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    SAMJ: South African Medical Journal

    versión impresa ISSN 0256-9574

    SAMJ, S. Afr. med. j. vol.101 no.12 Cape Town dic. 2011

     

    SCIENTIFIC LETTER

     

    NDM-1 has arrived: first report of a carbapenem resistance mechanism in South Africa

     

     

    W LowmanI; C SriruttanII; T NanaIII; N BosmanIV; A DuseV; J VenturasVI; C ClayVII; J CoetzeeVIII

    IMB BCh, MMed (Microbiol), FCPath (SA) (Microbiol). Department of Clinical Microbiology and Infectious Diseases, School of Pathology of the National Health Laboratory Services and University of the Witwatersrand, Johannesburg
    IIMB BCh, DTM&H, FCPath (SA) (Microbiol). Department of Clinical Microbiology and Infectious Diseases, School of Pathology of the National Health Laboratory Services and University of the Witwatersrand, Johannesburg
    IIIMB BCh, DTM&H, FCPath (SA) (Microbiol). Department of Clinical Microbiology and Infectious Diseases, School of Pathology of the National Health Laboratory Services and University of the Witwatersrand, Johannesburg
    IVMB BCh, DTM&H, FCPath (SA) (Microbiol). Department of Clinical Microbiology and Infectious Diseases, School of Pathology of the National Health Laboratory Services and University of the Witwatersrand, Johannesburg
    VMB BCh, DTM&H, MSc (Med), MMed (Microbiol), FCPath (Microbiol) (SA). Department of Internal Medicine, Charlotte Maxeke Johannesburg Academic Hospital, University of the Witwatersrand, Johannesburg
    VIMB ChB, FCP (SA), Cert Pulmonology, Cert Critical Care. Department of Clinical Microbiology and Molecular Biology, National Referral Laboratory, Ampath National Laboratory Services, Centurion
    VIIPhD. Department of Clinical Microbiology and Infectious Diseases, School of Pathology of the National Health Laboratory Services and University of the Witwatersrand, Johannesburg
    VIIIMB ChB, FCPath (SA) (Microbiol)
    . Department of Clinical Microbiology and Infectious Diseases, School of Pathology of the National Health Laboratory Services and University of the Witwatersrand, Johannesburg

     

     


    ABSTRACT

    The New Delhi Metallo-β-lactamase (NDM) resistance mechanism in Enterobacteriaceae threatens to render serious Gram-negative infections untreatable. The NDM-1 enzyme hydrolyses all available penicillin, cephalosporin and carbapenem antibiotics, and is commonly accompanied by additional resistance mechanisms to multiple antibiotic classes. Initially identified as a significant healthcare risk on the Indian sub-continent, it has rapidly become a global problem, posing significant diagnostic and management challenges. Here we report the first laboratory-confirmed case of NDM-1 in South Africa.


     

     

    To the Editor: Resistance to β-lactam antibiotics in Enterobacteriaceae has steadily increased, with the emergence of carbapenem-resistant Enterobacteriaceae (CRE) seen in the past decade. Resistance to carbapenems may be mediated via a variety of mechanisms, but the development and spread of carbapenemases (β-lactamase enzymes that hydrolyse carbapenems and many other β-lactam antibiotics) in Enterobacteriaceae has caused global concern. One such carbapenemase, NDM-1 (New Delhi metallo-β-lactamase), first described in 2009,1 has rapidly emerged as the leading threat to the treatment of infections caused by Enterobacteriaceae.

    A Swedish patient of Indian origin, who travelled to New Delhi in 2007, developed an infection caused by a strain of Klebsiella pneumoniae harbouring the blaNDM-1 gene encoding NDM-1. A subsequent study demonstrated that NDM-1-positive isolates were already present in Indian hospitals in 2006.2 Dissemination of NDM-1positive bacteria in the environment and community-acquired infection with these resistant organisms in parts of India is well-documented.3,4 Enterobacteriaceae with NDM-1 have since been isolated from patients in the USA, Canada, UK, Europe, Australia, Oman, Japan, Singapore and Africa.5-7 The presence of NDM-1 was demonstrated in certain multidrug resistant (MDR) K. pneumoniae isolates from a Kenyan hospital, in strains archived over a 3-year period (2007 - 2009).5

    The blaNDM-1 gene has been found on conjugative plasmids, which are mobile genetic elements.4 This facilitates transfer of the gene between bacteria, resulting in the emergence of resistance in other unrelated genera, such as Acinetobacter and Vibrio.3,8 NDM-1positive bacteria often carry genes that confer resistance to other non-β-lactam antibiotics, like the fluoroquinolones, sulphonamides and aminoglycosides.4,7 Of additional concern is that resistance to tigecycline and colistin has been described, further limiting available treatment options.4,7 We report the first laboratory-confirmed case of an NDM-1-producing isolate from South Africa.

     

    Methods and results

    Case report

    A 63-year-old black man presented to the Charlotte Maxeke Johannesburg Academic Hospital, with a 2-month history of a productive cough, right-sided pleuritic chest pain, dyspnoea, fever, and weight loss. The patient had previously been well, but had recently been diagnosed with HIV (not started on antiretroviral treatment) and hypertension. He had 2 previous admissions to the same hospital in 2010, for a trauma-related injury and a diarrhoeal illness, respectively. No immediate family members sought healthcare in the recent preceding years. The patient's house was noted to have proper sanitation with running water. He was a truck driver by occupation and travelled primarily within South Africa, but had also recently travelled to Mozambique and Zambia.

    The patient appeared wasted with generalised lymphadenopathy and mild conjunctival pallor. He was apyrexial and normotensive. There were no chest scars or deformities, and he had clinical evidence of a pneumonic process in the right middle lobe. A chest X-ray (CXR) revealed an area of opacification in the right middle lobe, with an air-fluid level suggestive of either a complex pleural collection or a lung abscess.

    The patient was started on a course of intravenous amoxicillinclavulanate and oral azithromycin; treatment was changed after 5 days to oral ciprofloxacin (750 mg twice daily), after a carbapenemresistant Enterobacter cloacae was isolated from sputum cultures (refer to 'Laboratory testing'). Fluid collection was achieved with a pig-tail catheter under ultrasound guidance. Macroscopically, the collection appeared empyematous; the biochemistry was consistent with this observation. A total of 150 ml of fluid was drained over 3 days; the catheter was removed following complete resolution confirmed on CXR. The fluid was culture-negative and investigations eliminated the possibility of tuberculosis. The patient received HIVcounselling, was initiated on antiretroviral treatment, and discharged with follow-up scheduled at the outpatient clinic after 2 weeks.

    At the follow-up visit, the patient appeared to have recovered well. On re-culture of his sputum, an extended spectrum -lactamase (ESBL)-producing K. pneumoniae was isolated. No CRE were isolated with a screening rectal swab. The CXR showed complete resolution.

    Laboratory testing

    The E. cloacae isolated from the sputum was identified with a MicroScan Walkaway system (Siemens Healthcare Diagnostics, USA). To verify the initial result, additional antimicrobial susceptibility testing (AST) was performed for a variety of antimicrobial agents, including a combination of broth microdilution and Etest (bioMérieux Clinical Diagnostics, France) (Table I). With the exception of tigecycline, colistin and fosfomycin, all minimum inhibitory concentrations (MICs) were interpreted using the Clinical and Laboratory Standards Institute (CLSI) breakpoints.9 The presence of a carbapenemase was presumptively confirmed using a combination of phenotypic methods. Using the method described by Zarfel et al.,11 the isolate was genotypically analysed using specific primers (Inqaba Biotec, Pretoria) designed to detect the presence of the bla NDM-1 gene conferring carbapenem resistance. K. pneumoniae strain BAA-2146 (ATCC, Manassas, USA), harbouring the bla NDM-1 gene, was used as a positive control.

     

    Discussion

    The emergence of NDM-1 in Enterobacteriaceae has heightened global concern regarding antimicrobial resistance. The MDR nature, propensity for horizontal transfer, and rapidity of global spread and emergence of micro-organisms harbouring this gene means that the threat of untreatable infections has arrived. To our knowledge, this is the first laboratory-confirmed case of an NDM-1-producing isolate in South Africa.

    The implications of this are multifactorial, affecting the laboratory and the bedside. Treatment options are limited, with colistin and tigecycline currently the only feasible choices. Susceptibility to these agents is not guaranteed and numerous clinical issues relate to their use in treating severe MDR Gram-negative infections. A dearth of pharmaco-kinetic and - dynamic data on the use of colistin compromises optimal dosing; literature suggests that it should be used in combination with other agents such as rifampicin.12 Tigecycline, a broad-spectrum minocycline analogue, has a high volume of distribution with low serum levels, raising concern as to its efficacy in the treatment of bacteraemic patients. Furthermore, Pseudomonas aeruginosa and several Enterobacteriaceae are inherently resistant to this agent. The efficacy of these agents in the treatment of severe infections caused by the described isolates remains to be determined.

    Early identification of NDM-1-producing Enterobacteriaceae (NPE), and timely infection prevention and control intervention is imperative to limiting further emergence and spread of these micro-organisms.13 Measures to ensure early laboratory detection of CRE are crucial in alerting clinicians and infection control staff to a potential carbapenemase producer. Clinicians must be made aware of the possibility of a CRE being an NPE in patients who have epidemiological links to the Indian subcontinent, or other countries or hospitals where such isolates have emerged.14 In this case, there were no confirmed epidemiological links to the Indian sub-continent, therefore the validity of this epidemiological link requires further investigation. The patient had travelled widely within southern Africa and may have acquired the NPE from a neighbouring country. Heightened awareness and improved laboratory detection is mandatory and will give a clearer understanding of local epidemiology. CDC and HICPAC guidance for control of infections with carbapenem-resistant or carbapenemase-producing Enterobacteriaceae in acute care facilities recommends an aggressive infection control strategy encompassing laboratory testing, contact precautions and active surveillance.15

    Active surveillance is crucial to establishing the true prevalence of this resistance gene. The expression of NDM-1 in other significant hospital pathogens, such as A. baumannii, also requires consideration. From the perspective of laboratory detection, additional surveillance capacity is required given the characteristic carbapenem-resistant nature of such micro-organisms, which may otherwise allow NDM-1 producers to go undetected. Phenotypic tests have limitations in detecting NDM-1; molecular confirmation is considered the 'gold standard'.8 Other infection prevention and control measures, such as environmental cleaning and selective decontamination of the gastrointestinal tract, may prove useful in halting dissemination and containing outbreaks of NPE. Acute healthcare institutions are urged to devise situation-specific infection control strategies for CRE, in an effort to stem the spread of these pathogens in South Africa. Vigilance and rapid action are our greatest weapons in the restricted arsenal currently available for combating this globally emerging resistance mechanism.

     

    References

    1. Yong D, Toleman MA, Giske CG, et al. 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 2009;53:5046-5054.         [ Links ]

    2. Castanheira M, Deshpande LM, Mathai D, et al. Early dissemination of NDM-1- and OXA181-producing Enterobacteriaceae in Indian hospitals: report from the SENTRY Antimicrobial Surveillance Program, 2006-2007. Antimicrob Agents Chemother 2011;55:1274-1278.         [ Links ]

    3. Walsh TR, Weeks J, Livermore DM, Toleman MA. Dissemination of NDM-1 positive bacteria in the New Delhi environment and its implications for human health: an environmental point prevalence study. Lancet Infect Dis 2011;11:355-362.         [ Links ]

    4. Kumarasamy KK, Toleman MA, Walsh TR, et al. Emergence of a new antibiotic resistance mechanism in India, Pakistan, and the UK: a molecular, biological, and epidemiological study. Lancet Infect Dis 2010;10:597-602.         [ Links ]

    5. Poirel L, Revathi G, Bernabeu S, Nordmann P. Detection of NDM-1-producing Klebsiella pneumoniae in Kenya. Antimicrob Agents Chemother 2011;55:934-936.         [ Links ]

    6. Struelens MJ, Monnet DL, Magiorakos AP, Santos O'Connor F, Giesecke J. New Delhi metallobeta-lactamase-1-producing Enterobacteriaceae: emergence and response in Europe. Euro Surveill 2010;15(46):19716.         [ Links ]

    7. Pillai DR, McGeer A, Low DE. New Delhi metallo-beta-lactamase-1 in Enterobacteriaceae: emerging resistance. CMAJ 2011;183:59-64.         [ Links ]

    8. Nordmann P, Poirel L, Carrer A, Toleman MA, Walsh TR. How to detect NDM-1 producers. J Clin Microbiol 2011;49:718-721.         [ Links ]

    9. Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing; Twenty First Informational Supplement, M100-S21. Pennsylvania: CLSI, 2011:31(1);M100-S21.         [ Links ]

    10. European Committee on Antimicrobial Susceptibility Testing (EUCAST). Växjö, Sweden: EUCAST, 2011. http://www.eucast.org (accessed 30 October 2011).         [ Links ]

    11. Zarfel G, Hoenigl M, Leitner E, et al. Emergence of New Delhi metallo-β-lactamase, Austria. Emerg Infect Dis, 2011;17(1):129-130.         [ Links ]

    12. Giamarellou H. Multidrug-resistant Gram-negative bacteria: how to treat and for how long. Int J Antimicrob Agents 2010;36(S2):S50-S54.         [ Links ]

    13. Spellberg B, Guidos R, Gilbert D, et al. The epidemic of antibiotic-resistant infections: a call to action for the medical community from the Infectious Diseases Society of America. Clin Infect Dis 2008;46:155-164.         [ Links ]

    14. Centers for Disease Control and Prevention (CDC). Detection of Enterobacteriaceae isolates carrying metallo-β-lactamase - United States, 2010. MMWR Morb Mortal Wkly Rep 2010;59(24):750.         [ Links ]

    15. Centers for Disease Control and Prevention (CDC), Guidance for control of infections with carbapenem-resistant or cabapenamase-producing Enterobacteriaceae in acute care facilities. MWR Morb Wkly Rep 2009;58(10):256-260.         [ Links ]

     

     

    Accepted 31 October 2011.

     

     

    Corresponding author: W Lowman (warren.lowman@wits.ac.za)