Molecular identification and genotyping of hepatitis E virus from Southern Punjab, Pakistan

• Published in: Scientific reports Vol. 14; no. 1; p. 223
• Main Authors: Ali, Muhammad Muddassir, Gul, Mehek, Imran, Muhammad, Ijaz, Muhammad, Azeem, Shahan, Ullah, Arif, Yaqub, Hafiz Muhammad Farooq
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 02-01-2024; Nature Publishing Group; Nature Portfolio
• Subjects: 631/326; 631/337; 631/601; Animals; Capsid protein; DNA biosynthesis; Genotype; Genotype & phenotype; Genotypes; Genotyping; Global health; Hepatitis; Hepatitis Antibodies; Hepatitis E; Hepatitis E virus; Homology; Humanities and Social Sciences; Humans; Immunoglobulin M; Infections; multidisciplinary; Pakistan - epidemiology; Phylogeny; Polymerase chain reaction; Protein structure; Proteins; Public health; RNA, Viral - analysis; RNA, Viral - genetics; Sanitation; Science; Science (multidisciplinary); Sequence analysis; Viruses; Pakistan; Punjab Pakistan
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-50514-5

Hepatitis E is a global health concern. Hepatitis E virus (HEV) infection is endemic in Pakistan. HEV has four genotypes: HEV-1 through HEV-4. The genotypes HEV-1 and HEV-2 are associated with infection in humans, especially in countries with poor sanitation. The genotypes HEV
-
3 and HEV-4 are zoonotic and human infection takes place by consuming undercooked meat or being in contact with animals. The present study was designed to ascertain the presence of HEV in the Southern Punjab region of Pakistan. First, blood samples (n = 50) were collected from patients suspected of infection with the hepatitis E virus from the Multan District. The serum was separated and the samples were initially screened using an HEV IgM-ELISA. Second, the ELISA-positive samples were subjected to PCR and were genetically characterized. For PCR, the RNA extraction and complementary DNA synthesis were done using commercial kits. The HEV ORF2 (Open Reading Frame-2, capsid protein) was amplified using nested PCR targeting a 348 bp segment. The PCR amplicons were sequenced and an evolutionary tree was constructed using MEGA X software. A protein model was built employing the SWISS Model after protein translation using ExPASy online tool. The positivity rate of anti-HEV antibodies in serum samples was found as 56% (28/50). All Pakistani HEV showed homology with genotype 1 and shared common evolutionary origin and ancestry with HEV isolates of genotype 1 of London (MH504163), France (MN401238), and Japan (LC314158). Sequence analysis of motif regions assessment and protein structure revealed that the sequences had a similarity with the reference sequence. These data suggest that genotype 1 of HEV is circulating in Pakistan. This finding could be used for the diagnosis and control of HEV in the specific geographic region focusing on its prevalent genotype.