Vertical transmission in Aedes aegypti and Aedes albopictus is considered a maintenance mechanism for dengue virus (DENV) during unfavorable conditions and may be implicated in dengue outbreaks. Since DENV infection dynamics vary among wild-type viruses and vector populations, vertical transmission rates can also vary between regions. However, even though São Paulo is the most populous city in the Americas and has experienced major dengue epidemics, natural vertical transmission had never been detected in this area before. Here we confirm and describe for the first time natural vertical transmission of DENV-3 in two pools of male Ae. albopictus from the city of São Paulo. The detection of DENV-3 in years when no human autochthonous cases of this serotype were recorded suggests that silent circulation of DENV-3 is occurring and indicates that green areas may be maintaining serotypes that are not circulating in the human population, possibly by a vertical transmission mechanism.
Dengue is considered the most serious re-emergent viral disease transmitted by arthropods, with approximately 390 million infections worldwide each year, 7% of which occur in Brazil1,2. The etiological agent of the disease is an arbovirus of the genus Flavivirus and family Flaviviridae with four antigenically distinct serotypes (DENV-1, DENV-2, DENV-3 and DENV-4)1,3,4 which is mainly transmitted by the mosquito Aedes aegypti5 although Aedes albopictus plays an important role in transmission of this virus in numerous countries around the world, especially in Southeast Asia5,6.
In the Americas, the dengue cycle is essentially urban, having as fundamental elements of its transmission dynamics the etiological agent (DENV), the anthropophilic diurnal mosquito Ae. aegypti and the vertebrate host5 (humans). Aedes albopictus is considered an exophilic mosquito with eclectic feeding behavior7,8, but some degree of anthropophily has recently been shown for this species9. Because of its vector competence under laboratory conditions, Ae. albopictus is considered a potential vector of DENV5,10. The species has already been found naturally infected with DENV in a pineapple plantation in Costa Rica11, but this evidence is not sufficient for it to be considered an actual vector.
The most common way mosquito females become infected with an arbovirus is by blood feeding on a viremic host, which is known as horizontal transmission12. Another route of infection is transmission from the parents to part of the offspring, which is known as vertical transmission13,14. While in endemic areas the ability of DENV to persist in the environment during periods that are unfavorable for horizontal transmission or when there is a low mosquito density is not clearly understood, there are indications that vertical transmission is an important maintenance mechanism for DENV circulation during these periods15. Indeed, vertical transmission of this virus was observed in seven and three consecutive generations of Ae. aegypti and Ae. albopictus, respectively, under laboratory conditions16,17, confirming the importance of this phenomenon.
A recent review15 showed that Asia and South America are the main continents where vertical transmission of DENV in Ae. aegypti and Ae. albopictus under natural conditions has been reported. While Brazil is the leading country in the Americas on studies of natural vertical transmission of DENV, few studies have investigated this phenomenon in the state of São Paulo18,19.
The state of São Paulo is the most populous in Brazil, with approximately 45 million inhabitants, representing about 21.5% of the entire Brazilian population (209 million inhabitants)20,21. Despite the fact that São Paulo, the capital of the state, is the most populous city in Brazil and Latin America22 and in recent years has experienced major dengue epidemics, such as those in 2014 and 201523, natural vertical transmission has never been detected in the city15.
The green areas in municipal parks in the city of São Paulo are remnants of Atlantic Forest vegetation. These parks are used for recreation and provide habitats for several species of mosquitoes of medical importance, such as those of the Culex, Aedes and Anopheles genera24. Previous studies performed in Piqueri Municipal Park, for example, reported a great abundance of Ae. albopictus24,25, followed by Culex quinquefasciatus, Aedes fluviatilis, Aedes scapularis, Culex nigripalpus and Ae. aegypti25, corroborating the findings of studies that showed that Ae. albopictus is usually present in areas with vegetation cover7,26. Despite the body of knowledge on mosquito fauna in green areas in São Paulo, little is known about the pathogens circulating in these locations. Investigation into the occurrence of natural vertical transmission of DENV in Ae. aegypti and Ae. albopictus populations is therefore of critical importance for an understanding of the transmission dynamics of this virus and can provide a new outlook on the maintenance of this pathogen in urban green areas and its possible implications for public health.
This study therefore sought to investigate the occurrence of natural vertical transmission of DENV in Ae. aegypti and Ae. albopictus mosquito populations in the city of São Paulo.
To detect natural vertical transmission of DENV in Ae. aegypti and Ae. albopictus during two seasons (spring and autumn), a total of 5,730 mosquito specimens were analyzed. Of these, 3,270 were Ae. albopictus (1,790 males and 1,480 females) and 2,460 Ae. aegypti (940 males and 1,520 females) (Table 1). Of the 5,730 specimens, 1,570 were collected in spring 2014, 2,090 in autumn 2015, 1,440 in spring 2015 and 630 in autumn 2016 (Fig. 1.)
Detection of positive pools
Of all the 573 pools tested, two of male Ae. albopictus were positive for DENV-3, showing a 290 bp band on agarose gel. One of the pools of male Ae. albopictus was collected in spring 2014 and the other in autumn 2015 (Fig. 2; Supplementary Figs. S1 and S2).
The two positive samples were sequenced, edited, aligned with each other and compared with GenBank sequences using BLAST. They had high degree of identity with DENV-3 serotype sequences from GenBank, as shown in the Neighbor Joining tree (Fig. 3), and only three differences in nucleotide sequence were found between the two samples. Both showed high identity with strains found in the city of Guarujá, SP, Brazil, and Belo Horizonte, MG, Brazil. The positive control sample, which was also sequenced and aligned with GenBank sequences, showed high identity with strains of completely different origin. The DENV-3 sequences found in this study and the positive control sequence were deposited in GenBank, respectively, under accession numbers (MN025404/MN025405/MN025406), as well as the data of the sequences used for construction of the Neighbor Joining tree are described in Supplementary Table S1.
Minimum infection rate (MIR)
We compared the overall Minimum Infection Rate (MIR = 0.35), which was calculated based on all the seasons and specimens studied, with the MIR for Ae. albopictus only (MIR = 0.61) and the MIR for Ae. albopictus only from each season that had positive pools (MIR spring 2014 = 1.47; MIR autumn 2015 = 0.44). The MIR for spring 2014 was higher than for autumn 2015.
Since the first reports of vertical transmission under natural conditions, the role of this phenomenon in the persistence and maintenance of arboviruses in nature has been the subject of much discussion27,28. The first report of natural vertical transmission of DENV in the Americas was described in specimens from Trinidad and Tobago29 and was subsequently reported in South American countries, including Bolivia30, Argentina31 and Peru32. In Brazil, the first report of natural vertical transmission was of DENV-1 in Ae. albopictus from the state of Minas Gerais33. Subsequently, other occurrences in this species involving other dengue serotypes were also reported in Brazil18,34,35,36. Natural vertical transmission of DENV in Ae. aegypti has been demonstrated in the states of Minas Gerais35,37,38,39, Pernambuco40, Ceará36, Mato Grosso40,41,42 Rio de Janeiro43 and Amazonas44.
Here, we report natural vertical transmission of DENV in Ae. albopictus for the first time in the city of São Paulo. Specifically, DENV-3 was detected in two pools of male Ae. albopictus. To date, only three studies have demonstrated natural vertical transmission of DENV-3 in Brazilian populations of Ae. albopictus, one in the state of Minas Gerais35, another in the state of Ceará36 and another in Santos (a coastal city in the state of São Paulo)18. Despite both DENV-3 positive samples of males of Ae. albopictus showed differences in nucleotide sequences, they exhibited high identity with strains found in the city of Guarujá, SP, Brazil, and Belo Horizonte, MG, Brazil, whereas the sequence of the positive control showed similarity with strains of the city of Ribeirão Preto, SP. The differences found between the three sequences indicate that the positive samples were not products of laboratory contamination.
Under laboratory conditions, females of Ae. albopictus were able to transmit all four DENV serotypes vertically to the offspring. The transmission rates varied according to the virus serotype and strain, and the lowest rate found was for DENV-345. Although the maintenance of DENV-1 was observed in three consecutive generations of Ae. albopictus by vertical transmission17, there is no data about the DENV-3 maintenance over successive generations in this species under laboratory conditions. However, the persistence of DENV-3 was demonstrated in Ae. aegypti during seven successive generations16.
Vertical transmission was also observed in Ae. aegypti although at a low rate, even for strains known to be more susceptible to oral infection45. Similar results were found for a Brazilian DENV strain and populations of Ae. aegypti and Ae. albopictus46, indicating that despite the importance of Ae. aegypti for horizontal transmission this species may be less relevant in the maintenance of DENV during periods of low vector density45,47. Our results corroborate these findings as we found positive Ae. albopictus pools but no positive Ae. aegypti pools. Other hypothesis for the absence of positive pools of Ae. aegypti in our study is related to the smaller number of specimens analyzed compared to Ae. albopictus. In addition, green areas favor the presence and abundance of Ae. albopictus when compared to Ae. aegypti24,25,48 which maintains DENV circulation in areas with high concentrations of human beings and houses49,50. This may have increased the chances of finding viral circulation in Ae. albopictus and not in Ae. aegypti. The presence of DENV-3 in Ae. albopictus from Piqueri Municipal Park suggests that this mosquito may be acting in the transmission dynamics of DENV, thereby maintaining circulation of the arbovirus in this environment.
In a study conducted with the DENV-2 serotype and strains of Ae. aegypti mosquitoes with high and low susceptibility to infection, Mourya et al.51 argue that vertical transmission is more frequent in eggs allowed to hatch after longer periods, probably because of an increase in viral copy numbers in the eggs. It seems, therefore, that unfavorable environmental conditions, such as low availability of water, and the consequent increase in the time required for the eggs to hatch, favor vertical transmission. This may explain our findings of DENV-3 in Ae. albopictus during spring 2014 and autumn 2015, when there was lower rainfall (spring 2014: 5.1 mm; autumn 2015: 3.3 mm) than in the other periods (spring 2015: 26.5 mm; autumn 2016: 15.0 mm)48. Another possible explanation for our findings is that during these two periods more specimens were tested.
Interestingly, no autochthonous human cases of DENV-3 have been reported in the city of São Paulo since 201023 (Supplementary Fig. S3). In fact, DENV-3 circulation was detected in the city of São Paulo in 201052, but this serotype was not identified in this area during the epidemic of 201453. This strengthens the hypothesis that vertical transmission could help maintain viral circulation during interepidemic periods and suggests that there is silent circulation of DENV-3 in green areas of São Paulo, a city with no detected autochthonous cases of infection by this serotype.
It is important to highlight that for natural vertical transmission to be detected under the conditions established in this study, an infected female had to have laid eggs in the ovitrap and successfully transmitted the virus vertically and the larvae had to have survived until adulthood to finally be analyzed. When mosquito infection rates are low, more specimens are required for a higher chance of virus detection. For example, for an infection rate of 1, a minimum of 1,609 and 2,301 mosquitoes are needed for an 80% and 90% chance of virus detection, respectively54. Although in our study we analyzed 2,460 Ae. aegypti adults and 3,270 Ae. albopictus adults that were raised in the laboratory from eggs collected in the park, if we consider that both species lay their eggs in more than one container in the same gonotrophic cycle55,56, it is possible that most of the mosquitoes analyzed originated from the same mother. Nevertheless, considering the difficulty in detecting this phenomenon in natural environments, the successful detection of natural vertical transmission of a serotype with no recent autochthonous cases in São Paulo23 in Ae. albopictus males in two different seasons indicates that the virus is circulating at significant rates in this vector population and being transmitted vertically.
The MIR values found in the present study are similar to those previously described in the literature, which are mainly low and vary considerably according to the mosquito population57. In addition, the fact that the MIR typically exhibits considerable temporal variability in vector populations58 explains the different results for the various seasons analyzed in this study.
As urban parks are open to the public, infected visitors can contribute to the expansion of several arboviruses. Furthermore, the continuous contact between humans, competent vectors and viruses make these parks high-risk areas for infection by DENV and other arboviruses, raising the question of the relevance of urban green areas in the transmission and maintenance dynamics of arboviruses59,60,61. Bearing in mind the biological characteristics of Ae. albopictus, such as its vector competence for dengue, yellow fever, Zika and chikungunya viruses in laboratory conditions46,62,63,64, our findings reinforce the importance of surveillance and control of this species as it may be playing a role in maintaining circulation of DENV, favoring infection of those who live close to parks or visitors to these parks and expanding the distribution of the virus to other areas.
To investigate the occurrence of vertical transmission of DENV in female and male Ae. aegypti and Ae. albopictus mosquitoes, adults were raised under laboratory conditions from eggs collected in urban green areas of Piqueri Municipal Park (23°31′39.98″S and 46°34′24.88″W), in Tatuapé district, in the east of the city of São Paulo, Brazil (Fig. 4). This park was selected as the study area because it is in the region of São Paulo that had one of the highest numbers of autochthonous human cases of dengue during the last major epidemic of the disease, in 2014/201523. The park, which extends over approximately 100,000 m² and has dense vegetation, harbors approximately 90 species of animals63 and receives an estimated 36,000 visitors a month63,64.
Field collections were undertaken during six consecutive weeks in spring 2014 and spring 2015 and six consecutive weeks in autumn 2015 and autumn 2016. These seasons were chosen because of the moderate temperatures, which favor each species equally48.
Thirty-six ovitraps distributed around Piqueri Municipal Park were used to collect Ae. aegypti and Ae. albopictus eggs. All the paddles were collected and replaced weekly and taken to the Public Health Entomology Laboratory at the School of Public Health, University of São Paulo (FSP/USP).
The paddles were allowed to dry at room temperature for 3–4 days, assessed for the presence of eggs under a stereoscope and placed individually in plastic trays containing 500 mL of water and ground fish food (Tretramin®) for larval hatching. All larvae in the L4 stage were identified and separated by species (Ae. aegypti or Ae. albopictus). Pupae were placed individually in small glass containers, and after the adults emerged they were killed by freezing and separated by species, season and sex into pools of 10 individuals, which were placed in 1.5 mL polypropylene microtubes. All 573 pools were kept at −80 °C until used to isolate DENV.
Isolation of viral genetic material
To detect the presence of DENV, each pool was initially macerated in 1 mL of Leibovitz’s L-15 medium and centrifuged for 15 minutes at 6000 rpm. A volume of 140 μL of the supernatant from each pool and the commercial QIAamp® Viral RNA Mini Kit (250) (QIAGEN, Hilden, Germany) were used for RNA extraction according to the manufacturer’s instructions. To avoid non-specific amplification, we treated the viral RNA with amplification-grade DNase I (Invitrogen, California, USA) following the manufacturer’s protocol.
RT-PCR was performed according to Lanciotti et al.65 with a second round of PCR amplification (semi-nested PCR) that allows simultaneous detection of the four DENV serotypes by generating DNA products of unique sizes, which can be used to differentiate the four serotypes (Table 2).
The target sequence of the viral RNA was initially converted to cDNA by reverse transcriptase (RT) and then amplified using the consensus primers D1 and D2 and SuperScript® III One-Step RT-PCR with Platinum® Taq polymerase (Invitrogen, California, USA) according to the manufacturer’s protocol: 30 minutes at 50 °C and 2 minutes at 94 °C, followed by 35 cycles of denaturation (94 °C, 15 s), annealing (60 °C, 30 s) and extension (72 °C, 30 s). Semi-nested PCR was then performed using GoTaq Green Master Mix 2 ×(Promega, USA) and the following cycling conditions: 25 cycles of denaturation (95 °C, 30 s), annealing (60 °C, 30 s) and extension (72 °C, 1 min). RNA from the four DENV serotypes and ultrapure water were used as positive and negative controls, respectively. Bands were visualized under UV light on a 2% agarose gel stained with 5 μL of Gel-Red (Biotium). For double confirmation, all samples showing positive bands were reanalyzed from the extracted RNA using only the oligonucleotides specific to the serotype detected.
The resulting PCR products were purified with Exosap-IT (GE) following the manufacturer’s instructions. The purified DNA was then sequenced by the Sanger method using the Big Dye Terminator Sequencing Kit (ABI) and DENV serotype specific primers (Table 2) in the ABI 3100 Automated DNA Sequencer (ABI). The double-stranded DNA fragments were sequenced in both directions to generate a consensus double-stranded sequence for each sample. Editing, analysis and alignment of the nucleotides were conducted using version 6.0.7 of Bioedit Sequence Alignment Editor. All nucleotide sequences were aligned using ClustalW66, and sequence polymorphisms within the amplified region were identified by comparing our sequences with a variety of sequences of the four dengue virus serotypes available from GenBank (Supplementary Table S1). A similarity tree was built (Fig. 3) with Neighbor Joining algorithm, based on a Kimura 2-parameter model, nucleotide distances, determined by MEGA software (Molecular Evolutionary Genetics Analysis, version 6.0), with 1,000 replications in the bootstrap test67.
The proportion of infected specimens is commonly estimated from the MIR (number of infected pools/total number of specimens x 1000 mosquitoes tested) based on the assumption of only one infected mosquito per positive pool13,68. This ratio is reasonable for estimates based on low-occurrence data and small pools, as observed in this study of natural vertical transmission13,68.
For the purposes of comparison, we calculated a general MIR for both species considering all the seasons studied (number of infected pools/total number of specimens for all the seasons analyzed x 1000), a MIR for Ae. albopictus only (number of infected pools of Ae. albopictus/total number of specimens analyzed for all seasons x 1000) and a MIR for Ae. albopictus for each season with positive pools (number of infected pools of Ae. albopictus/total number of specimens analyzed for each season with positive pools x 1,000).
All data generated or analyzed during this study are included in the manuscript.
Tauil, P. L. Aspectos críticos do controle do dengue no Brasil. Cad. Saude Publica 18, 867–871 (2002).
Bhatt, S. et al. The global distribution and burden of dengue. Nature 496, 504–507 (2013).
Bennett, S. N. Taxonomy and evolutionary relationships of flaviviruses. in Dengue and dengue hemorrhagic fever (eds. Gubler, D. J. & Kuno, G.) 322–333 (CABI https://doi.org/10.1079/9781845939649.0322 (1997).
Gubler, D. J. Dengue and dengue hemorrhagic fever. Clin. Microbiol. Rev. 11, 480–96 (1998).
Chouin-Carneiro, T. & dos Santos, F. B. Transmission of Major Arboviruses in Brazil: The Role of Aedes aegypti and Aedes albopictus Vectors. in Biological Control of Pest and Vector Insects vol. 2 Ch. 11 (InTech (2017).
Lima-Camara, T. N. Emerging arboviruses and public health challenges in Brazil. Rev. Saude Publica 50, 1–7 (2016).
Lima-Camara, T. N., Honório, N. A. & Lourenço-de-Oliveira, R. Freqüência e distribuição espacial de Aedes aegypti e Aedes albopictus (Diptera, Culicidae) no Rio de Janeiro, Brasil. Cad. Saude Publica 22, 2079–2084 (2006).
Consoli, R. A. G. B. & Lourenço-De-Oliveira, R. Principais mosquitos de importância sanitária no Brasil. (Fiocruz (1994).
Stenn, T., Peck, K. J., Rocha Pereira, G. & Burkett-Cadena, N. D. Vertebrate Hosts of Aedes aegypti, Aedes albopictus, and Culex quinquefasciatus (Diptera: Culicidae) as Potential Vectors of Zika Virus in Florida. J. Med. Entomol. 56, 10–17 (2019).
Degallier, N. et al. Aedes albopictus may not be vector of dengue virus in human epidemics in Brazil. Rev. Saude Publica 37, 386–387 (2003).
Calderón-Arguedas, O., Troyo, A., Moreira-Soto, R. D., Marín, R. & Taylor, L. Dengue viruses in Aedes albopictus Skuse from a pineapple plantation in Costa Rica. J. Vector Ecol. 40, 184–186 (2015).
Teixeira, M. G., Barreto, M. L. & Guerra, Z. Epidemiologia e medidas de prevenção do dengue. Inf Epidemiol Sus 8, 5–33 (1999).
Clements, A. N. Arboviruses - characteristics and concepts. in The biology of mosquitoes: Transmission of viruses and interactions with bacteria (ed. Clements, A. N.) 90–173 (CABI). https://doi.org/10.1079/9781845932428.0090 (2012).
Rosen, L. Mechanism of vertical transmission of the dengue virus in mosquitoes. C. R. Acad. Sci. III. 304, 347–50 (1987).
Ferreira-de-Lima, V. H. & Lima-Camara, T. N. Natural vertical transmission of dengue virus in Aedes aegypti and Aedes albopictus: a systematic review. Parasit. Vectors 11, 77 (2018).
Joshi, V., Mourya, D. T. & Sharma, R. C. Persistence of dengue-3 virus through transovarial transmission passage in successive generations of Aedes aegypti mosquitoes. Am. J. Trop. Med. Hyg. 67, 158–161 (2002).
Shroyer, D. A. Vertical maintenance of dengue-1 virus in sequential generations of Aedes albopictus. J. Am. Mosq. Control Assoc. 6, 312–4 (1990).
de Figueiredo, M. L. et al. Mosquitoes infected with dengue viruses in Brazil. Virol. J. 7, 152 (2010).
Moraes, A. et al. Transovarial transmission of dengue 1 virus in Aedes aegypti larvae: real-time PCR analysis in a Brazilian city with high mosquito population density. Can. J. Microbiol. 64, 393–400 (2018).
Instituto Brasileiro de Geografia e Estatística. Brasil em Síntese: São Paulo. https://cidades.ibge.gov.br/brasil/sp/panorama (2017).
Instituto Brasileiro de Geografia e Estatística. Projeção da população. https://www.ibge.gov.br/apps/populacao/projecao/ (2018).
Demographia World Urban Areas (Built-Up Urban Areas or Urban Agglomerations). Demographia 1–120 http://demographia.com/db-worldua.pdf (2018).
Sistema Único de Saúde/Coordenação de Vigilância em Saúde/Prefeitura de São Paulo. Plano de Contingência Municipal da Dengue: Município de São Paulo - 2015/2016. https://www.prefeitura.sp.gov.br/cidade/secretarias/upload/chamadas/plano_contigencia_final_1462895236.pdf (2016).
Medeiros-Sousa, A. R. et al. Mosquito Fauna in Municipal Parks of São Paulo City, Brazil: A Preliminary Survey. J. Am. Mosq. Control Assoc. 29, 275–279 (2013).
Wilke, A. B. B., Medeiros-Sousa, A. R., Ceretti-Junior, W. & Marrelli, M. T. Mosquito populations dynamics associated with climate variations. Acta Trop. 166, 343–350 (2017).
Braks, M. A. H., Honório, N. A., Lourenço-De-Oliveira, R., Juliano, S. A. & Lounibos, L. P. Convergent Habitat Segregation of Aedes aegypti and Aedes albopictus (Diptera: Culicidae) in Southeastern Brazil and Florida. J. Med. Entomol. 40, 785–794 (2003).
Khin, M. M. & Than, K. A. Transovarial Transmission of Dengue 2 Virus by Aedes aegypti in Nature. Am. J. Trop. Med. Hyg. 32, 590–594 (1983).
Watts, D. M., Harrison, B. A., Pantuwatana, S., Klein, T. A. & Burke, D. S. Failure to Detect Natural Transovarial Transmission of Dengue Viruses by Aedes aegypti and Aedes albopictus (Diptera: Culicidae). J. Med. Entomol. 22, 261–265 (1985).
Hull, B., Tikasingh, E., de Souza, M. & Martinez, R. Natural Transovarial Transmission of Dengue 4 Virus in Aedes aegypti in Trinidad. Am. J. Trop. Med. Hyg. 33, 1248–1250 (1984).
Le Goff, G. et al. Natural vertical transmission of dengue viruses by Aedes aegypti in Bolivia. Parasite 18, 277–280 (2011).
Espinosa, M., Giamperetti, S., Abril, M. & Seijo, A. Vertical transmission of dengue virus in Aedes aegypti collected in Puerto Iguazú, Misiones, Argentina. Rev. Inst. Med. Trop. Sao Paulo 56, 165–167 (2014).
Cabezas, C. et al. Transmisión vertical del virus del dengue en el Aedes aegypti, Perú. Rev. Peru. Med. Exp. Salud Publica 32, 191 (2015).
Serufo, J. C. et al. Isolation of dengue virus type 1 from larvae of Aedes albopictus in Campos Altos city, State of Minas Gerais, Brazil. Mem. Inst. Oswaldo Cruz 88, 503–504 (1993).
Cecílio, A. B., Campanelli, E. S., Souza, K. P. R., Figueiredo, L. B. & Resende, M. C. Natural vertical transmission by Stegomyia albopicta as dengue vector in Brazil. Braz. J. Biol. 69, 123–7 (2009).
Pessanha, J. E. M. et al. Cocirculation of two dengue virus serotypes in individual and pooled samples of Aedes aegypti and Aedes albopictus larvae. Rev. Soc. Bras. Med. Trop. 44, 103–105 (2011).
Martins, V. E. P. et al. Occurrence of Natural Vertical Transmission of Dengue-2 and Dengue-3 Viruses in Aedes aegypti and Aedes albopictus in Fortaleza, Ceará, Brazil. Plos One 7, e41386 (2012).
Cecílio, A. B. et al. Transovarial transmission of dengue vírus 1 and 2 as showed by detection in Aedes aegypti larvae. Soc Path 9, 57–60 (2004).
Vilela, A. P. P. et al. Dengue Virus 3 Genotype I in Aedes aegypti Mosquitoes and Eggs, Brazil, 2005–2006. Emerg. Infect. Dis. 16, 989–992 (2010).
Cecílio, S. G. et al. Dengue virus detection in Aedes aegypti larvae from southeastern Brazil. J. Vector Ecol. 40, 71–74 (2015).
Cruz, L. C. & de, T. A. da et al. Natural transovarial transmission of dengue virus 4 in Aedes aegypti from Cuiabá, State of Mato Grosso, Brazil. Rev. Soc. Bras. Med. Trop. 48, 18–25 (2015).
Serra, O. P., Cardoso, B. F., Ribeiro, A. L. M., Santos, F. A. L. Dos & Slhessarenko, R. D. Mayaro virus and dengue virus 1 and 4 natural infection in culicids from Cuiabá, state of Mato Grosso, Brazil. Mem. Inst. Oswaldo Cruz 111, 20–29 (2016).
Maia, L. M. S. et al. Natural vertical infection by dengue virus serotype 4, Zika virus and Mayaro virus in Aedes (Stegomyia) aegypti and Aedes (Stegomyia) albopictus. Med. Vet. Entomol. https://doi.org/10.1111/mve.12369 (2019).
dos Santos, T. P. et al. Dengue serotype circulation in natural populations of Aedes aegypti. Acta Trop. 176, 140–143 (2017).
da Costa, C. F. et al. Transovarial transmission of DENV in Aedes aegypti in the Amazon basin: a local model of xenomonitoring. Parasit. Vectors 10, 249 (2017).
Rosen, L., Shroyer, D. A., Lien, J. C., Freier, J. E. & Tesh, R. B. Transovarial Transmission of Dengue Viruses by Mosquitoes: Aedes albopictus and Aedes aegypti. Am. J. Trop. Med. Hyg. 32, 1108–1119 (1983).
Castro, M. G., de, Nogueira, R. M. R., Schatzmayr, H. G., Miagostovich, M. P. & Lourenço-de-Oliveira, R. Dengue virus detection by using reverse transcription-polymerase chain reaction in saliva and progeny of experimentally infected Aedes albopictus from Brazil. Mem. Inst. Oswaldo Cruz 99, 809–14 (2004).
Buckner, E. A., Alto, B. W. & Lounibos, L. P. Vertical transmission of Key West dengue-1 virus by Aedes aegypti and Aedes albopictus (Diptera: Culicidae) mosquitoes from Florida. J. Med. Entomol. 50, 1291–7 (2013).
Heinisch, M. R. S. et al. Seasonal and spatial distribution of Aedes aegypti and Aedes albopictus in a municipal urban park in São Paulo, SP, Brazil. Acta Trop. 189, 104–113 (2019).
Ayllón, T. et al. Dispersion and oviposition of Aedes albopictus in a Brazilian slum: Initial evidence of Asian tiger mosquito domiciliation in urban environments. Plos One 13, e0195014 (2018).
Natal, D. B. do Aedes aegypti. Biológico 64, 205–207 (2002).
Mourya, D. T. et al. Horizontal and vertical transmission of dengue virus type 2 in highly and lowly susceptible strains of Aedes aegypti mosquitoes. Acta Virol. 45, 67–71 (2001).
Paulo, SdeEdaSdeS., Endemias, SdeCde & Lutz, I. A. Dengue no Estado de São Paulo. Bol. epidemiol. paul. 9, 22–40 (2012).
Fares, R. C. G., Souza, K. P. R., Añez, G. & Rios, M. Epidemiological Scenario of Dengue in Brazil. Biomed Res. Int. 2015, 1–13 (2015).
Gu, W. & Novak, R. J. Short report: detection probability of arbovirus infection in mosquito populations. Am. J. Trop. Med. Hyg. 71, 636–8 (2004).
Apostol, B. L., Black, W. C., Reiter, P. & Miller, B. R. Use of randomly amplified polymorphic DNA amplified by polymerase chain reaction markers to estimate the number of Aedes aegypti families at oviposition sites in San Juan, Puerto Rico. Am. J. Trop. Med. Hyg. 51, 89–97 (1994).
Colton, Y. M., Chadee, D. D. & Severson, D. W. Natural skip oviposition of the mosquito Aedes aegypti indicated by codominant genetic markers. Med. Vet. Entomol. 17, 195–204 (2003).
Grunnill, M. & Boots, M. How Important is Vertical Transmission of Dengue Viruses by Mosquitoes (Diptera: Culicidae)? J. Med. Entomol. 53, 1–19 (2016).
Thongrungkiat, S., Maneekan, P., Wasinpiyamongkol, L. & Prummongkol, S. Prospective field study of transovarial dengue-virus transmission by two different forms of Aedes aegypti in an urban area of Bangkok, Thailand. J. Vector Ecol. 36, 147–152 (2011).
Carvalho, G. C. et al. Composition and diversity of mosquitoes (Diptera: Culicidae) in urban parks in the South region of the city of São Paulo, Brazil. Biota Neotrop. 17, (2017).
Miller, B. R. & Ballinger, M. E. Aedes albopictus mosquitoes introduced into Brazil: vector competence for yellow fever and dengue viruses. Trans. R. Soc. Trop. Med. Hyg. 82, 476–477 (1988).
Vega-Rua, A., Zouache, K., Girod, R., Failloux, A.-B. & Lourenco-de-Oliveira, R. High Level of Vector Competence of Aedes aegypti and Aedes albopictus from Ten American Countries as a Crucial Factor in the Spread of Chikungunya Virus. J. Virol. 88, 6294–6306 (2014).
Chouin-Carneiro, T. et al. Differential Susceptibilities of Aedes aegypti and Aedes albopictus from the Americas to Zika. Virus. Plos Negl. Trop. Dis. 10, e0004543 (2016).
Prefeitura de São Paulo. Piqueri. https://www.prefeitura.sp.gov.br/cidade/secretarias/meio_ambiente/parques/regiao_leste/index.php?p=5761 (2018).
Ferraz, I. & Rocha, L. Estudo dos parques paulistanos. http://sinaenco.com.br/wp-content/uploads/2016/08/ParquesPaulistanos2008.pdf (2008).
Lanciotti, R. S., Calisher, C. H., Gubler, D. J., Chang, G. J. & Vorndam, A. V. Rapid detection and typing of dengue viruses from clinical samples by using reverse transcriptase-polymerase chain reaction. J. Clin. Microbiol. 30, 545–51 (1992).
Thompson, J. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 25, 4876–4882 (1997).
Tamura, K., Stecher, G., Peterson, D., Filipski, A. & Kumar, S. MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0. Mol. Biol. Evol. 30, 2725–2729 (2013).
Gu, W., Lampman, R. & Novak, R. J. Assessment of arbovirus vector infection rates using variable size pooling. Med. Vet. Entomol. 18, 200–204 (2004).
We would like to thank the São Paulo Research Foundation (FAPESP) (Grant No. 2016/12140–0; 2017/12434–6), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001 and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (Grant No. 53689/2016-1) for providing funding for this research. The authors also thank Dr. Renato Pereira de Souza for providing positive controls of dengue virus and Colin Bowles for the help with the English in the manuscript.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Ferreira-de-Lima, V.H., Andrade, P.d.S., Thomazelli, L.M. et al. Silent circulation of dengue virus in Aedes albopictus (Diptera: Culicidae) resulting from natural vertical transmission. Sci Rep 10, 3855 (2020). https://doi.org/10.1038/s41598-020-60870-1
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