Detection of Autochthonous Zika Virus Transmission in Sincelejo, Colombia

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To the Editor: Zika virus (ZIKV) is an arthropodborne member of the genus Flavivirus of the Spondweni serocomplex and is transmitted by Aedes mosquitoes (primarily Ae. aegypti in urban and periurban cycles). ZIKV emerged in Africa and has caused outbreaks of febrile disease that clinically resemble dengue fever and other arboviral diseases (1) but has been linked to neurologic syndromes and congenital malformation (2). Outbreaks have been reported in the Yap islands of the Federated States of Micronesia (3), French Polynesia (4), and Oceania; Brazil is currently experiencing the first reported local transmission of ZIKV in the Americas (5).

The future spread of ZIKV is unpredictable, but the history of ZIKV has been reminiscent of chikungunya virus (CHIKV), which reemerged in Africa and now circulates on all inhabited continents and is a major global health problem. ZIKV has been found in Colombia and is likely following the path of CHIKV, which reached the country in August 2014 (6). The virus co-circulates with other Ae. aegypti–transmitted arboviruses, including dengue virus (DENV) and yellow fever virus. We report ZIKV infection in Colombia and a recent ongoing outbreak in Sincelejo, Colombia, with resulting illness characterized by maculopapular rash, fever, myalgia/arthralgia, and conjunctivitis.

During October–November 2015, a total of 22 patients received a presumptive diagnosis of an acute viral illness by emergency department physicians at the Centro de Diagnostico Medico-Universidad de Sucre in Sincelejo. The patients began treatment for a dengue-like illness, and blood samples were obtained for diagnosis. The samples were analyzed at the Universidad de Sucre by using reverse transcription PCR (RT-PCR) to detect DENV, CHIKV, or ZIKV. Viral RNA was extracted from the serum samples by using the ZR Viral RNA Kit (Zymo Research, Irvine, CA, USA); reverse transcription was performed by using the Protoscript First Strand cDNA Synthesis Kit (New England Biolabs, Ipswich, MA, USA). Amplicons were produced by using the OneTaq Quick-Load 2X Master Mix (New England Biolabs) with primers specific to DENV (7), CHIKV (forward: 5′-CGCCAACATTCTGCTTACAC-3′; reverse: 5′-AGGATGCCGGTCATTTGAT-3′), and ZIKV. The CHIKV amplification target was 649 bp of nonstructural protein 1 (NS1). A positive PCR for a partial region of the envelope (E) gene with primers ZIKVENVF and ZIKVENVR (8) was considered indicative of ZIKV infection. ZIKV primers specific for the E gene and NS1 were designed and used to amplify the E gene and NS1 for phylogenetic analyses, and amplicons were produced by using the OneTaq One-Step RT-PCR Kit (New England Biolabs). E gene and NS1 PCR products were sequenced at the University of Wisconsin–Madison Biotechnology Center (Madison, WI, USA).

Thumbnail of Majority-rule consensus tree based on Zika virus envelope and nonstructural protein 1 gene sequences (2,604 nt) of isolates from patients in Sincelejo, Colombia, October–November 2015, compared with reference isolates. The tree was constructed on the basis of Bayesian phylogenetic analysis with 8 million generations and a general time-reversible substitution model using MrBayes software version 3.2 (http://mrbayes.sourceforge.net). Numbers to the right of nodes represent posterior p

Figure. Majority-rule consensus tree based on Zika virus envelope and nonstructural protein 1 gene sequences (2,604 nt) of isolates from patients in Sincelejo, Colombia, October–November 2015, compared with reference isolates. The tree...

Samples from all patients were negative by RT-PCR for DENV and CHIKV; samples from 9 (41%) patients were positive for ZIKV. Among those 9 patients, 7 (78%) were male; median age was 23; and none had a history of international travel. ZIKV was analyzed by sequencing the E gene and NS1 of 2 isolates. Phylogenetic analyses rooted with Spondweni virus showed that the ZIKV sequences (GenBank accession nos. KU646827 and KU646828) belonged to the Asian lineage (Figure) and were closely related to strains isolated during the 2015 outbreak in Brazil (5). The sequences also showed 99% identity with sequences from a ZIKV isolate from French Polynesia (GenBank accession no. KJ776791) (9). These data suggest that ZIKV circulating in Colombia could have been imported from Brazil, most likely as a result of tourism activities on Colombia’s northern coast, where the first reported case was identified (the state of Bolivar).

We report ZIKV infection in Colombia in association with an ongoing outbreak of acute maculoexantematic illness. Since detection of ZIKV in Sincelejo, a total of 13,500 cases have been identified in 28 of the country’s 32 territorial entities (10), all of which have abundant populations of Ae. aegypti mosquitoes and co-circulation of DENV and CHIKV. These circumstances highlight the need for accurate laboratory diagnostics and suggest that monitoring whether the virus spreads into neighboring countries (e.g., Ecuador, Peru, Venezuela, and Panama) is imperative.

Erwin Camacho, Margaret Paternina-Gomez, Pedro J. Blanco, Jorge E. Osorio, and Matthew T. Aliota

Author affiliations: University of Wisconsin–Madison, Madison, Wisconsin, USA (E. Camacho, J.E. Osorio, M.T. Aliota); Universidad de Sucre, Sincelejo, Colombia (M. Paternina-Gomez, P.J. Blanco)

Acknowledgment

We thank the University of Wisconsin–Madison for partially funding this study. E.C. was supported by the University of Wisconsin–Madison Global Health Institute.

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Figure. Majority-rule consensus tree based on Zika virus envelope and nonstructural protein 1 gene sequences (2,604 nt) of isolates from patients in Sincelejo, Colombia, October–November 2015, compared with reference isolates. The...

Suggested citation for this article: Camacho E, Paternina-Gomez M, Blanco PJ, Osorio JE, Aliota MT. Detection of autochthonous Zika virus transmission in Sincelejo, Colombia [letter]. Emerg Infect Dis. 2016 May [date cited]. http://dx.doi.org/10.3201/eid2205.160023

DOI: 10.3201/eid2205.160023