2010
DOI: 10.1371/journal.pntd.0000753
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Evaluation of Chikungunya Diagnostic Assays: Differences in Sensitivity of Serology Assays in Two Independent Outbreaks

Abstract: BackgroundThe sensitivity and specificity of two in-house MAC-ELISA assays were tested and compared with the performance of commercially-available CTK lateral flow rapid test and EUROIMMUN IFA assays for the detection of anti-Chikungunya virus (CHIKV) IgM. Each MAC-ELISA assay used a whole virus-based antigen derived from genetically distinct CHIKV strains involved in two chikungunya disease outbreaks in Singapore (2008); a January outbreak strain with alanine at amino acid residue 226 of the E1 glycoprotein (… Show more

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Cited by 100 publications
(76 citation statements)
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References 22 publications
(33 reference statements)
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“…The two isolates D2/Singapore/0904aTw and D2/ Singapore/0904bTw, derived from case 1 and case 2, respectively, had 100% nucleotide identity in their envelope genes and belonged to the Cosmopolitan genotype. Our data are in agreement with recent reports that E1-226V mutant CHIKV strains grouped into the Central/East/South African genotype and DENV-2 strains grouped into the Cosmopolitan genotype were predominant epidemic strains circulating in Singapore in 2009 (7,19). As various genotypic strains may differ in epidemic potential and virulence, molecular epidemiological surveillance can provide valuable information in decision making regarding patient care, outbreak investigation, and control measures (2,4).…”
supporting
confidence: 92%
“…The two isolates D2/Singapore/0904aTw and D2/ Singapore/0904bTw, derived from case 1 and case 2, respectively, had 100% nucleotide identity in their envelope genes and belonged to the Cosmopolitan genotype. Our data are in agreement with recent reports that E1-226V mutant CHIKV strains grouped into the Central/East/South African genotype and DENV-2 strains grouped into the Cosmopolitan genotype were predominant epidemic strains circulating in Singapore in 2009 (7,19). As various genotypic strains may differ in epidemic potential and virulence, molecular epidemiological surveillance can provide valuable information in decision making regarding patient care, outbreak investigation, and control measures (2,4).…”
supporting
confidence: 92%
“…A laboratory-developed indirect immunofluorescence assay (IFA) based on the Titerplane system (Euroimmun US, Inc., Morris Plains, NJ) was used to measure CHIKV IgG (26,27). Sera diluted 1:10 in phosphate-buffered saline (PBS) were added to reaction fields of a reagent tray, and a slide containing mounted glass biochips coated with CHIKV (strain EU 14)-infected Vero cells or uninfected Vero cells was placed into the recesses of the reagent tray.…”
Section: Chikv Igg Ifamentioning
confidence: 99%
“…An approach similar to that described for CHIKV IgG detection was used to measure CHIKV IgM (26,27). Sera were diluted 1:10 in PBS containing goat anti-human IgG (Focus Diagnostics Products, Cypress, CA), and after 15 min at room temperature, diluted sera were transferred to reagent tray reaction fields.…”
Section: Chikv Igg Ifamentioning
confidence: 99%
“…In the acute phase of illness, detection of viral nucleic acid in serum by RT-PCR is possible [6]. After this period, diagnosis relies on detection of specific antibodies against CHIKV [7][8]. Laboratory confirmation of CHIKV infection is usually achieved by detection of viral genome or demonstration of seroconversion in paired serum samples [9].…”
Section: Diagnosismentioning
confidence: 99%