Molecular epidemiology of hepatitis B, hepatitis C, and HIV-1 co-infections in Ethiopia: Implications for disease burden and intervention strategies

被引:1
作者
Weldemariam, Atsbeha Gebreegziabxier [1 ]
Lin, Su-, I [1 ,2 ]
Li, Wei-You [3 ]
Wolday, Dawit [1 ,4 ]
Yang, Ming-Hui [5 ]
Alemu, Yibeltal Assefa [6 ]
Sarusi, Deborah [7 ]
Maayan, Shlomo [8 ]
Chen, Yi-Ming Arthur [3 ,8 ,9 ]
Chuang, Kuo-Pin [11 ]
Tyan, Yu-Chang [10 ,11 ,12 ,13 ]
Dai, Chia-Yen [14 ,15 ,16 ]
机构
[1] Ethiopian Publ Hlth Inst, Addis Ababa, Ethiopia
[2] LumiSTAR Biotechnol Inc, Taipei, Taiwan
[3] Fu Jen Catholic Univ, Grad Inst Biomed & Pharmaceut Sci, Coll Med, New Taipei City, Taiwan
[4] McMaster Univ, Dept Biochem & Biomed Sci, Hlth Sci, Hamilton, ON, Canada
[5] Kaohsiung Med Univ, Div Gen & Digest Surg, Dept Surg, Kaohsiung Med Univ Hosp, Kaohsiung, Taiwan
[6] Univ Queensland, Sch Publ Hlth, Brisbane, Australia
[7] Barzilai Univ, Div Infect Dis, Med Ctr, Ashqelon, Israel
[8] Fu Jen Catholic Univ, Sch Med, Dept Med, Lab Important Infect Dis & Canc, New Taipei City, Taiwan
[9] Natl Inst Infect Dis & Vaccinol, Natl Hlth Res Inst, Miaoli Cty, Taiwan
[10] Natl Pingtung Univ Sci & Technol, Grad Inst Anim Vaccine Technol, Coll Vet Med, Pingtung, Taiwan
[11] Kaohsiung Med Univ, Ctr Trop Med & Infect Dis Res, Kaohsiung, Taiwan
[12] Kaohsiung Med Univ, Dept Med Imaging & Radiol Sci, Kaohsiung, Taiwan
[13] Kaohsiung Med Univ Hosp, Dept Med Res, Kaohsiung, Taiwan
[14] Kaohsiung Med Univ, Sch Med & Drug Dev, Kaohsiung, Taiwan
[15] Kaohsiung Med Univ, Value Creat Res Ctr, Kaohsiung, Taiwan
[16] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Internal Med, Hepatobiliary Div, Kaohsiung, Taiwan
关键词
Hepatitis B virus; Co-infections; Molecular epidemiology; Genotype; Ethiopia; HUMAN-IMMUNODEFICIENCY-VIRUS; LIVER-DISEASE; GENOTYPES; INFECTION; CANCER; HBV;
D O I
10.1016/j.actatropica.2024.107318
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Background: Hepatitis B virus (HBV) exhibits high prevalence rates within Ethiopia. The genetic diversity of HBV, marked by mixed genotype infections, may hold significant implications for the trajectory of disease and responses to treatment. Ethiopia grapples with a substantial public health challenge posed by co-infections involving HBV, hepatitis C virus (HCV), and human immunodeficiency virus 1 (HIV-1), particularly among vulnerable populations. Methods: A comprehensive investigation into HBV, HCV, and HIV-1 co-infection was conducted. A total of 7,789 blood samples were meticulously analyzed, among which 815 exhibited HBV positivity. Among the HBV-positive samples, 630 were subjected to genotyping procedures, resulting in the identification of a prevalent trend of mixed infections characterized by HBV genotypes A/E/F (67.30%). Serological assessments were performed on 492 specimens to ascertain the presence of HCV and HIV-1 co-infections, revealing respective co-infection rates of 13.02% for HBV/HIV, 3.31% for HBV/HCV, and 2.07% for triple infection. Results: The investigation revealed the intricate prevalence of co-infections in Ethiopia, notably underlining the continued transmission of viruses. The prominent occurrence of mixed HBV genotypes A/E/F suggests dynamic viral interactions and ongoing transmission pathways. These findings accentuate the necessity for targeted interventions and enhanced patient care, as co-infections carry significant clinical complexities. Conclusions: This study furnishes crucial insights into the molecular epidemiology of HBV, HCV, and HIV-1 co- infections in Ethiopia. The acquired knowledge can contribute to the advancement of strategies for clinical management and the formulation of public health interventions aimed at ameliorating the burden of viral infections within the nation.
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