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. 2019 Dec 9;9:18596. doi: 10.1038/s41598-019-55160-4

Table 1.

Investigation of arboviral infections by molecular and serological methods during an outbreak occurred in Midwest Brazil, 2016.

Specimen Molecular diagnosis Serological diagnosis
rtRT-PCR for ZIKV
(Lanciotti et al., 2008) Positive/Tested (%)
rtRT-PCR for DENV
(Johnson et al., 2005) Positive/Tested (%)
SEROTYPE
Simplexa™ Dengue rtRT-PCR
Positive/Tested (%)
SEROTYPE
Platelia Dengue NS1
Positive/Tested (%)
Anti-DENV IgM Capture
Positive/Tested (%)
Serum (n = 76, all mono-infections) 33/76 (43.42)a 0/76b 0/76 5/76 (6.57) 0/76
Plasma (n = 132; 108 mono-infections and 24 co-infections) 12/132 (9.09)

22/132 (16.66)c

14 DENV-1 (14/22; 63.63)

8 DENV-4 (8/22; 36.37)

22/132 (16.66)c

14 DENV-1 (14/22; 63.63)

8 DENV-4 (8/22; 36.37)

58/132 (43.93) 29/132 (21.96)
Urine (n = 19, all mono-infections) 12/19 (63.15) 0/19 0/19 0/19 0/19
TOTAL 57/227 (25.11) 22/227 (9.69) 22/227 (9.69) 63/227 (27.75) 29/227 (12.77)

aAll 33 positive serum samples by rtRT-PCR for ZIKV, were negative for Dengue (NS1 and IgM), chikununya and mayaro.

bFrom 76 dengue negative serum samples by rtRT-PCR, only 5 were positive for Dengue NS1. Those 5 samples were negative for Zika, chikungunya and mayaro.

cBy either rtRT-PCR for DENV and Simplexa™ Dengue rtRT-PCR, 22 plasmas were positive for dengue and from those, 14 were characterized as DENV-1 and 8 as DENV-4.