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Citation: Ascencio EJ, Carcamo PM, Carrasco-Escobar G (2025) Rapid geographic expansion of local dengue community transmission in Peru. PLoS Negl Trop Dis 19(4): e0013001. https://doi.org/10.1371/journal.pntd.0013001
Editor: William B. Messer, Oregon Health and Science University, UNITED STATES OF AMERICA
Published: April 17, 2025
Copyright: © 2025 Ascencio et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: GCE is funded by the Wellcome Trust (https://wellcome.org/) under the HARMONIZE project. The project award reference is 224694/C/21/Z. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Dengue is currently the most significant vector-borne disease in Peru, with its incidence increasing markedly over the past few years. In particular, 2023 saw a substantial rise, with 251,605 confirmed cases reported, making it the highest incidence recorded in the country’s history [1]. Although cases were reported in Peru during the 1950s, the epidemic in 1990 was the first laboratory confirmation of dengue indigenous transmission in Peru [2]. Confirmed cases in 2023 were approximately 9-fold the average number during the previous 5 years (29,841 confirmed cases) and 4.2-fold the number during 2017 (59,303 confirmed cases), the year of the largest previous national dengue outbreak [3]. We hypothesized that, in Peru, the apparent confluence of urbanization, climate change, and increased human migration has led to the worst dengue epidemic in the country’s history, peaking in recent years. In this comment, we aimed to describe the rapid geographic expansion of local community transmission of dengue in distinct natural regions of Peru over the past two decades, particularly toward districts that have historically been free of dengue transmission.
We used the reported probable and confirmed dengue cases from 2000 to 2023 (Peruvian Ministry of Health) to estimate the daily effective reproductive number (Rt) in each district, using intrinsic incubation period and generation interval distributions from the literature [4–6]. Districts with less than 12 cumulative cases in the study period were excluded from the analysis, and we discarded Rt estimates obtained before 12 cumulative cases were reported [7]. We computed 95% confidence intervals (95% CI) for each Rt using an overlapping block bootstrap method and identified periods of local community transmission if the lower bound of the 95% CI was Rt > 1 for two subsequent weeks or more. We used the estimateR package (R software) to develop the analysis.
The result is concerning. In the last 5 years, a total of 119 districts have detected local community dengue transmission for the first time (Fig 1A). Between 2000 and 2020, the rate of increase in new districts was relatively stable, with a mean of 6.8 new districts per year, and most new districts located in the Amazon rainforest region. However, in 2023 alone, there were 60 new districts with dengue transmission. Compared to previous periods, the most significant difference is observed along the coastal region, where the number of new districts with dengue jumped from an average of 5.6 per year to 48 in 2023 (Fig 1B). Overall, three primary geographic areas of dengue expansion are clearly defined in Peru: the Amazon rainforest, the northern coast, and now the central and southern coast. Finally, the mean daily Rt was 1.4 (standard deviation [SD] = 2.5), while the daily mean of the 95% CI lower and upper bound were 0.08 (SD = 0.6) and 10.6 (SD = 9.5), respectively.
It has been described that dengue transmission optimal conditions in the Amazon rainforest and northern coast were 21–29 °C and >70% humidity [8]. However, rapid urbanization and the rise in frequency and magnitude of meteorological anomalies such as El Niño-Southern Oscillation (ENSO) influence the report of new dengue community transmission geographic areas [9,10]. Peru has extensive experience in the surveillance and controlling of dengue and other vector-borne diseases such as malaria in the Amazon rainforest region. However, this accumulated experience is not uniformly distributed across the country, and areas without previous exposure to dengue are struggling with the sudden surge in cases. In addition, the expansion of the dengue transmission area along the central and southern coast is worrisome due to the increasing susceptible population, especially in Lima, the most populated and urban city in the country (29.2% of the Peruvian population). Highlands have not been affected yet due to altitude and low temperatures; however, climate change could alter these fragile environmental conditions [11]. In addition, it is important to notice some limitations of data. This data was collected as part of passive case detection (i.e., not all cases of dengue are presented to a health facility). Therefore, case notification depends on the completion of the epidemiological form and samples taken by healthcare personnel; however, in resource-limited settings, this scenario is not feasible in 100% of patients.
Our findings are useful to underscore that, for example, ENSO during 2023 could influence dengue rapid expansion to new geographic areas. The observed phenomenon may be attributed to the dissemination of the dengue virus in previously non-endemic regions where the vector was already established. For instance, in Lima, the capital of Peru—historically considered non-endemic for dengue—the presence of the vector was documented in certain districts several years ago, with reports of vector reemergence dating back to the year 2000 [12]. Within this context, the ENSO may facilitate the rapid expansion of dengue, particularly in densely populated urban areas. Therefore, we advocate for the development of new tools to monitor the dissemination of arboviruses, including the large-scale implementation of trap-based mosquito surveillance, sentinel surveillance of syndromic cases, forecasting models and early warning systems, and effective risk communication, including international cooperation. Such efforts are crucial to increasing the precision of preventive and control actions, ultimately saving lives.
References
- 1. Pan American Health Organization. Situation report N.1: dengue epidemiological situation in the Americas—14 December 2023. 2023 [cited 6 Jul 2024. ]. Available from: https://www.paho.org/en/documents/situation-report-n1-dengue-epidemiological-situation-americas-14-december-2023
- 2. U.S. Centers for Disease Control and Prevention. International Notes Dengue Epidemic—Peru, 1990. 1991 [cited 1 Aug 2024. ]. Available from: https://www.cdc.gov/mmwr/preview/mmwrhtml/00001924.htm
- 3. Munayco CV, Valderrama Rosales BY, Mateo Lizarbe SY, Yon Fabian CR, Peña Sánchez R, Vásquez Sánchez CH, et al. Notes from the field: dengue outbreak—Peru, 2023. MMWR Morb Mortal Wkly Rep. 2024;73(4):86–8. pmid:38300858
- 4. Scire J, Huisman JS, Grosu A, Angst DC, Lison A, Li J, et al. estimateR: an R package to estimate and monitor the effective reproductive number. BMC Bioinformatics. 2023;24(1):310. pmid:37568078
- 5. Chan M, Johansson MA. The incubation periods of Dengue viruses. PLoS One. 2012;7(11):e50972. pmid:23226436
- 6. Siraj AS, Oidtman RJ, Huber JH, Kraemer MUG, Brady OJ, Johansson MA, et al. Temperature modulates dengue virus epidemic growth rates through its effects on reproduction numbers and generation intervals. PLoS Negl Trop Dis. 2017;11(7):e0005797. pmid:28723920
- 7. Cori A, Ferguson NM, Fraser C, Cauchemez S. A new framework and software to estimate time-varying reproduction numbers during epidemics. Am J Epidemiol. 2013;178(9):1505–12. pmid:24043437
- 8. Campbell KM, Haldeman K, Lehnig C, Munayco CV, Halsey ES, Laguna-Torres VA, et al. Weather regulates location, timing, and intensity of dengue virus transmission between humans and mosquitoes. PLoS Negl Trop Dis. 2015;9(7):e0003957. pmid:26222979
- 9. Kolimenakis A, Heinz S, Wilson ML, Winkler V, Yakob L, Michaelakis A, et al. The role of urbanisation in the spread of Aedes mosquitoes and the diseases they transmit—a systematic review. PLoS Negl Trop Dis. 2021;15(9):e0009631. pmid:34499653
- 10. Dostal T, Meisner J, Munayco C, García PJ, Cárcamo C, Pérez Lu JE, et al. The effect of weather and climate on dengue outbreak risk in Peru, 2000-2018: a time-series analysis. PLoS Negl Trop Dis. 2022;16(6):e0010479. pmid:35771874
- 11. Kamal M, Kenawy MA, Rady MH, Khaled AS, Samy AM. Mapping the global potential distributions of two arboviral vectors Aedes aegypti and Ae. albopictus under changing climate. PLoS One. 2018;13(12):e0210122. pmid:30596764
- 12. Andrade CS, Cáceres AG, Vaquerizo A, Ibañez-Bernal S, Cachay LS. Reappearance of Aedes aegypti (Diptera: Culicidae) in Lima, Peru. Mem Inst Oswaldo Cruz. 2001;96(5):657–8. pmid:11500764