New Delhi metallo-beta-lactamase 1

Klebsiella pneumoniae, the bacterium in which NDM-1 was first identified.

New Delhi Metallo-beta-lactamase-1 (NDM-1)[1] is an enzyme that makes bacteria resistant to a broad range of beta-lactam antibiotics. These include the antibiotics of the carbapenem family, which are a mainstay for the treatment of antibiotic-resistant bacterial infections. The gene for NDM-1 is one member of a large gene family that encodes beta-lactamase enzymes called carbapenemases. Bacteria that produce carbapenemases are often referred to in the news media as "superbugs" because infections caused by them are difficult to treat. Such bacteria are usually susceptible only to polymyxins and tigecycline.[2]

NDM-1 was first detected in a Klebsiella pneumoniae isolate from a Swedish patient of Indian origin in 2008. It was later detected in bacteria in India, Pakistan, the United Kingdom, the United States,[3] Canada,[4] and Japan.[5]

The most common bacteria that make this enzyme are Gram-negative such as Escherichia coli and Klebsiella pneumoniae, but the gene for NDM-1 can spread from one strain of bacteria to another by horizontal gene transfer.[6]

Enzyme function

Structure of the carbapenem backbone.

Carbapenems are a class of beta-lactam antibiotics that are capable of killing most bacteria by inhibiting the synthesis of one of their cell wall layers. The carbapenems were developed to overcome antibiotic resistance mediated by bacterial beta-lactamase enzymes. However, the blaNDM-1 gene produces NDM-1, which is a carbapenemase beta-lactamase - an enzyme that hydrolyzes and inactivates these carbapenem antibiotics.

Carbapenemases are particularly dangerous resistance mechanisms, since they can inactivate a wide range of different antibiotics.[7] The NDM-1 enzyme is one of the class B metallo-beta-lactamase; other types of carbapenemase are class A or class D beta-lactamases.[8] (The class A Klebsiella pneumoniae carbapenemase (KPC) is currently the most common carbapenemase, which was first detected in North Carolina, United States, in 1996 and has since spread worldwide.[9] A later publication indicated that Enterobacteriaceae that produce KPC were becoming common in the United States.[10])

The resistance conferred by this gene (blaNDM-1), therefore, aids the expansion of bacteria that carry it throughout a human host, since they will face less opposition/competition from populations of antibiotic-sensitive bacteria, which will be diminished by the original antibacterial treatment.

Origin and spread

The NDM-1 enzyme was named after New Delhi, the capital city of India, as it was first described by Yong et al. in December 2009 in a Swedish national who fell ill with an antibiotic-resistant bacterial infection that he acquired in India.[11] The infection was identified as a carbapenem-resistant Klebsiella pneumoniae strain bearing the novel gene blaNDM-1. The authors concluded that the new resistance mechanism "clearly arose in India, but there are few data arising from India to suggest how widespread it is".[11] Its exact geographical origin, however, has not been conclusively verified. In March 2010, a study in a hospital in Mumbai found that most carbapenem-resistant bacteria isolated from patients carried the blaNDM-1 gene.[12] Later, the journal authority apologized for using the name of New Delhi, India to describe a pathogen.

NDM-1 β-lactamase was also found in an K. pneumoniae isolate from Croatia, and the patient arrived from Bosnia and Herzegovina. The second geographical origin is considered to be eastern Balkans.[13]

In May 2010, a case of infection with E. coli expressing NDM-1 was reported in Coventry in the United Kingdom.[14] The patient was a man of Indian origin who had visited India 18 months previously, where he had undergone dialysis. In initial assays the bacterium was fully resistant to all antibiotics tested, while later tests found that it was susceptible to tigecycline and colistin. The authors warned that international travel and patients' use of multiple countries' healthcare systems could lead to the "rapid spread of NDM-1 with potentially serious consequences".

As of June 2010, there were three reported cases of Enterobacteriaceae isolates bearing this newly described resistance mechanism in the US, the Centers for Disease Control and Prevention (CDC) stated that "All three U.S. isolates were from patients having received recent medical care in India."[15] However, US experts stated that it is unclear as to whether this strain is any more dangerous than existing antibiotic-resistant bacteria such as methicillin-resistant Staphylococcus aureus, which are already common in the USA.[16]

Structure of colistin, one of the few antibiotics able to treat NDM-1 positive bacterial infections.

In July 2010, a team in New Delhi reported a cluster of three cases of Acinetobacter baumannii bearing blaNDM-1 that were found in the intensive care unit of a hospital in Chennai, India, in April 2010. As previously, the bacteria were fully resistant to all the aminoglycoside β-lactam and quinolone antibiotics, but were susceptible to tigecycline and colistin. This particularly broad spectrum of antibiotic resistance was heightened by the strain's expressing several different resistance genes in addition to blaNDM-1.[17]

A study by a multi-national team was published in the August 2010 issue of the journal The Lancet Infectious Diseases. This examined the emergence and spread of bacteria carrying the blaNDM-1 gene. This reported on 37 cases in the United Kingdom, 44 isolates with NDM-1in Chennai, 26 in Haryana, and 73 in various other sites in Pakistan and India.[1] The authors' analysis of the strains showed that many carried blaNDM-1 on plasmids, which will allow the gene to be readily transferred between different strains of bacteria by horizontal gene transfer. All the isolates were resistant to multiple different classes of antibiotics, including beta-lactam antibiotics, fluoroquinolones, and aminoglycosides, but most were still susceptible to the polymyxin antibiotic colistin.

On 21 August 2010, Ontario, Canada, had its first confirmed case of the "superbug" in Brampton. There were other confirmed cases in British Columbia and Alberta.[18] These confirmed NDM-1 infected cases have no relationship with New Delhi, India. The patients or their relatives never travelled India in the last decade.

In August 2010, a chemical compound GSK 299423 was found to significantly fight against antibiotic-resistant bacteria by making such bacteria unable to reproduce, citing a likely treatment to the NDM-1 strain.[19][20][21][22]

On 6 September 2010, Japan detected its first ever case of the NDM-1 enzyme. In May 2009, a Japanese man in his 50s who had recently returned from vacation in India was struck with a fever and hospitalized, later making a full recovery. Hospital officials confirmed that tests carried out after the patient's recovery were positive for the NDM-1 enzyme.[23]

An environmental point prevalence study conducted between 26 September and 10 October 2010 found bacteria with the NDM-1 gene in drinking water and seepage samples in New Delhi. 50 tap water samples and 171 seepage samples were collected from sites within 12 km of central New Delhi. Of these samples, 20 strains of bacteria were found to contain NDM-1 gene in 51 out of 171 seepage samples and 2 out of 50 tap water samples.[24]

On 8 May 2012, the presence of NDM was found in a patient who died at Royal Alexandra Hospital in Edmonton, Alberta. The patient was also found to be carrying an Acinetobacter strain. The patient contracted the bacteria after another patient, who had surgery on the Indian subcontinent, traveled to Canada and was admitted to hospital with an infection.[25]

Science Daily reported on the 16 December 2013 that a team of scientists from Rice, Nankai and Tianjin universities found NDM-1 in two wastewater treatment plants in northern China.[26][27]

In June 2014 it was reported that the molecule aspergillomarasmine A from the Aspergillus fungus turns off the resistance mechanism of NDM-1 and thus makes bacteria once again sensitive to traditional antibiotics. It has been shown to be effective in mice and rats but has not yet been tested in humans for safety or effectiveness. [28]

Phenotypic detection of NDM-1

Detection of NDM-1 gene depends upon the phenotypic determination of the enzyme activity. These enzymes are zinc dependent and therefore termed as metallo-beta-lactamase. Indian studies have been done which demonstrate their dependency on zinc and the ability of zinc chelating agents like EDTA to decrease their activity. The Modified Hodge Test and a newly developed Re-Modified Hodge Test were developed for detection on a routine basis in resource limited laboratories,[29]

Indian response

The Indian health ministry has disputed the conclusion of the August 2010 Lancet study that the gene originated in India, describing this conclusion as "unfair" and stating that Indian hospitals are perfectly safe for treatment.[30][31] Indian politicians have described linking this new drug resistance gene to India as "malicious propaganda" and blamed multinational corporations for what they describe as selective malignancy.[30][32] A Bharatiya Janata Party politician has instead argued that the journal article is bogus and represented an attempt to scare medical tourists away from India.[33] The Indian Ministry of Health released a statement "strongly refut[ing]" naming the enzyme "New Delhi".[34] A co-author of the 2010 Lancet study, who is based in the University of Madras, has stated that he does not agree with the part of the article that advises people to avoid elective surgeries in India.[35]

In contrast, an editorial in the March 2010 issue of the Journal of Association of Physicians of India blamed the emergence of this gene on the widespread misuse of antibiotics in the Indian healthcare system, stating that Indian doctors have "not yet taken the issue of antibiotic resistance seriously" and noting little control over the prescription of antibiotics by doctors and even pharmacists.[36] The Times of India states that there is general agreement among experts that India needs both an improved policy to control the use of antibiotics and a central registry of antibiotic-resistant infections.[35]

The Lancet naming apology and aftermath

The British journal The Lancet refused to publish a rebuttal from the Indian National Centre for Disease Control, claiming lack of space and that the journal's editors felt it would be better placed elsewhere.[37] However, on 12 January 2011, the editor of The Lancet, Richard Horton, apologized and acknowledged that naming a superbug after New Delhi was an "error".[38] Following this, Ajai R. Singh, editor of Mens Sana Monographs, demanded that such 'geographic names giving' be abandoned and replaced by 'scientific name giving'. He proposed changing NDM-1 to PCM (plasmid-encoding carbapenem-resistant metallo-beta-lactamase).[39]

First death

In August 2010, the first reported death due to bacteria expressing the NDM-1 enzyme was recorded after a Belgian man, who had become infected while being treated in a hospital in Pakistan, died despite being administered colistin. A doctor involved in his treatment said: "He was involved in a car accident during a trip to Pakistan. He was hospitalised with a major leg injury and then repatriated to Belgium, but he was already infected".[40]

See also

References

  1. 1 2 Kumarasamy KK, Toleman MA, Walsh TR, et al. (August 2010). "Emergence of a new antibiotic resistance mechanism in India, Pakistan, and the UK: a molecular, biological, and epidemiological study". Lancet Infect Dis. 10 (9): 597–602. doi:10.1016/S1473-3099(10)70143-2. PMC 2933358Freely accessible. PMID 20705517.
  2. ↑ "Health Protection Report". Health Protection Agency. 3 July 2009.
  3. ↑ Stephen Smith (13 September 2010). "New drug-resistant 'superbug' arrives in Mass.". The Boston Globe. Retrieved 18 September 2010.
  4. ↑ "Superbug detected in GTA". Toronto Star. 22 August 2010.
  5. ↑ Shino Yuasa (8 September 2010). "Japan confirms first case of superbug gene". The Boston Globe. Associated Press. Retrieved 14 February 2016.
  6. ↑ Hudson, Corey; Bent, Zachary; Meagher, Robert; Williams, Kelly (June 7, 2014). "Resistance Determinants and Mobile Genetic Elements of an NDM-1-Encoding Klebsiella pneumoniae Strain". PLOS ONE. 9: e99209. doi:10.1371/journal.pone.0099209. PMC 4048246Freely accessible. PMID 24905728.
  7. ↑ Queenan AM, Bush K (July 2007). "Carbapenemases: the versatile beta-lactamases". Clinical Microbiology Reviews. 20 (3): 440–458. doi:10.1128/CMR.00001-07. PMC 1932750Freely accessible. PMID 17630334.
  8. ↑ Miriagou V, Cornaglia G, Edelstein M, et al. (February 2010). "Acquired carbapenemases in Gram-negative bacterial pathogens: detection and surveillance issues". Clin. Microbiol. Infect. 16 (2): 112–122. doi:10.1111/j.1469-0691.2009.03116.x. PMID 20085605.
  9. ↑ Nordmann P, Cuzon G, Naas T (April 2009). "The real threat of Klebsiella pneumoniae carbapenemase-producing bacteria". Lancet Infect Dis. 9 (4): 228–236. doi:10.1016/S1473-3099(09)70054-4. PMID 19324295.
  10. ↑ Cuzon G, Naas T, Nordmann P (February 2010). "KPC carbapenemases: what is at stake in clinical microbiology?" [KPC carbapenemases: what is at stake in clinical microbiology?]. Pathol Biol (Paris) (in French). 58 (1): 39–45. doi:10.1016/j.patbio.2009.07.026. PMID 19854586.
  11. 1 2 Yong D, Toleman MA, Giske CG, Cho HS, Sundman K, Lee K, Walsh TR (December 2009). "Characterization of a new metallo-beta-lactamase gene, bla(NDM-1), and a novel erythromycin esterase gene carried on a unique genetic structure in Klebsiella pneumoniae sequence type 14 from India". Antimicrob Agents Chemother. 53 (12): 5046–5054. doi:10.1128/AAC.00774-09. PMC 2786356Freely accessible. PMID 19770275.
  12. ↑ Deshpande Payal; Rodrigues Camilla; Shetty Anjali; Kapadia Farhad; Hedge Ashit; Soman Rajeev (2010). "New Delhi Metallo-β lactamase (NDM-1) in Enterobacteriaceae: Treatment options with Carbapenems Compromised". Journal of Association of Physicians of India. 58: 147–150.
  13. ↑ Kalenić, Smilja (2013). Medicinska mikrobiologija [Medical Microbiology] (in Croatian). Zagreb: Medicinska naklada. ISBN 978-953-176-637-1.
  14. ↑ Muir A, Weinbren MJ (July 2010). "New Delhi metallo-beta-lactamase: a cautionary tale". J. Hosp. Infect. 75 (3): 239–240. doi:10.1016/j.jhin.2010.02.005. PMID 20435372.
  15. ↑ "Detection of Enterobacteriaceae Isolates Carrying Metallo-Beta-Lactamase --- United States, 2010". MMWR. Centers for Disease Control.
  16. ↑ McNeil Jr., Donald G. (11 August 2010). "Antibiotic-Resistant Bacteria Moving From South Asia to U.S.". The New York Times. Retrieved 13 August 2010.
  17. ↑ Karthikeyan K, Thirunarayan MA, Krishnan P (July 2010). "Coexistence of blaOXA-23 with blaNDM-1 and armA in clinical isolates of Acinetobacter baumannii from India". J Antimicrob Chemother. 65 (10): 2253–2254. doi:10.1093/jac/dkq273. PMID 20650909.
  18. ↑ First NDM-1 superbug case confirmed in Ontario - CTV News
  19. ↑ 299423: GSK cites progress with a new-gen antibiotic - FierceBiotech
  20. ↑ Bax BD; et al. (4 August 2010). "Type IIA topoisomerase inhibition by a new class of antibacterial agents". Nature. 466 (7309): 935–940. doi:10.1038/nature09197. PMID 20686482. (primary source)
  21. ↑ Alazraki, Melly (6 August 2010). "GlaxoSmithKline Finds Compound That Could Help Fight 'Superbugs'". dailyfinance.com. Retrieved 13 August 2010.
  22. ↑ NDM1 - Origin, Symtoms and Cure for NDM1
  23. ↑ Japan detects its first case of NDM-1 superbug - Channel NewsAsia
  24. ↑ Walsh, Timothy R; Janis Weeks; David M Livermore; Mark A Toleman (7 April 2011). "Dissemination of NDM-1 positive bacteria in the New Delhi environment and its implications for human health: an environmental point prevalence study". The Lancet Infectious Diseases. 11 (5): 355–362. doi:10.1016/S1473-3099(11)70059-7. PMID 21478057. Retrieved 7 April 2011.
  25. ↑
  26. ↑ Yi Luo, Fenxia Yang, Jacques Mathieu, Daqing Mao, Qing Wang, and P.J.J. Alvarez (December 4, 2013), Proliferation of Multidrug-Resistant New Delhi Metallo-β-lactamase Genes in Municipal Wastewater Treatment Plants in Northern China, Environmental Science & Technology Letters, doi:10.1021/ez400152e
  27. ↑
  28. ↑ Antibiotic-resistant bacteria disarmed with fungus compound CBC News, June 25, 2014
  29. ↑ Rai, S; Manchanda, V; Singh, NP; Kaur, IR (Jul–Sep 2011). "Zinc-dependent carbapenemases in clinical isolates of family Enterobacteriaceae.". Indian journal of medical microbiology. 29 (3): 275–9. doi:10.4103/0255-0857.83912. PMID 21860109.
  30. 1 2 Pandey, Geeta (12 August 2010). "India rejects UK scientists' 'superbug' claim". BBC News. Retrieved 13 August 2010.
  31. ↑ Telegraph.co.uk: Indian Government angry over claims its hospitals are fuelling global superbug
  32. ↑ "Linking India to superbug unfair and wrong, says India". Hindustan Times. 12 August 2010. Retrieved 13 August 2010.
  33. ↑ 'Superbug' an MNC conspiracy: BJP leader | SS Ahluwalia | superbug | Indian Express
  34. ↑ Sharma, Sanchita (13 August 2010). "'Don't blame superbug on India, it's everywhere'". Hindustan Times. Retrieved 13 August 2010.
  35. 1 2 Narayan, Pushpa (13 August 2010). "Indian author says superbug report is fudged". The Times of India. Retrieved 13 August 2010.
  36. ↑ Abdul Ghafur K (March 2010). "An obituary- On the Death of antibiotics!". Journal of Association of Physicians of India. 58.
  37. ↑ Lancet won't publish India's rebuttal, NEW DELHI, Special Correspondent, April 13, 2011, thehindu.com
  38. ↑ "Lancet says sorry for 'Delhi bug'". The Times Of India. 12 January 2011. Retrieved 2011-01-12.
  39. ↑ "Science, names giving and names calling: Change NDM-1 to PCM". Mens Sana Monographs. Retrieved 2011-03-11.
  40. ↑ AFP: Belgian man dies of South Asian superbug
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