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Sunday, 29 January 2017

Kuman dari Tanah

Kuman dari Tanah


Burkholderia pseudomallei (also known as Pseudomonas pseudomallei) is a Gram-negative, bipolar, aerobic, motile rod-shaped bacterium.[2] It is a soil-dwelling bacterium endemic in tropical and subtropical regions worldwide, particularly in Thailand and northern Australia.[3] It infects humans and animals and causes the disease melioidosis. It is also capable of infecting plants.[4]
B. pseudomallei measures 2–5 μm in length and 0.4–0.8 μm in diameter and is capable of self-propulsion using flagella. The bacteria can grow in a number of artificial nutrient environments, especially betaine- and arginine-containing ones.
In vitro, optimal proliferation temperature is reported around 40 °C in neutral or slightly acidic environments (pH 6.8–7.0). The majority of strains are capable of fermentation of sugars without gas formation (most importantly, glucose and galactose; older cultures are reported to also metabolize maltose and starch). Bacteria produce both exo- and endotoxins. The role of the toxins identified in the process of melioidosis symptom development has not been fully elucidated.[5]
B. pseudomallei is susceptible to numerous disinfectants, including benzalkonium chloride, iodine, mercuric chloride, potassium permanganate, 1% sodium hypochlorite, 70% ethanol, 2% glutaraldehyde, and to a lesser extent, phenolic preparations.[29] B. pseudomallei is effectively killed by the commercial disinfectants, Perasafe and Virkon.[30] The microorganism can also be destroyed by heating to above 74 °C for 10 min or by ultraviolet irradiation.[31] B. pseudomallei is not reliably disinfected by chlorine.[32][33]
B. pseudomallei infection in humans is called melioidosis; its mortality is 20 to 50% even with treatment.[22]

The antibiotic of choice is ceftazidime.[22] While various antibiotics are active in vitro (e.g., chloramphenicol, doxycycline, co-trimoxazole), they have been proven to be inferior in vivo for the treatment of acute melioidosis.[34] Disc diffusion tests are unreliable when looking for co-trimoxazole resistance in B. pseudomallei (they greatly overestimate resistance) and Etests or agar dilution tests should be used in preference.[35][36] The actions of co-trimoxazole and doxycycline are antagonistic, which suggests these two drugs ought not to be used together.[37]
The organism is intrinsically resistant to gentamicin[38] and colistin, and this fact is helpful in the identification of the organism.[39] Kanamycin is used to kill B. pseudomallei in the laboratory, but the concentrations used are much higher than those achievable in humans.[40]
B. pseudomallei is an opportunistic pathogen. An environmental organism, it has no requirement to pass through an animal host to replicate. From the point of view of the bacterium, human infection is an developmental "dead end".[41]
Strains which cause disease in humans differ from those causing disease in other animals, by possessing certain genomic islands.[42] It may have the ability to cause disease in humans because of DNA it has acquired from other microorganisms.[42] Its mutation rate is also high, and the organism continues to evolve even after infecting a host.[43]
B. pseudomallei is able to invade cells (it is an intracellular pathogen).[44] It is able to polymerise actin, and to spread from cell to cell, causing cell fusion and the formation of multinucleated giant cells.[45] It possesses a uniquely fusogenic type-6 secretion system that is required for cell-cell spread and virulence in mammalian hosts.[46] The bacterium also expresses a toxin called lethal factor 1.[47] B. pseudomallei is one of the first Proteobacteria to be identified as containing an active type-6 secretion system. it is also the only organism identified that contains up to six different type-6 secretion systems.[48]
B. pseudomallei is intrinsically resistant to a large number of antimicrobial agents by virtue of its efflux pump mechanism. This mediates resistance to aminoglycosides (AmrAB-OprA), tetracyclines, fluoroquinolones, and macrolides (BpeAB-OprB).[49]


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