Antimicrobial resistance in Neisseria gonorrhoeae and Treponema pallidum: evolution, therapeutic challenges and the need to strengthen global surveillance
- 1Sexually Transmitted Infections Reference Centre, National Institute for Communicable Diseases, National Health Laboratory Service, Johannesburg, South Africa
- 2Department of Internal Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
- 3Division of Microbiology, University of Cape Town, Cape Town, South Africa
- 4London School of Hygiene and Tropical Medicine, London, UK
- 5Departments of Medicine and Global Health, University of Washington, Seattle, Washington, USA
- Correspondence to Professor David Lewis, STI Reference Centre, National Institute for Communicable Diseases, Private Bag X4, Sandringham 2131, South Africa;
Contributors Both authors co-wrote and revised the paper.
- Accepted 18 May 2011
The emergence of drug resistance among bacterial, viral and protozoan sexually transmitted infections (STI) in recent years threatens to undermine global STI control programmes. While this review will focus on microbiological resistance determinants for two important bacterial STI pathogens, namely Neisseria gonorrhoeae and Treponema pallidum, it is important to appreciate that a number of non-microbiological determinants may also directly influence both the emergence and transmission of antimicrobial resistant STI pathogens (table 1). This short paper describes the historical development of antibiotic resistance in N gonorrhoeae and T pallidum, outlines the challenges of identifying and treating these resistant infections, and highlights the requirement for the strengthening of global microbiological surveillance programmes for STI.
N gonorrhoeae infection
Gonorrhoea treatment in the pre-cephalosporin era
The gonococcus is characterised by a remarkable ability to develop and acquire antibiotic resistance mechanisms (table 2).1 Following the rapid demise of sulphonamides in treating gonorrhoea in the early 1940s, penicillins became the mainstay of global therapy for almost 40 years, initially at very low dosage and subsequently given at higher doses with probenecid. Tetracyclines or erythromycin were used during this period for the management of penicillin allergic patients and sometimes for cases of chromosomally mediated penicillin-resistant N gonorrhoeae infection. The global spread of high-level plasmid-mediated penicillin and tetracycline resistance among N gonorrhoeae isolates in the 1980s effectively sealed the fate of these antibiotics in terms of gonorrhoea treatment.1
Spectinomycin provided a temporary solution to the problem of penicillinase-producing N gonorrhoeae but resistance rapidly developed with first-line use.2 Spectinomycin is now seldom used due to the high cost and practical unavailability but remains useful in special instances, such as treating pregnant women with severe penicillin allergy or cephalosporin-resistant gonorrhoea. In most countries, quinolones rather than intramuscular ceftriaxone replaced penicillins and spectinomycin as first-line oral therapy for gonorrhoea in the 1980s and were used with success for over a decade before resistance developed, initially in the Asia Pacific region and subsequently in the USA, Europe and Africa.1 3
Modern treatment of gonorrhoea
With the demise of quinolones, physicians treating gonorrhoea turned to the last remaining class of effective antigonococcal antibiotics, namely cephalosporins. Oral third generation cephalosporins, such as cefixime and cefpodoxime, are still being used with success as single-dose oral agents in many countries. Reports of gonococci exhibiting decreased susceptibility and resistance to oral cephalosporins have been seen in Japan since 2001, and more recently in other countries in the western Pacific region and Europe.4–7 Although the genetic basis of resistance to oral cephalosporins has yet to be fully elucidated, the presence of a mosaic penA gene appears to be the predominant mechanism.1 8 At present, intramuscular ceftriaxone is the only antibiotic that still offers reliable cure for genital gonorrhoea, and it is likely to continue to do so unless the gonococcus acquires the ability to express an extended spectrum β-lactamase. Such an event is viewed with trepidation, as it will herald an era of extensively drug-resistant gonorrhoea and, unless new therapeutic agents are made available, gonorrhoea may potentially become untreatable.
Methods of detecting drug-resistant gonorrhoea
The traditional method of antimicrobial susceptibility testing relies on the presence of viable N gonorrhoeae isolates, which can be tested using disc diffusion or minimum inhibitory concentration assays using either Etest or agar dilution methodologies. Molecular assays for the detection of key antibiotic resistance genetic mutations or resistance-encoding plasmids have been described but are not yet in routine clinical use.9 10 Although molecular techniques offer enormous potential for the diagnosis of gonorrhoea, their use in antimicrobial susceptibility testing has several limitations. First, such an approach is not practical for those antibiotics for which several different resistance mechanisms exist and, second, molecular resistance assays will not detect new mechanisms of resistance for which phenotypic culture-based assays are required.
Surveillance systems for monitoring the prevalence of antimicrobial-resistant N gonorrhoeae
One key challenge to effective gonococcal control in the current era of multidrug-resistant gonorrhoea is that few countries have effective gonococcal sentinel surveillance programmes in place. The problem is being compounded due to the replacement of traditional culture and susceptibility testing with nucleic acid amplification tests as the diagnostic method of choice in high-income countries and the practice of treating patients with suspected gonorrhoea without laboratory testing, as occurs, for example, in those countries using the syndromic management approach.
Examples of sustainable and on-going national programmes include the Gonococcal Isolate Surveillance Project (GISP, 1986–date), coordinated by the US Centers for Disease Control and Prevention, and the Gonococcal Resistance to Antimicrobials Surveillance Programme (GRASP, 2000–date), now coordinated by the UK Health Protection Agency. At a regional level, examples of surveillance networks include the WHO's Western Pacific Region Gonococcal Antimicrobial Surveillance Programme (GASP, 1992–date), the European Surveillance of STI (ESSTI) Programme (2001–date), which is now coordinated by the European Centre for Disease Prevention and Control, and the WHO/Pan-American Health Organisation GASP (1992–date), which formerly involved a network of more than 35 countries in Latin America and the Caribbean. In an attempt to provide an up-to-date global picture of gonococcal resistance, the WHO is currently supporting, renewing and initiating additional GASP activities in South East Asia, Africa, Latin America and eastern Europe.5 11 In a similar manner to the national and regional surveillance programmes mentioned above, the WHO's GASP initiative is supported by surveillance protocols, definitions for multidrug-resistant and extensively drug-resistant N gonorrhoeae and a new panel of control gonococcal strains appropriate for the global antibiotic resistance patterns now observed.5 12
Potential treatment strategies in an era of multidrug-resistant gonorrhoea
In terms of the treatment of gonorrhoea resistant to oral cephalosporins, single-dose intramuscular ceftriaxone 250 mg still remains effective. Single-dose intramuscular spectinomycin 2 g and oral azithromycin 2 g are alternative second-line agents, although neither should be used as first-line agents due to the ease with which gonococci may develop resistance to these two antibiotics. Several strategies, which have yet to be evaluated in clinical trials, have been proposed to prolong the usefulness of current effective antibiotics, including higher cephalosporin doses, multidose cephalosporin regimens, multidrug regimens, microbiologically directed treatment and, should an alternative effective first-line antibiotic become available, drug cycling.13 Engagement with research funders and the pharmaceutical industry is urgently required in order to highlight the need for new therapeutic agents to treat N gonorrhoeae infections in the future.
T pallidum infection
Syphilis treatment in the pre-antibiotic era
Several potentially toxic treatments, including mercury salves and inunctions, and arsenic and bismuth compounds, were used in the pre-antibiotic era to ward off the possibility of very serious, sometimes fatal, late manifestations of syphilis. The discovery and introduction of penicillin in the 1940s revolutionised the treatment of syphilis, providing for the first time a safe and highly effective remedy.
Penicillin-based treatment for syphilis
The causative agent of syphilis, T pallidum, divides very slowly, and treponemacidal levels of penicillin must be maintained for approximately 10–14 days to cure early syphilis, or up to 30 days for late syphilis. A single dose of the currently recommended benzathine penicillin G (BPG) provides effective levels of penicillin for at least 2–3 weeks, thus making single-dose therapy possible for early syphilis. Unfortunately, BPG has minimal ability to cross the blood–brain barrier and viable T pallidum, as well as T pallidum DNA, have been detected in the cerebrospinal fluid (CSF) of infected persons following BPG treatment.14 15 The possible presence of viable treponemes in CSF following treatment is of concern, particularly in HIV-infected individuals. Although serological and microbiological treatment failures have been reported following BPG treatment, these may be due to sequestration of treponemes protected in the central nervous system or to re-infection. There has been no documented case of penicillin-resistant T pallidum.
Alternative antibiotic therapies for syphilis
For persons who are allergic to penicillin, the tetracyclines (eg, tetracycline and doxycycline), macrolides (eg, erythromycin, and more recently, azithromycin), chloramphenicol, and third-generation cephalosporins (eg, ceftriaxone) have been used and, except for chloramphenicol, are recommended by international experts. Higher failure rates have been seen with tetracycline and erythromycin, compared with BPG, but it is unclear whether these failures were due to biological causes or to lack of compliance with the more complicated dosing schedule for the oral drugs. The efficacy, safety and ease of use of azithromycin made it appropriate to use partner-delivered therapy approaches to control syphilis outbreaks in defined populations; this approach was implemented in men who have sex with men in San Francisco beginning in 1999–2000. However, in 2002, the first of several cases of clinical failure following azithromycin treatment for syphilis was identified in San Francisco.16
Recognition of T pallidum macrolide resistance
Historically, a single strain of erythromycin-resistant T pallidum (called Street Strain 14) was isolated by John Clark at the US Centers for Disease Control and Prevention from a man who had failed intensive erythromycin treatment for secondary syphilis. Stamm and Bergen17 subsequently demonstrated that this resistance was associated with an A→G transition in both copies of the 23S rRNA gene in this strain. Following the appearance of azithromycin treatment failures in San Francisco, laboratory analysis of swab samples from syphilis-infected patients showed the presence of an A2058G mutation in the 23S rRNA gene of some circulating T pallidum strains, identical to that identified in the Street Strain 14. Molecular analysis of isolated historical strains and swab samples collected from a variety of geographical sites (including San Francisco, Seattle, Baltimore and Dublin) revealed identical mutations in a subset of samples.18 Importantly, the proportion of samples containing this mutation has increased over time in both San Francisco and Seattle, with recent levels greater than 80% in men who have sex with men.
Following these reports, A2058G mutations in T pallidum were reported from Vancouver and Alberta, Canada, as well as Shanghai, China. Zhou et al19 reported the failure of azithromycin treatment of pregnant women to prevent congenital syphilis in five infants born in Shanghai between 1998 and 2004, but it is unclear whether this failure occurred because of the poor penetration of the placenta by the drug or because of the unrecognised presence of macrolide-resistant T pallidum strains at that time. Matějková and colleagues20 recently described a clinical failure of spiramycin, another macrolide antibiotic used for the treatment of syphilis in the Czech Republic, in a patient with secondary syphilis. This strain contained a different mutation (A2059G), which was also identified in additional samples collected from 2005 to 2008.
The origin of strains with macrolide resistance mutations is unknown. Several possible theories exist, including the unrecognised existence of such strains for many years, with selection due to the widespread use of azithromycin for the treatment of Chlamydia trachomatis or for prophylaxis of Mycobacterium avium complex, and the real-time selection of spontaneous mutants by antibiotic pressure. Marra and coworkers21 demonstrated that T pallidum strains containing the A2058G mutation were more likely to be found in persons who had taken macrolide antibiotics in the preceding year; importantly, strains containing the resistance mutation can be divided into multiple molecular types, indicating that the mutation is not restricted to a single strain type, even within a city.
Global challenges in the detection of resistance mutations in T pallidum
The identified macrolide resistance mutations can be identified in strains by restriction digestion of PCR products.18 Because these techniques are available in only a limited number of laboratories, samples from most geographical regions cannot readily be tested. There is a need for an international surveillance programme to determine the current geographical distribution of resistant strains and to assess the prevalence of resistant strains in many geographical areas periodically. This could be achieved most economically at a regional reference laboratory level using DNA extracts from ulcer swabs found to be positive for T pallidum by molecular testing. A global surveillance programme would require the establishment of a network of laboratories with expertise in molecular testing and sequencing of T pallidum, commitment by countries to send appropriate samples and adequate funding to support the network and testing. Published successful azithromycin treatment trials from Africa have led to the naive belief that resistant strains may not be present on that continent.22–24 It is important to recognise that these trials were conducted in 1994–7, 2000–3 and 2000–7, either before or very early in the recognition of such resistant strains elsewhere. There are no recent data on macrolide resistance from Africa.
Recommendations for syphilis treatment in light of the emergence of resistance
Penicillin G remains the preferred treatment for syphilis of all stages. Doxycycline or tetracycline should be considered as second-line drugs for uncomplicated syphilis, to be used when penicillin treatment is not possible (table 3). Macrolides, including azithromycin, should be used only in regions where the prevalence of resistant strains is known to be low, and treated patients require close follow-up.
As antimicrobial resistance increases on a global scale, treatments for gonorrhoea and syphilis need to be tailored to ensure that over 95% of clinical infections respond to first-line treatment regimens in accordance with WHO recommendations. This can be achieved only by the determination of antibiotic susceptibility phenotypes or genotypes for these pathogens through national and regional surveillance activities. For most of the world, such activities are weak or non-existent. Globally, surveillance efforts require significant strengthening through capacity building of laboratories, enhanced sharing of information between surveillance units, and the provision of sustainable funding from both governments and donor agencies. Finally, there is a need to prioritise funding for research into new therapeutic agents for STI pathogens, particularly in the case of N gonorrhoeae, before existing treatment options disappear.
Due to editorial constraints, the authors were unable to reference all of the relevant publications related to this topic.
Competing interests DAL is a member of the Merck Serono Advisory Board for the planned launch of Fixime (cefixime) within South Africa in 2011. SAL has no competing interests.
Provenance and peer review Commissioned; externally peer reviewed.
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.