Drug resistance

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Drug resistance is the reduction in effectiveness of a drug such as an antimicrobial or an antineoplastic [1] in curing a disease or condition. When the drug is not intended to kill or inhibit a pathogen, then the term is equivalent to dosage failure or drug tolerance. More commonly, the term is used in the context of resistance acquired by pathogens. When an organism is resistant to more than one drug, it is said to be multidrug resistant.

Introduction

Drug or toxin or chemical resistance is a consequence of evolution and is a response to pressures imposed on any living organism. Individual organisms vary in their sensitivity to the drug used and some with greater fitness may be capable of surviving drug treatment. Drug resistant traits are accordingly inherited by subsequent offspring, resulting in a population that is more drug resistant. Unless the drug used makes sexual reproduction or cell-division or horizontal gene transfer impossible in the entire target population, resistance to the drug will inevitably follow. This can be seen in cancerous tumours where some cells may develop resistance to the drugs used in chemotherapy. [2] A quicker process of sharing resistance exists among single-celled organisms, and is termed horizontal gene transfer in which there is a direct exchange of genes. Some processes that destroy 100% of pathogens make use of high sugar concentrations as in fruit canning or high salt and vinegar concentrations as in pickling. Strong sugar and salt solutions have a high osmotic gradient, destroying pathogens by dehydration through their permeable cell walls. Other methods include irradiation, or high temperatures as in canning and pasteurisation. Examples of drug-resistant strains are to be found in microorganisms [3] such as bacteria and viruses, parasites both endo- and ecto-, plants, fungi, arthropods [4], mammals [5], birds [6], reptiles [7], fish and amphibians [8].

In the domestic environment, drug-resistant strains of organism may arise from seemingly innocent activities such as tooth-brushing and mouthwashing [9], the use of disinfectants and detergents, shampoos and soaps, particularly antibacterial soaps, [10][11] hand-washing [12], surface sprays, application of deodorants, sunblocks and any cosmetic or health-care product, insecticides and dips [13]. The chemicals contained in these preparations, besides harming beneficial organisms, may intentionally or inadvertently target organisms that have the potential to develop resistance and thereby become increasingly problematic. [14]

"The use and misuse of antimicrobials in human medicine and animal husbandry over the past 70 years has led to a relentless rise in the number and types of microorganisms resistant to these medicines - leading to death, increased suffering and disability, and higher healthcare costs." - World Health Organisation 2010

"Deaths from acute respiratory infections, diarrhoeal diseases, measles, AIDS, malaria and tuberculosis account for more than 85% of the mortality from infection worldwide. Resistance to first-line drugs in most of the pathogens causing these diseases ranges from zero to almost 100%. In some instances resistance to second- and thirdline agents is seriously compromising treatment outcome. Added to this is the significant global burden of resistant hospital-acquired infections, the emerging problems of antiviral resistance and the increasing problems of drug resistance in the neglected parasitic diseases of poor and marginalized populations." - WHO Global Strategy for Containment of Antimicrobial Resistance 2010

Mechanisms

The four main mechanisms by which microorganisms exhibit resistance to antimicrobials are:

  1. Drug inactivation or modification: e.g. enzymatic deactivation of Penicillin G in some penicillin-resistant bacteria through the production of β-lactamases.
  2. Alteration of target site: e.g. alteration of PBP—the binding target site of penicillins—in MRSA and other penicillin-resistant bacteria.
  3. Alteration of metabolic pathway: e.g. some sulfonamide-resistant bacteria do not require para-aminobenzoic acid (PABA), an important precursor for the synthesis of folic acid and nucleic acids in bacteria inhibited by sulfonamides. Instead, like mammalian cells, they turn to utilizing preformed folic acid.
  4. Reduced drug accumulation: by decreasing drug permeability and/or increasing active efflux (pumping out) of the drugs across the cell surface.[15]

Metabolic price

Biological cost or metabolic price is a measure of the increased energy metabolism required to achieve a function.

Drug resistance has a high metabolic price,[16] in pathogens for which this concept is relevant (bacteria[17], endoparasites, and tumor cells.) In viruses, an equivalent "cost" is genomic complexity.

Treatment

The chances of drug resistance can sometimes be minimised by using multiple drugs simultaneously. This works because individual mutations can be independent and may only tackle one drug at a time, if the individuals are still killed by the other drugs, then the mutations cannot persist. This was used successfully in tuberculosis. However, cross resistance where mutations confer resistance to two or more treatments can be problematic.

See also

References

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External links

et:Ravimresistentsus

fa:مقاومت دارویی it:Farmaco-resistenza ja:薬剤耐性 no:Resistens ru:Резистентность (иммунитет) sv:Resistens

zh:抗药性
  1. MeSH Drug+Resistance
  2. http://www.merck.com/mmhe/sec02/ch013/ch013d.html
  3. http://www.tulane.edu/~wiser/protozoology/notes/drugs.html
  4. http://horizon.documentation.ird.fr/exl-doc/pleins_textes/pleins_textes_5/b_fdi_12-13/15697.pdf
  5. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480843/pdf/bullwho00185-0069.pdf
  6. http://www.jstor.org/pss/3808656
  7. Reptile Channel
  8. Reptile Channel
  9. http://www.healthstores.com/dentists/new_dental_products.htm
  10. http://www.cbc.ca/marketplace/webextras/triclosan/antibacterial.html?triclosan
  11. http://health.howstuffworks.com/skin-care/cleansing/myths/antibacterial-soap-outlawed.htm
  12. http://www.journals.uchicago.edu/doi/abs/10.1086/507964
  13. Kyong Sup Yoon, Deok Ho Kwon, Joseph P. Strycharz, Craig S. Hollingsworth, Si Hyeock Lee, J. Marshall Clark (2008). Biochemical and Molecular Analysis of Deltamethrin Resistance in the Common Bed Bug (Hemiptera: Cimicidae) Journal of Medical Entomology, 45 (6), 1092-1101 DOI: 10.1603/0022-2585(2008)45[1092:BAMAOD]2.0.CO;2
  14. http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Antibacterial_cleaning_products
  15. Li, X, Nikadio H (2009). "Efflux-mediated drug resistance in bacteria: an update". Drug. 69 (12): 1555–623. doi:10.2165/11317030-000000000-00000. PMC 2847397Freely accessible. PMID 19678712. 
  16. The biological cost of antimicrobial resistance Stephen H. Gillespie*, and Timothy D. McHugh
  17. Wichelhaus TA, Böddinghaus B, Besier S, Schäfer V, Brade V, Ludwig A (2002). "Biological cost of rifampin resistance from the perspective of Staphylococcus aureus". Antimicrob. Agents Chemother. 46 (11): 3381–5. doi:10.1128/AAC.46.11.3381-3385.2002. PMC 128759Freely accessible. PMID 12384339.