Abstract:
Hepatitis E virus (HEV) is an emergent source of enterically transmitted viral hepatitis and
an imminent public health concern. HEV has a substantial disease burden in areas afflicted
with humanitarian emergencies such as flood-affected regions, externally or internally
displaced populations, and densely packed areas where access to proper sanitation and safe
drinking water is challenging. Although outbreaks and sporadic cases are linked to
waterborne transmission, zoonosis has also been linked to the emergence of disease. It
usually presents itself as a self-resolving aliment, but chronic HEV infections prove to be
devastating in immunocompromised patients and pregnant females where the infection is
associated with high maternal mortality and frequent fetal loss. HEV-related clinical
complications are often undetected and not considered in the differential diagnosis.
Pakistan is the fifth most populous nation in the world and is faced with several challenges
including recent devastating floods, sub-optimal sanitary conditions, cluster
accommodation, and unregulated cross-border movements. These drastic shifts in
population dynamics make these territories vulnerable to proficient disease spread. The
current study thus sought to analyze the epidemiological and viral genotype characteristics
of the Hepatitis E virus, to assess the genetic variants circulating in the population.
Consecutive patients presenting with symptoms associated with acute liver disease were
sampled from three metropolitan cities including Lahore, Peshawar, and Karachi. HEV
infection was confirmed by ELISA. ELISA-positive samples (75 samples) were further
subjected to viral RNA extraction, followed by the amplification of the HEV Rdrp region
using Nested PCR and degenerate primers. 40% of the samples (33 samples) were found
to be positive for HEV RNA indicating an active infectious state. Sequencing and
phylogenetic analysis revealed that HEV isolates cluster with genotype 1. Subtype 1g was
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found to be the prevailing subtype as compared to the previously documented subtype 1a
reported from Karachi. Thus, our results indicate the presence of a newly abundant
circulating subtype and thus merit a thorough investigation to further evaluate the impacts
of this shift on clinical manifestation and disease severity.