Arbovirus
Arbovirus is an informal name for any virus that is transmitted by arthropod vectors. The term arbovirus is a portmanteau word. Tibovirus is sometimes used to more specifically describe viruses transmitted by ticks, a superorder within the arthropods. Arboviruses can affect both animals and plants. In humans, symptoms of arbovirus infection usually occur 3–15 days after exposure to the virus and last three or four days. The most common clinical features of infection are fever, headache, and malaise, but other features of viral hemorrhagic fever syndrome and encephalitis may also occur.
Signs and symptoms
The incubation period – the time between when infection occurs and when symptoms appear – varies from virus to virus, but is usually limited between 2 and 15 days for arboviruses. The majority of infections, however, are asymptomatic. Among cases in which symptoms do appear, symptoms tend to be non-specific, resembling a flu-like illness, and are not indicative of a specific causative agent. These symptoms include fever, headache, malaise, rash and fatigue. Rarely, vomiting and hemorrhagic fever may occur. The central nervous system can also be affected by infection, as encephalitis and meningitis are sometimes observed. Prognosis is good for most people, but is poor in those who develop severe symptoms, with up to a 20% mortality rate in this population depending on the virus. The very young, elderly, pregnant women, and people with immune deficiencies are more likely to develop severe symptoms.| Arbovirus | Disease | Incubation period | Symptoms | Duration of symptoms | Complications | Case fatality rate | Vector | Primary host | Geographic distribution | Does infection provide lifelong immunity? |
| Dengue virus | Dengue fever | 3–14 days | Asymptomatic in most cases; fever, headache, rash, muscle, and joint pains | 7–10 days | Shock, internal bleeding, and organ damage | <1% with treatment, 1–5% without; about 25% in severe cases | Aedes mosquitoes, especially Aedes aegypti | Humans | Near the equator globally | Varies |
| Japanese encephalitis virus | Japanese encephalitis | 5–15 days | Asymptomatic in most cases; fever, headache, fatigue, nausea, and vomiting | Encephalitis, seizures, paralysis, coma, and long-term brain damage | 20–30% in encephalitis cases | Culex mosquitoes, especially Culex tritaeniorhynchus | Domestic pigs and wading birds | Southeast and East Asia | Yes | |
| Rift Valley fever virus | Rift Valley fever | 2–6 days | Fever, headache, myalgia and liver abnormalities | 4–7 days | Hemorrhagic fever, meningoencephalitis | 1% in humans; in pregnant livestock, 100% fatality rate for fetuses | Culex tritaeniorhynchus and Aedes vexans | Micropteropus pusillus and Hipposideros abae | Eastern, Southern, and Western Africa | Yes |
| Tick-borne encephalitis virus | Tick-borne encephalitis | 7–14 days | Fever, headache, muscle pain, nausea, vomiting, meningitis, and encephalitis | Paralysis and long-term brain damage | 1–2% | Ixodes scapularis, Ixodes ricinus, and Ixodes persulcatus | Small rodents | Eastern Europe and Southern Russia | Yes | |
| West Nile virus | West Nile fever, encephalitis | 2–15 days | Asymptomatic in most cases; fever, headache, fatigue, nausea, vomiting, rash | 3–6 days | Swollen lymph nodes, meningitis, encephalitis, acute flaccid paralysis | 3–15% in severe cases | Culex mosquitoes | Passerine birds | North America, Europe, West and Central Asia, Oceania, and Africa | Yes |
| Yellow fever virus | Yellow fever | 3–6 days | Fever, headache, back pain, loss of appetite, nausea, and vomiting | 3–4 days | Jaundice, liver damage, gastrointestinal bleeding, recurring fever | 3% in general; 20% in cases with severe complications | Aedes mosquitoes, especially Aedes aegypti | Primates | Tropical and subtropical regions of South America and Africa | Yes |
| Zika virus | Zika fever | 3–14 days | Fever, rash, joint pain, nausea and vomiting | 2–7 days | Neurological complications | <1% | Aedes mosquitoes | Primates | Africa, the Americas, Asia and the Pacific | Yes |
Cause
Transmission
Arboviruses maintain themselves in nature by going through a cycle between a host, an organism that carries the virus, and a vector, an organism that carries and transmits the virus to other organisms. For arboviruses, vectors are commonly mosquitoes, ticks, sandflies and other arthropods that consume the blood of vertebrates for nutritious or developmental purposes. Vertebrates which have their blood consumed act as the hosts, with each vector generally having an affinity for the blood of specific species, making those species the hosts.Transmission between the vector and the host occurs when the vector feeds on the blood of the vertebrate, wherein the virus that has established an infection in the salivary glands of the vector comes into contact with the host's blood. While the virus is inside the host, it undergoes a process called amplification, where the virus replicates at sufficient levels to induce viremia, a condition in which there are large numbers of virions present in the blood. The abundance of virions in the host's blood allows the host to transmit the virus to other organisms if its blood is consumed by them. When uninfected vectors become infected from feeding, they are then capable of transmitting the virus to uninfected hosts, resuming amplification of virus populations. If viremia is not achieved in a vertebrate, the species can be called a "dead-end host", as the virus cannot be transmitted back to the vector.
An example of this vector-host relationship can be observed in the transmission of the West Nile virus. Female mosquitoes of the genus Culex prefer to consume the blood of passerine birds, making them the hosts of the virus. When these birds are infected, the virus amplifies, potentially infecting multiple mosquitoes that feed on its blood. These infected mosquitoes may go on to further transmit the virus to more birds. If the mosquito is unable to find its preferred food source, it will choose another. Human blood is sometimes consumed, but since the West Nile virus does not replicate that well in mammals, humans are considered a dead-end host.
In humans
Person-to-person transmission of arboviruses is not common, but can occur. Blood transfusions, organ transplantation, and the use of blood products can transmit arboviruses if the virus is present in the donor's blood or organs. Because of this, blood and organs are often screened for viruses before being administered. Rarely, vertical transmission, or mother-to-child transmission, has been observed in infected pregnant and breastfeeding women. Exposure to used needles may also transmit arboviruses if they have been used by an infected person or animal. This puts intravenous drug users and healthcare workers at risk for infection in regions where the arbovirus may be spreading in human populations.Virology
Arboviruses are a polyphyletic group, belonging to various viral genera and therefore exhibiting different virologic characteristics.| Arbovirus | Genome type | Genome length | Diameter | Capsid shape | Enveloped? | Viral entry | Replication site | Viral shedding | Infected cell | Genetic variability |
| African swine fever virus | dsDNA | 170-190 kilobases | ~200 nm | Icosahedral | Yes | Endocytosis | Nucleus | Budding | Endothelial cells and red and white blood cells | 22 genotypes |
| Chikungunya virus | +ssRNA | 11.6 kilobases | 60 - 70 nm | Icosahedral | Yes | Membrane fusion | Cell cytoplasm | Budding | Epithelial cells, endothelial cells, primary fibroblasts and macrophages | Three genotypes |
| Dengue virus | +ssRNA | ~11,000 nucleobases | ~50 nm | Icosahedral | Yes | Membrane fusion | Cell cytoplasm | Budding | Langerhans and white blood cells | Four serotypes |
| Japanese encephalitis virus | +ssRNA | ~11,000 nucleobases | ~50 nm | Icosahedral | Yes | Membrane fusion | Cell cytoplasm | Budding | Five genotypes | |
| Rift Valley fever virus | -ssRNA | Spherical | Yes | Cell cytoplasm | Budding | - | ||||
| Tick-borne encephalitis virus | +ssRNA | ~11,000 nucleobases | 40-50 nm | Icosahedral | Yes | Membrane fusion | Cell cytoplasm | Budding | Neural cells | Five genotypes |
| West Nile virus | +ssRNA | ~11,000 nucleobases | 45-50 nm | Icosahedral | Yes | Membrane fusion | Cell cytoplasm | Budding | ||
| Yellow fever virus | +ssRNA | ~11,000 nucleobases | 40-60 nm | Icosahedral | Yes | Membrane fusion | Cell cytoplasm | Budding | Hepatocytes and white blood cells | |
| Zika virus | +ssRNA | 10794 nucleobases | 40 nm | Icosahedral | Yes | Membrane fusion | Cell cytoplasm | Budding |