First Molecular Characterization of Chronic Hepatitis B Carriers in Timbuktu, Mali

Author:

Lawrence Philip,Chabane Mawlouda,Abrouk Lucie,Thiesson Adrien,Berthé Diakaridia,Diarra Amadou B.,Bengaly Karim,Traoré BrehimaORCID,Kassogué Djibril,Durand Geoffroy,Voegele Catherine,Le Calvez-Kelm Florence,Steenkeste Nicolas,Hainaut Pierre,Kouriba BouremaORCID,Gormally Emmanuelle

Abstract

In Mali, hepatocellular carcinoma (HCC) is the third and sixth most common cancer in men and women, respectively. Mali comprises several distinct climato-ecological zones. Most studies to date have been conducted in the sub-Sahelian zone of southern Mali, including the capital city Bamako. In this part of the country, the main risk factors for HCC are chronic hepatitis B virus (HBV) carriage and dietary exposure to aflatoxins, a well-known hepatocarcinogen. Data are scarce for other ecological zones, but our preliminary data from 721 blood donors in the area of Timbuktu, presented in this study, suggest that chronic HBV carriage is also endemic in the northern Saharan zone of Mali. For further study, 29 healthy HBV chronic carrier volunteers were recruited from the blood transfusion center in Timbuktu. Successful viral genotyping in 20 volunteers revealed HBV genotype E in 13 cases and D in 7 cases, suggesting that this geographical and anthropological transition zone may also represent a transition zone between HBV genotypes that dominate sub-Saharan and northern Africa, respectively. Sequencing of circulating cell-free plasma DNA (cfDNA) from donors did not reveal the presence of the TP53 R249S mutation in these donors, a marker of dietary exposure to aflatoxins in sub-Saharan Africa. These results suggest that the geo-epidemiological distribution of the risk factors for HCC is not uniform across Mali, but is dependent upon climatic, socioeconomic and anthropological factors that might have an impact on patterns of chronic liver disease and cancer.

Funder

French Région Auvergne Rhône-Alpes

IARC funds for NGS experiments

Publisher

MDPI AG

Subject

Clinical Biochemistry

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