Yellow fever
Yellow fever | |
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Other names | Yellow jack, yellow plague,[1]bronze john[2] |
ATEMmicrographofyellow fever virus(234,000× magnification) | |
Specialty | Infectious disease |
Symptoms | Fever,chills,muscle pain,headache,yellow skin[3] |
Complications | Liver failure,bleeding[3] |
Usual onset | 3–6 days post exposure[3] |
Duration | 3–4 days[3] |
Causes | Yellow fever virusspread bymosquitoes[3] |
Diagnostic method | Blood test[4] |
Prevention | Yellow fever vaccine[3] |
Treatment | Supportive care[3] |
Frequency | ~130,000 severe cases in Africa alone (2013)[3][5] |
Deaths | ~78,000 in Africa alone (2013)[3][5] |
Yellow feveris aviraldiseaseof typicallyshort duration.[3]In most cases, symptoms includefever,chills,loss of appetite,nausea,muscle pains—particularly in the back—andheadaches.[3]Symptoms typically improve within five days.[3]In about 15% of people, within a day of improving the fever comes back, abdominal pain occurs, andliverdamage begins causingyellow skin.[3][6]If this occurs, the risk of bleeding andkidney problemsis increased.[3][7]
The disease is caused by theyellow fever virusand is spread by the bite of an infectedmosquito.[3][8]It infects humans, otherprimates,[9]and several types of mosquitoes.[3]In cities, it is spread primarily byAedes aegypti,a type of mosquito found throughout thetropicsandsubtropics.[3]The virus is anRNA virusof the genusFlavivirus.[10][11]The disease may be difficult to tell apart from other illnesses, especially in the early stages.[3]To confirm a suspected case, blood-sample testing with apolymerase chain reactionis required.[4]
A safe and effectivevaccine against yellow feverexists, and some countries require vaccinations for travelers.[3]Other efforts to prevent infection include reducing the population of the transmitting mosquitoes.[3]In areas where yellow fever is common, early diagnosis of cases and immunization of large parts of the population are important to preventoutbreaks.[3]Once a person is infected, management is symptomatic; no specific measures are effective against the virus.[3]Death occurs in up to half of those who get severe disease.[3][12]
In 2013, yellow fever was estimated to have caused 130,000 severe infections and 78,000 deaths in Africa.[3][5]Approximately 90 percent of an estimated 200,000 cases of yellow fever per year occur in Africa.[13]Nearly a billion people live in an area of the world where the disease is common.[3]It is common in tropical areas of the continents of South America and Africa,[14]but not in Asia.[3][15]Since the 1980s, the number of cases of yellow fever has been increasing.[3][16]This is believed to be due to fewer people being immune, more people living in cities, people moving frequently, andchanging climateincreasing the habitat for mosquitoes.[3]
The disease originated in Africa and spread to the Americas starting in the 17th century with the European trafficking ofenslaved Africansfrom sub-Saharan Africa.[1][17]Since the 17th century, several majoroutbreaksof the disease have occurred in the Americas, Africa, and Europe.[1]In the 18th and 19th centuries, yellow fever was considered one of the most dangerousinfectious diseases;numerous epidemics swept through major cities of the US and in other parts of the world.[1]
In 1927, yellow fever virus became the first human virus to be isolated.[10][18]
Signs and symptoms
[edit]Yellow fever begins after an incubation period of three to six days.[19]Most cases cause only mild infection with fever, headache, chills, back pain, fatigue, loss of appetite, muscle pain, nausea, and vomiting.[20]In these cases, the infection lasts only three to six days.[21]
But in 15% of cases, people enter a second, toxic phase of the disease characterized by recurring fever, this time accompanied byjaundicedue toliver damage,as well asabdominal pain.[22]Bleeding in the mouth, nose, eyes, and thegastrointestinal tractcausevomit containing blood,hence one of the names in Spanish for yellow fever,vómito negro( "black vomit" ).[23]There may also be kidney failure, hiccups, and delirium.[24][25]
Among those who develop jaundice, the fatality rate is 20 to 50%, while the overallfatality rateis about 3 to 7.5%.[26]Severe cases may have a mortality rate greater than 50%.[27]
Surviving the infection provides lifelongimmunity,[28]and normally results in no permanent organ damage.[29][30]
Complication
[edit]Yellow fever can lead to death for 20% to 50% of those who develop severe disease. Jaundice, fatigue, heart rhythm problems, seizures and internal bleeding may also appear as complications of yellow fever during recovery time.[8][31]
Cause
[edit]Yellow fever virus | |
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Flavivirus structure and genome | |
Virus classification | |
(unranked): | Virus |
Realm: | Riboviria |
Kingdom: | Orthornavirae |
Phylum: | Kitrinoviricota |
Class: | Flasuviricetes |
Order: | Amarillovirales |
Family: | Flaviviridae |
Genus: | Flavivirus |
Species: | Yellow fever virus
|
Yellow fever is caused byyellow fever virus(YFV), an envelopedRNA virus40–50nmin width, the type species and namesake of the familyFlaviviridae.[10]It was the first illness shown to be transmissible by filtered human serum and transmitted by mosquitoes, by American doctorWalter Reedaround 1900.[32]The positive-sense,single-strandedRNAis around 10,862nucleotideslong and has a singleopen reading frameencoding apolyprotein.[33]Hostproteasescut this polyprotein into three structural (C, prM, E) and seven nonstructural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, NS5); the enumeration corresponds to the arrangement of the protein codinggenesin thegenome.[34]Minimal YFV 3′UTR region is required for stalling of the host 5′-3′exonuclease XRN1.[35]The UTR contains PKS3 pseudoknot structure, which serves as a molecular signal to stall the exonuclease and is the only viral requirement for subgenomic flavivirus RNA (sfRNA) production.[36]The sfRNAs are a result of incomplete degradation of the viral genome by the exonuclease and are important for viral pathogenicity.[37]Yellow fever belongs to the group ofhemorrhagic fevers.[38]
The viruses infect, amongst others,monocytes,macrophages,Schwann cells,anddendritic cells.They attach to the cell surfaces via specificreceptorsand are taken up by an endosomalvesicle.[39]Inside theendosome,the decreased pH induces the fusion of the endosomal membrane with thevirus envelope.[40]Thecapsidenters thecytosol,decays, and releases the genome.[41]Receptor binding, as well as membrane fusion, arecatalyzedby the protein E, which changes its conformation at low pH, causing a rearrangement of the 90 homodimersto 60 homotrimers.[34][42]
After entering the host cell, the viral genome is replicated in the roughendoplasmic reticulum(ER) and in the so-called vesicle packets.[43]At first, an immature form of the virus particle is produced inside the ER, whose M-protein is not yet cleaved to its mature form, so is denoted as precursor M (prM) and forms a complex with protein E.[44]The immature particles are processed in theGolgi apparatusby the host proteinfurin,which cleaves prM to M.[45]This releases E from the complex, which can now take its place in the mature, infectiousvirion.[34]
Transmission
[edit]Yellow fever virus is mainly transmitted through the bite of the yellow fever mosquitoAedes aegypti,but other mostlyAedesmosquitoes such as the tiger mosquito (Aedes albopictus) can also serve as avectorfor this virus.[46]Like otherarboviruses,which are transmitted by mosquitoes,yellow fever virusis taken up by a female mosquito when it ingests the blood of an infected human or another primate.[47]Viruses reach the stomach of the mosquito, and if the virus concentration is high enough, the virions can infectepithelial cellsand replicate there. From there, they reach thehaemocoel(the blood system of mosquitoes) and from there thesalivary glands.[48]When the mosquito next sucks blood, it injects its saliva into the wound, and the virus reaches the bloodstream of the bitten person.[49]Transovarial transmissionial andtransstadial transmissionof yellow fever virus withinA. aegypti,that is, the transmission from a female mosquito to its eggs and then larvae, are indicated.[50]This infection of vectors without a previous blood meal seems to play a role in single, sudden breakouts of the disease.[51]
Three epidemiologically different infectious cycles occur[16]in which the virus is transmitted from mosquitoes to humans or other primates.[52]In the "urban cycle", only the yellow fever mosquitoA. aegyptiis involved. It is well adapted to urban areas, and can also transmit other diseases, includingZika fever,dengue fever,andchikungunya.[53]The urban cycle is responsible for the major outbreaks of yellow fever that occur in Africa. Except for an outbreak in Bolivia in 1999, this urban cycle no longer exists in South America.[54]
Besides the urban cycle, both in Africa and South America, asylvatic cycle(forest or jungle cycle) is present, whereAedes africanus(in Africa) or mosquitoes of the genusHaemagogusandSabethes(in South America) serve as vectors.[55]In the jungle, the mosquitoes infect mainly nonhuman primates; the disease is mostly asymptomatic in African primates.[49]In South America, the sylvatic cycle is currently the only way unvaccinated humans can become infected, which explains the low incidence of yellow fever cases on the continent.[46]People who become infected in the jungle can carry the virus to urban areas, whereA. aegyptiacts as a vector. Because of this sylvatic cycle, yellow fever cannot be eradicated except by eradicating the mosquitoes that serve as vectors.[16]
In Africa, a third infectious cycle known as "savannah cycle" or intermediate cycle, occurs between the jungle and urban cycles.[56]Different mosquitoes of the genusAedesare involved. In recent years, this has been the most common form of transmission of yellow fever in Africa.[57]
Concern exists about yellow fever spreading to southeast Asia, where its vectorA. aegyptialready occurs.[58]
Pathogenesis
[edit]After transmission from a mosquito, the viruses replicate in thelymph nodesand infectdendritic cellsin particular. From there, they reach the liver and infecthepatocytes(probably indirectly viaKupffer cells), which leads toeosinophilic degradationof these cells and to the release ofcytokines.Apoptotic masses known asCouncilman bodiesappear in thecytoplasmof hepatocytes.[59][60]
Fatality may occur whencytokine storm,shock,andmultiple organ failurefollow.[26]
Diagnosis
[edit]Yellow fever is most frequently a clinicaldiagnosis,based onsymptomatologyand travel history. Mild cases of the disease can only be confirmed virologically.[47]Since mild cases of yellow fever can also contribute significantly to regional outbreaks, every suspected case of yellow fever (involving symptoms of fever, pain, nausea, and vomiting 6–10 days after leaving the affected area) is treated seriously.[47]
If yellow fever is suspected, the virus cannot be confirmed until 6–10 days following the illness. A direct confirmation can be obtained byreverse transcription polymerase chain reaction,where the genome of the virus is amplified.[4]Another direct approach is the isolation of the virus and its growth in cell culture usingblood plasma;this can take 1–4 weeks.[61][13]
Serologically, anenzyme-linked immunosorbent assayduring the acute phase of the disease using specificIgMagainst yellow fever or an increase in specificIgGtiter(compared to an earlier sample) can confirm yellow fever.[62]Together with clinical symptoms, the detection of IgM or a four-fold increase in IgG titer is considered sufficient indication for yellow fever. As these tests can cross-react with other flaviviruses, such asdengue virus,these indirect methods cannot conclusively prove yellow fever infection.[63]
Liverbiopsycan verifyinflammationandnecrosisof hepatocytes and detect viralantigens.Because of the bleeding tendency of yellow fever patients, a biopsy is only advisablepost mortemto confirm the cause of death.[64]
In adifferential diagnosis,infections with yellow fever must be distinguished from other feverish illnesses such asmalaria.Otherviral hemorrhagic fevers,such asEbola virus,Lassa virus,Marburg virus,andJunin virus,must be excluded as the cause.[65]
Prevention
[edit]Personal prevention of yellow fever includes vaccination and avoidance of mosquito bites in areas where yellow fever is endemic.[46]Institutional measures for prevention of yellow fever include vaccination programmes and measures to control mosquitoes. Programmes for distribution of mosquito nets for use in homes produce reductions in cases of both malaria and yellow fever. Use of EPA-registered insect repellent is recommended when outdoors. Exposure for even a short time is enough for a potential mosquito bite. Long-sleeved clothing, long pants, and socks are useful for prevention. The application of larvicides to water-storage containers can help eliminate potential mosquito breeding sites. EPA-registered insecticide spray decreases the transmission of yellow fever.[66]
- Use insect repellent when outdoors such as those containingDEET,picaridin,ethyl butylacetylaminopropionate(IR3535), oroil of lemon eucalyptuson exposed skin.[67]
- Mosquitoes may bite through thin clothing, so spraying clothes with repellent containingpermethrinor another EPA-registered repellent gives extra protection.[68]Clothing treated with permethrin is commercially available. Mosquito repellents containing permethrin are not approved for application directly to the skin.[69]
- The peak biting times for many mosquito species are dusk to dawn. However,A. aegypti,one of the mosquitoes that transmit yellow fever virus, feeds during the daytime.[70]Staying in accommodations with screened or air-conditioned rooms, particularly during peak biting times, also reduces the risk of mosquito bites.[70]
Vaccination
[edit]Vaccinationis recommended for those traveling to affected areas, because non-native people tend to develop more severe illness when infected. Protection begins by the 10th day after vaccine administration in 95% of people,[72]and had been reported to last for at least 10 years. TheWorld Health Organization(WHO) now states that a single dose of vaccine is sufficient to confer lifelong immunity against yellow fever disease.[73]The attenuated live vaccine stem 17D was developed in 1937 byMax Theiler.[72]The WHO recommends routine vaccination for people living in affected areas between the 9th and 12th month after birth.[4]
Up to one in four people experience fever, aches, and local soreness and redness at the site of injection.[74]In rare cases (less than one in 200,000 to 300,000),[72]the vaccination can cause yellow fever vaccine-associated viscerotropic disease, which is fatal in 60% of cases. It is probably due to the genetic morphology of the immune system. Another possible side effect is an infection of the nervous system, which occurs in one in 200,000 to 300,000 cases, causing yellow fever vaccine-associated neurotropic disease, which can lead tomeningoencephalitisand is fatal in less than 5%[72]of cases.[4][26]
The Yellow Fever Initiative, launched by the WHO in 2006, vaccinated more than 105 million people in 14 countries in West Africa.[75]No outbreaks were reported during 2015. The campaign was supported by theGAVIalliance and governmental organizations in Europe and Africa.[76]According to the WHO, mass vaccination cannot eliminate yellow fever because of the vast number of infected mosquitoes in urban areas of the target countries, but it will significantly reduce the number of people infected.[77]
Demand for yellow fever vaccine has continued to increase due to the growing number of countries implementing yellow fever vaccination as part of their routine immunization programmes.[78]Recent upsurges in yellow fever outbreaks in Angola (2015), the Democratic Republic of Congo (2016), Uganda (2016), and more recently in Nigeria and Brazil in 2017 have further increased demand, while straining global vaccine supply.[78][79]Therefore, to vaccinate susceptible populations in preventive mass immunization campaigns during outbreaks,fractional dosingof the vaccine is being considered as a dose-sparing strategy to maximize limited vaccine supplies.[78]Fractional dose yellow fever vaccination refers to administration of a reduced volume of vaccine dose, which has been reconstituted as per manufacturer recommendations.[78][80]The first practical use of fractional dose yellow fever vaccination was in response to a large yellow fever outbreak in the Democratic Republic of the Congo in mid-2016.[78]Available evidence shows that fractional dose yellow fever vaccination induces a level of immune response similar to that of the standard full dose.[81]
In March 2017, the WHO launched a vaccination campaign in Brazil with 3.5 million doses from an emergency stockpile.[82]In March 2017 the WHO recommended vaccination for travellers to certain parts of Brazil.[83]In March 2018, Brazil shifted its policy and announced it planned to vaccinate all 77.5 million currently unvaccinated citizens by April 2019.[84]
Compulsory vaccination
[edit]Some countries in Asia are considered to be potentially in danger of yellow fever epidemics, as both mosquitoes with the capability to transmit yellow fever as well as susceptible monkeys are present.[85]The disease does not yet occur in Asia. To prevent introduction of the virus, some countries demand previous vaccination of foreign visitors who have passed through yellow fever areas.[86]Vaccination has to be proved by a vaccination certificate, which is valid 10 days after the vaccination and lasts for 10 years. Although the WHO on 17 May 2013 advised that subsequent booster vaccinations are unnecessary, an older (than 10 years) certificate may not be acceptable at all border posts in all affected countries. A list of the countries that require yellow fever vaccination is published by the WHO.[71]If the vaccination cannot be given for some reason, dispensation may be possible. In this case, an exemption certificate issued by a WHO-approved vaccination center is required. Although 32 of 44 countries where yellow fever occurs endemically do have vaccination programmes, in many of these countries, less than 50% of their population is vaccinated.[4]
Vector control
[edit]Control of the yellow fever mosquitoA. aegyptiis of major importance, especially because the same mosquito can also transmitdenguefever andchikungunyadisease.[87]A. aegyptibreeds preferentially in water, for example, in installations by inhabitants of areas with precarious drinking water supplies, or in domestic refuse, especially tires, cans, and plastic bottles. These conditions are common in urban areas in developing countries.[88]
Two main strategies are employed to reduceA. aegyptipopulations.[89]One approach is to kill the developing larvae. Measures are taken to reduce the water accumulations in which the larvae develop.Larvicidesare used, along with larvae-eating fish andcopepods,which reduce the number of larvae.[90]For many years, copepods of the genusMesocyclopshave been used inVietnamfor preventing dengue fever.[91]This eradicated the mosquito vector in several areas. Similar efforts may prove effective against yellow fever.Pyriproxyfenis recommended as a chemical larvicide, mainly because it is safe for humans and effective in small doses.[4]
The second strategy is to reduce populations of the adult yellow fever mosquito.Lethal ovitrapscan reduceAedespopulations, using lesser amounts of pesticide because it targets the pest directly.[92]Curtains and lids of water tanks can be sprayed with insecticides, but application inside houses is not recommended by the WHO.[93]Insecticide-treatedmosquito netsare effective, just as they are against theAnophelesmosquito that carries malaria.[4]
Treatment
[edit]As with otherFlavivirusinfections, no cure is known for yellow fever. Hospitalization is advisable and intensive care may be necessary because of rapid deterioration in some cases. Certain acute treatment methods lack efficacy:passive immunizationafter the emergence of symptoms is probably without effect;ribavirinand otherantiviral drugs,as well as treatment withinterferons,are ineffective in yellow fever patients.[26]Symptomatic treatment includes rehydration and pain relief with drugs such asparacetamol(acetaminophen). However,aspirinand othernon-steroidal anti-inflammatory drugs(NSAIDs) are often avoided because of an increased risk of gastrointestinal bleeding due to their anticoagulant effects.[94]
Epidemiology
[edit]Yellow fever iscommonin tropical and subtropical areas of South America and Africa.[95]Worldwide, about 600 million people live in endemic areas. The WHO estimates 200,000 cases of yellow fever worldwide each year.[96]About 15% of people infected with yellow fever progress to a severe form of the illness, and up to half of those will die, as there is no cure for yellow fever.[97]
Africa
[edit]An estimated 90% of yellow fever infections occur on the African continent.[4]In 2016,a large outbreak originated in Angolaand spread to neighboring countries before being contained by a massive vaccination campaign.[98]In March and April 2016, 11 imported cases of the Angola genotype in unvaccinated Chinese nationals were reported in China, the first appearance of the disease in Asia in recorded history.[99][100]
Phylogeneticanalysis has identified sevengenotypesof yellow fever viruses, and they are assumed to be differently adapted to humans and to the vectorA. aegypti.Five genotypes (Angola, Central/East Africa, East Africa, West Africa I, and West Africa II) occur only in Africa. West Africa genotype I is found inNigeriaand the surrounding region.[101]West Africa genotype I appears to be especially infectious, as it is often associated with major outbreaks. The three genotypes found outside of Nigeria and Angola occur in areas where outbreaks are rare. Two outbreaks, in Kenya (1992–1993) and Sudan (2003 and 2005), involved the East African genotype, which had remained undetected in the previous 40 years.[102]
South America
[edit]In South America, two genotypes have been identified (South American genotypes I and II).[16]Based on phylogenetic analysis these two genotypes appear to have originated in West Africa[103]and were first introduced into Brazil.[104]The date of introduction of the predecessor African genotype which gave rise to the South American genotypes appears to be 1822 (95% confidence interval 1701 to 1911).[104]The historical record shows an outbreak of yellow fever occurred in Recife, Brazil, between 1685 and 1690. The disease seems to have disappeared, with the next outbreak occurring in 1849.[105]It was likely introduced with the trafficking of slaves through theslave tradefrom Africa. Genotype I has been divided into five subclades, A through E.[106]
In late 2016, a large outbreak began inMinas Geraisstate of Brazil that was characterized as a sylvatic or jungleepizootic.[107]Real-time phylogenetic investigations at the epicentre of the outbreak revealed that the outbreak was caused by the introduction of a virus lineage from the Amazon region into the southeast region around July 2016,[108]spreading rapidly across several neotropical monkey species, includingbrown howlermonkeys,[109]which serve as asentinel speciesfor yellow fever. No cases had been transmitted between humans by theA. aegyptimosquito, which can sustain urban outbreaks that can spread rapidly. In April 2017, the sylvatic outbreak continued moving toward the Brazilian coast, where most people were unvaccinated.[83]By the end of May the outbreak appeared to be declining after more than 3,000 suspected cases, 758 confirmed and 264 deaths confirmed to be yellow fever.[110]The Health Ministry launched a vaccination campaign and was concerned about spread during theCarnivalseason in February and March. The CDC issued aLevel 2 alert (practice enhanced precautions.)[111]
A Bayesian analysis of genotypes I and II has shown that genotype I accounts for virtually all the current infections inBrazil,Colombia,Venezuela,andTrinidadandTobago,while genotype II accounted for all cases inPeru.[112]Genotype I originated in the northern Brazilian region around 1908 (95% highest posterior density interval [HPD]: 1870–1936). Genotype II originated in Peru in 1920 (95% HPD: 1867–1958).[113]The estimated rate of mutation for both genotypes was about 5 × 10−4 substitutions/site/year, similar to that of other RNA viruses.[114]
Asia
[edit]The main vector (A. aegypti) also occurs in tropical and subtropical regions of Asia, the Pacific, and Australia, but yellow fever had never occurred there until jet travel introduced 11 cases from the2016 Angola and DR Congo yellow fever outbreakin Africa. Proposed explanations include:[115]
- That the strains of the mosquito in the east are less able to transmityellow fever virus.[116]
- That immunity is present in the populations because of other diseases caused by related viruses (for example,dengue).[117]
- That the disease was never introduced because the shipping trade was insufficient.
But none is considered satisfactory.[118][119]Another proposal is the absence of a slave trade to Asia on the scale of that to the Americas.[120]Thetrans-Atlantic slave tradeprobably introduced yellow fever into the Western Hemisphere from Africa.[121]
History
[edit]Early history
[edit]The evolutionary origins of yellow fever most likely lie in Africa, with transmission of the disease from nonhuman primates to humans.[122][123]The virus is thought to have originated in East or Central Africa and spread from there to West Africa. As it was endemic in Africa, local populations had developed some immunity to it. When an outbreak of yellow fever would occur in an African community where colonists resided, most Europeans died, while the indigenous Africans usually developed nonlethal symptoms resemblinginfluenza.[124]This phenomenon, in which certain populations develop immunity to yellow fever due to prolonged exposure in their childhood, is known asacquired immunity.[125]The virus, as well as the vectorA. aegypti,were probably transferred to North and South America with the trafficking ofslavesfrom Africa, part of theColumbian exchangefollowing European exploration and colonization.[126]However, some researchers have argued that yellow fever might have existed in the Americas during the pre-Columbian period as mosquitoes of the genusHaemagogus,which is indigenous to the Americas, have been known to carry the disease.[127]
The first definitive outbreak of yellow fever in the New World was in 1647 on the island ofBarbados.[128]An outbreak was recorded by Spanish colonists in 1648 in theYucatán Peninsula,where theindigenousMayan peoplecalled the illnessxekik( "blood vomit" ). In 1685, Brazil suffered its first epidemic inRecife.The first mention of the disease by the name "yellow fever" occurred in 1744.[129]
- (John Mitchell) (1805)(Mitchell's account of the Yellow Fever in Virginia in 1741–2)Archived2017-02-23 at theWayback Machine,The Philadelphia Medical Museum,1 (1): 1–20.
- (John Mitchell) (1814)"Account of the Yellow fever which prevailed in Virginia in the years 1737, 1741, and 1742, in a letter to the late Cadwallader Colden, Esq. of New York, from the late John Mitchell, M.D.F.R.S. of Virginia,"Archived2017-02-23 at theWayback MachineAmerican Medical and Philosophical Register,4:181–215. The term "yellow fever" appears on p. 186. On p. 188, Mitchell mentions "... the distemper was what is generally called yellow fever in America." However, on pages 191–192, he states "... I shall consider the cause of the yellowness which is so remarkable in this distemper, as to have given it the name of the Yellow Fever. Unfortunately, Mitchell misidentified the cause ofyellow fever,believing it was transmitted through "putrid miasma" in the air. "[citation needed]
However, Dr. Mitchell misdiagnosed the disease that he observed and treated, and the disease was probably Weil's disease or hepatitis.[130]McNeill argues that the environmental and ecological disruption caused by the introduction ofsugar plantationscreated the conditions for mosquito and viral reproduction, and subsequent outbreaks of yellow fever.[131]Deforestation reduced populations of insectivorous birds and other creatures that fed on mosquitoes and their eggs.[132]
InColonial timesand during theNapoleonic Wars,the West Indies were known as a particularly dangerous posting for soldiers due to yellow fever being endemic in the area.[133]The mortality rate in British garrisons inJamaicawas seven times that of garrisons in Canada, mostly because of yellow fever and other tropical diseases.[134]Both English and French forces posted there were seriously affected by the "yellow jack."[135]Wanting to regain control of the lucrative sugar trade inSaint-Domingue(Hispaniola), and with an eye on regaining France's New World empire, Napoleon sent an army under the command of his brother-in-law GeneralCharles Leclercto Saint-Domingue to seize control after a slave revolt.[136]The historian J. R. McNeill asserts that yellow fever accounted for about 35,000 to 45,000 casualties of these forces during the fighting.[137]Only one-third of the French troops survived for withdrawal and return to France. Napoleon gave up on the island and his plans for North America, selling theLouisiana Purchaseto the US in 1803. In 1804,Haitiproclaimed its independence as the second republic in the Western Hemisphere.[138]Considerable debate exists over whether the number of deaths caused by disease in theHaitian Revolutionwas exaggerated.[139]
Although yellow fever is most prevalent in tropical-like climates, the northern United States were not exempt from the fever. The first outbreak in English-speaking North America occurred inNew York Cityin 1668.[140]English colonists inPhiladelphiaand the French in theMississippi River Valleyrecorded major outbreaks in 1669, as well as additional yellow fever epidemics in Philadelphia,Baltimore,and New York City in the 18th and 19th centuries. The disease traveled alongsteamboatroutes from New Orleans, causing some 100,000–150,000 deaths in total.[141]Theyellow fever epidemic of 1793in Philadelphia, which was then the capital of the United States, resulted in the deaths of several thousand people, more than 9% of the population.[142]One of these deaths wasJames Hutchinson,a physician helping to treat the population of the city. Thenational government fledthe city to Trenton, New Jersey, including PresidentGeorge Washington.[143]
The southern city ofNew Orleanswas plagued with major epidemics during the 19th century, most notably in 1833 and 1853.[144]A major epidemic occurred in both New Orleans andShreveport, Louisiana,in 1873. Its residents called the disease "yellow jack". Urban epidemics continued in the United States until 1905, with the last outbreak affecting New Orleans.[145][16][146]
At least 25 major outbreaks took place in the Americas during the 18th and 19th centuries, including particularly serious ones inCartagena, Chile,in 1741; Cuba in 1762 and 1900;Santo Domingoin 1803; andMemphis, Tennessee,in 1878.[147]
In the early 19th century, the prevalence of yellow fever in the Caribbean "led to serious health problems" and alarmed theUnited States Navyas numerous deaths and sickness curtailed naval operations and destroyed morale.[148]One episode began in April 1822 when the frigateUSSMacedonianleftBostonand became part of Commodore James Biddle's West India Squadron. Unbeknownst to all, they were about to embark on a cruise to disaster and their assignment "would prove a cruise through hell".[149]Secretary of the NavySmith Thompsonhad assigned the squadron to guard United States merchant shipping and suppress piracy.[150]During their time on deployment from 26 May to 3 August 1822, 76 of theMacedonian's officers and men died, including John Cadle, surgeon USN. Seventy-four of these deaths were attributed to yellow fever. Biddle reported that another 52 of his crew were on sick-list. In their report to the secretary of the Navy, Biddle and Surgeon's Mate Charles Chase stated the cause as "fever". As a consequence of this loss, Biddle noted that his squadron was forced to return to Norfolk Navy Yard early. Upon arrival, theMacedonian's crew were provided medical care and quarantined atCraney Island, Virginia.[151][152][153]
In 1853,Cloutierville, Louisiana,had a late-summer outbreak of yellow fever that quickly killed 68 of the 91 inhabitants. A local doctor concluded that some unspecified infectious agent had arrived in a package from New Orleans.[154][155]In 1854, 650 residents ofSavannah, Georgia,died from yellow fever.[156]In 1858,St. Matthew's German Evangelical Lutheran ChurchinCharleston, South Carolina,had 308 yellow fever deaths, reducing the congregation by half.[157]A ship carrying persons infected with the virus arrived inHampton Roadsin southeasternVirginiain June 1855.[158]The disease spread quickly through the community, eventually killing over 3,000 people, mostly residents ofNorfolkandPortsmouth.[159]In 1873, Shreveport, Louisiana, lost 759 citizens in an 80-day period to a yellow fever epidemic, with over 400 additional victims eventually succumbing. The total death toll from August through November was approximately 1,200.[160][161]
In 1878, about 20,000 people died in a widespreadepidemic in the Mississippi River Valley.[162]That year, Memphis had an unusually large amount of rain, which led to an increase in the mosquito population. The result was a huge epidemic of yellow fever.[163]The steamship John D. Porter took people fleeing Memphis northward in hopes of escaping the disease, but passengers were not allowed to disembark due to concerns of spreading yellow fever. The ship roamed the Mississippi River for the next two months before unloading her passengers.[164]
Major outbreaks have also occurred in southern Europe.Gibraltarlost many lives to outbreaks in 1804, 1814, and 1828.[165]Barcelonasuffered the loss of several thousand citizens during an outbreak in 1821. TheDuke de Richelieudeployed 30,000 French troops to the border betweenFranceandSpainin thePyrenees Mountains,to establish acordon sanitairein order to prevent the epidemic from spreading from Spain into France.[166]
Causes and transmission
[edit]Ezekiel Stone Wiggins,known as the Ottawa Prophet, proposed that the cause of a yellow fever epidemic inJacksonville, Florida,in 1888, was astrological.[167]
The planets were in the same line as the sun and earth and this produced, besides Cyclones, Earthquakes, etc., a denser atmosphere holding more carbon and creating microbes. Mars had an uncommonly dense atmosphere, but its inhabitants were probably protected from the fever by their newly discoveredcanals,which were perhaps made to absorb carbon and prevent the disease.[168]
In 1848,Josiah C. Nottsuggested that yellow fever was spread by insects such as moths or mosquitoes, basing his ideas on the pattern of transmission of the disease.[169]Carlos Finlay,a Cuban-Spanish doctor and scientist, proposed in 1881 that yellow fever might be transmitted by previously infectedmosquitoesrather than by direct contact from person to person, as had long been believed.[170][171]Since the losses from yellow fever in theSpanish–American Warin the 1890s were extremely high, U.S. Army doctors began research experiments with a team led byWalter Reed,and composed of doctorsJames Carroll,Aristides Agramonte,andJesse William Lazear.They successfully proved Finlay's "mosquito hypothesis". Yellow fever was the first virus shown to be transmitted by mosquitoes. The physicianWilliam Gorgasapplied these insights and eradicated yellow fever fromHavana.He also campaigned against yellow fever during the construction of thePanama Canal.A previous effort of canal building by the French had failed in part due to mortality from the high incidence of yellow fever and malaria, which killed many workers.[16]
Although Reed has received much of the credit in United States history books for "beating" yellow fever, he had fully credited Finlay with the discovery of the yellow fever vector, and how it might be controlled. Reed often cited Finlay's papers in his own articles, and also credited him for the discovery in his personal correspondence.[172]The acceptance of Finlay's work was one of the most important and far-reaching effects of the U.S. Army Yellow Fever Commission of 1900.[173]Applying methods first suggested by Finlay, the United States government and Army eradicated yellow fever in Cuba and later in Panama, allowing completion of the Panama Canal. While Reed built on the research of Finlay, historian François Delaporte notes that yellow fever research was a contentious issue. Scientists, including Finlay and Reed, became successful by building on the work of less prominent scientists, without always giving them the credit they were due.[174]Reed's research was essential in the fight against yellow fever. He is also credited for using the first type ofmedical consentform during his experiments in Cuba, an attempt to ensure that participants knew they were taking a risk by being part of testing.[175]
Like Cuba and Panama, Brazil also led a highly successful sanitation campaign against mosquitoes and yellow fever. Beginning in 1903, the campaign led byOswaldo Cruz,then director general of public health, resulted not only in eradicating the disease but also in reshaping the physical landscape of Brazilian cities such as Rio de Janeiro.[176]During rainy seasons, Rio de Janeiro had regularly suffered floods, as water from the bay surrounding the city overflowed into Rio's narrow streets. Coupled with the poor drainage systems found throughout Rio, this created swampy conditions in the city's neighborhoods. Pools of stagnant water stood year-long in city streets and proved to be a fertile ground for disease-carrying mosquitoes. Thus, under Cruz's direction, public health units known as "mosquito inspectors" fiercely worked to combat yellow fever throughout Rio by spraying, exterminating rats, improving drainage, and destroying unsanitary housing. Ultimately, the city's sanitation and renovation campaigns reshaped Rio de Janeiro's neighborhoods. Its poor residents were pushed from city centers to Rio's suburbs, or to towns found in the outskirts of the city. In later years, Rio's most impoverished inhabitants would come to reside infavelas.[177]
During 1920–1923, theRockefeller Foundation'sInternational Health Boardundertook an expensive and successful yellow fever eradication campaign in Mexico.[178]The IHB gained the respect of Mexico's federal government because of the success. The eradication of yellow fever strengthened the relationship between the US and Mexico, which had not been very good in the years prior. The eradication of yellow fever was also a major step toward better global health.[179]
In 1927, scientists isolated theyellow fever virusin West Africa.[180]Following this, twovaccineswere developed in the 1930s.Max Theilerled the completion of the 17Dyellow fever vaccinein 1937, for which he was subsequently awarded theNobel Prize in Physiology or Medicine.[181]That vaccine, 17D, is still in use, although newer vaccines, based onvero cells,are in development (as of 2018).[4][182][183]
-
A painting depictingyellow fever in Buenos Aires,1871
Current status
[edit]Using vector control and strict vaccination programs, the urban cycle of yellow fever was nearly eradicated from South America.[184]Since 1943, only a single urban outbreak inSanta Cruz de la Sierra,Bolivia, has occurred. Since the 1980s, however, the number of yellow fever cases has been increasing again, andA. aegyptihas returned to the urban centers of South America. This is partly due to limitations on available insecticides, as well as habitat dislocations caused by climate change. It is also because the vector control program was abandoned. Although no new urban cycle has yet been established, scientists believe this could happen again at any point. An outbreak inParaguayin 2008 was thought to be urban in nature, but this ultimately proved not to be the case.[4]
In Africa, virus eradication programs have mostly relied upon vaccination.[185]These programs have largely been unsuccessful because they were unable to break thesylvatic cycleinvolving wild primates. With few countries establishing regular vaccination programs, measures to fight yellow fever have been neglected, making the future spread of the virus more likely.[4]
Research
[edit]In the hamster model of yellow fever, early administration of the antiviralribavirinis an effective treatment of many pathological features of the disease.[186]Ribavirin treatment during the first five days after virus infection improved survival rates, reduced tissue damage in the liver andspleen,prevented hepatocellularsteatosis,and normalised levels of alanine aminotransferase, a liver damage marker. The mechanism of action of ribavirin in reducing liver pathology inyellow fever virusinfection may be similar to its activity in treatment ofhepatitis C,a related virus.[186]Because ribavirin had failed to improve survival in a virulent rhesus model of yellow fever infection, it had been previously discounted as a possible therapy.[187]Infection was reduced in mosquitoes with the wMel strain ofWolbachia.[188]
Yellow fever has been researched by several countries as a potentialbiological weapon.[189]
Notes
[edit]- ^Also required for travellers having transited (more than 12 hours) through a risk country's airport.
- ^Not required for travellers having transited through a risk country's airport.
- ^The WHO has designated (parts of) Argentina, Brazil and Peru as risk countries, but these countries do not require incoming travellers to vaccinate against yellow fever.
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Further reading
[edit]- Crosby M (2006).The American Plague: The Untold Story of Yellow Fever, the Epidemic that Shaped Our History.New York: The Berkley Publishing Group.ISBN978-0-425-21202-8.
- Espinosa M (2009).Epidemic Invasions: Yellow Fever and the Limits of Cuban Independence, 1878–1930.Chicago: University of Chicago Press.ISBN978-0-226-21811-3.
- Finlay CJ (January 2012)."The Mosquito Hypothetically Considered as the Transmitting Agent of Yellow Fever".MEDICC Review.14(1): 56–59.doi:10.37757/MR2012V14.N1.10.PMID34503309.
- Gessner I (2016).Yellow Fever Years: An Epidemiology of Nineteenth-Century American Literature and Culture.Frankfurt on Main: Peter Lang.ISBN978-3-631-67412-3.
- Harcourt-Smith S (1974). "'Yellow Jack': Caribbean Fever ".History Today.23(9): 618–624.
- Murphy J (2003).An American Plague: The True and Terrifying Story of the Yellow Fever Epidemic of 1793.New York: Clarion Books.ISBN978-0-395-77608-7.
- Nuwer DS (2009).Plague Among the Magnolias: The 1878 Yellow Fever Epidemic in Mississippi.University of Alabama Press.ISBN978-0-8173-1653-2.
External links
[edit]- "U.S. Army Yellow Fever Commission."Claude Moore Health Sciences Library,University of Virginia
- "Yellow fever virus".NCBI Taxonomy Browser.11089.