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Limited potential for transmission of live dengue virus vaccine candidates by Aedes aegypti and Aedes albopictus.

To evaluate the transmission risk of four live dengue (DEN) vaccine candidates developed by the U.S. Army (DEN-1, 45AZ5 PDK 20; DEN-2, S16803 PDK 50; DEN-3, CH53489 PDK 20; and DEN-4, 341750 PDK 20), we tested 3,010 Aedes aegypti and 1,576 Aedes albopictus mosquitoes blood-fed on 21 volunteers who had been administered one of the four vaccine candidates or the licensed yellow fever (YF) vaccine (17D). We used an indirect immunofluorescence assay (IFA) to detect DEN or YF viral antigen in the heads of mosquitoes. Corresponding to the lack of a detectable viremia among volunteers inoculated 8-13 days previously with live DEN-1 or DEN-2 vaccine candidates, only six mosquitoes developed disseminated infections after feeding on these volunteers. These six mosquitoes included 4 of 247 Ae. albopictus fed on volunteers inoculated with the DEN-1 vaccine candidate and 2 of 528 Ae. aegypti fed on volunteers inoculated with the DEN-2 vaccine candidate. Infection was confirmed in each of these IFA-positive mosquitoes by isolating infectious virus from the mosquito's body in Vero-cell culture. None of the 1,252 or the 969 mosquitoes fed on DEN-3 or DEN-4 recipients, respectively, were infected. Overall, dissemination rates in Ae. albopictus and Ae. aegypti were low. Dissemination rates were 0.5%, 0.3%, < 0.1%, and < 0.1% for the DEN-1 through DEN-4 vaccine candidates, respectively. Because of the observed low dissemination rates, it is unlikely that these vaccine viruses would be transmitted under natural conditions.

Aedes↗

Growth characteristics of ChimeriVax-DEN2 vaccine virus in Aedes aegypti and Aedes albopictus mosquitoes.

The chimeric yellow fever (YF) 17D-dengue type 2 (ChimeriVax-DEN2) vaccine virus developed by Acambis, Inc. (Cambridge, MA) contains the prM and E genes of wild-type (wt) dengue 2 (DEN-2) (strain PUO-218) virus in the YF vaccine virus (strain 17D) backbone. The potential of ChimeriVax-DEN2 virus to infect and be transmitted by Aedes aegypti, the principal DEN and YF virus mosquito vector, and Aedes albopictus, a species that occurs in areas of active transmission of YF and DEN viruses, was evaluated. Mosquitoes were intrathoracically (IT) inoculated with virus or were fed a virus-laden blood meal, and the replication kinetics of ChimeriVax-DEN2 were compared with the wt DEN-2 and YF 17D vaccine viruses. Replication of YF 17D virus is attenuated in cultured Ae. albopictus C6/36 mosquito cells and in Ae. aegypti and Ae. albopictus mosquitoes. Growth of ChimeriVax-DEN2 virus similarly was restricted in C6/36 cells and in mosquitoes. ChimeriVax-DEN2 replicated in 56% of IT inoculated Ae. aegypti, and virus disseminated to head tissue in 36%, with a mean viral titer of 1.8 log10 PFU/mosquito. Of mosquitoes, 16% of Ae. aegypti and 24% of Ae. albopictus were infected 14 days after a blood meal containing ChimeriVax-DEN2, but virus did not disseminate to head tissue. In contrast, DEN-2 replicated in all IT inoculated and orally infected Ae. aegypti (mean titer 5.5 log10 PFU/mosquito), and virus disseminated to head tissue in 95%. Of Ae. albopictus, 84% were infected after a blood meal containing DEN-2 virus; dissemination occurred in 36%. Replication of ChimeriVax-DEN2 virus in mosquitoes corresponded to that of YF 17D vaccine virus, which is restricted in its ability to infect and replicate in mosquitoes. Therefore, transmission of ChimeriVax-DEN2 virus by vector mosquitoes is unlikely.

Aedes↗

Laboratory studies on the vector capability of Aedes (neomelaniconion) unidentatus McIntosh and Aedes (Aedimorphus/ dentatus (Theobald) with West Nile and Sindbis viruses.

Laboratory tests were made with Aedes (Neomelaniconion) unidentatus McIntosh and Aedes (Aedimorphus) dentatus (Theobald) collected from the Highveld region of the Transvaal, South Africa, to determine their ability of transmit West Nile and Sindbis viruses. Viraemic hamsters or a viraemic chick were exposed to the mosquitoes as infective meals. Infection of mosquitoes was determined by testing mosquitoes individually for the presence of virus 10-26 days later. Transmission of virus, attempted between the 10-20th days by exposing hamsters to groups of mosquitoes, was not achieved. With West Nile virus, the high concentrations of virus required to infect each species led to the conclusion that neither is an important vector of this virus. With Sindbis virus and A. unidentatus the 10 per cent infection threshold was less than 2,6 logs of virus, while with A. dentatus it was about 3,5 logs. This suggests that both species, but more particularly A. unidentatus, could be vectors of this virus.

Aedes↗

Current status of Aedes albopictus and Aedes atropalpus in Italy.

Eight years after the 1st record in Italy, scattered foci of Aedes albopictus are reported in 9 regions and 107 municipalities belonging to 22 provinces, mainly located in the northeastern part of the country (Veneto region). In almost all infested areas the species is well controlled and at low levels of density, through source reduction and antilarval treatments. Aedes atropalpus, 1st recorded in 1996, remains limited to the original focus in the province of Treviso. Surveillance and control of both species are carried out by local health agencies within a national program coordinated by Istituto Superiore di Sanità (national Institute of Public Health).

Aedes↗

Does temperature affect the outcome of larval competition between Aedes aegypti and Aedes albopictus?

The superior larval competitive ability of Aedes albopictus has been proposed to explain the recent displacement of Aedes aegyptiby the former species inparts of the southeastern U.S. Ae. aegypti persists, however, in sympatry with Ae. albopictus in urban areas of southern Louisiana, Florida, and Texas, and the impact of larval competition between these species has not been investigated at higher temperatures that may be characteristic of these urban environments. We compared growth and survivorship of the two species at controlled temperatures of 24 degrees and 30 degrees C in water-containing tires under conditions of intra- and interspecific competition and with or without leaf litter. When other variables were controlled statistically, the estimated finite rate of increase (lambda') was significantly higher for both species at the higher temperature, and the proportional increases in lambda' did not differ between species. Therefore, our experiment predicts that by itself, temperatures between 24 degrees and 30 degrees C would not alter the outcome of larval competition. Overall, response measures of Ae. albopictus were more sensitive than those of Ae. aegypti to the litter and species/density variables, although the development ofAe. aegypti females was uniquely retarded by a high density of its own species.

Adaptation, Physiological↗

Low oral receptivity for dengue type 2 viruses of Aedes albopictus from Southeast Asia compared with that of Aedes aegypti.

Dengue hemorrhagic fever has been a major health problem in Asia since the 1950s. During this period, the former principal vector of dengue viruses in Asia, Aedes albopictus, was replaced by Aedes aegypti in most major cities of the area. Ae. aegypti is now considered the main vector of dengue viruses in Asia. Surprisingly, however, this mosquito has been described as having a relatively low oral receptivity for dengue viruses compared with Ae. albopictus. In the present study, we compared the relative oral receptivities of Ae. aegypti and Ae. albopictus collected in southeast Asia from both sympatric and allopatric breeding sites. In all instances, the oral receptivity of Ae. aegypti to the dengue type 2 virus used was significantly higher than that of Ae. albopictus. We also compared the relative oral receptivity of Ae. aegypti and Ae. albopictus for two other low-passage strains of dengue 2. In all instances, Ae. aegypti was significantly more receptive than Ae. albopictus. It should be noted, however, that the difference was found only for Ae. albopictus recently collected from the field (Ta Promh strain, Cambodia, 2001) and not for an Ae. albopictus strain that had been colonized for many years (Oahu strain, Hawaii, 1971). We also observed a significant increase in the infection rate of Ae. albopictus of the Ta Promh strain with increasing generations in the laboratory. These observations demonstrate the importance of considering the colonization history of mosquitoes when assessing their susceptibility to infection with dengue viruses and, perhaps, other arboviruses.

Aedes↗

Laboratory evaluation of 18 repellent compounds as oviposition deterrents of Aedes albopictus and as larvicides of Aedes aegypti, Anopheles quadrimaculatus, and Culex quinquefasciatus.

Among 18 experimental skin repellent compounds tested at five concentrations in the laboratory as oviposition deterrents against Aedes albopictus. 12 compounds showed significant activity, with median effective dose values ranging from 0.005 to 0.052%. The test compounds also were evaluated in the laboratory as larvicides against laboratory-reared 4th instars of Aedes aegypti, Anopheles quadrimaculatus, and Culex quinquefasciatus with the same concentrations employed for the oviposition deterrency tests against Ae. albopictus. Larval mortality data at 24 and 48 h after treatment indicated that 12 test repellents caused larval mortalities in the range of 67 to 100% against An. quadrimaculatus, 10 compounds induced 55-100% larval mortalities of Ae. aegypti, whereas larval mortality caused by 9 compounds ranged from 74 to 100% against Cx. quinquefasciatus. These mortality data did not fit the linear model of the statistical analysis. However, multiway analysis of variance of these data showed that the repellent compounds, concentrations used, species of mosquitoes, and exposure times affect the degree of larval mortalities.

Aedes↗

A comparison of seven traps used for collection of Aedes albopictus and Aedes aegypti originating from a large tire repository in Harris County (Houston), Texas.

Among 7 traps tested, significantly higher (P < 0.01) mean numbers of Aedes albopictus (269) and Aedes aegypti (55) females were collected within the Mosquito Magnet Liberty trap compared with the remaining traps. The second highest mean captures for both species were obtained from omnidirectional Fay-Prince (77 Ae. albopictus) and Dragonfly (13 Ae. aegypti) traps, which were not significantly different (P > 0.01) from an experimental moving-target trap that produced mean captures of 40 Ae. albopictus and 6 Ae. aegypti (alpha = 0.01). In terms of Ae. albopictus capture, no significant differences (P > 0.01) existed between Dragonfly, CDC without light (CDC -), and CDC with light (CDC +) captures, which were significantly different (P < 0.01) from Mosquito Deleto. No statistical significance existed between moving-target, omnidirectional, CDC +, CDC -, and Mosquito Deleto traps in terms of Ae. aegypti capture (P > 0.01), individual trap positions, or number of Ae. albopictus and Ae. aegypti females collected throughout the 21-day test (P > 0.05). Mosquito Magnet Liberty collected 7,208 Ae. albopictus, 1467 Ae. aegypti, and 13 other species representing 5 genera, which comprised the largest total (9662) and percentage (62.5%) of mosquitoes collected by all traps combined. Omnidirectional and moving-target traps captured 1941 and 1050 Ae. albopictus, 138 and 220 Ae. aegypti, and 2171 (14.0%) and 1397 (9.0%) of the total mosquitoes captured by all traps, with 8 and 10 species representing 5 genera, respectively, included in these collections. The Dragonfly captured 476 Ae. albopictus, 376 Ae. aegypti, and 1008 total specimens (6.5%) representing 8 species and 4 genera in these collections. CDC + and CDC - traps collected nearly identical numbers of Ae. albopictus (431, 450) and Ae. aegypti (71, 71) with 537 (3.4%) and 551 (3.5%) total specimens, respectively. Eight species representing 5 genera were captured from CDC +, whereas CDC - captured 6 species representing 4 genera. Mosquito Deleto captured 118 mosquitoes, including 19 Ae. albopictus and 62 Ae. aegypti females (0.7%), with 6 species representing 4 genera. Battery-powered traps with contrasting color schemes and movement worked considerably better than stationary CDC miniatures without color or movement. Omnidirectional Fay-Prince and moving-target traps without octenol captured Ae. albopictus and Ae. aegypti females as frequently as some commercial traps. Additionally, costs incurred per mosquito trapped, future trap design, and important consumer-centered issues are briefly discussed.

Aedes↗

Surveillance and behavioral investigations of Aedes aegypti and Aedes polynesiensis in Moorea, French Polynesia, using a sticky ovitrap.

The effectiveness of the sticky ovitrap was assessed for the container-breeding Aedes aegypti and Aedes polynesiensis in Moorea, French Polynesia. These mosquitoes are the primary vectors of dengue viruses and Bancroftian filariasis, respectively, in the area. Both Ae. aegypti and Ae. polynesiensis were collected in greatest numbers in sticky ovitraps baited with water or grass infusions rather than leaf infusions. Sticky ovitrap collections were significantly higher for both species in the 12 h post-midday than pre-midday and in traps set in shaded compared with open locations. More females of Ae. aegypti were collected in ovitraps at west-facing walls, although Ae. polynesiensis collected at east- or west-facing traps did not differ in number. Female Ae. aegypti (bloodfed, marked, and released for oviposition) were readily recaptured (19-26%) by sticky ovitraps, exhibiting movement of up to 30 m, and between outdoor and indoor situations. Overall, the sticky ovitrap proved an effective tool for investigating the oviposition behavior and dispersal of these container-breeding species.

Aedes↗

Insecticide resistance development in Culex quinquefasciatus (Say), Aedes aegypti (L.) and Aedes albopictus (Skuse) larvae against malathion, permethrin and temephos.

Laboratory-bred females of Culex quinquefasciatus, Aedes aegypti and Aedes albopictus from the insectarium, Unit of Medical Entomology, Institute for Medical Research were used in the experiment. The late third stage of the F0 larvae which survived the high selection pressure of malathion, permethrin and temephos were reared and colonies were established from adults that emerged. Cx. quinquefasciatus larvae were subjected to selection by malathion and permethrin for 40 generations, Ae. aegypti larvae to malathion, permethrin and temephos for 32 generations and Ae. albopictus larvae were selected against malathion and permethrin for 32 generations and 20 generations against temephos. The rate of resistance development was measured by LC50 value. Cx. quinquefasciatus larvae developed higher resistance to malathion and permethrin compared to Ae. aegypti and Ae. albopictus. On the whole, permethrin resistance developed at a faster rate than malathion and temephos.

Aedes↗

Protein synthesized by dengue infected Aedes aegypti and Aedes albopictus.

The main objective of this study was to compare protein profiles of whole mosquitoes of Malaysian Aedes aegypti and Aedes albopictus after infection with virus and to investigate whether dengue virus would induce protein secretion in Ae. aegypti and Ae. albopictus. Using SDS -PAGE, it was shown that in uninfected Ae. aegypti and Ae. albopictus, the protein bands were within the range of 14 - 80 kDa with most of the bands overlapping for the two species. Comparison of the protein profile of infected and uninfected Ae. aegypti and Ae. albopictus showed five distinct molecular weight grouping at 73 - 76 kDa (Group 1), 44 - 50 kDa (Group 2), 28 - 31 kDa (Group 3), 20 - 25 kDa (Group 4) and 14 - 17 kDa (Group 5). Predominant bands for both species (infected and uninfected) were between 21 - 25 kDa and 44 - 50 kDa. Protein bands having a molecular weight of 70 kDa were only present in infected Ae. albopictus and those bands having molecular weight of 21 kDa were observed only in infected Ae. aegypti. The rate of digestion of blood meals was more rapid in Ae. albopictus than Ae. aegypti. Uninfected Ae. albopictus completed the blood digestion 2 days after ingestion of a blood meal whereas Ae. aegypti needed 3 days to complete the digestion. The rate of digestion for blood meals was slower for both mosquito species when fed with dengue virus infected blood. The digestion processes were completed 3 and 4 days after blood ingestion for Ae. albopictus and Ae. aegypti, respectively. This could be due to the presence of dengue virus in the blood, which slow down the digestion process. Appearance and disappearance of new protein bands was also observed even after the digestion has completed for both infected mosquito species. In conclusion, dengue virus was shown to induce specific proteins in both Ae. aegypti and Ae. albopictus.

Aedes↗

[Seasonal variation of Aedes aegypti and Aedes albopictus in a city of Southeastern Brazil].

OBJECTIVE: To assess the seasonal variation of Aedes aegypti and Aedes albopictus and to estimate the association between the species abundance and abiotic factors. METHODS: Tire-traps were kept for a period of 15 days monthly in an urban area of the city of Potim in the state of São Paulo, Southeastern Brazil, from November 2002 to October 2003. Samples of immature forms were followed up under laboratory conditions for 29 days and species were identified. The association between abundance and temperature, rainfall and air relative humidity was tested using Spearman correlations (r s). The descriptive statistics were presented by the average and the standard error (alpha=0.05). RESULTS: From a total of 20,727 immatures collected, 95.3% were Ae. aegypti and 4.7%, Ae. albopictus. Ae. aegypti was found throughout the whole year while Ae. albopictus was found from November to July. The association between these species and abiotic factors was significant for Ae. aegypti (p=0.04) as for maximum temperature and for Ae. albopictus as for maximum temperature (p=0.01) and rainfall (p=0.02). CONCLUSIONS: Both species presented seasonal variation. However, Ae. aegypti was found throughout the whole year showing a decrease between April and May and June and July. Ae. albopictus, less abundant, was found only between November, 2002 and July, 2003 with a peak in April, 2003. The higher abundance of Ae. aegypti compared to Ae. albopictus in an urban area showed Ae. aegypti has greater capacity of colonizing tires. Such a breeding site in the environment may be important to the maintenance and abundance of Ae. aegypti.

Aedes↗

Replacement of Aedes aegypti by Aedes albopictus in Mobile, Alabama.

Aedes albopictus was first detected in Mobile, AL, in 1987 during a CDC sponsored ovitrap survey in the Historic District. A comparison of ovitrap and larval surveys, done in 1957, 1984, 1987 and 1990, indicates that Ae. albopictus had replaced Aedes aegypti in urban Mobile. Possible explanations of this replacement, including displacement, are discussed.

Aedes↗

Nectar feeding activity of Aedes mosquitoes, with special reference to Aedes communis females.

A total of 5,721 mosquitoes (6% males) of 16 species were collected with an aerial net, when attracted to the investigator, during May-August 1984 at 2 sites in central Sweden. The majority of the mosquitoes collected (63%) were Aedes communis. Aedes communis females at both localities showed peak flight activity at evening twilight. At one site, a diel pattern of nectar feeding was correlated with host seeking activity; at the other site no correlation was found. Seasonal differences in mean fructose content of the mosquitoes were found. Among the 94 blood-fed females (belonging to 6 species) that were collected, 71% were fructose positive (n = 67) and in different ovarian stages.

Aedes↗

Relative suitability of Aedes albopictus and Aedes aegypti in North Carolina to support development of Dirofilaria immitis.

The relative suitability of two colonies established from local strains of Aedes albopictus (Wilmington and Rockingham) and a local (Raleigh) and laboratory (Liverpool) strain of Ae. aegypti to support development of Dirofilaria immitis was investigated. High levels of mortality occurred 1-2 days after mosquitoes fed on a heavily microfilaremic (28,617 microfilariae/ml) dog but not when mosquitoes were fed on a dog exhibiting a moderate microfilaremia (3,300 microfilariae/ml). At 15-16 days postfeeding, development of D. immitis to the third larval stage occurred to some extent in mosquitoes of all four strains. Microfilariae were only found in the Raleigh strain of Ae. aegypti. Aedes albopictus most frequently contained first and second stage larvae that were deteriorated which suggested that their development had been arrested. Third stage larvae were found most often in the Liverpool strain of Ae. aegypti. Colonies established from local strains of Ae. albopictus and Ae. aegypti do not appear to be suitable hosts of D. immitis.

Aedes↗

Alteration in Aedes togoi susceptibility to Brugia pahangi microfilariae induced by Aedes albopictus thoracic homogenate.

Refractoriness to Brugia pahangi microfilarial infection could be induced in the normally susceptible Aedes togoi mosquitoes by intrathoracic injection with crude thoracic homogenate of the refractory Aedes albopictus mosquitoes. The crude thoracic homogenate contained three Sephadex G-200 protein profiles of which the first profile showed strongest inhibition to the parasite development.

Aedes↗

Occurrence and ovitrap site preference of tree hole mosquitoes: Aedes triseriatus and Aedes hendersoni in eastern Kentucky.

This ovitrap study examined the effects of altitude above sea level, tree species, and tree trunk diameter on the distribution of eggs of the 2 tree hole mosquitoes, Aedes hendersoni and Ae. triseriatus. Only tree species and trunk diameter affected the distribution significantly. Aedes hendersoni eggs were found more frequently associated with trees of border and sunny habitat, while Ae. triseriatus eggs were more frequently found in association with trees of mesic habitat. Oviposition of Ae. hendersoni occurred more often at trees with smaller diameter at breast height than did Ae. triseriatus. These differences in ovipositing frequency appear to be related to the microhabitat associated with different sample sites.

Aedes↗

Filariasis transmission in Samoa. I. Relation between density of microfilariae and larval density in laboratory-bred and wild-caught Aedes (Stegomyia) polynesiensis (Marks) and wild-caught Aedes (Finlaya) samoanus (Gruenberg).

Transmission experiments of laboratory-bred and wild-caught Aedes polynesiensis and wild-caught Ae. samoanus on carriers with different levels of microfilaraemia showed that the percentage of mosquitoes infected, the average number and range of larvae found in each infected mosquito were directly proportional to the microfilarial densities in the carrier at the time of feeding. There was no difference between the results for laboratory-bred and wild-caught mosquitoes. Aedes polynesiensis fed on low carriers (around 20 Mf ml-1 and less) gave an average infection rate of 4.9%. Each infected mosquito harboured only one larva. A plot of the probit of percentage Ae. polynesiensis positive against the logarithm of microfilarial density showed a linear relationship. Using the regression line, at 95% confidence interval, a microfilarial density of 1 ml-1 would give an infection rate of 0.22-2.51%, a density of 0.1 Mf ml-1 an infection rate of 0.01-1.0%. The concentrating capacity of Ae. polynesiensis ranged from 0.70 to 4.74. As microfilaria densities decreased, concentration increased. The microfilarial intake, the subsequent worm burden and concentrating capacity were less in Ae. samoanus than Ae. polynesiensis. There was no evidence of any association between microfilarial density and concentration in Ae. samoanus.

Adolescent↗