Wolbachia wMel strain-mediated effects on dengue virus vertical transmission from Aedes aegypti to their offspring

Background Dengue virus serotypes (DENV-1 to -4) can be transmitted vertically in Aedes aegpti mosquitoes. Whether infection with the wMel strain of the endosymbiont Wolbachia can reduce the incidence of vertical transmission of DENV from infected females to their offspring is not well understood. Methods A laboratory colony of Vietnamese Ae. aegypti, both with and without wMel infection, were infected with DENV-1 by intrathoracic injection (IT) to estimate the rate of vertical transmission (VT) of the virus. VT in the DENV-infected mosquitoes was calculated via the infection rate estimation from mosquito pool data using maximum likelihood estimation (MLE). Results In 6047 F1 Vietnamese wild-type Ae. aegypti, the MLE of DENV-1 infection was 1.49 per 1000 mosquitoes (95% confidence interval [CI] 0.73–2.74). In 5500 wMel-infected Ae. aegypti, the MLE infection rate was 0 (95% CI 0–0.69). The VT rates between mosquito lines showed a statistically significant difference. Conclusions The results reinforce the view that VT is a rare event in wild-type mosquitoes and that infection with wMel is effective in reducing VT. Graphical Abstract Supplementary Information The online version contains supplementary material available at 10.1186/s13071-023-05921-y.


Background
Dengue is a mosquito-borne viral infection caused by one of four dengue virus serotypes (DENV-1 to -4) that is endemic in many tropical and sub-tropical countries [1].The global incidence of dengue has increased dramatically in the last 50 years, with approximately 50-100 million symptomatic infections and 20,000 deaths reported annually in over 125 countries [2,3].DENV is transmitted between humans through the bite of an infected female Aedes sp.mosquito (Ae.aegypti or Ae.albopictus).However, DENV can also be transmitted vertically, from the DENV-infected female mosquito to her offspring during follicle development or oviposition [4][5][6].This latter transmission mode is hypothesized to contribute to DENV persistence in the mosquito population [7].A sign of vertical transmission (VT) of DENV in a mosquito populations is the presence of infected male mosquitoes (which do not blood feed) and the presence of viruses in immature forms of mosquitoes of any sex.VT is a rare event in nature [8][9][10][11] but it has been observed in laboratory studies in both Ae.aegypti and Ae.albopictus [12,13].Several studies have also shown that VT is influenced by a number of factors, including mosquito-rearing temperature, mosquito strain and virus strain [14][15][16][17][18].
Although there are two licensed dengue vaccines, vector control has been the mainstay of dengue control efforts for decades.However, it is obvious that existing vector control methods have not removed the public health burden of dengue in any endemic country.A new approach that involves the insect endosymbiont Wolbachia (wMel or wAlbB strains) is being applied to render Ae. aegypti populations much less competent at transmitting DENV between humans [19][20][21].Wolbachia inhibits virus replication in mosquito cells via multiple mechanisms, including altering the intracellular environment, activating the innate immune system and interacting with the cell machinery involved in RNA virus infection [22].Multiple epidemiological studies, including a cluster randomized trial, have shown a large decrease in dengue cases in communities with wMel-Wolbachia-treated mosquitoes, demonstrating that wMel introgression is an effective disease control measure [23,24].
We previously found a very low DENV VT rate (0.23%) among wild-type (Wt) Ae. aegypti orally infected with DENV after feeding on viremic blood from dengue patients [9].To assess whether wMel would eliminate VT of DENV, we established an experimental model system to measure VT in the presence and absence of wMel infection.

Generating DENV-infected F0 mosquitoes
Both Wt and wMet-infected adult female mosquitoes, aged 2-3 days, were injected intrathoracically with 1 µl of solution containing DENV-1 grown in cell culture (10 5 pfu/ml; Genbank Accession Number: FJ432735).DENV-1 was used to establish infection based on the findings of our previous study which indicated that this serotype was less inhibited by wMel than the other three DENV serotypes [28].Ten injected females were then kept in cups containing 10 male mosquitoes (female:male ratio = 1:1) where they were maintained on sucrose for 10 days.
A human blood meal (non-infectious blood provided via a membrane feeder) was provided to surviving F0 females on day 10 post-injection [28].After 30 min of blood feeding, fully engorged females were isolated and placed into separate cups (isofemales) containing wet cotton balls for oviposition.Sugar (a piece of cotton soaked in 10% sucrose) was provided for 14 days.On day 14 post non-infectious blood meal, individual F0 females were harvested for testing of their DENV infection status.

Hatching and harvesting F1 mosquitoes
F1 eggs were collected at 5-7 days after the F0 females had taken their non-infectious blood meal and placed in trays filled with fresh water; the trays were kept in incubators at 28 °C under a 12/12-h light/dark cycle.Each tray was provided with one 100 mg tablet of fish food.The larval density was maintained at approximately 3300-3500 larvae per 1.5 l of water.F1 mosquitoes were individually stored and sorted by sex within cohorts originating from the same mother.
F0 and F1 mosquitoes homogenized in a TissueLyser II instrument (Qiagen, Hilden, Germany) at 30 Hz for 2-5 min.Each F0 mosquito homogenate was stored individually, while F1 mosquito homogenates (50 µl from each sample) were pooled before conducting the reverse transcriptase PCR (RT-PCR) assays to detect the presence of Wolbachia [27] and DENV [29].The positive pooled samples were then un-pooled to determine the number of infected individuals using the remaining volume of mosquito homogenate.

Estimating VT of DENV-1 in colonized Ae. aegypti with and without wMel infection
To estimate the VT of DENV-1 in a large number of F1 mosquitoes, we utilized the maximum likelihood estimate (MLE) method.This method estimated the proportion of DENV-infected individuals in pooled samples, defined as the infection rate most likely observed given the test results and an assumed probabilistic model (binomial distribution of infected individuals in a positive pool) [30][31][32][33][34][35].To account for biases, we utilized bias-corrected likelihood methods and calculated a skew-corrected score confidence interval (95% CI) [36].The infection rate was reported as the number of infected mosquitoes per 1000 individuals.In addition, to perform comparisons of CIs, we utilized the Wilson score-based interval of the Newcombe method, which relies on exact calculations of coverage probabilities [37].This approach allowed us to assess the statistical significance of the differences in infection rates between populations.
To accurately estimate the proportion of infected individuals in a population using MLE, determining the appropriate pool size is crucial to minimize the likelihood of false-negative results.In this study, the pool size was examined using a sample-media pooling approach, adapted from the Clinical and Laboratory Standards Institute (CLSI) document EP12 (CLSI EP12 [38]).The positive percent agreement (PPA) and negative percent agreement (NPA) values were calculated for different pool sizes.The highest PPA value (96%) was obtained with a pool size of four mosquitoes, whereas a pool size of eight mosquitoes showed a PPA of 89% (95% CI 0.8-0.9)and a pool size of sixteen showed only 68% agreement [39].All three sizes showed 100% agreement fir NPA values.Therefore, a pool size of eight was selected [39].
A total of 6047 F1 adults emerged from the approximately 10,328 eggs collected from 343 virus-infected Wt F0 females.Similarly, the approximately 12,027 F1 eggs from 304 virusinfected wMel-Ae.aegypti F0 females completed their development, providing 5500 wMel-Ae.aegypti F1 adults (Fig. 1).All Wt F1 adult mosquitoes were grouped into 785 pools, and 5500 wMel-Ae.aegypti F1 adult mosquitoes were grouped into 712 pools (for details, see Additional file 1: Table S1).These pools were tested for DENV-1, and nine positive pools were detected from the Wt group, while no positive pools were found in the wMel-Ae.aegypti group.The MLE for the VT rate of DENV-1 in Wt mosquitoes was estimated to be 1.49(95% CI 0.73-2.74)per 1000 adults.However, in wMel-Ae.aegypti mosquitoes, the transmission rate was estimated to be zero (95% CI 0-0.69).The observed difference in the infection rates between the Wt group and the wMel-Ae.aegypti group is 1.49 (95% CI 0.67-5.05).As the 95% CI is entirely above 0, the null hypothesis of no difference (H0: Wt − wMel = 0) can be rejected at a significance level of P < 0.05.Consequently, it can be concluded that the VT rate of the Wt group is significantly higher than that of the wMel group.
Thirteen DENV-1 infected Wt F1 individuals were identified from the nine positive pools, of which 10 were females.When assessing the frequency of mothers transmitting the virus to their progeny and determining the proportion of progeny born to DENV-infected mothers [9] based on positive pools, we observed a slight increase in rates compared to those found in fieldcollected mosquitoes [9].Our estimates indicated that for every 343 DENV-infected Wt Ae. aegypti female mosquitoes that survived and laid eggs, 11 individuals (3.21%) transmitted the virus to their offspring.However, experimentally we found that only 0.13% of progeny born to DENV-infected mothers would be infected with DENV-1(13 out of 10,328 eggs acquiring the infection).This proportion increased to 0.21% when calculated based on 6047 F1 adults.The frequency of mothers transmitting the virus to any of their progeny in Wt Ae. aegypti (3.21%) compared to the frequency identified in field-collected Ae. aegypti (2.43%) using patientderived blood meals [9] might be attributed to the direct introduction of virus into systemic tissues via IT inoculation.
The MLE of DENV-1 infection rate observed in wMel-infected Ae. aegypti was comparable to that found in wMel-infected Ae. aegypti from Brazil [40].In our study, we optimized the conditions to increase the probability of a VT event in Wt Ae. aegypti, by employing IT inoculation of virus and a long extrinsic incubation period.Furthermore, our study was conducted with a large sample size, approximately 11,547 total F1 Ae. aegypti (6047 Wt and 5500 wMel-Ae.aegypti).Despite these advantages, the VT event was not recorded in wMel-infected Ae. aegypti.The absence of DENV infection in wMel-infected F1 mosquitoes and the observed difference in VT rates between mosquito lines provide evidence that wMel is effective in reducing VT.The ability of wMel to decrease DENV replication in wMel-carrying mosquitoes has been used to reduce the incidence of dengue through the deployment of Wolbachia mosquitoes in endemic areas [23,24].The ability of wMel to reduce the VT of DENV can be attributed to various mechanisms, including resource competition, immune system activation and interference with viral replication in the reproductive tissues of mosquitoes [41][42][43][44].These mechanisms are recognized for their ability to reduce the replication of DENV and could therefore limit its transmission from one generation to the next generation.The capacity of wMel to diminish dengue transmission in both horizontal and vertical modes of transmission is critical in mitigating the incidence of dengue, ultimately decreasing the overall disease burden.

Conclusions
The results of the present study support the belief that VT is a rare phenomenon.wMel infection reduces VT in wMel-carrying Ae. aegypti population.• support for research data, including large and complex data types • gold Open Access which fosters wider collaboration and increased citations maximum visibility for your research: over 100M website views per year

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Fig. 1
Fig. 1 Flowchart of vertical transmission estimation of DENV-1 in Wt and wMel-infected Ae. aegypti with a Vietnamese background.Shown is the fate of mosquitoes as they were processed in order to determine the frequency of vertical transmission of F0 females after being infected by microinjection of DENV-1 (strain FJ432735).The orange boxes represent Wt Ae. aegypti, the green boxes represent wMel-Ae.aegypti and the red boxes indicate excluded samples.The asterisk (*) indicates the numbers are estimated.DENV-1, Dengue virus serotype 1; MLE, maximum likelihood estimate of infection rate; RT-PCR, reverse transcriptase-PCR; wMel, Wolbachia strain wMel-infected Ae. aegypti; Wt, wild type

Fig. 2
Fig. 2 DENV-1 copy numbers in F0 female Ae.aegypti with and without wMel infection.The infectivity of DENV-1 by intrathoracic injection in F0 females represents log10 viral genome copy numbers.Wt mosquitoes are shown in orange and wMel-mosquitoes are shown in green.wMel, Wolbachia strain wMel-infected Ae. aegypti; Wt, wild type

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