Out of the bush: the Asian bush mosquito Aedes japonicus japonicus (Theobald, 1901) (Diptera, Culicidae) becomes invasive

Systematics of the Japonicus Group

Aedes japonicus occurs with four morphologically very similar subspecies: Ae. j. japonicus (Theobald, 1901), Ae. j. shintienensis Tsai & Lien, 1950, Ae. j. amamiensis Tanaka, Mizusawa & Saugstad, 1979, and Ae. j. yaeyamensis Tanaka, Mizusawa & Saugstad, 1979. These varieties may be differentiated by the presence/absence and the particular design of a sub-basal dark band on their hind femora. Secondary characteristics are the colour, alignment and shape of the scales on their posterior pronotal lobes, on their subspiracular areas, on their costae and on their fourth hind tarsomeres [41]. The four subspecies are genetically distinct and form a monophyletic group together with Aedes koreicus[42].

Distribution and spread

The Ae. japonicus subspecies have characteristic distribution areas in Asia. Aedes j. japonicus is most wide-spread and has been recorded from Palaearctic Japan (Hokkaido, Honshu, Shikoku, Kyushu, Yakushima, Tsushima), the Ryukyu Archipelago, Korea (including both the Korean peninsula and Cheju Island), southern China including Hong Kong, Taiwan and southeastern Siberia (Primorskiy Kray). Aedes j. shintienensis is more restricted to the Oriental region, including Taiwan and Korea, while Ae. j. amamiensis occurs on Amami Guntô and Ae. j. yaeyamensis on Yaeyama Guntô, Okinawa Guntô and associated islands of the Ryukyu Archipelago [41, 43, 44].

For reasons not quite understood, only Ae. j. japonicus has become invasive. In principal, it is supposed to use the same transportation mechanisms as Ae. albopictus, primarily the second-hand tyre trade for intercontinental/long-distance overseas movement of the desiccation-resistant eggs [45] and land-based trade and vehicle transport for the dispersal of eggs, larvae and adults on the ground [6, 46]. Of course, land-based transport is also possible through displacement of tyres, and it is hypothesized that initial introductions into Ohio and Illinois could be attributed to interstate used tyre commerce [7, 27]. It is assumed, however, that a major mode of spread across the USA might be connected to land-based vehicle transport and transit of adult mosquitoes via the Standardbred horse trade [6, 47]. Furthermore, Gray et al. [17] and Bevins [48], who found Ae. j. japonicus larvae in rock pools associated with all major rivers in the Appalachians and Blue Ridge Mountains of the USA, discuss the possibility of active expansion along river corridors.

For Ae. albopictus, introduction of larvae through the lucky bamboo (Dracaena spec.) and machinery water and of adults on airplanes has been identified in addition to the used tyre pathway [49, 50]. Similarly, Ae. j. japonicus was found in used machinery and water tankers arriving in New Zealand [51].

Aedes j. japonicus was first detected outside its native distribution range in New Zealand in 1993 [3]. Up to 2003, eight additional introductions were reported but all of them remained interceptions [51]. To date, no establishment of the species in New Zealand has become public.

In the US, three states notified collections of Ae. j. japonicus in 1998, New Jersey, New York and Connecticut [4, 5]. Retrospectively, it is not clear when introduction had taken place but it is assumed that it must have been after 1992 since no Ae. j. japonicus specimens had been encountered during a previous intense monitoring programme for Ae. albopictus[52]. By 2011, Ae. j. japonicus was demonstrated in 33 US states including Hawaii (Figure 1, Table 1).

Early phylogenetic investigations by Fonseca et al. [6] on mosquitoes from the eastern US states suggest that there had been at least two independent introductions, since samples from New York, New Jersey and Connecticut represented genetic signatures significantly different from samples from Pennsylvania and Maryland. A more detailed study on mosquitoes collected up to 2005 provided evidence for continuous merging of the initial populations, thus producing increased genetic diversity [53].

While the spread of Ae. j. japonicus continued on the eastern US coast and gradually included more central states, establishment of the species was reported from Washington State on the western coast as early as in 2001 [15]. It remained unclear whether this was a result from movement of contaminated products (e.g. tyres) from the eastern states or from another intercontinental introduction event. In 2006, Oregon was the second western state to report occurrence of Ae. j. japonicus[28].

In 2001, the northeastern distribution area expanded towards Canada (Figure 1), and the rock pool mosquito was subsequently demonstrated in southern Quebec and southern Ontario [34, 35].

In Europe, Aedes j. japonicus was first detected in 2000 in the form of two larvae in a storage yard of recycled tyres in a town in northwestern France [36]. According to Schaffner et al. [38], this introduction could be eliminated. In 2002, a used tyre-trading company in Central Belgium was found infested by Ae. j. japonicus, and in 2008 the species was discovered on the premises of another Belgian company involved in the second-hand tyre business in the same area [37]. From 2003 onwards, the bush mosquito was regularly collected in Belgium suggesting the establishment of a local population. Interestingly, a spatial spread beyond the companies’ properties was observed only exceptionally although natural breeding sites were accepted in addition to discarded tyres [37]. Control efforts were only initiated in 2012 and continued in 2013, but final eradication could not be confirmed so far (Schaffner, pers. comm.).

Schaffner et al. [38] reported the presence of another European distribution area of Ae. j. japonicus in 2008 from northern Switzerland, spreading cross-border into Germany. Prompted by this finding, a monitoring programme carried out in southern Germany demonstrated a wide-spread population in 2009 with further expansion up to 2012 [54–56], (Becker, pers. comm.). Additional populations were found in 2012 in western Germany [57] and in 2013 in northern Germany [58] after individual mosquitoes were submitted to the authors for identification by private persons. Since the West German area was considerably larger and more densely populated than the North German one, it was assumed to be older. Most of the positive sites in northern Germany were located close to a motorway connecting the two distribution areas, suggesting that the North German population was probably an offshoot of the West German one [58]. Apparently, the Swiss/South German population expands westwards as Ae. j. japonicus specimens were detected in southern Alsace in 2013 (Schaffner, pers. comm.).

In 2011, immature bush mosquito stages were also collected in the border region of Austria (Styria) and Slovenia [39]. During a monitoring in Slovenia carried out in 2013, the whole north-eastern half of Slovenia was found colonized by Ae. j. japonicus[59], with frontier crossing to Croatia where several specimens were detected in 2013 close to the Slovenian border (Merdić, pers. comm.).

A single Ae. j. japonicus specimen was trapped in the Central Netherlands during routine monitoring in 2012, prompting a more thorough surveillance in the affected municipality with a closer trap grid in 2013. When several females were found, a site inspection produced numerous breeding sites containing preimaginal stages [40].

In summary, it appears that six spatially separated colonization areas exist in Europe: Belgium (being treated), northern Switzerland/France/southern Germany, western Germany, northern Germany, Austria/Slovenia/Croatia and the Central Netherlands (Figure 2). Except for Belgium, it is not known where the mosquitoes came from and how they were imported [e.g. [38, 57]. It is also not clear whether the various European populations are related to each other and whether they go back to different introduction events. Population genetic analyses using microsatellite signatures are underway to shed light on their relationships and geographic origins.

Biology

Aedes j. japonicus is a mosquito species adapted to temperate climates, capable of withstanding cold and snowy winters as occuring in its endemic home range in northern Japan. According to Kamimura [60], overwintering takes place as eggs in northeastern Japan and as larvae in southwestern Japan. In the southern Appalachians, USA, larvae were found at altitudes of up to 1,500 m where winter temperatures can reach −18°C [48].

The life-cycle is multivoltine both in Japan [61] and in the eastern US [52]. During a five-year period in southern New Hampshire, Burger & Davis [9] observed hatching of larvae at the end of March, as soon as breeding sites lost their ice cover, at water temperatures of 4.0-4.5°C. Larvae were present until freezing produced a new ice cover in late October or early November. In laboratory studies larvae were demonstrated to hatch at 5°C water temperature and to be able to survive extended periods at low temperatures (e.g. 141 days at 10°C [8]). These observations suggest that Ae. j. japonicus can indeed overwinter in the larval stage as communicated by Kamimura [60] for southern Japan.

The activity period of adults may last from May to October [62, 63] or, at mild temperatures, even to early December [64]. At 22°C under laboratory conditions, preimaginal development, i.e. the period from larval hatching to adult emergence, takes two to four weeks [8]. Females exhibit a crepuscular/diurnal biting habit [65, 66] and are assumed to have a relatively short flight range [6].

Aedes j. japonicus has a preference for forested and bushy areas, be they in agricultural, rural, suburban or urban settings [41, 52]. Being essentially a rock-hole breeder in its native range [41], streamside rock pools are among numerous other natural and movable or stationary artificial containers colonized elsewhere. Larvae can be found in tree-holes, leaf axils, tree stumps, rain water pools, ditches, subterranean catch basins, used tyre casings, stone vessels, drainage pipes, drinking fountains, tin cans, bath tubs, bird baths, roof gutters, flower vases, water dishes for pot plants, plastic cartons, vinyl tarpaulins, street gutters, rain water barrels, buckets, pans, etc. [16, 38, 48, 52, 62, 67–72]. Strikingly, the breeding habitats often contain decaying leaves, twigs, other decomposing organic matter and algae [41, 52, 62]. Larval collections in extremely dirty artificial containers, such as used ashtrays, indicate a high tolerance to environmental pollutants [35].

Breeding sites are selected in both sun-lit and shaded environments [41, 52], suggesting that the larvae and pupae can tolerate a wide range of water temperatures [71]. However, confirming the mosquito’s distribution boundaries in Japan [41], the frequent lack of Ae. j. japonicus in warm water pools fully exposed to the sun in some areas led Andreadis & Wolfe [73] to suggest that a temperature barrier may exist for this species preventing the colonization of regions with relatively high summer temperatures. This may explain the present, more northerly distribution areas in Europe and North America. In the southern US state Alabama, for example, a single Ae. j. japonicus female was trapped in the northeasternmost corner in 2005, whereas no specimens at all were encountered in any other county during a state-wide survey of tyre-breeding mosquitoes [74]. Also in Europe, establishment has as yet been demonstrated only in the central countries where a temperate climate prevails, but not in southern subtropical regions.

In Japan, Ae. j. japonicus females are said to be reluctant to bite humans [41, 62], whereas they readily feed on chicken and mice in the laboratory, but not on reptiles or amphibians [75]. Williges et al. [76] feed their laboratory colony on guinea pigs, and Takashima & Rosen [77], Sardelis & Turell [11] and Sardelis et al. [78–80] used chickens, hamsters and mice, respectively, as blood hosts for transmission studies. In contrast to extensive biting study observations in the field by LaCasse & Yamaguti [62] where Ae. j. japonicus was never encountered, Iriarte et al. [61] reported Ae. j. japonicus to be abundant near human dwellings in urban areas, and Kamimura [81] and Andreadis et al. [52] actually observed attraction to, and even attacks on, humans in the field, indicating a feeding purpose. Knight [67] also argues that the species will readily bite humans entering their habitats. While analyzing blood meals from wild-caught Ae. j. japonicus, Apperson et al. [82] found that all tested samples were of mammalian but none of human origin. Molaei et al. [83], however, demonstrated acquisition of blood from human hosts in a third of examined blood-engorged females. In summary, there is evidence that the bush mosquito feeds on both avian and mammalian, including human, hosts. Vector competence provided, this indiscriminant behaviour makes it a potential bridge vector of zoonotic viruses such as West Nile virus (WNV).

Once established under adequate climatic conditions, Aedes j. japonicus may quickly propagate. In some newly infested areas, the invader was detected quite early, either by chance or as a consequence of routine mosquito surveillance, when population densities were still low and distribution was limited. It has commonly been observed that detection frequency, together with breeding site numbers and spatial distribution, will usually increase significantly within one to three years after the initial phase of colonization, resulting from considerable population growth [9, 20, 22, 27, 35]. However, the initial phase of colonization is missed in some areas, and the mosquito’s presence is only recognized with some delay, probably a few years, when high population numbers and a wide-spread distribution have already been reached [e.g. [5, 11, 52].

Along with the observed adaptive capacity and successful proliferation of Ae. j. japonicus in many areas of North America and Europe comes evidence that it represses the population densities of other culicids [9, 57, 73, 84]. Such a displacement of indigenous mosquito species would of course directly affect the biodiversity and may also have direct or indirect effects on the epidemiology of mosquito-borne diseases [48, 85]. While competitive advantage could not be proven so far or remains anecdotal in Europe [38, 57], there is evidence from the US that Ae. j. japonicus larvae outcompete larvae of other species. A decline in relative abundances as compared to Ae. j. japonicus has been reported for Aedes atropalpus, Aedes triseriatus, Culex restuans and even Culex pipiens[22, 72, 73, 84–86]. Handicaps of Ae. atropalpus, for example, are hypothesized to be autogeny and a longer larval development [85]. Aedes triseriatus is inferior in sunlit peridomestic locations [72] and Cx. pipiens when decaying leaves and algae are the only food sources [86]. Similar negative effects with weak support for Ae. j. japonicus over Ae. triseriatus with regard to development time were also observed by Alto [87] when these two species were co-bred under artificial conditions. These observations contrast somewhat with studies which indicate that Cx. pipiens maintained similar larval populations in tyres before and after the introduction of Ae. j. japonicus in Connecticut [73] and with studies of larval competition between Ae. j. japonicus and Cx. pipiens reared on laboratory diets which indicate that the two species are equivalent competitors [88].

Being possibly superior in competition to a number of native culicid species, Ae. j. japonicus larvae have been shown in laboratory experiments to be inferior to the Asian tiger mosquito Ae. albopictus[89], another invasive container-breeding culicid species which had started its worldwide spread long before the Asian bush mosquito [90–92]. This would be unfortunate if transferable to natural conditions since Ae. albopictus is a highly efficient vector of dirofilarial nematodes and more than 20 arboviruses including many of public health relevance [93]. It is therefore thought to pose a considerably greater threat to invaded countries than Ae. j. japonicus. Field observations made by Bartlett-Healy et al. [94] do not necessarily support the laboratory results of Armistead et al. [89]. They rather suggest that species abundance depends on urban, suburban or rural surroundings, with Ae. albopictus being more abundant in urban and suburban settings, and Ae. j. japonicus being more abundant in rural settings when both are sympatric.

There are most likely numerous factors to be considered simultaneously when larval competition is to be determined, such as food resource availability and quality, water quality, shade and insolation, and temperature [94]. Thus, the competition between Ae. j. japonicus and Aedes epactius, another US resident mosquito species, appears to be clearly dependent on season-associated temperature [32]. Early in the year, when temperatures are cooler, Ae. j. japonicus is the dominating species in rock hole habitats while later in the year, during the hotter months, Ae. epactius is more frequent.

Vector potential

Thus, Mitamura et al. [98] reported experimental JEV infection and subsequent transmission by Ae. j. japonicus in Japan decades ago, whereas the mosquitoes became infected but did not transmit the virus in a Russian study by Petrischeva & Shubladse [99]. Specimens positive for JEV were also found in the field in Russia [100]. Takashima & Rosen [77] have later shown the capability of Ae. j. japonicus of transmitting the virus both horizontally and vertically in the laboratory. In the field, its vector role for JEV may be obscured by the principal vector, Culex tritaeniorhynchus, which breeds in the countless Asian rice fields. Aedes j. japonicus probably may only gain some significance as a vector in areas devoid of rice fields and Cx. tritaeniorhynchus[104]. JEV causes serious encephalitides in humans and horses and abortion in pigs [105].

Turell et al. [95, 96] and Sardelis & Turell [11] have shown laboratory transmission of WNV by feeding Ae. j. japonicus on viremic chickens and re-feeding them on naïve chickens after a period of two weeks. WNV affects birds, equines and humans, where infections may go asymptomatically or cause encephalitis, meningitis, flaccid paralysis and even death. Epidemics have occurred in Europe, Africa, North and Central America, the Middle East and parts of Asia [106]. Major WNV vectors are Culex species but the virus was found in numerous field-collected pools of Ae. j. japonicus from at least nine different US states between 2000 and 2009 [83, 97].

Sardelis et al. [78–80] also described experimental transmission of eastern equine encephalitis virus (EEEV), La Crosse virus (LACV) and St. Louis encephalitis virus (SLEV) by Ae. j. japonicus fed on viremic chickens or hamsters first and on naïve chickens or suckling mice one to three weeks later, respectively. Most human infections with all three viruses remain subclinical or inapparent, while in some cases they may involve the central nervous system and cause severe encephalitides and death. LACV and EEEV are restricted to North America where the principal mosquito vectors are Culiseta melanura and Ae. triseriatus, respectively [107, 108]. SLEV is distributed throughout the Americas and is transmitted by various Culex species [109].

Quite recently, Turell et al. [101] also demonstrated efficient laboratory transmission of Rift Valley fever virus (RVFV) by Ae. j. japonicus. More than 90% of all mosquitoes fed on viremic hamsters had disseminated infections from seven days post infection onwards, and virus transmission to susceptible hamsters readily occurred. RVFV virus is highly pathogenic to humans and ruminants [110, 111] and raises great concern that it might be imported into Europe and North America [112, 113]. It has long been endemic to sub-Saharan Africa but epidemics have increasingly been occurring in North Africa and the Middle East [112]. Notably, RVFV is also transmitted transovarially by some mosquito species. Infected females pass the virus over to the next generation via the eggs resulting in the fact that the virus can persist in the mosquito population over extended periods of time without involvement of a vertebrate host [114].

Susceptibility to infection, but not virus transmission, has been shown for chikungunya and dengue viruses by Schaffner et al. [102], by artificial feeding of Ae. j. japonicus on viremic blood through chicken skin and saliva titration 14 days later. Occurrence of the viral particles in the saliva indicated vector competence. Both viruses have been proven to be transmitted by synanthropic Aedes species, such as Ae. albopictus and Aedes aegypti, and have recently caused large unexpected outbreaks in northern Italy (chikungunya [115]) and on the Portuguese island of Madeira (dengue [116]), respectively. Chikungunya may be associated with long-lasting and painful polyarthralgia [117] while dengue may present with a hemorrhagic fever or a shock syndrome and be fatal [118].

Getah virus occurs in southeastern Asia and Australia, is transmitted by various Aedes and Culex species, and has been described as causing disease in horses, characterized by pyrexia, urticaria, rash and oedema of the hind legs [119]. Aedes j. japonicus showed susceptible to the virus when fed on viremic blood through pig skin membrane as demonstrated by titration of whole mosquito homogenates 21 days after blood ingestion [103].