During 2009–2010, serum samples from patients with suspected dengue were received by the FDOH for dengue diagnostic testing; the samples came from 16 of Florida’s 67counties. All samples were tested by using DENV serotype–specific, real-time RT-PCR (8) and IgM anti-DENV ELISA (9). Samples with highly positive RT-PCR results were spread onto cultured Ae. albopictus C6/36 cells, and the presence of virus and genome were confirmed by immunofluorescence (10) and RT-PCR, respectively (11). Isolates were further propagated and viral RNA was extracted from culture supernatants by using the Universal BioRobot System (QIAGEN, Valencia, CA, USA). The envelope glycoprotein (E) gene was amplified (Technical Appendix), and the E gene open-reading frame (1,485 bp) was sequenced. All sequences were submitted to GenBank; accession numbers are shown in Technical Appendix. Multiple sequence alignments were performed by using the MUSCLE module available in MEGA 5 (www.megasoftware.net). Evolutionary history was inferred by using maximum likelihood and phylogenetic trees constructed by using neighbor-joining methods. Evolutionary distances were computed, and several E gene sequences from GenBank were included in the phylogenetic tree to support tree topology by genotype (Technical Appendix).

In 2009, five DENV-1–positive cases were identified by RT-PCR in Key West. Subsequently, in 2010, the FDOH tested 195 serum samples by real-time RT-PCR. Fifty-six (29%) samples were positive for DENV RNA: DENV-1 (37 [66%] samples), DENV-2 (13 [23%] samples), DENV-3 (3 [5%] samples), and DENV-4 (3 [5%] samples). Monroe County submitted 73 serum samples, of which 31 (42%) had results positive for recent dengue infection: DENV-1 was detected in 22 by RT-PCR, and 9 had positive IgM anti-DENV ELISA results. No other DENV serotype was identified in Key West. None of the DENV-1 patients from Monroe County had a history of recent travel to a dengue-endemic region before the onset of symptoms. Fifteen other Florida counties submitted serum samples: 13 counties submitted <10 specimens, 1 submitted 20–30 specimens, and 1 submitted >60specimens. DENV-1 was found in 15 serum samples from 6 of these counties; however, all the patients had a history of recent international travel.

We sequenced the E gene of 12 DENV-1 strains isolated in Florida during 2009–2010 to determine their genetic relatedness; of the 12 strains, 8 were from Key West and 1 each was from Dade, Broward, Orange, and Pinellas Counties. In addition, 23 DENV-1 E sequences published in GenBank, including the 2010 Key West isolates obtained from a blood donor and a mosquito pool (6,7), were used to construct a maximum-likelihood phylogenetic tree. The significance of branch lengths and taxa relationships was tested by 1,000 bootstrap replications. This phylogenetic analysis showed that all the Florida DENV-1 isolates belong to the American–African genotype (genotype V) (12,13) together with other viruses isolated throughout the Americas (Figure 1).

Key West DENV-1 viruses grouped among Central American viruses, which configure a distinct lineage separate from the Caribbean viruses. This divergence between the Central American and Caribbean lineages is well supported by high bootstrap values. Moreover, the Key West and Monroe County viruses grouped together and indicated a distinct sublineage supported by a high bootstrap value (99%), separating them from viruses isolated in Dade, Orange, Pinellas, and Broward Counties that were more closely related to other Central American viruses (Figure 1). One 2009 isolate (IQ425062) from a Key West patient is related to this group, suggesting a separate introduction of DENV-1 in Key West. The sequence similarity between the 2009 and 2010 Key West strains was <0.9%; however, the evolutionary distance and taxa positions between the 2009 and 2010 strains presented in the phylogenetic tree suggests that the 2010 strains diverged from the 2009 strains. The observed differences between E gene sequences for the Key West strains (2009–2010) and the rest of the strains in this phylogeny were <2.1% with the other Florida strains, <1.2% with Central American strains, and <4.8% with the rest of the American–African genotype.

Evolutionary distances and the topology of the Central American lineage suggest this lineage is the genetic origin of the Florida DENV-1 strain. Most viruses isolated in Monroe County diverged from the Central American lineage into a distinct sublineage—the Key West DENV-1 strain associated with the 2009–2010 outbreak. The high level of genetic similarity among the viruses isolated in Monroe County, their close evolutionary distances, and the lack of recent international travel for the case-patients suggest endemic transmission and microevolution of this DENV. Conversely, the scattered and separate phylogenetic positioning of virus strains from patients with travel-associated cases from other Florida counties indicates a different origin from the majority of Key West isolates. Although the 2009 Broward isolate (JQ425067) is positioned near the Central American lineage, the low bootstrap value (53%) does not support lineage ancestry.

The epidemiologic and phylogenetic evidence suggests that the 2010 cases appeared to be a continuation of the 2009 outbreak. Unlike cases along the Texas–Mexico border (14), all DENV-1 infections in Key West seem to have been locally acquired. Ae. aegypti mosquitoes collected by the FDOH were positive for DENV-1. In addition, DENV-1 was detected in a blood donation from the Monroe County in 2010, further supporting local transmission of DENV (7). Collectively, these findings indicate that endemic DENV-1 was transmitted in Key West over a period of >2 years.

Table showing the dengue virus type 1 (DENV-1) envelope gene reverse transcription PCR and another showing DENV-1 strains used in a study of the genetic relatedness of dengue viruses in Key West, Florida, USA, 2009–2010.