, 4, 5a, and 6a [J].
Ohno, T ;
Mizokami, M ;
Wu, RR ;
Saleh, MG ;
Ohba, K ;
Orito, E ;
Mukaide, M ;
Williams, R ;
Lau, JYN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (01) :201-207
[10]  
Pybus OG, 2000, GENETICS, V155, P1429