TY - JOUR
T1 - Development and validation of a rapid lateral flow E1/E2-antigen test and ELISA in patients infected with emerging Asian strain of Chikungunya virus in the Americas
AU - Reddy, Ankita
AU - Bosch, Irene
AU - Salcedo, Nol
AU - Herrera, Bobby Brooke
AU - de Puig, Helena
AU - Narváez, Carlos F.
AU - Caicedo-Borrero, Diana María
AU - Lorenzana, Ivette
AU - Parham, Leda
AU - García, Kimberly
AU - Mercado, Marcela
AU - Rico Turca, Angélica María
AU - Villar-Centeno, Luis A.
AU - Gélvez-Ramírez, Margarita
AU - Gómez Ríos, Natalia Andrea
AU - Hiley, Megan
AU - García, Dawlyn
AU - Diamond, Michael S.
AU - Gehrke, Lee
N1 - Publisher Copyright:
© 2020 by the authors.
PY - 2020/9
Y1 - 2020/9
N2 - Since its 2013 emergence in the Americas, Chikungunya virus (CHIKV) has posed a serious threat to public health. Early and accurate diagnosis of the disease, though currently lacking in clinics, is integral to enable timely care and epidemiological response. We developed a dual detection system: a CHIKV antigen E1/E2-based enzyme-linked immunosorbent assay (ELISA) and a lateral flow test using high-affinity anti-CHIKV antibodies. The ELISA was validated with 100 PCR-tested acute Chikungunya fever samples from Honduras. The assay had an overall sensitivity and specificity of 51% and 96.67%, respectively, with accuracy reaching 95.45% sensitivity and 92.03% specificity at a cycle threshold (Ct) cutoff of 22. As the Ct value decreased from 35 to 22, the ELISA sensitivity increased. We then developed and validated two lateral flow tests using independent antibody pairs. The sensitivity and specificity reached 100% for both lateral flow tests using 39 samples from Colombia and Honduras at Ct cutoffs of 20 and 27, respectively. For both lateral flow tests, sensitivity decreased as the Ct increased after 27. Because CHIKV E1/E2 are exposed in the virion surfaces in serum during the acute infection phase, these sensitive and specific assays demonstrate opportunities for early detection of this emerging human pathogen.
AB - Since its 2013 emergence in the Americas, Chikungunya virus (CHIKV) has posed a serious threat to public health. Early and accurate diagnosis of the disease, though currently lacking in clinics, is integral to enable timely care and epidemiological response. We developed a dual detection system: a CHIKV antigen E1/E2-based enzyme-linked immunosorbent assay (ELISA) and a lateral flow test using high-affinity anti-CHIKV antibodies. The ELISA was validated with 100 PCR-tested acute Chikungunya fever samples from Honduras. The assay had an overall sensitivity and specificity of 51% and 96.67%, respectively, with accuracy reaching 95.45% sensitivity and 92.03% specificity at a cycle threshold (Ct) cutoff of 22. As the Ct value decreased from 35 to 22, the ELISA sensitivity increased. We then developed and validated two lateral flow tests using independent antibody pairs. The sensitivity and specificity reached 100% for both lateral flow tests using 39 samples from Colombia and Honduras at Ct cutoffs of 20 and 27, respectively. For both lateral flow tests, sensitivity decreased as the Ct increased after 27. Because CHIKV E1/E2 are exposed in the virion surfaces in serum during the acute infection phase, these sensitive and specific assays demonstrate opportunities for early detection of this emerging human pathogen.
KW - Acute phase diagnosis
KW - Alphavirus
KW - Chikungunya fever
KW - E1/E2 antigen detection
KW - ELISA
KW - Lateral flow
KW - Latin America
KW - Rapid diagnosis
UR - http://www.scopus.com/inward/record.url?scp=85090320234&partnerID=8YFLogxK
U2 - 10.3390/v12090971
DO - 10.3390/v12090971
M3 - Article
C2 - 32882998
AN - SCOPUS:85090320234
SN - 1999-4915
VL - 12
JO - Viruses
JF - Viruses
IS - 9
M1 - 971
ER -