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Volume 31, Number 11—November 2025

Research Letter

Detection of Aedes (Fredwardsius) vittatus Mosquitoes, Yucatán Peninsula, Mexico, 2025

Author affiliation: Center for Research and Advanced Studies (Cinvestav), Mérida Unit, Mérida, Mexico

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Abstract

We report detection of Aedes (Fredwardsius) vittatus mosquitoes in continental North America, in Yucatán, Mexico. Phylogenetic analysis clustered the sequence from mosquitoes collected in Mexico with Caribbean mosquito lineages, suggesting species introduction via the Caribbean. Given its arbovirus competence, urgent inclusion of the Ae. vittatus mosquito in surveillance programs is warranted.

Mosquitoborne arboviruses, such as dengue, Zika, chikungunya, and yellow fever, have expanded dramatically over the past 5 decades, driven by urbanization, globalization, and human mobility (1). Dengue and chikungunya alone now cause >50 million infections annually, reflecting a 30-fold increase linked to demographic and ecologic change (2). Although Aedes aegypti and Ae. albopictus mosquitoes remain the primary invasive vectors under surveillance and control, other species of epidemiologic relevance are gaining increased attention as potential emerging threats (3).

Ae. (Fredwardsius) vittatus is one such mosquito, notable for its expanding range and proven arboviral vector competence (4). Described from Corsica, France, in 1977 (5), Ae. vittatus is now distributed across Africa, the Mediterranean Basin, the Middle East, and South and Southeast Asia, and sporadic detections have been reported in southern Europe and the Caribbean. Ae. vittatus mosquitoes are highly adaptable, breeding in both natural and artificial containers, and thrive in sylvatic, rural, agricultural, and periurban environments (6). Laboratory and field studies confirm the species’ ability to transmit dengue, chikungunya, Zika, and yellow fever viruses and its additional potential to transmit Japanese encephalitis and West Nile viruses (7).

Figure

Map of Aedes (Fredwardsius) vittatus mosquito detection and GHMI, Yucatán Peninsula, Mexico, 2025. White circles show sites where mosquitoes were detected in this study; gray circle shows site of mosquito detection from another study (J.C. Tzuc-Dzul et al., unpub. data, https://doi.org/10.21203/rs.3.rs-6786909/v1). Inset shows Mexico with study region marked. Map is overlaid with the GHMI (0.09 km2 resolution). GHMI measures landscape modified by humans and values range from 0 (unmodified) to 1 (completely modified). Gray lines indicate main federal and state roads. GHMI, Global Human Modification Index.

Figure. Map of Aedes (Fredwardsius) vittatusmosquito detection and GHMI, Yucatán Peninsula, Mexico, 2025. White circles show sites where mosquitoes were detected in this study; gray...

During entomological surveillance in August–September 2025, we collected 67 adult Ae. vittatus mosquitoes in traditional Mayan cornfields (milpa) (Appendix Figure 1) on the outskirts of the Mama and Teabo municipalities of Yucatán, Mexico (Table; Figure). We aspirated adult mosquitoes as they attempted to bite field personnel (Appendix Figure 2, panel A). We collected both sexes (Table; Appendix Figure 2, panels B, C), supporting evidence of local reproduction and establishment in rural agricultural environments.

We morphologically identified specimens by using standard taxonomic keys (4,5) and deposited 7 voucher individuals (nos. AR-0734–40), in the Arthropod Collection (ECOSUR, https://colecciones.ecosur.mx), Chetumal Unit. Ae. vittatus mosquitoes can be distinguished from other Aedes species mosquitoes by their dark proboscis with pale yellowish scales, small bilateral patches of white scales on the clypeus, 3 pairs of narrow white patches on the anterior scutum, a short maxillary palp with apical white scaling, and a distinct white patch at the midpoint of the third tibia (Appendix Figure 2, panels B–E).

To confirm species identity, we sequenced a fragment of the mitochondrial cytochrome oxidase 1 (COX1) gene from an Ae. vittatus mosquito we collected in Yucatán, Mexico (GeneBank accession no. PX418072), and analyzed it with global reference sequences. Bayesian phylogenetic inference placed the mosquito specimen from Mexico within the American–Caribbean lineage, clustering with sequences from Cuba and the Dominican Republic (Appendix Figure 3). Although the history of Ae. vittatus mosquito invasion is only beginning to unfold, this regional pattern resembles the early stages of Ae. aegypti mosquito expansion, for which the Caribbean acted as a bridgehead before dispersal into the Americas and beyond (8). Although the 0.8–0.9 posterior support for the Ae. vittatus subclade in North America was moderate, the overall tree was well resolved (Appendix Figure 3), strengthening confidence in this inference. The case of Ae. aegypti mosquitoes illustrates how the Caribbean can serve as an intermediate launch point for Old World mosquitoes, underscoring the importance of acting now to monitor Ae. vittatus mosquitoes and prevent wider establishment as a new invasive vector in the Americas.

We also characterized the ecologic context of the Ae. vittatus mosquito using the Global Human Modification Index (The Nature Conservancy, https://gdra-tnc.org/current). High human modification index scores in the Yucatán Peninsula reflect intense land-use change from urbanization, agriculture, and infrastructure projects, highlighting conditions favorable for mosquito establishment and spread (Figure). As a flat landmass with few natural biogeographic barriers, the peninsula provides little resistance to dispersal of habitat-tolerant invasive species. Studies of Ae. aegypti mosquitoes have shown that flat, highly connected regions with dense human activity enhance mosquito gene flow and facilitate spread (9). By analogy, regions where Ae. vittatus mosquitoes are now reported, including the Yucatán Peninsula, present similar ecologic and sociological conditions that could accelerate its population increase and dispersal.

Detection of Ae. vittatus mosquitoes in southeastern Mexico highlights the potential emergence of a new arbovirus vector in the Americas. The Yucatán Peninsula is undergoing profound anthropogenic change, where deforestation, agricultural expansion, and large-scale infrastructure projects like the Tren Maya (10) are rapidly reshaping landscapes. Beyond their economic and social goals, such megaprojects can intensify ecosystem degradation, reduce ecologic barriers, and enhance human connectivity, thereby creating ideal conditions for the establishment and spread of invasive mosquitoes. Those dynamics underscore the need to integrate health considerations into land-use planning, recognizing that environmental transformation can amplify the risk for vectorborne diseases.

In conclusion, detection of Ae. vittatus mosquitoes in continental North America, specifically in Mexico’s Yucatán Peninsula, highlights the species’ ecologic plasticity and the urgent need to investigate introduction pathways and its potential role in arboviral transmission. Including the Ae. vittatus mosquito in regional surveillance and control programs will be essential to anticipate its spread and mitigate future public health impacts.

This article was preprinted at https://www.biorxiv.org/content/10.1101/2025.10.29.684036v1.

Dr. Chan-Chablé is a postdoctoral researcher at the Center for Research and Advanced Studies, Mérida Unit, Mexico. His research focuses on the natural history, taxonomy, and ecology of mosquitoes (Diptera: Culicidae) and other arthropods of public health importance in the Yucatán Peninsula.

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Acknowledgment

We thank Fernando Chan-Poot for assistance with fieldwork and Humberto Bahena-Basave for photographing Aedes (Fredwardsius) vittatus mosquitoes. We also thank Marysol Trujano Ortega and Noemí Salas Suárez for their support with entomologic laboratory materials at the ECOSUR Zoology Museum.

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References

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Figures
Table

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Suggested citation for this article: Chan-Chable RJ, Rodríguez-Luna CR, Espinal-Palomino R, Ibarra-Cerdeña CN. Detection of Aedes (Fredwardsius) vittatus mosquitoes, Yucatán Peninsula, Mexico, 2025. Emerg Infect Dis. 2025 Nov [date cited]. https://doi.org/10.3201/eid3111.251358

DOI: 10.3201/eid3111.251358

Original Publication Date: November 18, 2025

Table of Contents – Volume 31, Number 11—November 2025

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Please use the form below to submit correspondence to the authors or contact them at the following address:

Carlos N. Ibarra-Cerdeña, Human Ecology Department, Center for Research and Advanced Studies (Cinvestav), Carretera Mérida-Progreso, Loma Bonita, 97205 Mérida, Yucatán, Mexico

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Page created: November 17, 2025
Page updated: November 18, 2025
Page reviewed: November 18, 2025
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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