Melioidosis is an infectious disease caused by the bacterium Burkholderia pseudomallei. While many exposed individuals remain asymptomatic, others develop a range of symptoms, from mild fever and skin changes to severe pneumonia, abscesses, and potentially fatal septic shock. A subset of patients, around 10%, experience chronic melioidosis, characterized by symptoms persisting for over two months. The severity and diverse presentation of melioidosis highlight its potential for significant morbidity and mortality.
In 1912, Pathologist Alfred Whitmore and his assistant Krishnaswami first reported melioidosis among beggars and morphine addicts at autopsy in Rangoon, present-day Myanmar.
In 1913, Arthur Conan Doyle may have alluded to melioidosis in a Sherlock Holmes story, and an outbreak occurred at the Institute for Medical Research in Kuala Lumpur.
In 1917, Fletcher isolated an organism similar to Whitmore's bacillus from a Tamil rubber estate worker, confirming the presence of the new species of bacteria.
In 1921, the term "melioidosis" was first coined, derived from Greek roots meaning "a condition similar to glanders."
In 1927, the first human case of melioidosis in South Asia was reported in Sri Lanka.
In 1932, Thomas and Fletcher compiled a collection of 83 cases of melioidosis from various sources. The case series indicated a high mortality rate, with only two survivors.
In 1936, the first animal (pig) case of melioidosis in Africa was reported in Madagascar.
In 1937, water was first identified as the natural habitat of B. pseudomallei, which was a key discovery.
In 1949, the first case of Australian melioidosis was described during an outbreak in sheep in North Queensland.
In 1950, the first case of human melioidosis in Australia was reported in Townsville, following the outbreak in sheep the previous year.
In the United States, two historical cases (1950 and 1971) have been reported amongst people that did not travel overseas.
In 1955, the first case of local human melioidosis was reported in Thailand.
From 1961–2017, fifty-one cases of melioidosis were reported in Bangladesh. Nonetheless, lack of awareness and resources gives rise to underdiagnosis of the disease in the country.
In the United States, two historical cases (1950 and 1971) have been reported amongst people that did not travel overseas.
In 1982 and 1984, the Soviet Union reportedly used B. mallei during the Soviet–Afghan War.
In 1982 and 1984, the Soviet Union reportedly used B. mallei during the Soviet–Afghan War.
Before 1989, the standard treatment for acute melioidosis was a three-drug combination of chloramphenicol, co-trimoxazole, and doxycycline; this regimen is associated with a mortality rate of 80% and is no longer used unless no other alternatives are available.
In 1989, studies in Thailand demonstrated ceftazidime as an effective antibiotic against melioidosis, reducing the risk of death from 74% to 37%.
In 1990, Vanaporn Wuthiekanun found a non-virulent 'arabinose-positive B. pseudomallei', later reclassified as B. thailandensis, which became a useful tool for studying the pathogenesis of B. pseudomallei.
Since 1991, a total of 583 cases were reported in India, with most Indian cases located in Karnataka and Tamil Nadu.
In 1992, the pathogen previously classified under Pseudomonas was formally named Burkholderia pseudomallei.
In 1994, the First International Symposium on melioidosis was held in Kuala Lumpur, attended by 80 delegates, with presented papers later published as a book.
In 2002, B. pseudomallei was classified as a "Category B agent".
In 2004, the complete genome of B. pseudomallei was published, marking a significant advancement in understanding the bacterium.
According to a review of case reports in 2005, lifelong therapy with co-trimoxazole may be needed for those with prosthetic vascular grafts due to mycotic aneurysm.
In the United States, four recent cases (2010, 2011, 2013, 2020) have been reported amongst people that did not travel overseas.
Since 2010, in the United Kingdom, 41.3% of imported melioidosis cases reported by laboratories were not officially notified.
Since 2010, under-reporting is a common problem as only 1,300 cases have been reported worldwide, which is less than 1% of the projected incidence based on modelling.
In the United States, four recent cases (2010, 2011, 2013, 2020) have been reported amongst people that did not travel overseas.
In 2012, B pseudomallei was classified as a "Tier 1 select agent" by the U.S. Centers for Disease Control, highlighting its potential threat.
In the United States, four recent cases (2010, 2011, 2013, 2020) have been reported amongst people that did not travel overseas.
A study from 2014 to 2018 showed no significant differences in whether behavioral changes can reduce the risk of contracting melioidosis. Modification of behavioural changes or more frequent interventions may be needed to ensure a definite reduction in the risk of getting melioidosis.
In 2014, co-trimoxazole was established as the only oral eradication therapy, replacing the previous combination therapy with doxycycline.
In 2014, the Royal Darwin Hospital guidelines recommended granulocyte colony-stimulating factor (G-CSF) as immunomodulating therapy for those with septic shock at 300 ug daily as soon as the bacteriological laboratory flag the culture as possibly Burkholderia pseudomallei.
Recurrent melioidosis is rare since 2014 due to improved antibiotic therapy and prolongation of the intensive phase of therapy as evident in Darwin Prospective Melioidosis Study.
In 2015, the International Melioidosis Society was formed to raise disease awareness of Melioidosis.
In June 2016, melioidosis became a notifiable condition in Thailand, allowing for monitoring of the disease burden. However, the official notification system initially underestimated the true incidence and mortality.
In 2016, a mathematical model estimated that approximately 165,000 people are infected with melioidosis annually, resulting in about 89,000 deaths. The model also highlighted diabetes as a major risk factor.
In 2016, a statistical model was developed to predict the occurrence of global melioidosis per year, aiding in disease monitoring and prevention efforts.
In 2016, a statistical model was developed, predicting approximately 165,000 melioidosis cases per year, with a significant portion in East and South Asia and the Pacific. The model estimated a high mortality rate.
From 1961–2017, fifty-one cases of melioidosis were reported in Bangladesh. Nonetheless, lack of awareness and resources gives rise to underdiagnosis of the disease in the country.
In 2017, whole genome sequencing of B. pseudomallei suggested Australia as the early reservoir for melioidosis, disproving previous hypotheses about its spread from Southeast Asia.
A study from 2014 to 2018 showed no significant differences in whether behavioral changes can reduce the risk of contracting melioidosis. Modification of behavioural changes or more frequent interventions may be needed to ensure a definite reduction in the risk of getting melioidosis.
In 2018, a study determined that co-trimoxazole could potentially prevent melioidosis in high-risk renal failure patients undergoing haemodialysis.
According to the 2020 Revised Royal Darwin Hospital Guideline, the dosage for intravenous ceftazidime is 2g 6-hourly in adults (50 mg/kg up to 2g in children less than 15 years old). The dosage for meropenem is 1g 8-hourly in adults (25 mg/kg up to 1g in children).
In the United States, four recent cases (2010, 2011, 2013, 2020) have been reported amongst people that did not travel overseas.
In 2021, the European Committee on Antimicrobial Susceptibility Testing (EUCAST) released a new guideline on interpreting the susceptibility of B pseudomallei towards various antibiotics on disc susceptibility testing.
In 2021, there was a melioidosis outbreak in several states in the United States due to usage of contaminated aromatherapy spray imported from India.
As of 2022, melioidosis is not included in the WHO list of neglected tropical diseases.
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