1.Monoclonal antibody-escape variant of dengue virus serotype 1: Genetic composition and envelope protein expression
Chem, Y.K. ; Chua, K.B. ; Malik, Y. ; Voon, K.
Tropical Biomedicine 2015;32(2):344-351
Monoclonal antibody-escape variant of dengue virus type 1 (MabEV DEN-1) was
discovered and isolated in an outbreak of dengue in Klang Valley, Malaysia from December
2004 to March 2005. This study was done to investigate whether DEN152 (an isolate of
MabEV DEN-1) is a product of recombination event or not. In addition, the non-synonymous
mutations that correlate with the monoclonal antibody-escape variant were determined in
this study. The genomes of DEN152 and two new DEN-1 isolates, DENB04 and DENK154
were completely sequenced, aligned, and compared. Phylogenetic tree was plotted and the
recombination event on DEN152 was investigated. DEN152 is sub-grouped under genotype I
and is closely related genetically to a DEN-1 isolated in Japan in 2004. DEN152 is not a
recombinant product of any parental strains. Four amino acid substitutions were unique only
to DEN 152. These amino acid substitutions were Ser[326]Leu, Ser[340]Leu at the deduced E
protein, Ile[250]Thr at NS1 protein, and Thr[41]Ser at NS5 protein. Thus, DEN152 is an isolate of
the emerging monoclonal antibody-escape variant DEN-1 that escaped diagnostic laboratory
detection.
2.Detection of enteroviruses during a 2018 hand, foot and mouth disease outbreak in Malaysia
Lee, M.H.P. ; Chong, Y.M. ; Tay, C.G. ; Koh, M.T. ; Chem, Y.K. ; Noordin, N. ; Jahis, R. ; Sam, I.C. ; Chan, Y.F.
Tropical Biomedicine 2021;38(No.1):150-153
Hand, foot, and mouth disease (HFMD) is a common childhood disease caused by
enteroviruses. In 2018, a HFMD outbreak in Malaysia affected over 76,000 children. In this
study, we used RT-qPCR and CODEHOP PCR to detect the causative agents in 89 clinically
diagnosed HFMD patients in Kuala Lumpur and Selangor. Most (62.9%) of the children were
below 3 years old. PCR with either assay detected enteroviruses in 84.2% (75/89) and CODEHOP
PCR successfully typed 66.7% (50/75) of the enteroviruses. Sequencing of CODEHOP amplicons
showed co-circulation of multiple enteroviruses with coxsackievirus A6 (CV-A6) and A16 as
the predominant serotypes, but not the neurovirulent enterovirus A71. CV-A6 infection was
more common in children less than 12 months old (p=0.01) and was more likely to cause
vesicles in the gluteal area (p=0.01) compared to other enteroviruses. Establishing a robust
identification method during HFMD outbreaks is important for patient management and
public health responses.