| Mosquito | |
|---|---|
| Female Culiseta longiareolata | |
| Scientific classification  | |
| Kingdom: | Animalia | 
| Phylum: | Arthropoda | 
| Class: | Insecta | 
| Order: | Diptera | 
| Superfamily: | Culicoidea | 
| Family: | Culicidae Meigen, 1818  | 
| Subfamilies | |
| Diversity | |
| 41 genera | |
Mosquitoes (alternate spelling mosquitos) comprise a group of about 3,500 species of small insects that are flies (order Diptera). Within Diptera they constitute the family Culicidae (from the Latin culex meaning "gnat"). The word "mosquito" (formed by mosca and diminutive -ito) is Spanish for "little fly". Mosquitoes have a slender segmented body, one pair of wings, one pair of halteres, three pairs of long hair-like legs, and elongated mouthparts.
The mosquito life cycle consists of egg, larva, pupa, and adult stages. Eggs are laid on the water surface; they hatch into motile larvae that feed on aquatic algae and organic material. The adult females of most species have tube-like mouthparts (called a proboscis) that can pierce the skin of a host and feed on blood, which contains protein and iron needed to produce eggs. Thousands of mosquito species feed on the blood of various hosts — vertebrates, including mammals, birds, reptiles, amphibians, and some fish; along with some invertebrates, primarily other arthropods. This loss of blood is seldom of any importance to the host.
The mosquito's saliva is transferred to the host during the bite, and can cause an itchy rash. In addition, many species can ingest pathogens while biting, and transmit them to future hosts. In this way, mosquitoes are important vectors of diseases such as malaria, yellow fever, Chikungunya, West Nile, dengue fever, filariasis, Zika and other arboviruses. By transmitting diseases, mosquitoes cause the deaths of more people than any other animal taxon: over 700,000 each year and as many as half of the people who have ever lived.
Fossil record and evolution
The oldest known mosquito with an anatomy similar to modern species was found in 79-million-year-old Canadian amber from the Cretaceous. An older sister species with more primitive features was found in Burmese amber that is 90 to 100 million years old.
 Two mosquito fossils have been found that show very little 
morphological change in modern mosquitoes against their counterpart from
 46 million years ago. These fossils are also the oldest ever found to have blood preserved within their abdomens.
 Despite no fossils being found earlier than the Cretaceous, recent 
studies suggest that the earliest divergence of mosquitoes between the 
lineages leading to Anophelinae and Culicinae occurred 226 million years ago.
The mosquito Anopheles gambiae is currently undergoing speciation
 into the M(opti) and S(avanah) molecular forms. Consequently, some 
pesticides that work on the M form no longer work on the S form.
Over 3,500 species of the Culicidae have already been described.
 They are generally divided into two subfamilies which in turn comprise 
some 43 genera. These figures are subject to continual change, as more 
species are discovered, and as DNA studies compel rearrangement of the 
taxonomy of the family. The two main subfamilies are the Anophelinae and
 Culicinae, with their genera as shown in the subsection below.
 The distinction is of great practical importance because the two 
subfamilies tend to differ in their significance as vectors of different
 classes of diseases. Roughly speaking, arboviral diseases such as yellow fever and dengue fever tend to be transmitted by Culicine species, not necessarily in the genus Culex. Some transmit various species of avian malaria, but it is not clear that they ever transmit any form of human malaria. Some species do however transmit various forms of filariasis, much as many Simuliidae do.
Taxonomy
Family
Mosquitoes are members of a family of nematocerid flies: the Culicidae (from the Latin culex, genitive culicis, meaning "midge" or "gnat"). Superficially, mosquitoes resemble crane flies (family Tipulidae) and chironomid flies (family Chironomidae).
Subfamilies
Genera
Mosquitoes have been classified in 112 genera.
- Aedeomyia
 - Aedes
 - Anopheles
 - Armigeres
 - Ayurakitia
 - Borachinda
 - Coquillettidia
 - Culex
 - Culiseta
 - Deinocerites
 - Eretmapodites
 - Ficalbia
 - Galindomyia
 - Haemagogus
 - Heizmannia
 - Hodgesia
 - Isostomyia
 - Johnbelkinia
 - Kimia
 - Limatus
 - Lutzia
 - Malaya
 - Mansonia
 - Maorigoeldia
 - Mimomyia
 - Onirion
 - Opifex
 - Orthopodomyia
 - Psorophora
 - Runchomyia
 - Sabethes
 - Shannoniana
 - Topomyia
 - Toxorhynchites
 - Trichoprosopon
 - Tripteroides
 - Udaya
 - Uranotaenia
 - Verrallina
 - Wyeomyia
 
Species
Over 3,500 species of mosquitoes have thus far been described in the scientific literature.
Morphology
As
 true flies, mosquitoes have one pair of wings, with distinct scales on 
the surface. Their wings are long and narrow, same with their long, thin
 legs. They have slender and dainty bodies of length typically from 3 mm
 to 6 mm, with a color of dark grey to black, some species have specific
 patterns. When at rest, they tend to hold their first pair of legs 
outward. They look similar to midge flies (Chironomidae), another ancient family of flies. Tokunagayusurika akamusi,
 for example, is a midge fly that look very much alike mosquitoes in 
that they also have slender and dainty bodies of similar colors, though 
larger in size. They also have only one pair of wings, but without 
scales on the surface. Another distinct feature to tell the two families
 of flies apart is the way they hold their first pair of legs - 
mosquitoes hold them outward, while midges hold them forward.
Life cycle
Image of pitcher plant mosquito Wyeomyia smithii, showing segmentation and partial anatomy of circulatory system
Overview
Like all flies, mosquitoes go through four stages in their life cycles: egg, larva, pupa, and adult or imago.
 The first three stages—egg, larva, and pupa—are largely aquatic. Each 
of the stages typically lasts 5 to 14 days, depending on the species and
 the ambient temperature, but there are important exceptions. Mosquitoes living in regions where some seasons are freezing or waterless spend part of the year in diapause;
 they delay their development, typically for months, and carry on with 
life only when there is enough water or warmth for their needs. For 
instance, Wyeomyia larvae typically get frozen into solid lumps 
of ice during winter and only complete their development in spring. The 
eggs of some species of Aedes remain unharmed in diapause if they dry out, and hatch later when they are covered by water.
Eggs hatch to become larvae, which grow until they are able to change into pupae.
 The adult mosquito emerges from the mature pupa as it floats at the 
water surface. Bloodsucking mosquitoes, depending on species, sex, and 
weather conditions, have potential adult lifespans ranging from as short
 as a week to as long as several months. Some species can overwinter as 
adults in diapause.
Breeding
In 
most species, adult females lay their eggs in stagnant water: some lay 
near the water's edge while others attach their eggs to aquatic plants. 
Each species selects the situation of the water into which it lays its 
eggs and does so according to its own ecological adaptations. Some breed
 in lakes, some in temporary puddles. Some breed in marshes, some in 
salt-marshes. Among those that breed in salt water, some are equally at 
home in fresh and salt water up to about one-third the concentration of 
seawater, whereas others must acclimatize themselves to the salinity.
 Such differences are important because certain ecological preferences 
keep mosquitoes away from most humans, whereas other preferences bring 
them right into houses at night.
Some species of mosquitoes prefer to breed in phytotelmata (natural reservoirs on plants), such as rainwater accumulated in holes in tree trunks, or in the leaf-axils of bromeliads. Some specialize in the liquid in pitchers of particular species of pitcher plants, their larvae feeding on decaying insects that had drowned there or on the associated bacteria; the genus Wyeomyia provides such examples — the harmless Wyeomyia smithii breeds only in the pitchers of Sarracenia purpurea.
However, some of the species of mosquitoes that are adapted to 
breeding in phytotelmata are dangerous disease vectors. In nature, they 
might occupy anything from a hollow tree trunk to a cupped leaf. Such 
species typically take readily to breeding in artificial water 
containers. Such casual puddles are important breeding places for some 
of the most serious disease vectors, such as species of Aedes
 that transmit dengue and yellow fever. Some with such breeding habits 
are disproportionately important vectors because they are well-placed to
 pick up pathogens
 from humans and pass them on. In contrast, no matter how voracious, 
mosquitoes that breed and feed mainly in remote wetlands and salt 
marshes may well remain uninfected, and if they do happen to become 
infected with a relevant pathogen, might seldom encounter humans to 
infect, in turn.
Eggs and oviposition
Electron micrograph of a mosquito egg
Mosquito habits of oviposition, the ways in which they lay their eggs, vary considerably between species, and the morphologies of the eggs vary accordingly. The simplest procedure is that followed by many species of Anopheles; like many other gracile
 species of aquatic insects, females just fly over the water, bobbing up
 and down to the water surface and dropping eggs more or less singly. 
The bobbing behavior occurs among some other aquatic insects as well, 
for example mayflies and dragonflies; it is sometimes called "dapping". The eggs of Anopheles
 species are roughly cigar-shaped and have floats down their sides. 
Females of many common species can lay 100–200 eggs during the course of
 the adult phase of their life cycles. Even with high egg and 
intergenerational mortality, over a period of several weeks, a single 
successful breeding pair can create a population of thousands. 
An egg raft of a Culex species, partly broken, showing individual egg shapes
Some other species, for example members of the genus Mansonia, lay their eggs in arrays, attached usually to the under-surfaces of waterlily pads. Their close relatives, the genus Coquillettidia,
 lay their eggs similarly, but not attached to plants. Instead, the eggs
 form layers called "rafts" that float on the water. This is a common 
mode of oviposition, and most species of Culex are known for the habit, which also occurs in some other genera, such as Culiseta and Uranotaenia. Anopheles
 eggs may on occasion cluster together on the water, too, but the 
clusters do not generally look much like compactly glued rafts of eggs. 
In species that lay their eggs in rafts, rafts do not form adventitiously; the female Culex
 settles carefully on still water with its hind legs crossed, and as it 
lays the eggs one by one, it twitches to arrange them into a head-down 
array that sticks together to form the raft.
Aedes females generally drop their eggs singly, much as Anopheles
 do, but not as a rule into water. Instead, they lay their eggs on damp 
mud or other surfaces near the water's edge. Such an oviposition site 
commonly is the wall of a cavity such as a hollow stump or a container 
such as a bucket or a discarded vehicle tire. The eggs generally do not 
hatch until they are flooded, and they may have to withstand 
considerable desiccation before that happens. They are not resistant to 
desiccation straight after oviposition, but must develop to a suitable 
degree first. Once they have achieved that, however, they can enter 
diapause for several months if they dry out. Clutches of eggs of the 
majority of mosquito species hatch as soon as possible, and all the eggs
 in the clutch hatch at much the same time. In contrast, a batch of Aedes
 eggs in diapause tends to hatch irregularly over an extended period of 
time. This makes it much more difficult to control such species than 
those mosquitoes whose larvae can be killed all together as they hatch. 
Some Anopheles species do also behave in such a manner, though not to the same degree of sophistication.
Larva
Anatomy of a Culex larva
The mosquito larva has a well-developed head with mouth brushes used for feeding, a large thorax with no legs, and a segmented abdomen.
Larvae breathe through spiracles
 located on their eighth abdominal segments, or through a siphon, so 
must come to the surface frequently. The larvae spend most of their time
 feeding on algae, bacteria, and other microbes in the surface microlayer.
Mosquito larvae have been investigated as prey of other Dipteran flies. Species such as Bezzia nobilis within the family Ceratopogonidae have been observed in experiments to prey upon mosquito larvae.
They dive below the surface when disturbed. Larvae swim either through propulsion
 with their mouth brushes, or by jerky movements of their entire bodies,
 giving them the common name of "wigglers" or "wrigglers". 
Larvae develop through four stages, or instars, after which they metamorphose into pupae. At the end of each instar, the larvae molt, shedding their skins to allow for further growth.
- Anopheles larva from southern Germany, about 8 mm long
 
Pupa
As seen in its lateral aspect, the mosquito pupa is comma-shaped. The head and thorax are merged into a cephalothorax,
 with the abdomen curving around underneath. The pupa can swim actively 
by flipping its abdomen, and it is commonly called a "tumbler" because 
of its swimming action. As with the larva, the pupa of most species must
 come to the surface frequently to breathe, which they do through a pair
 of respiratory trumpets on their cephalothoraxes. However, pupae do not
 feed during this stage; typically they pass their time hanging from the
 surface of the water by their respiratory trumpets. If alarmed, say by a
 passing shadow, they nimbly swim downwards by flipping their abdomens 
in much the same way as the larvae do. If undisturbed, they soon float 
up again.
After a few days or longer, depending on the temperature and other circumstances, the dorsal
 surface of its cephalothorax splits, and the adult mosquito emerges. 
The pupa is less active than the larva because it does not feed, whereas
 the larva feeds constantly.
Adult
Anatomy of an adult mosquito
The period of development from egg to adult varies among species and 
is strongly influenced by ambient temperature. Some species of 
mosquitoes can develop from egg to adult in as few as five days, but a 
more typical period of development in tropical conditions would be some 
40 days or more for most species. The variation of the body size in 
adult mosquitoes depends on the density of the larval population and 
food supply within the breeding water. 
Adult mosquitoes usually mate within a few days after emerging from the pupal stage. In most species, the males form large swarms, usually around dusk, and the females fly into the swarms to mate. 
Males typically live for about 5–7 days, feeding on nectar and other sources of sugar.
 After obtaining a full blood meal, the female will rest for a few days 
while the blood is digested and eggs are developed. This process depends
 on the temperature, but usually takes two to three days in tropical 
conditions. Once the eggs are fully developed, the female lays them and 
resumes host-seeking.
The cycle repeats itself until the female dies. While females can
 live longer than a month in captivity, most do not live longer than one
 to two weeks in nature. Their lifespans depend on temperature, 
humidity, and their ability to successfully obtain a blood meal while 
avoiding host defenses and predators. 
The length of the adult is typically between 3 mm and 6 mm. The 
smallest known mosquitoes are around 2 mm (0.1 in), and the largest 
around 19 mm (0.7 in).
 Mosquitoes typically weigh around 5 mg. All mosquitoes have slender 
bodies with three segments: a head, a thorax and an abdomen. 
The head is specialized for receiving sensory information and for feeding. It has eyes and a pair of long, many-segmented antennae.
 The antennae are important for detecting host odors, as well as odors 
of breeding sites where females lay eggs. In all mosquito species, the 
antennae of the males in comparison to the females are noticeably 
bushier and contain auditory receptors to detect the characteristic 
whine of the females.
Adult yellow fever mosquito Aedes aegypti, typical of subfamily Culicinae. Note bushy antennae and longer palps of male on left vs. females at right.
The compound eyes
 are distinctly separated from one another. Their larvae only possess a 
pit-eye ocellus. The compound eyes of adults develop in a separate 
region of the head. New ommatidia
 are added in semicircular rows at the rear of the eye. During the first
 phase of growth, this leads to individual ommatidia being square, but 
later in development they become hexagonal. The hexagonal pattern will 
only become visible when the carapace of the stage with square eyes is 
molted.
The head also has an elongated, forward-projecting, stinger-like proboscis
 used for feeding, and two sensory palps. The maxillary palps of the 
males are longer than their proboscises, whereas the females’ maxillary 
palps are much shorter. In typical bloodsucking species, the female has 
an elongated proboscis.
The thorax is specialized for locomotion. Three pairs of legs and a pair of wings are attached to the thorax. The insect wing is an outgrowth of the exoskeleton. The Anopheles mosquito can fly for up to four hours continuously at 1 to 2 km/h (0.6–1 mph), traveling up to 12 km (7.5 mi) in a night. Males beat their wings between 450 and 600 times per second.
The abdomen is specialized for food digestion and egg 
development; the abdomen of a mosquito can hold three times its own 
weight in blood. This segment expands considerably when a female takes a blood meal. The blood is digested over time, serving as a source of protein for the production of eggs, which gradually fill the abdomen.
Feeding by adults
Typically, both male and female mosquitoes feed on nectar, aphid honeydew, and plant juices, but in many species the mouthparts of the females are adapted for piercing the skin of animal hosts and sucking their blood as ectoparasites.
 In many species, the female needs to obtain nutrients from a blood meal
 before it can produce eggs, whereas in many other species, obtaining 
nutrients from a blood meal only makes it so that the mosquito can lay 
more eggs. A mosquito has a variety of ways of finding nectar or its 
prey, including chemical, visual, and heat sensors.
 Both plant materials and blood are useful sources of energy in the form
 of sugars, and blood also supplies more concentrated nutrients, such as
 lipids, but the most important function of blood meals is to obtain proteins as materials for egg production.
Among humans, the feeding preferences of mosquitoes typically include: those with type O blood, heavy breathers, an abundance of skin bacteria, high body heat, and pregnant women. Individuals' attractiveness to mosquitoes also has a heritable, genetically-controlled component.
When a female reproduces without such parasitic meals, it is said to practice autogenous reproduction, as in Toxorhynchites; otherwise, the reproduction may be termed anautogenous, as occurs in mosquito species that serve as disease vectors, particularly Anopheles and some of the most important disease vectors in the genus Aedes. In contrast, some mosquitoes, for example, many Culex,
 are partially anautogenous: they do not need a blood meal for their 
first cycle of egg production, which they produce autogenously; however,
 subsequent clutches of eggs are produced anautogenously, at which point
 their disease vectoring activity becomes operative.
Here an Anopheles stephensi
 female is engorged with blood and beginning to pass unwanted liquid 
fractions of the blood to make room in its gut for more of the solid 
nutrients.
Female mosquitoes hunt their blood host by detecting organic substances such as carbon dioxide (CO2) and 1-octen-3-ol (mushroom alcohol,
 found in exhaled breath) produced from the host, and through visual 
recognition. Mosquitoes prefer some people over others. The preferred 
victim's sweat smells more attractive than others' because of the 
proportions of the carbon dioxide, octenol, and other compounds that make up body odor. The most powerful semiochemical that triggers the keen sense of smell of Culex quinquefasciatus is nonanal. Another compound identified in human blood that attracts mosquitoes is sulcatone or 6-methyl-5-hepten-2-one, especially for Aedes aegypti mosquitoes with the odor receptor gene Or4.
 A large part of the mosquito's sense of smell, or olfactory system, is 
devoted to sniffing out blood sources. Of 72 types of odor receptors on 
its antennae, at least 27 are tuned to detect chemicals found in 
perspiration. In Aedes,
 the search for a host takes place in two phases. First, the mosquito 
exhibits a nonspecific searching behavior until the perception of a 
host's stimulants, then it follows a targeted approach.
Most mosquito species are crepuscular (dawn or dusk)
 feeders. During the heat of the day, most mosquitoes rest in a cool 
place and wait for the evenings, although they may still bite if 
disturbed. Some species, such as the Asian tiger mosquito, are known to fly and feed during daytime.
Prior to and during blood feeding, blood-sucking mosquitoes inject saliva into the bodies of their source(s) of blood. This saliva serves as an anticoagulant;
 without it the female mosquito's proboscis might become clogged with 
blood clots. The saliva also is the main route by which mosquito physiology offers passenger pathogens access to the hosts' bloodstream. The salivary glands are a major target to most pathogens, whence they find their way into the host via the saliva.
A mosquito bite often leaves an itchy weal, a raised bump, on the victim's skin, which is caused by histamines trying to fight off the protein left by the attacking insect.
Mosquitoes of the genus Toxorhynchites never drink blood. This genus
 includes the largest extant mosquitoes, the larvae of which prey on the
 larvae of other mosquitoes. These mosquito eaters have been used in the
 past as mosquito control agents, with varying success.
Hosts of blood-feeding mosquito species
Video of Anopheline mosquito locating and feeding on a caterpillar
Mosquitoes feeding on a reptile
Many, if not all, blood-sucking species of mosquitoes are fairly 
selective feeders that specialise in particular host species, though 
they often relax their selectivity when they experience severe 
competition for food, defensive activity on the part of the hosts, or 
starvation. Some species feed selectively on monkeys, while others 
prefer particular kinds of birds, but they become less selective as 
conditions become more difficult. For example, Culiseta melanura sucks the blood of passerine birds for preference, and such birds are typically the main reservoir of the Eastern equine encephalitis virus
 in North America. Early in the season while mosquito numbers are low, 
they concentrate on passerine hosts, but as mosquito numbers rise and 
the birds are forced to defend themselves more vigorously, the 
mosquitoes become less selective of hosts. Soon the mosquitoes begin 
attacking mammals more readily, thereby becoming the major vector of the
 virus, and causing epidemics of the disease, most conspicuously in 
humans and horses.
Even more dramatically, in most of its range in North America, the main vector for the Western equine encephalitis virus is Culex tarsalis,
 because it is known to feed variously on mammals, birds, reptiles, and 
amphibians. Even fish may be attacked by some mosquito species if they 
expose themselves above water level, as mudskippers do.
Some species of blood-sucking flies, such as many of the Ceratopogonidae, will attack large, live insects and suck their haemolymph and others, such as the so-called "jackal flies" (Milichiidae), will attack the recently dead prey of say, crab spiders (Thomisidae). In 1969 it was reported that some species of anautogenous mosquitoes would feed on the haemolymph of caterpillars. Other observations include mosquitoes feeding on cicadas and mantids.
 In 2014, it was shown that malaria-transmitting mosquitoes actively 
seek out some species of caterpillars and feed on their haemolymph, and do so to the caterpillar's apparent physical detriment.
Mouthparts
Mosquito
 mouthparts are very specialized, particularly those of the females, 
which in most species are adapted to piercing skin and then sucking 
blood. Apart from bloodsucking, the females generally also drink 
assorted fluids rich in dissolved sugar, such as nectar and honeydew, to
 obtain the energy they need. For this, their blood-sucking mouthparts 
are perfectly adequate. In contrast, male mosquitoes are not 
bloodsuckers; they only drink sugary fluids. Accordingly, their 
mouthparts do not require the same degree of specialization as those of 
females.
Externally, the most obvious feeding structure of the mosquito is
 the proboscis. More specifically, the visible part of the proboscis is 
the labium,
 which forms the sheath enclosing the rest of the mouthparts. When the 
mosquito first lands on a potential host, its mouthparts are enclosed 
entirely in this sheath, and it will touch the tip of the labium to the 
skin in various places. Sometimes, it will begin to bite almost straight
 away, while other times, it will prod around, apparently looking for a 
suitable place. Occasionally, it will wander for a considerable time, 
and eventually fly away without biting. Presumably, this probing is a 
search for a place with easily accessible blood vessels, but the exact 
mechanism is not known. It is known that there are two taste receptors 
at the tip of the labium which may well play a role.
The female mosquito does not insert its labium into the skin; it 
bends back into a bow when the mosquito begins to bite. The tip of the 
labium remains in contact with the skin of the victim, acting as a guide
 for the other mouthparts. In total, there are six mouthparts besides 
the labium: two mandibles, two maxillae, the hypopharynx, and the labrum. 
The mandibles and the maxillae are used for piercing the skin. 
The mandibles are pointed, while the maxillae end in flat, toothed 
"blades". To force these into the skin, the mosquito moves its head 
backwards and forwards. On one movement, the maxillae are moved as far 
forward as possible. On the opposite movement, the mandibles are pushed 
deeper into the skin by levering against the maxillae. The maxillae do 
not slip back because the toothed blades grip the skin.
The hypopharynx and the labrum are both hollow. Saliva with 
anticoagulant is pumped down the hypopharynx to prevent clotting, and 
blood is drawn up the labrum.
To understand the mosquito mouthparts, it is helpful to draw a comparison with an insect that chews food, such as a dragonfly.
 A dragonfly has two mandibles, which are used for chewing, and two 
maxillae, which are used to hold the food in place as it is chewed. The 
labium forms the floor of the dragonfly's mouth, the labrum forms the 
top, while the hypopharynx is inside the mouth and is used in 
swallowing. Conceptually, then, the mosquito's proboscis is an 
adaptation of the mouthparts that occur in other insects. The labium 
still lies beneath the other mouthparts, but also enfolds them, and it 
has been extended into a proboscis. The maxillae still "grip" the "food"
 while the mandibles "bite" it. The top of the mouth, the labrum, has 
developed into a channeled blade the length of the proboscis, with a 
cross-section like an inverted "U". Finally, the hypopharynx has 
extended into a tube that can deliver saliva at the end of the 
proboscis. Its upper surface is somewhat flattened so, when the lower 
part of the hypopharynx is pressed against it, the labrum forms a closed
 tube for conveying blood from the victim.
Saliva
For the mosquito to obtain a blood meal, it must circumvent the vertebrate's physiological responses. The mosquito, as with all blood-feeding arthropods, has mechanisms to effectively block the hemostasis system with their saliva, which contains a mixture of secreted proteins. Mosquito saliva acts to reduce vascular constriction, blood clotting, platelet aggregation, angiogenesis and immunity, and creates inflammation.
 Universally, hematophagous arthropod saliva contains at least one 
anti-clotting, one anti-platelet, and one vasodilatory substance. 
Mosquito saliva also contains enzymes that aid in sugar feeding, and antimicrobial agents to control bacterial growth in the sugar meal. The composition of mosquito saliva is relatively simple, as it usually contains fewer than 20 dominant proteins. As of the early 2000s, scientists still were unable to ascribe functions to more than half of the molecules found in arthropod saliva.
 One promising application of components of mosquito saliva is the 
development of anti-clotting drugs, such as clotting inhibitors and 
capillary dilators, that could be useful for cardiovascular disease.
It is now well recognized that feeding ticks, sandflies, and, more recently, mosquitoes, have an ability to modulate the immune response of the animals (hosts) on which they feed.
 The presence of this activity in vector saliva is a reflection of the 
inherent overlapping and interconnected nature of the host hemostatic 
and inflammatory/immunological responses and the intrinsic need to 
prevent these host defenses from disrupting successful feeding. The 
mechanism for mosquito saliva-induced alteration of the host immune 
response is unclear, but the data have become increasingly convincing 
that such an effect occurs. Early work described a factor in saliva that
 directly suppresses TNF-α release, but not antigen-induced histamine secretion, from activated mast cells. Experiments by Cross et al. (1994) demonstrated that the inclusion of Ae. aegypti mosquito saliva into naïve cultures led to a suppression of interleukin (IL)-2 and IFN-γ production, while the cytokines IL-4 and IL-5 are unaffected. Cellular proliferation in response to IL-2 is clearly reduced by prior treatment of cells with mosquito salivary gland extract. Correspondingly, activated splenocytes isolated from mice fed upon by either Ae. aegypti or Cx. pipiens mosquitoes produce markedly higher levels of IL-4 and IL-10 concurrent with suppressed IFN-γ production.
 Unexpectedly, this shift in cytokine expression is observed in 
splenocytes up to 10 days after mosquito exposure, suggesting natural 
feeding of mosquitoes can have a profound, enduring, and systemic effect
 on the immune response.
T cell
 populations are decidedly susceptible to the suppressive effect of 
mosquito saliva, showing increased mortality and decreased division 
rates. Parallel work by Wasserman et al. (2004) demonstrated that T and B cell proliferation was inhibited in a dose dependent manner with concentrations as low as 1/7 of the saliva in a single mosquito.
 Depinay et al. (2005) observed a suppression of antibody-specific T 
cell responses mediated by mosquito saliva and dependent on mast cells 
and IL-10 expression.
A 2006 study suggests mosquito saliva can also decrease expression of interferon−α/β during early mosquito-borne virus infection. The contribution of type I interferons (IFN) in recovery from infection with viruses has been demonstrated in vivo by the therapeutic and prophylactic effects of administration of IFN inducers or IFN itself, and different research suggests mosquito saliva exacerbates West Nile virus infection, as well as other mosquito-transmitted viruses.
Studies in humanized mice
 bearing a reconstituted human immune system have suggested potential 
impact of mosquito saliva in humans. Work published in 2018 from the Baylor College of Medicine using such humanized mice came to several conclusions, among them being that mosquito saliva led to an increase in natural killer T cells in peripheral blood; to an overall decrease in ex vivo cytokine production by peripheral blood mononuclear cells
 (PBMCs); changes to proportions of subsets of PBMCs; changes in the 
prevalence of T cell subtypes across organs; and changes to circulating 
levels of cytokines.
Egg development and blood digestion
Most
 species of mosquito require a blood meal to begin the process of egg 
development. Females with poor larval nutrition may need to ingest sugar
 or a preliminary blood meal bring ovarian follicles to their resting 
stage. Once the follicles have reached the resting stage, digestion of a
 sufficiently large blood meal triggers a hormonal cascade that leads to
 egg development. Upon completion of feeding, the mosquito withdraws her proboscis, and as the gut fills up, the stomach lining secretes a peritrophic membrane
 that surrounds the blood. This membrane keeps the blood separate from 
anything else in the stomach. However, like certain other insects that 
survive on dilute, purely liquid diets, notably many of the Hemiptera, many adult mosquitoes must excrete unwanted aqueous fractions even as they feed. (See the photograph of a feeding Anopheles stephensi:
 Note that the excreted droplet patently is not whole blood, being far 
more dilute). As long as they are not disturbed, this permits mosquitoes
 to continue feeding until they have accumulated a full meal of nutrient
 solids. As a result, a mosquito replete with blood can continue to 
absorb sugar, even as the blood meal is slowly digested over a period of
 several days.
 Once blood is in the stomach, the midgut of the female synthesizes 
proteolytic enzymes that hydrolyze the blood proteins into free amino 
acids. These are used as building blocks for the synthesis of vitellogenin, which are the precursors for egg yolk protein.
In the mosquito Anopheles stephensi,
 trypsin activity is restricted entirely to the posterior midgut lumen. 
No trypsin activity occurs before the blood meal, but activity increases
 continuously up to 30 hours after feeding, and subsequently returns to 
baseline levels by 60 hours. Aminopeptidase is active in the anterior 
and posterior midgut regions before and after feeding. In the whole 
midgut, activity rises from a baseline of approximately three enzyme 
units (EU) per midgut to a maximum of 12 EU at 30 hours after the blood 
meal, subsequently falling to baseline levels by 60 hours. A similar 
cycle of activity occurs in the posterior midgut and posterior midgut 
lumen, whereas aminopeptidase in the posterior midgut epithelium 
decreases in activity during digestion. Aminopeptidase in the anterior 
midgut is maintained at a constant, low level, showing no significant 
variation with time after feeding. Alpha-glucosidase is active in 
anterior and posterior midguts before and at all times after feeding. In
 whole midgut homogenates, alpha-glucosidase activity increases slowly 
up to 18 hours after the blood meal, then rises rapidly to a maximum at 
30 hours after the blood meal, whereas the subsequent decline in 
activity is less predictable. All posterior midgut activity is 
restricted to the posterior midgut lumen. Depending on the time after 
feeding, greater than 25% of the total midgut activity of 
alpha-glucosidase is located in the anterior midgut. After blood meal 
ingestion, proteases are active only in the posterior midgut. Trypsin is
 the major primary hydrolytic protease and is secreted into the 
posterior midgut lumen without activation in the posterior midgut 
epithelium. Aminopeptidase activity is also luminal in the posterior 
midgut, but cellular aminopeptidases are required for peptide processing
 in both anterior and posterior midguts. Alpha-glucosidase activity is 
elevated in the posterior midgut after feeding in response to the blood 
meal, whereas activity in the anterior midgut is consistent with a 
nectar-processing role for this midgut region.
Ecology
Female Ochlerotatus notoscriptus feeding on a human arm, Tasmania, Australia
Distribution
Mosquitoes are cosmopolitan (world-wide): they are in every land region except Antarctica and a few islands with polar or subpolar climates. Iceland is such an island, being essentially free of mosquitoes.
The absence of mosquitoes from Iceland and similar regions is 
probably because of quirks of their climate, which differs in some 
respects from mainland regions. At the start of the uninterrupted continental
 winter of Greenland and the northern regions of Eurasia and America, 
the pupa enters diapause under the ice that covers sufficiently deep 
water. The imago emerges
 only after the ice breaks in late spring. In Iceland however, the 
weather is less predictable. In mid-winter it frequently warms up 
suddenly, causing the ice to break, but then to freeze again after a few
 days. By that time the mosquitoes will have emerged from their pupae, 
but the new freeze sets in before they can complete their life cycle. 
Any anautogenous
 adult mosquito would need a host to supply a blood meal before it could
 lay viable eggs; it would need time to mate, mature the eggs and 
oviposit in suitable wetlands. These requirements would not be realistic
 in Iceland and in fact the absence of mosquitoes from such subpolar 
islands is in line with the islands' low biodiversity; Iceland has fewer
 than 1,500 described species of insects, many of them probably 
accidentally introduced by human agency. In Iceland most ectoparasitic 
insects live in sheltered conditions or actually on mammals; examples 
include lice, fleas and bedbugs, in whose living conditions freezing is 
no concern, and most of which were introduced inadvertently by humans.
Some other aquatic Diptera, such as Simuliidae,
 do survive in Iceland, but their habits and adaptations differ from 
those of mosquitoes; Simuliidae for example, though they, like 
mosquitoes, are bloodsuckers, generally inhabit stones under running 
water that does not readily freeze and which is totally unsuited to 
mosquitoes; mosquitoes are generally not adapted to running water.
Eggs of species of mosquitoes from the temperate zones are more tolerant of cold than the eggs of species indigenous to warmer regions.
 Many even tolerate subzero temperatures. In addition, adults of some 
species can survive the winter by taking shelter in suitable 
microhabitats such as buildings or hollow trees.
Pollination
Several flowers are pollinated by mosquitoes, including some members of the Asteraceae, Roseaceae and Orchidaceae.
Activity
In 
warm and humid tropical regions, some mosquito species are active for 
the entire year, but in temperate and cold regions they hibernate or 
enter diapause. Arctic or subarctic mosquitoes, like some other arctic midges in families such as Simuliidae and Ceratopogonidae
 may be active for only a few weeks annually as melt-water pools form on
 the permafrost. During that time, though, they emerge in huge numbers 
in some regions and may take up to 300 ml of blood per day from each 
animal in a caribou herd.
Means of dispersal
Worldwide
 introduction of various mosquito species over large distances into 
regions where they are not indigenous has occurred through human 
agencies, primarily on sea routes, in which the eggs, larvae, and pupae 
inhabiting water-filled used tires and cut flowers
 are transported. However, apart from sea transport, mosquitoes have 
been effectively carried by personal vehicles, delivery trucks, trains, 
and aircraft. Man-made areas such as storm water retention basins,
 or storm drains also provide sprawling sanctuaries. Sufficient 
quarantine measures have proven difficult to implement. In addition, 
outdoor pool areas make a perfect place for them to grow.
Climate and global distribution
Seasonality
In order for a mosquito to transmit a disease to the host there must be favorable conditions, referred to as transmission seasonality.
 Seasonal factors that impact the prevalence of mosquitos and 
mosquito-borne diseases are primarily humidity, temperature, and 
precipitation. A positive correlation between malaria outbreaks and these climatic variables has been demonstrated in China; and El Niño has been shown to impact the location and number of outbreaks of mosquito-borne diseases observed in East Africa, Latin America, Southeast Asia and India. Climate change impacts each of these seasonal factors and in turn impacts the dispersal of mosquitos.
Past and future patterns
Climatology
 and the study of mosquito-borne disease have been developed only over 
the past 100 years; however historical records of weather patterns and 
distinct symptoms associated with mosquito-borne diseases can be 
utilized to trace the prevalence of these diseases in relation to the 
climate over longer time periods.
 Further, statistical models are being created to predict the impact of 
climate change on vector-borne diseases using these past records, and 
these models can be utilized in the field of public health in order to create interventions to reduce the impact of these predicted outcomes.
Two types of models are used to predict mosquito-borne disease spread in relation to climate: correlative models and mechanistic models. Correlative models
 focus primarily on vector distribution, and generally function in 3 
steps. First, data is collected regarding geographical location of a 
target mosquito species. Next, a multivariate regression model 
establishes the conditions under which the target species can survive. 
Finally, the model determines the likelihood of the mosquito species to 
become established in a new location based on similar living conditions.
 The model can further predict future distributions based on 
environmental emissions data. Mechanistic models tend to be broader and include the pathogens and hosts
 in the analysis. These models have been used to recreate past outbreaks
 as well as predict the potential risk of a vector-borne disease based 
on an areas forecasted climate.
Mosquito-borne diseases are currently most prevalent in East Africa, Latin America, Southeast Asia, and India;
 however, emergence of vector-borne diseases in Europe have recently 
been observed. A weighted risk analysis demonstrated associations to 
climate for 49% of infectious diseases in Europe including all 
transmission routes. One statistical model predicts by 2030, the climate
 of southern Great Britain will be climatically-suitable for malaria transmission Plasmodium vivax malaria for 2 months of the year. By 2080 it is predicted that the same will be true for southern Scotland.
Vectors of disease
Anopheles albimanus mosquito feeding on a human arm – this mosquito is a vector of malaria, and mosquito control is a very effective way of reducing the incidence of malaria.
Mosquitoes can act as vectors for many disease-causing viruses and parasites. Infected mosquitoes carry these organisms from person to person without exhibiting symptoms themselves. Mosquito-borne diseases include:
- Viral diseases, such as yellow fever, dengue fever, and chikungunya, transmitted mostly by Aedes aegypti. Dengue fever is the most common cause of fever in travelers returning from the Caribbean, Central America, South America, and South Central Asia. This disease is spread through the bites of infected mosquitoes and cannot be spread person to person. Severe dengue can be fatal, but with good treatment, fewer than 1% of patients die from dengue. Work published in 2012 from Baylor College of Medicine suggested that for some diseases, such as dengue fever, which can be transmitted via mosquitoes and by other means, the severity of the mosquito-transmitted disease could be greater.
 - The parasitic diseases collectively called malaria, caused by various species of Plasmodium, carried by female mosquitoes of the genus Anopheles
 - Lymphatic filariasis (the main cause of elephantiasis) which can be spread by a wide variety of mosquito species
 - West Nile virus is a concern in the United States, but there are no reliable statistics on worldwide cases.
 - Equine encephalitis viruses, such as Eastern equine encephalitis virus, Western equine encephalitis virus, and Venezuelan equine encephalitis virus, can be spread by mosquito vectors such as Aedes taeniorhynchus.
 - Tularemia, a bacterial disease caused by Francisella tularensis, is variously transmitted, including by biting flies. Culex and Culiseta are vectors of tularemia, as well as arbovirus infections such as West Nile virus.
 - Zika, recently notorious, though rarely deadly. It causes fever, joint pain, rashes and conjunctivitis. The most serious consequence appears when the infected person is a pregnant woman, since during pregnancy this virus can originate a birth defect called microcephaly.
 - St. Louis Encephalitis, a mosquito-borne disease that is characterized by fever and headaches upon initial onset of infection, arises from mosquitos who feed on birds who are infected with the illness, and can result in death if fatal. The most common vector of this disease is Culex pipiens, also known as the common house mosquito.
 
Potential transmission of HIV
 was originally a public health concern, but practical considerations 
and detailed studies of epidemiological patterns suggest that any 
transmission of the HIV virus by mosquitoes is at worst extremely 
unlikely.
Various species of mosquitoes are estimated to transmit various 
types of disease to more than 700 million people annually in Africa, 
South America, Central America, Mexico, Russia, and much of Asia, with 
millions of resultant deaths. At least two million people annually die 
of these diseases, and the morbidity rates are many times higher still.
Methods used to prevent the spread of disease, or to protect individuals in areas where disease is endemic, include:
- Vector control aimed at mosquito control or eradication
 - Disease prevention, using prophylactic drugs and developing vaccines
 - Prevention of mosquito bites, with insecticides, nets, and repellents
 
Since most such diseases are carried by "elderly" female mosquitoes, 
some scientists have suggested focusing on these to avoid the evolution 
of resistance.
Control
Mosquitofish Gambusia affinis, a natural mosquito predator
Many measures have been tried for mosquito control, including the elimination of breeding places, exclusion via window screens and mosquito nets, biological control with parasites such as fungi and nematodes, or predators such as fish, copepods, dragonfly nymphs and adults, and some species of lizard and gecko. Another approach is to introduce large numbers of sterile males.
 Genetic methods including cytoplasmic incompatibility, chromosomal 
translocations, sex distortion and gene replacement have been explored. 
They are cheaper and not subject to vector resistance.
According to an article in Nature discussing the idea of 
totally eradicating mosquitoes, "Ultimately, there seem to be few things
 that mosquitoes do that other organisms can’t do just as well — except 
perhaps for one. They are lethally efficient at sucking blood from one 
individual and mainlining it into another, providing an ideal route for 
the spread of pathogenic microbes." The control of disease-carrying mosquitoes may in the future be possible using gene drives.
Repellents
Insect repellents are applied on skin and give short-term protection against mosquito bites. The chemical DEET repels some mosquitoes and other insects. Some CDC-recommended repellents are picaridin, eucalyptus oil (PMD) and ethyl butylacetylaminopropionate (IR3535). Others are indalone, dimethyl phthalate, dimethyl carbate, and ethyl hexanediol. 
There are also electronic insect repellent devices which produce ultrasounds
 that were developed to keep away insects (and mosquitoes). However, no 
scientific research based on the EPA's as well as the many universities'
 studies has ever provided evidence that these devices prevent a human 
from being bitten by a mosquito.
Bites
Video of a mosquito biting on leg
Mosquito bites lead to a variety of mild, serious, and, rarely, life-threatening allergic reactions. These include ordinary wheal and flare reactions and mosquito bite allergies
 (MBA). The MBA, also termed hypersensitivity to mosquito bites (HMB), 
are excessive reactions to mosquito bites that are not caused by any toxin or pathogen in the saliva injected by a mosquito at the time it takes its blood-meal. Rather, they are allergic hypersensitivity reactions caused by the non-toxic allergenic proteins contained in the mosquito's saliva. Studies have shown or suggest that numerous species of mosquitoes can trigger ordinary reactions as well as MBA. These include Aedes aegypti, Aedes vexans, Aedes albopictus, Anopheles sinensis, Culex pipiens, Aedes communis, Anopheles stephensi, Culex quinquefasciatus, Ochlerotatus triseriatus, and Culex tritaeniorhynchus.
 Furthermore, there is considerable cross-reactivity between the 
salivary proteins of mosquitoes in the same family and, to a lesser 
extent, different families. It is therefore assumed that these allergic 
responses may be caused by virtually any mosquito species (or other 
biting insect).
The mosquito bite allergies are informally classified as 1) the Skeeter syndrome, i.e. severe local skin reactions sometimes associated with low-grade fever; 2) systemic reactions that range from high-grade fever, lymphadenopathy, abdominal pain, and/or diarrhea to, very rarely, life-threatening symptoms of anaphylaxis; and 3) severe and often systemic reactions occurring in individuals that have an Epstein-Barr virus-associated lymphoproliferative disease, Epstein-Barr virus-negative lymphoid malignancy, or another predisposing condition such as Eosinophilic cellulitis or chronic lymphocytic leukemia.
Mechanism
Visible, irritating bites are due to an immune response from the binding of IgG and IgE antibodies to antigens in the mosquito's saliva.
 Some of the sensitizing antigens are common to all mosquito species, 
whereas others are specific to certain species. There are both immediate
 hypersensitivity reactions (types I and III) and delayed hypersensitivity reactions (type IV) to mosquito bites.
 Both reactions result in itching, redness and swelling. Immediate 
reactions develop within a few minutes of the bite and last for a few 
hours. Delayed reactions take around a day to develop, and last for up 
to a week.
Treatment
Several anti-itch medications are commercially available, including those taken orally, such as diphenhydramine, or topically applied antihistamines and, for more severe cases, corticosteroids, such as hydrocortisone and triamcinolone. A common topical remedy in camping gear is aqueous ammonia. 
Both topical heat and cool may be useful to treat mosquito bites.
In human culture
Greek mythology
Ancient Greek
 beast fables including "The Elephant and the Mosquito" and "The Bull 
and the Mosquito", with the general moral that the large beast does not 
even notice the small one, derive ultimately from Mesopotamia.
Origin myths
The peoples of Siberia have origin myths surrounding the mosquito - one Ostiak myth tells of a man eating giant, Punegusse,
 who is killed by a hero but will not stay dead, the hero eventually 
burns the giant, but the ashes of the fire become mosquitos that 
continue to plague mankind.
Other myths from the Yakuts, Goldes (Nanai people), and Samoyed
 have the insect arising from the ashes or fragments of some giant 
creature or demon. Similar tales are found in North American Indian 
myth, with the mosquito arising from the ashes of a man-eater - 
suggesting a common origin. The Tatars of the Altai had a similar myth, thought to be of Indian origin, involving the fragments of the dead giant Andalma-Muus, becoming mosquitos and other insects.
Modern era
Winsor McCay's 1912 film How a Mosquito Operates
 was one of the earliest works of animation, far ahead of its time in 
technical quality. It depicts a giant mosquito tormenting a sleeping 
man.
The de Havilland Mosquito was a high-speed aircraft manufactured between 1940 and 1950, and used in many roles.