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Typhoid fever

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Template:Short description Template:Cs1 config Template:Distinguish Template:Infobox medical condition (new) Typhoid fever, also known simply as typhoid, is a disease caused by Salmonella enterica serotype Typhi bacteria, also called Salmonella Typhi.<ref name="Lancet2015" /><ref>Template:Cite journal</ref> Symptoms vary from mild to severe, and usually begin six to 30 days after exposure.<ref name="Yellow2014" /><ref name="CDC2013" /> Often there is a gradual onset of a high fever over several days.<ref name="Yellow2014">Template:Cite book</ref> This is commonly accompanied by weakness, abdominal pain, constipation, headaches, and mild vomiting.<ref>Template:Cite web</ref><ref name="CDC2013" /><ref name="CDC2013Tech" /> Some people develop a skin rash with rose colored spots.<ref name="CDC2013">Template:Cite web</ref> In severe cases, people may experience confusion.<ref name="CDC2013Tech" /> Without treatment, symptoms may last weeks or months.<ref name="CDC2013" /> Diarrhea may be severe, but is uncommon.<ref name="CDC2013Tech" /> Other people may carry it without being affected, but are still contagious.<ref name="WHO2008" /> Typhoid fever is a type of enteric fever, along with paratyphoid fever.<ref name="Lancet2015" /> Salmonella enterica Typhi is believed to infect and replicate only within humans.<ref name="Pitzer S395–S401">Template:Cite journal</ref>

Typhoid is caused by the bacterium Salmonella enterica subsp. enterica serovar Typhi growing in the intestines, Peyer's patches, mesenteric lymph nodes, spleen, liver, gallbladder, bone marrow and blood.<ref name="CDC2013" /><ref name="CDC2013Tech">Template:Cite web</ref> Typhoid is spread by eating or drinking food or water contaminated with the feces of an infected person.<ref name="WHO2008">Template:Cite journal</ref> Risk factors include limited access to clean drinking water and poor sanitation.<ref name="Lancet2015" /> Those who have not yet been exposed to it and ingest contaminated drinking water or food are most at risk for developing symptoms.<ref name="CDC2013Tech" /> Only humans can be infected; there are no known animal reservoirs.<ref name="WHO2008" /> Salmonella Typhi which causes typhoid fever is different from the other Salmonella bacteria that usually cause salmonellosis, a common type of food poisoning.<ref>Template:Cite web</ref>

Diagnosis is performed by culturing and identifying S. Typhi from patient samples or detecting an immune response to the pathogen from blood samples.<ref name="CDC2013" /><ref name="Lancet2015" /><ref name="Crump2010">Template:Cite journal</ref> Recently, new advances in large-scale data collection and analysis have allowed researchers to develop better diagnostics, such as detecting changing abundances of small molecules in the blood that may specifically indicate typhoid fever.<ref>Template:Cite book</ref> Diagnostic tools in regions where typhoid is most prevalent are quite limited in their accuracy and specificity, and the time required for a proper diagnosis, the increasing spread of antibiotic resistance, and the cost of testing are also hardships for under-resourced healthcare systems.<ref name="Pitzer S395–S401"/>

A typhoid vaccine can prevent about 40–90% of cases during the first two years.<ref name=Mil2018>Template:Cite journal</ref> The vaccine may have some effect for up to seven years.<ref name=Lancet2015/> For those at high risk or people traveling to areas where it is common, vaccination is recommended.<ref name=WHO2008/> Other efforts to prevent it include providing clean drinking water, good sanitation, and handwashing.<ref name=CDC2013/><ref name=WHO2008/> Until an infection is confirmed as cleared, the infected person should not prepare food for others.<ref name=CDC2013/> Typhoid is treated with antibiotics such as azithromycin, fluoroquinolones, or third-generation cephalosporins.<ref name=Lancet2015/> Resistance to these antibiotics has been developing, which has made treatment more difficult.<ref name=Lancet2015>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref>

In 2015, 12.5 million new typhoid cases were reported.<ref name=GBD2015Pre>Template:Cite journal</ref> The disease is most common in India.<ref name=Lancet2015/> Children are most commonly affected.<ref name=Lancet2015/><ref name=WHO2008/> Typhoid decreased in the developed world in the 1940s as a result of improved sanitation and the use of antibiotics.<ref name=WHO2008/> Every year about 400 cases are reported in the U.S. and an estimated 6,000 people have typhoid.<ref name=CDC2013Tech/><ref>Template:Cite journal</ref> In 2015, it resulted in about 149,000 deaths worldwide – down from 181,000 in 1990.<ref name=GBD2015De>Template:Cite journal</ref><ref name=GBD204>Template:Cite journal</ref> Without treatment, the risk of death may be as high as 20%.<ref name=WHO2008/> With treatment, it is between 1% and 4%.<ref name=Lancet2015/><ref name=WHO2008/>

Typhus is a different disease, caused by unrelated species of bacteria.<ref>Template:Cite journal</ref> Owing to their similar symptoms, they were not recognized as distinct diseases until the 1800s. "Typhoid" means "resembling typhus".<ref>Template:Cite book</ref>

Signs and symptoms

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Classically, the progression of untreated typhoid fever has three distinct stages, each lasting about a week. Over the course of these stages, the patient becomes exhausted and emaciated.<ref>Template:Cite web</ref>Template:Better source

  • In the first week, the body temperature rises slowly, and fever fluctuations are seen with relative bradycardia (Faget sign), malaise, headache, and cough. A bloody nose (epistaxis) is seen in a quarter of cases, and abdominal pain is also possible. A decrease in the number of circulating white blood cells (leukopenia) occurs with eosinopenia and relative lymphocytosis; blood cultures are positive for S. enterica subsp. enterica serovar Typhi. The Widal test is usually negative.<ref name="pmid27796818">Template:Cite journal</ref>
  • In the second week, the person is often too tired to get up, with high fever in plateau around Template:Convert and bradycardia (sphygmothermic dissociation or Faget sign), classically with a dicrotic pulse wave. Delirium can occur, where the patient is often calm, but sometimes becomes agitated. This delirium has given typhoid the nickname "nervous fever". Rose spots appear on the lower chest and abdomen in around a third of patients. Rhonchi (rattling breathing sounds) are heard in the base of the lungs. The abdomen is distended and painful in the right lower quadrant, where a rumbling sound can be heard. Diarrhea can occur in this stage, but constipation is also common. The spleen and liver are enlarged (hepatosplenomegaly) and tender, and liver transaminases are elevated. The Widal test is strongly positive, with antiO and antiH antibodies. Blood cultures are sometimes still positive.Template:Cn
  • In the third week of typhoid fever, possible complications include:

Causes

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File:ForskeligeVeje ad hvilkenBroen kan inficeres medTyfusbaciller.png
A 1939 conceptual illustration showing various ways that typhoid bacteria can contaminate a water well (center)

Bacteria

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The Gram-negative bacterium that causes typhoid fever is Salmonella enterica subsp. enterica serovar Typhi. Based on the MLST subtyping scheme, the two main sequence types of the S. Typhi are ST1 and ST2, which are widespread globally.<ref name="Yap et al 2016">Template:Cite journal</ref> Global phylogeographical analysis showed dominance of a haplotype 58 (H58), which probably originated in India during the late 1980s and is now spreading through the world with multi-drug resistance.<ref>Template:Cite journal</ref> A more detailed genotyping scheme was reported in 2016 and is now widely used. This scheme reclassified the nomenclature of H58 to genotype 4.3.1.<ref>Template:Cite journal</ref>

Transmission

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Unlike other strains of Salmonella, humans are the only known typhoid carriers.<ref name=Eng2015 /> S. enterica subsp. enterica serovar Typhi is spread by the fecal-oral route from people who are infected and from asymptomatic carriers of the bacterium.<ref name=Eng2015>Template:Cite journal</ref> An asymptomatic human carrier is someone who is still excreting typhoid bacteria in stool a year after the acute stage of the infection.<ref name=Eng2015 />

File:STyphipathogenesisdiagram.jpg
Pathogenesis of typhoid fever

Diagnosis

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Diagnosis is made by any blood, bone marrow, or stool cultures and with the Widal test (demonstration of antibodies against Salmonella antigens O-somatic and H-flagellar). In epidemics and less wealthy countries, after excluding malaria, dysentery, or pneumonia, a therapeutic trial time with chloramphenicol is generally undertaken while awaiting the results of the Widal test and blood and stool cultures.<ref name="Sherris">Template:Cite book</ref>

Widal test

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File:Widal Test Slide.jpg
Widal test card

The Widal test is used to identify specific antibodies in the serum of people with typhoid by using antigen-antibody interactions.<ref>Template:Cite journal</ref>

In this test, the serum is mixed with a dead bacterial suspension of Salmonella with specific antigens. If the patient's serum contains antibodies against those antigens, they get attached to them, forming clumps. If clumping does not occur, the test is negative. The Widal test is time-consuming and prone to significant false positives. It may also be falsely negative in recently infected people. But unlike the Typhidot test, the Widal test quantifies the specimen with titres.<ref>Template:Cite book</ref>

Rapid diagnostic tests

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Rapid diagnostic tests such as Tubex, Typhidot, and Test-It have shown moderate diagnostic accuracy.<ref>Template:Cite journal</ref>

Typhidot

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Typhidot is based on the presence of specific IgM and IgG antibodies to a specific 50Kd OMP antigen. This test is carried out on a cellulose nitrate membrane where a specific S. typhi outer membrane protein is attached as fixed test lines. It separately identifies IgM and IgG antibodies. IgM shows recent infection; IgG signifies remote infection.<ref>Template:Cite journal</ref>

The sample pad of this kit contains colloidal gold-anti-human IgG or gold-anti-human IgM. If the sample contains IgG and IgM antibodies against those antigens, they will react and turn red. The typhidot test becomes positive within 2–3 days of infection.<ref>Template:Cite journal</ref>

Two colored bands indicate a positive test. A single control band indicates a negative test. A single first fixed line or no band at all indicates an invalid test. Typhidot's biggest limitation is that it is not quantitative, just positive or negative.<ref>Template:Cite journal</ref>

Tubex test

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The Tubex test contains two types of particles: brown magnetic particles coated with antigen and blue indicator particles coated with O9 antibody. During the test, if antibodies are present in the serum, they will attach to the brown magnetic particles and settle at the base, while the blue indicator particles remain in the solution, producing a blue color, which means the test is positive.Template:Citation needed

If the serum does not have an antibody in it, the blue particles attach to the brown particles and settle at the bottom, producing a colorless solution, which means the test is negative.<ref>Template:Cite web</ref>

Prevention

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File:Typhoid inoculation2.jpg
Doctor administering a typhoid vaccination at a school in San Augustine County, Texas, 1943

Sanitation and hygiene are important to prevent typhoid. It can spread only in environments where human feces can come into contact with food or drinking water. Careful food preparation and washing of hands are crucial to prevent typhoid. Industrialization contributed greatly to the elimination of typhoid fever, as it eliminated the public health hazards associated with having horse manure in public streets, which led to a large number of flies,<ref>Template:Cite web</ref> which are vectors of many pathogens, including Salmonella spp.<ref>Template:Cite journal</ref> According to statistics from the U.S. Centers for Disease Control and Prevention, the chlorination of drinking water has led to dramatic decreases in the transmission of typhoid fever.<ref>Template:Cite web</ref>

Vaccination

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Two typhoid vaccines are licensed for use in the prevention of typhoid:<ref name=Mil2018/> the live, oral Ty21a vaccine (sold as Vivotif by Crucell Switzerland AG) and the injectable typhoid polysaccharide vaccine (sold as Typhim Vi by Sanofi Pasteur and Typherix by GlaxoSmithKline). Both are efficacious and recommended for travelers to areas where typhoid is endemic. Boosters are recommended every five years for the oral vaccine and every two years for the injectable form.<ref name="Mil2018"/> An older, killed whole-cell vaccine is still used in countries where the newer preparations are not available, but this vaccine is no longer recommended for use because it has more side effects (mainly pain and inflammation at the site of the injection).<ref>Template:Cite journal</ref>

File:Vivotif-typhoid-live-oral-vaccine.JPG
Vivotif – oral typhoid vaccine of live-attenuated S. enterica Typhi strain Ty21a

To help decrease rates of typhoid fever in developing nations, the World Health Organization (WHO) endorsed the use of a vaccination program starting in 1999. Vaccination has proven effective at controlling outbreaks in high-incidence areas and is also very cost-effective: prices are normally less than US$1 per dose. Because the price is low, poverty-stricken communities are more willing to take advantage of the vaccinations.<ref name=":0">Template:Cite journal</ref> Although vaccination programs for typhoid have proven effective, they alone cannot eliminate typhoid fever.<ref name=":0" /> Combining vaccines with public health efforts is the only proven way to control this disease.<ref name=":0" />

Since the 1990s, the WHO has recommended two typhoid fever vaccines. The ViPS vaccine is given by injection and the Ty21a by capsules. Only people over age two are recommended to be vaccinated with the ViPS vaccine, and it requires a revaccination after 2–3 years, with a 55–72% efficacy. The Ty21a vaccine is recommended for people five and older, lasting 5–7 years with 51–67% efficacy. The two vaccines have proved safe and effective for epidemic disease control in multiple regions.<ref name=":0"/>

A version of the vaccine combined with a hepatitis A vaccine is also available.<ref>Template:Cite web</ref>

Results of a phase 3 trial of typhoid conjugate vaccine (TCV) in December 2019 reported 81% fewer cases among children.<ref>Template:Cite news</ref><ref>Template:Cite journal</ref>

Treatment

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Oral rehydration therapy

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The rediscovery of oral rehydration therapy in the 1960s provided a simple way to prevent many of the deaths of diarrheal diseases in general.<ref>Template:Cite web</ref>

Antibiotics

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Where resistance is uncommon, the treatment of choice is a fluoroquinolone such as ciprofloxacin.<ref name="BMJ2009">Template:Cite journal</ref><ref name="pmid21975746">Template:Cite journal</ref> Otherwise, a third-generation cephalosporin such as ceftriaxone or cefotaxime is the first choice.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> Cefixime is a suitable oral alternative.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref>

Properly treated, typhoid fever is not fatal in most cases. Antibiotics such as ampicillin, chloramphenicol, trimethoprim-sulfamethoxazole, amoxicillin, and ciprofloxacin have been commonly used to treat it.<ref>Baron S et al.</ref> Treatment with antibiotics reduces the case-fatality rate to about 1%.<ref>Template:Cite web</ref>

Without treatment, some patients develop sustained fever, bradycardia, hepatosplenomegaly, abdominal symptoms, and occasionally pneumonia. In white-skinned patients, pink spots, which fade on pressure, appear on the skin of the trunk in up to 20% of cases. In the third week, untreated cases may develop gastrointestinal and cerebral complications, which may prove fatal in 10–20% of cases. The highest case fatality rates are reported in children under 4. Around 2–5% of those who contract typhoid fever become chronic carriers, as bacteria persist in the biliary tract after symptoms have resolved.<ref>Template:Cite web</ref>

Surgery

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Surgery is usually indicated if intestinal perforation occurs. One study found a 30-day mortality rate of 9% (8/88), and surgical site infections at 67% (59/88), with the disease burden borne predominantly by low-resource countries.<ref name=GlobalSurg2>Template:Cite journal</ref>

For surgical treatment, most surgeons prefer simple closure of the perforation with drainage of the peritoneum. Small bowel resection is indicated for patients with multiple perforations. If antibiotic treatment fails to eradicate the hepatobiliary carriage, the gallbladder should be resected. Cholecystectomy is sometimes successful, especially in patients with gallstones, but is not always successful in eradicating the carrier state because of persisting hepatic infection.<ref>Template:Cite journal</ref><ref name="G Gonzalez-Escobedo, JM Marshall, JS Gunn 2010"/>

Resistance

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As resistance to ampicillin, chloramphenicol, trimethoprim-sulfamethoxazole, and streptomycin is now common, these agents are no longer used as first-line treatment of typhoid fever.<ref>Template:Cite web</ref> Typhoid resistant to these agents is known as multidrug-resistant typhoid.<ref>Template:Cite journal</ref>

Ciprofloxacin resistance is an increasing problem, especially in the Indian subcontinent and Southeast Asia. Many centres are shifting from ciprofloxacin to ceftriaxone as the first line for treating suspected typhoid originating in South America, India, Pakistan, Bangladesh, Thailand, or Vietnam. Also, it has been suggested that azithromycin is better at treating resistant typhoid than both fluoroquinolone drugs and ceftriaxone.<ref name="pmid21975746" /> Azithromycin can be taken by mouth and is less expensive than ceftriaxone, which is given by injection.<ref>Template:Cite journal</ref>

A separate problem exists with laboratory testing for reduced susceptibility to ciprofloxacin; current recommendations are that isolates should be tested simultaneously against ciprofloxacin (CIP) and against nalidixic acid (NAL), that isolates sensitive to both CIP and NAL should be reported as "sensitive to ciprofloxacin", and that isolates sensitive to CIP but not to NAL should be reported as "reduced sensitivity to ciprofloxacin". But an analysis of 271 isolates found that around 18% of isolates with reduced susceptibility to fluoroquinolones, the class to which CIP belongs (MIC 0.125–1.0 mg/L), would not be detected by this method.<ref>Template:Cite journal</ref>

Epidemiology

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File:Fievre typhoide.png
Typhoid fever incidence; most common in Asia, Africa, Central and South America
Template:LegendTemplate:Legend

In 2000, typhoid fever caused an estimated 21.7 million illnesses and 217,000 deaths.<ref name=Crump2010/> It occurs most often in children and young adults between 5 and 19 years old.<ref name="who">Template:Cite web</ref> In 2013, it resulted in about 161,000 deaths – down from 181,000 in 1990.<ref name=GBD204 /> Infants, children, and adolescents in south-central and Southeast Asia have the highest rates of typhoid.<ref name="Crump JA, Luby SP, Mintz ED 2004">Template:Cite journal</ref> Outbreaks are also often reported in sub-Saharan Africa and Southeast Asia.<ref name="Muyembe-Tamfum JJ, Veyi J, Kaswa M, Lunguya O, Verhaegen J, Boelaert M 2009">Template:Cite journal</ref><ref name="Baddam, Ramani, Narender Kumar, Kwai-Lin Thong, Soo-Tein Ngoi, Cindy Shuan Ju Teh, Kien-Pong Yap, Lay-Ching Chai, Tiruvayipati Suma Avasthi, and Niyaz Ahmed 2012">Template:Cite journal</ref><ref name="Yap et al 2012">Template:Cite journal</ref> In 2000, more than 90% of morbidity and mortality due to typhoid fever occurred in Asia.<ref>Template:Cite web</ref> In the U.S., about 400 cases occur each year, 75% of which are acquired while traveling internationally.<ref>Template:Cite journal</ref><ref>Template:Cite web</ref>

Before the antibiotic era, the case fatality rate of typhoid fever was 10–20%. Today, with prompt treatment, it is less than 1%,<ref>Heymann, David L., ed. (2008), Control of Communicable Diseases Manual, Washington, D.C.: American Public Health Association, pg 665. Template:ISBN.</ref> but 3–5% of people who are infected develop a chronic infection in the gall bladder.<ref name="Levine et al 1982">Template:Cite journal</ref> Since S. enterica subsp. enterica serovar Typhi is human-restricted, these chronic carriers become the crucial reservoir, which can persist for decades for further spread of the disease, further complicating its identification and treatment.<ref name="G Gonzalez-Escobedo, JM Marshall, JS Gunn 2010">Template:Cite journal</ref> Lately, the study of S. enterica subsp. enterica serovar Typhi associated with a large outbreak and a carrier at the genome level provides new insight into the pathogenesis of the pathogen.<ref name="Yap et al 2012-2">Template:Cite journal</ref><ref name="Yap et al 2014">Template:Cite journal</ref>

In industrialized nations, water sanitation and food handling improvements have reduced the number of typhoid cases.<ref>Template:Cite journal</ref> Third world nations have the highest rates. People in these areas often lack access to clean water, proper sanitation systems, and proper healthcare facilities. In these areas, such access to basic public-health needs is not expected in the near future.<ref>Template:Cite journal</ref>

In 2004–2005, an outbreak in the Democratic Republic of Congo resulted in more than 42,000 cases and 214 deaths.<ref name="who" /> Since November 2016, Pakistan has had an outbreak of extensively drug-resistant (XDR) typhoid fever.<ref>Template:Cite news</ref>

In Europe, a report based on data for 2017 retrieved from The European Surveillance System (TESSy) on the distribution of confirmed typhoid and paratyphoid fever cases found that 22 EU/EEA countries reported a total of 1,098 cases, 90.9% of which were travel-related, mainly acquired during travel to South Asia.<ref>Template:Cite web</ref>

Outbreaks

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File:TyphoidOutbreaksMap.pdf
Map of Typhoid Fever Outbreaks 1989–2018<ref name=":11">Template:Cite journal</ref>
  • Plague of Athens (suspected)<ref name=":10" />
  • Cocoliztli epidemics (suspected)<ref name="Krause 2018">Template:Cite journal</ref>
  • "Burning Fever" outbreak among indigenous Americans. Between 1607 and 1624, 85% of the population at the James River died from a typhoid epidemic. The World Health Organization estimates the death toll was over 6,000 during this time.<ref>Template:Cite web</ref>
  • Maidstone, Kent outbreak in 1897–1898: 1,847 patients were recorded to have typhoid fever. This outbreak is notable because it was the first time a typhoid vaccine was deployed during a civilian outbreak. Almoth Edward Wright's vaccine was offered to 200 healthcare providers, and of the 84 individuals who received the vaccine, none developed typhoid whereas 4 who had not been vaccinated became ill.<ref name=":1" />
  • American army in the Spanish-American war: government records estimate over 21,000 troops had typhoid, resulting in 2,200 deaths.<ref name=":1" />
  • In 1902, guests at mayoral banquets in Southampton and Winchester, England became ill and four died, including the Dean of Winchester, after consuming oysters. The infection was due to oysters sourced from Emsworth, where the oyster beds had been contaminated with raw sewage.<ref name="oyster1">Template:Cite web</ref><ref>Template:Cite report</ref>
  • Jamaica Plain neighborhood, Boston in 1908 – linked to milk delivery. See the history section, "carriers" for further details.<ref name=":2" />
  • Outbreak in upper-class New Yorkers who employed Mary Mallon – 51 cases and 3 deaths from 1907 to 1915.<ref name=":4" /><ref name=":7" />
  • Aberdeen, Scotland, in summer 1964 – traced back to contaminated canned beef sourced from Argentina sold in markets. More than 500 patients were quarantined in the hospital for a minimum of four weeks, and the outbreak was contained without any deaths.<ref>Template:Cite news</ref>
  • Dushanbe, Tajikistan, in 1996–1997: 10,677 cases reported, 108 deaths.<ref name=":11" />
  • Kinshasa, Democratic Republic of the Congo, in 2004: 43,000 cases and over 200 deaths.<ref name=":1" /> A prospective study of specimens collected in the same region between 2007 and 2011 revealed about one-third of samples obtained from patient samples were resistant to multiple antibiotics.<ref>Template:Cite journal</ref>
  • Kampala, Uganda in 2015: 10,230 cases reported.<ref name=":11" />

History

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Early descriptions

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The plague of Athens, during the Peloponnesian War, was most likely an outbreak of typhoid fever.<ref name=":1" /> During the war, Athenians retreated into a walled-in city to escape attack from the Spartans. This massive influx of humans into a concentrated space overwhelmed the water supply and waste infrastructure, likely leading to unsanitary conditions as fresh water became harder to obtain and waste became more difficult to collect and remove beyond the city walls.<ref name=":1" /> In 2006, examining the remains of a mass burial site from Athens from around the time of the plague (~430 B.C.) revealed that fragments of DNA similar to that of modern-day S. Typhi were detected, whereas Yersinia pestis (plague), Rickettsia prowazekii (typhus), Mycobacterium tuberculosis, cowpox virus, and Bartonella henselae were not detected in any of the remains tested.<ref name=":10">Template:Cite journal</ref>

Definition and evidence of transmission

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The French doctors Pierre-Fidele Bretonneau and Pierre-Charles-Alexandre Louis are credited with describing typhoid fever as a specific disease, unique from typhus. Both doctors performed autopsies on individuals who died in Paris due to fever – and indicated that many had lesions on the Peyer's patches which correlated with distinct symptoms before death.<ref name=":1">Template:Cite book</ref> British medics were skeptical of the differentiation between typhoid and typhus because both were endemic to Britain at that time. However, in France, only typhoid was present circulating in the population.<ref name=":1" /> Pierre-Charlles-Alexandre Louis also performed case studies and statistical analysis to demonstrate that typhoid was contagious – and that persons who already had the disease seemed to be protected.<ref name=":1" /> Afterward, several American doctors confirmed these findings, and then Sir William Jenner convinced any remaining skeptics that typhoid is a specific disease recognizable by lesions in the Peyer's patches by examining sixty-six autopsies from fever patients and concluding that the symptoms of headaches, diarrhea, rash spots, and abdominal pain were present only in patients who were found to have intestinal lesions after death; these observations solidified the association of the disease with the intestinal tract and gave the first clue to the route of transmission.<ref name=":1" />

In 1847, William Budd learned of an epidemic of typhoid fever in Clifton, and identified that all 13 of 34 residents who had contracted the disease drew their drinking water from the same well.<ref name=":1" /> Notably, this observation was two years before John Snow first published an early version of his theory that contaminated water was the central conduit for transmitting cholera. Budd later became health officer of Bristol ensured a clean water supply, and documented further evidence of typhoid as a water-borne illness throughout his career.<ref name=":1" />

Cause

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Polish scientist Tadeusz Browicz described a short bacillus in the organs and feces of typhoid victims in 1874.<ref>Template:Cite journal</ref> Browicz was able to isolate and grow the bacilli but did not go as far as to insinuate or prove that they caused the disease.<ref name=":1" />

In April 1880, three months before Eberth's publication, Edwin Klebs described short and filamentous bacilli in the Peyer's patches in typhoid victims.<ref>Template:Cite journal</ref> The bacterium's role in disease was speculated but not confirmed.<ref name=":1" />

In 1880, Karl Joseph Eberth described a bacillus that he suspected was the cause of typhoid.<ref> Template:Cite journal</ref><ref> Template:Cite journal</ref><ref> Eberth's findings were verified by Robert Koch Template:Cite journal</ref> Eberth is given credit for discovering the bacterium definitively by successfully isolating the same bacterium from 18 of 40 typhoid victims and failing to discover the bacterium present in any "control" victims of other diseases.<ref name=":1" /> In 1884, pathologist Georg Theodor August Gaffky (1850–1918) confirmed Eberth's findings.<ref>Template:Cite journal</ref> Gaffky isolated the same bacterium as Eberth from the spleen of a typhoid victim, and was able to grow the bacterium on solid media.<ref name=":1" /> The organism was given names such as Eberth's bacillus, Eberthella Typhi, and Gaffky-Eberth bacillus.<ref name=":1" /> Today, the bacillus that causes typhoid fever goes by the scientific name Salmonella enterica serovar Typhi.<ref>Template:Cite book</ref>

Chlorination of water

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Most developed countries had declining rates of typhoid fever throughout the first half of the 20th century due to vaccinations and advances in public sanitation and hygiene. In 1893, attempts were made to chlorinate the water supply in Hamburg, Germany, and in 1897 Maidstone, England, was the first town to have its entire water supply chlorinated.<ref>Template:Cite journal</ref> In 1905, following an outbreak of typhoid fever, the City of Lincoln, England, instituted permanent water chlorination.<ref>Template:Cite web</ref> The first permanent disinfection of drinking water in the US was made in 1908 to the Jersey City, New Jersey, water supply. Credit for the decision to build the chlorination system has been given to John L. Leal.<ref>Template:Cite book</ref> The chlorination facility was designed by George W. Fuller.<ref>Template:Cite book</ref>

Outbreaks in traveling military groups led to the creation of the Lyster bag in 1915: a bag with a faucet that can be hung from a tree or pole, filled with water, and comes with a chlorination tablet to drop into the water.<ref name=":1" /> The Lyster bag was essential for the survival of American soldiers in the Vietnam War.<ref name=":1" />

Direct transmission and carriers

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File:Mary Mallon in hospital.jpg
Mary Mallon ("Typhoid Mary") in a hospital bed (foreground): She was forcibly quarantined as a carrier of typhoid fever in 1907 for three years and then again from 1915 until she died in 1938.

There were several occurrences of milk delivery men spreading typhoid fever throughout the communities they served. Although typhoid is not spread through milk itself, there were several examples of milk distributors in many locations watering their milk down with contaminated water, or cleaning the glass bottles the milk was placed in with contaminated water.<ref name=":1" /><ref name=":2" /> Boston had two such cases around the turn of the 20th century.<ref name=":2">Template:Cite web</ref> In 1899, there were 24 cases of typhoid traced to a single milkman, whose wife had died of typhoid fever a week before the outbreak.<ref name=":2" /> In 1908, J.J. Fallon, who was also a milkman, died of typhoid fever.<ref name=":2" /> Following his death and confirmation of the typhoid fever diagnosis, the city conducted an investigation of typhoid symptoms and cases along his route and found evidence of a significant outbreak. A month after the outbreak was first reported, the Boston Globe published a short statement declaring the outbreak over, stating "[a]t Jamaica Plain there is a slight increase, the total being 272 cases. Throughout the city, there is a total of 348 cases."<ref name=":2" /> There was at least one death reported during this outbreak: Mrs. Sophia S. Engstrom, aged 46.<ref name=":2" /> Typhoid continued to ravage the Jamaica Plain neighborhood in particular throughout 1908, and several more people were reported dead due to typhoid fever, although these cases were not explicitly linked to the outbreak.<ref name=":2" /> The Jamaica Plain neighborhood at that time was home to many working-class and poor immigrants, mostly from Ireland.<ref>Template:Cite book</ref>

The most notorious carrier of typhoid fever, but by no means the most destructive, was Mary Mallon, known as Typhoid Mary.<ref name="Nova">Template:Cite web</ref><ref name=":7">Template:Cite web</ref> Although other cases of human-to-human spread of typhoid were known at the time, the concept of an asymptomatic carrier, who was able to transmit disease, had only been hypothesized and not yet identified or proven.<ref name=":1" /> Mary Mallon became the first known example of an asymptomatic carrier of an infectious disease, making typhoid fever the first known disease being transmissible through asymptomatic hosts.<ref name=":1" /> The cases and deaths caused by Mallon were mainly upper-class families in New York City.<ref name=":1" /> At the time of Mallon's tenure as a personal cook for upper-class families, New York City reported 3,000 to 4,500 cases of typhoid fever annually.<ref name=":1" /> In the summer of 1906, two daughters of a wealthy family and maids working in their home became ill with typhoid fever.<ref name=":1" /> After investigating their home water sources and ruling out water contamination, the family hired civil engineer George Soper to conduct an investigation of the possible source of typhoid fever in the home.<ref name=":1" /> Soper described himself as an "epidemic fighter".<ref name=":1" /> His investigation ruled out many sources of food, and led him to question if the cook the family hired just prior to their household outbreak, Mallon, was the source.<ref name=":1" /> Since she had already left and begun employment elsewhere, he proceeded to track her down in order to obtain a stool sample.<ref name=":1" /> When he was able to finally meet Mallon in person he described her by saying "Mary had a good figure and might have been called athletic had she not been a little too heavy."<ref name=":4">Template:Cite journal</ref> In recounts of Soper's pursuit of Mallon, his only remorse appears to be that he was not given enough credit for his relentless pursuit and publication of her personal identifying information, stating that the media "rob[s] me of whatever credit belongs to the discovery of the first typhoid fever carrier to be found in America."<ref name=":4"/> Ultimately, 51 cases and 3 deaths were suspected to be caused by Mallon.<ref>Template:Cite web</ref><ref name=":7" />

In 1924, the city of Portland, Oregon, experienced an outbreak of typhoid fever, consisting of 26 cases and 5 deaths, all deaths due to intestinal hemorrhage.<ref name=":3">Template:Cite journal</ref> All cases were concluded to be due to a single milk farm worker, who was shedding large amounts of the typhoid pathogen in his urine.<ref name=":3" /> Misidentification of the disease, due to inaccurate Widal test results, delayed identification of the carrier and proper treatment.<ref name=":3" /> Ultimately, it took four samplings of different secretions from all of the dairy workers in order to successfully identify the carrier.<ref name=":3" /> Upon discovery, the dairy worker was forcibly quarantined for seven weeks, and regular samples were taken, most of the time the stool samples yielding no typhoid and often the urine yielding the pathogen.<ref name=":3" /> The carrier was reported as being 72 years old and appearing in excellent health with no symptoms.<ref name=":3" /> Pharmaceutical treatment decreased the amount of bacteria secreted, however, the infection was never fully cleared from the urine, and the carrier was released "under orders never again to engage in the handling of foods for human consumption."<ref name=":3" /> At the time of release, the authors noted "for more than fifty years he has earned his living chiefly by milking cows and knows little of other forms of labor, it must be expected that the closest surveillance will be necessary to make certain that he does not again engage in this occupation."<ref name=":3" />

Overall, in the early 20th century the medical profession began to identify disease carriers and evidence of transmission independent of water contamination.<ref name=":1" /> In a 1933 American Medical Association publication, physicians' treatment of asymptomatic carriers is best summarized by the opening line "Carriers of typhoid bacilli are a menace".<ref name=":6">Template:Cite journal</ref> Within the same publication, the first official estimate of typhoid carriers is given: 2–5% of all typhoid patients, and distinguished between temporary carriers and chronic carriers.<ref name=":6" /> The authors further estimate that there are four to five chronic female carriers to every one male carrier, although offered no data to explain this assertion of a gender difference in the rate of typhoid carriers.<ref name=":6" /> As far as treatment, the authors suggest: "When recognized, carriers must be instructed as to the disposal of excreta as well as to the importance of personal cleanliness. They should be forbidden to handle food or drink intended for others, and their movements and whereabouts must be reported to the public health officers".<ref name=":6" />

File:Typhoid LAcounty 2016.jpg
New Typhoid carrier cases reported in L.A. County between 2006 and 2016<ref name="LA county typhoid 2016" />

Today, typhoid carriers exist all over the world, but the highest incidence of asymptomatic infection is likely to occur in South/Southeast Asian and Sub-Saharan countries.<ref name="LA county typhoid 2016" /><ref>Template:Cite journal</ref> The Los Angeles County department of public health tracks typhoid carriers and reports the number of carriers identified within the county yearly; between 2006 and 2016 0–4 new cases of typhoid carriers were identified per year.<ref name="LA county typhoid 2016" /> Cases of typhoid fever must be reported within one working day from identification. As of 2018, chronic typhoid carriers must sign a "Carrier Agreement" and are required to test for typhoid shedding twice yearly, ideally every 6 months.<ref name=":8">Template:Cite web</ref> Carriers may be released from their agreements upon fulfilling "release" requirements, based on completion of a personalized treatment plan designed with medical professionals.<ref name=":8" /> Fecal or gallbladder carrier release requirements: 6 consecutive negative feces and urine specimens submitted at 1-month or greater intervals beginning at least 7 days after completion of therapy.<ref name=":8" /> Urinary or kidney carrier release requirements: 6 consecutive negative urine specimens submitted at 1-month or greater intervals beginning at least 7 days after completion of therapy.<ref name=":8" />

Due to the nature of asymptomatic cases, many questions remain about how individuals can tolerate infection for long periods, how to identify such cases, and efficient options for treatment. Researchers are working to understand asymptomatic infection with Salmonella species by studying infections in laboratory animals, which will ultimately lead to improved prevention and treatment options for typhoid carriers. In 2002, John Gunn described the ability of Salmonella sp. to form biofilms on gallstones in mice, providing a model for studying carriage in the gallbladder.<ref>Template:Cite journal</ref> Denise Monack and Stanley Falkow described a mouse model of asymptomatic intestinal and systemic infection in 2004, and Monack went on to demonstrate that a subpopulation of superspreaders are responsible for the majority of transmission to new hosts, following the 80/20 rule of disease transmission, and that the intestinal microbiota likely plays a role in transmission.<ref name=":9">Template:Cite journal</ref><ref>Template:Cite journal</ref> Monack's mouse model allows long-term carriage of Salmonella in mesenteric lymph nodes, spleen and liver.<ref name=":9" />

Vaccine development

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File:Almroth Wright c1900.jpg
Almroth Edward Wright developed the first effective typhoid vaccine.

British bacteriologist Almroth Edward Wright first developed an effective typhoid vaccine at the Army Medical School in Netley, Hampshire. It was introduced in 1896 and used successfully by the British during the Second Boer War in South Africa.<ref>Template:Cite web</ref> At that time, typhoid often killed more soldiers at war than were lost due to enemy combat. Wright further developed his vaccine at a newly opened research department at St Mary's Hospital Medical School in London in 1902, where he established a method for measuring protective substances (opsonin) in human blood.<ref>Template:Cite journal</ref> Wright's version of the typhoid vaccine was produced by growing the bacterium at body temperature in broth, then heating the bacteria to 60 °C to "heat inactivate" the pathogen, killing it, while keeping the surface antigens intact. The heat-killed bacteria was then injected into a patient.<ref name=":1" /> To show evidence of the vaccine's efficacy, Wright then collected serum samples from patients several weeks post-vaccination, and tested their serum's ability to agglutinate live typhoid bacteria. A "positive" result was represented by clumping of bacteria, indicating that the body was producing anti-serum (now called antibodies) against the pathogen.<ref name=":1" />

Citing the example of the Second Boer War, during which many soldiers died from easily preventable diseases, Wright convinced the British Army that 10 million vaccine doses should be produced for the troops being sent to the Western Front, thereby saving up to half a million lives during World War I.<ref>Template:Cite webTemplate:Dead link</ref> The British Army was the only combatant at the outbreak of the war to have its troops fully immunized against the bacterium. For the first time, their casualties due to combat exceeded those from disease.<ref>Template:Cite web</ref>

In 1909, Frederick F. Russell, a U.S. Army physician, adopted Wright's typhoid vaccine for use with the Army, and two years later, his vaccination program became the first in which an entire army was immunized. It eliminated typhoid as a significant cause of morbidity and mortality in the U.S. military.<ref name="USAMRMC">Template:Cite book</ref> Typhoid vaccination for members of the American military became mandatory in 1911.<ref name=":1" /> Before the vaccine, the rate of typhoid fever in the military was 14,000 or greater per 100,000 soldiers. By World War I, the rate of typhoid in American soldiers was 37 per 100,000.<ref name=":1" />

During the Second World War, the United States Army authorized the use of a trivalent vaccine – containing heat-inactivated Typhoid, Paratyphi A and Paratyphi B pathogens.<ref name=":1" />

In 1934, the discovery of the Vi capsular antigen by Arthur Felix and Miss S. R. Margaret Pitt enabled the development of the safer Vi Antigen vaccine – which is widely in use today.<ref>Template:Cite journal</ref> Arthur Felix and Margaret Pitt also isolated the strain Ty2, which became the parent strain of Ty21a, the strain used as a live-attenuated vaccine for typhoid fever today.<ref>Template:Cite journal</ref>

Antibiotics and resistance

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Chloramphenicol was isolated from Streptomyces by David Gotlieb during the 1940s.<ref name=":1" /> In 1948, American army doctors tested its efficacy in treating typhoid patients in Kuala Lumpur, Malaysia.<ref name=":1" /> Individuals who received a full course of treatment cleared the infection, whereas patients given a lower dose had a relapse.<ref name=":1" /> Asymptomatic carriers continued to shed bacilli despite chloramphenicol treatment – only ill patients were improved with chloramphenicol.<ref name=":1" /> Resistance to chloramphenicol became frequent in Southeast Asia by the 1950s, and today chloramphenicol is only used as a last resort due to the high prevalence of resistance.<ref name=":1" />

Terminology

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The disease has been referred to by various names, often associated with symptoms, such as gastric fever, enteric fever, abdominal typhus, infantile remittent fever, slow fever, nervous fever, phytogenic fever,<ref>Template:Cite web</ref> drain fever, and low fever.<ref>Template:Cite news</ref>

Society and culture

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Notable people

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Further reading

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