Table 2.
CHIKV IgM+* | CHIKV IgM−† | |
---|---|---|
Number of samples tested | 100 | 147 |
Serology | ||
Confirmed by PRNT only | 54 | 0 |
Confirmed by real-time RT-PCR only | 10 | 0 |
Confirmed by HAI only | 13 | 0 |
Confirmed by both PRNT and HAI | 17 | 0 |
Confirmed by both real-time RT-PCR and HAI | 3 | 0 |
Confirmed by both PRNT and real-time RT-PCR | 2 | 0 |
Confirmed by PRNT, real-time RT-PCR, and HAI | 1 | 0 |
Travel history | ||
Travel to Americas‡ | 63 | 31 |
Travel to Asia | 2 | 4 |
Travel to Africa | 2 | 1 |
Travel to Oceania | 2 | 0 |
No travel history provided | 31 | 111 |
CHIKV = chikungunya virus; ELISA = enzyme-linked immunosorbent assay; HAI = hemagglutination inhibition assay; PRNT = plaque reduction neutralization assay; NML = the Public Health Agency of Canada National Microbiology Laboratory; RT-PCR = reverse transcription polymerase chain reaction.
Serum samples were classified as originating from confirmed cases of CHIKV infection if CHIK IgM+ and either PRNT and/or real-time RT-PCR and/or HAI positive. Samples were identified as either CHIKV IgM+ or IgM− using an in-house CDC-based IgM ELISA.
See Table 3 for description of sample panel with no detectable CHIK IgM antibodies.
South America, Central America, or the Caribbean; two CHIKV IgM samples with travel history to Mexico were also included.