1.Prevalence of Epstein-Barr virus infection in individuals with nasopharyngeal carcinoma in Malaysia: The first systematic review and meta-analysis
Engku Abd Rahman, E.N.S. ; Irekeola, A.A. ; Shueb, R.H. ; Mohamud, R. ; Mat Lazim, N. ; Abdullah, B. ; Chan, Y.Y.
Tropical Biomedicine 2022;39(No.1):89-98
Epstein-Barr virus (EBV) was the first herpesvirus associated to human malignancies. Despite
the well-known association between EBV and malignancies, the prevalence of EBV infection
in Malaysians with malignancies is unknown. Preferred Reporting Items for Systematic
Reviews and Meta-Analysis (PRISMA) was used to conduct a systematic review and metaanalysis of published data in this study. Studies reporting the occurrence of EBV infection in
Malaysian malignancy patients were searched in electronic databases like PubMed, Scopus,
ScienceDirect, and Google Scholar without year or language constraints. The study protocol
was filed in PROSPERO (CRD42021273769). A total of 21 studies were included, with 1,036 EBV
infection cases among 2,078 malignancy patients. The random-effects model was used to
produce summary estimates. The pooled prevalence of EBV infection in Malaysians with
malignancy was 36.3% (95% CI, 20.3 – 56.2). When the prevalence estimates were stratified by
malignancy type, nasopharyngeal carcinoma has the highest prevalence (90.5%), followed
by lymphoma (23.4%), and gastric carcinoma (10.0%). Male patients had a higher cases
prevalence and most patients were above the age of 40. In Malaysia, many malignancies are
increasingly linked to EBV infection. Screening for EBV infection in malignancy patients is
therefore important to determine disease recurrence and metastases.
2.A rare and unusual cause of Vibrio cholerae non-O1, non-O139 causing spontaneous peritonitis in a patient with cirrhosis
Engku Nur Syafirah, E.A.R. ; Che Azmi, N.A. ; Nik Hashim, N.H.H. ; Muhd Besari, A. ; Mustaffa, N. ; Harun, A. ; Chan, Y.Y.
Tropical Biomedicine 2021;38(No.1):183-186
Spontaneous bacterial peritonitis caused by Vibrio cholerae non-O1/ non-O139 is a rare
phenomenon. V. cholerae is known as a common aetiology of epidemic diarrheal disease
and rarely causes extra-gastrointestinal infections. In this report, a 52-year-old man presented
to our hospital with a clinical scenario for chronic liver cirrhosis with low grade fever and
loose stools. V. cholerae was isolated from peritoneal fluid culture, which was further
confirmed as non-O1/ non-O139 strain by multiplex polymerase chain reaction. The patient
was successfully treated with antimicrobial therapy and peritoneal drainage. This case
represents the first isolation of V. cholerae non-O1/ non-O139 strain from peritoneal fluid.
3.Development and validation of TaqMan real-time PCR for the detection of Burkholderia pseudomallei isolates from Malaysia
Mohd Ali, M.R ; Foo, P.C. ; Hassan, M. ; Maning, N. ; Hussin, A. ; Syed Ahmad Yunus, S.Z. ; Fauzi, M.H. ; Muhd Besar, A. ; Harun, A. ; Ismail, N. ; Chan, Y.Y.
Tropical Biomedicine 2019;36(2):379-389
Rapid detection of Burkholderia pseudomallei, the etiologic agent of melioidosis,
allows for timely initiation of appropriate treatment and better clinical outcomes. In the
current gold standard, the culture method is time consuming and suffers from low sensitivity.
Meanwhile, previously reported molecular assays are fast and sensitive, but their performance
on isolates from Malaysia, an endemic region of melioidosis is under reported. This study
designed oligonucleotides targeting orf2 of Type III secretion system (TTSS) genes cluster
for the detection of Malaysian B. pseudomallei isolates and evaluated the assay on 95 local
B. pseudomallei strains, 58 other microorganisms and 71 clinical specimens from patients.
The developed assay exclusively detected all tested B. pseudomallei isolates with a detection
limit of 20 fg per reaction (equivalent to ~2.5 copies). Subsequent testing on clinical samples
showed that the assay detected all confirmed specimens with the growth of B. pseudomallei
(n = 10/10). None of the negative specimens had a detectable signal of our TTSS-orf2 assay
(n = 0/61). In conclusion, the present study provides crucial preliminary data for a subsequent
study and should be considered as a potential alternative to current time-consuming culture
method for the detection of B. pseudomallei.