There is increasing concern about Mycoplasma genitalium as a cause of urethritis, cervicitis, pelvic inflammatory disease (PID), infertility and ectopic pregnancy. Commercial nucleic acid amplification tests (NAATs) are becoming available, and their use in screening for M. genitalium has been advocated, but M. genitalium’s natural history is poorly-understood, making screening’s effectiveness unclear. We used a transmission-dynamic compartmental model to synthesise evidence from surveillance data and epidemiological and behavioural studies to better understand M. genitalium’s natural history, and then examined the effects of implementing NAAT testing. Introducing NAAT testing initially increases diagnoses, by finding a larger proportion of infections; subsequently the diagnosis rate falls, due to reduced incidence. Testing only symptomatic patients finds relatively little infection in women, as a large proportion is asymptomatic. Testing both symptomatic and asymptomatic patients has a much larger impact and reduces cumulative PID incidence in women due to M. genitalium by 31.1% (95% range:13.0%-52.0%) over 20 years. However, there is important uncertainty in M. genitalium’s natural history parameters, leading to uncertainty in the absolute reduction in PID and sequelae. Empirical work is required to improve understanding of key aspects of M. genitalium’s natural history before it will be possible to determine the effectiveness of screening.
There is increasing concern about the sexually-transmitted bacterium, Mycoplasma genitalium, as a cause of a range of morbidities1,2 including mucopurulent cervicitis1,3,4,5,6, pelvic inflammatory disease (PID)1,5,6,7,8,9,10,11, tubal factor infertility1,12,13, and ectopic pregnancy in women7,8,9,10,12,13,14,15,16,17,18; urethritis, balanitis, posthitis and balanoposthitis in men19,20,21; and increased HIV acquisition and transmission22. An increasing array of commercial nucleic acid amplification tests (NAATs) are available, for example, the Bio-Rad Dx CT/NG/MG® assay23, many of which are non-invasive (urine-based), and using them to screen for M. genitalium has been advocated24, and this may reduce the incidence of serious, costly sequelae in women25.
However, there is uncertainty in its importance as a cause of disease, whether public health intervention is justified and, if so, how best to intervene14,25,26,27. Uncertainty in the natural history of M. genitalium needs to be accounted for in analyses of the likely impact of screening26. Extensive screening for Chlamydia trachomatis has been implemented by several countries – for more than a decade in England, and yet the impact of this screening is still poorly-understood28. In large part this is because natural history of C. trachomatis is still not well-understood, reflected by wide variation in the values of key parameters used in mathematical models29; only in recent years has evidence synthesis been used to improve estimates30,31.
As highlighted by Walker et al. “transmission dynamics and duration of infection [are] both important factors in understanding the management of [M. genitalium] in the population”14. We used a transmission-dynamic model to synthesise evidence32 from studies of the natural history and epidemiology of M. genitalium, and surveillance data, to identify the parameters that are most important in contributing to uncertainty in its transmission dynamics. We then examined the potential impact of using NAATs for (i) diagnostic testing of symptomatic patients, and (ii) diagnostic testing of symptomatic patients plus screening of asymptomatic patients, of both sexes, on incidence of infection and diagnoses in each sex and incidence of serious sequelae in women.
We developed a transmission-dynamic compartmental mathematical model in which M. genitalium’s epidemiology is represented by compartments for asymptomatic infected individuals, symptomatic infected individuals not seeking treatment, symptomatic infected individuals seeking treatment, and women with asymptomatic, symptomatic and treated PID33. The model is stratified by sex, and into ‘activity classes’ with low, medium, and high rates of sexual partner change. Interaction between activity classes is determined by a mixing matrix, with an assortativeness coefficient specifying the amount of like-with-like interaction34. The model is summarised by the flow diagram in Fig. 1; equations specifying the model are in the Appendix. Acquisition of infection causes individuals to move from the Susceptible state to the Latent state, from which they progress to one of the Infectious states. Infectious individuals may be Asymptomatic, Symptomatic but not seeking care despite their symptoms, or Symptomatic and seeking care. Individuals may seek care following partner notification: this applies to persons with and without infection and with and without symptoms. When an infected individual is diagnosed and treated successfully, they return to the Susceptible state. If treatment is unsuccessful, then the patient enters the Treatment Failure state; those individuals then seek further treatment due to continuing symptoms (this time treated successfully) or recover through natural immune processes. Infected individuals who do not receive treatment will recover eventually through natural immune processes, returning to the Susceptible state. If an Asymptomatic individual is treated and treatment fails, then they remain in the Asymptomatic infected state, and recover naturally – unless partner notification leads to their being diagnosed and treated again. In women, a proportion of cases of untreated infection and of treatment failure cases will progress to PID. A proportion of PID cases are symptomatic and seek care due, entering the Treated PID state, with successful treatment returning them to the Susceptible state. All cases of PID can recover through natural immune processes and return to the Susceptible state. Numbers of cases of ectopic pregnancy and tubal factor infertility were calculated by multiplying the number of untreated PID cases by the proportions of PID cases developing each sequela as reported in previous studies15,16,17,30.
We used surveillance data from England, where all symptomatic men and 5% of asymptomatic men attending sexual health clinics received screening for non-chlamydial non-gonococcal urethritis (NCNGU) with urethral gram stain microscopy35 and diagnosed cases were recorded. In general practice, microscopy is not used at all and people are managed according to symptoms. Women with symptoms of mucopurulent cervicitis would be treated (and the diagnosis recorded in surveillance), whilst asymptomatic women with infection would only be treated (and recorded in surveillance) through partner notification.
Symptomatic cases of NCNGU were given first-line treatment with azithromycin; a proportion of these cases (estimates are described below) will have been due to M. genitalium, and a proportion of those will have been cured by it. M. genitalium can be treated with azithromycin, doxycycline and cefoxitin, with treatment failure rates ranging from 5–60%9,36,37,38,39. Moxifloxacin is more effective but is often reserved as a second-line treatment38.
Sensitivity analysis to identify the most epidemiologically important parameters
To identify which parameters have the greatest impact on the model output (i.e. diagnoses in men and prevalence in women), prior ranges for parameters values were defined, based on literature and expert opinion (Table 1)8,9,36,40,41,42,43,44. Some parameter estimates were well-defined, including sexual partner change rates45; time-delays associated with seeking and receiving care46,47; the proportion of symptomatic patients abstaining from sexual activity whilst seeking care46,47,48; and the effectiveness of treatment41,49. Natural history parameters of M. genitalium were more uncertain, due to variation between studies of estimates or due to a lack of studies. These include the transmission probability; the proportion of infections that are symptomatic; the latent period and duration of infection; and the rate of progression to PID. In the univariate analysis, the model was run using intermediate values of all the ranges of the parameters while allowing one parameter at a time to vary between the minimum and maximum of the range. The most influential parameters were then varied in the model calibration step.
The model represents the UK population aged 18–40 years, with 10 million individuals of each sex. Since testing for M. genitalium is not routine, we use surveillance data on diagnoses of NCNGU in men from sexual health clinics in the UK in 2000–200950, complemented by estimates of the proportion of NCNGU that is due to M. genitalium (i.e. 10–46%19,20,51,52). In men in the UK, there were ~65,000 annual diagnoses of urethritis due to NCNGU, ~10% of which were asymptomatic epidemiologically-treated cases50. The model was calibrated to estimated numbers of annual M. genitalium diagnoses in men (including asymptomatic epidemiologically-treated cases), and the prevalence in women (i.e. 3.3% (95% CI: 2.6–4.1%))11. Candidate parameter sets were generated by Latin Hypercube Sampling from the prior ranges of parameters that were uncertain and influential. Parameter sets were accepted if both the annual diagnoses and prevalence fell within the specified ranges defined by the data: the female prevalence generated by the model had to fall in the range 2.6–4.1%, and the annual number of male diagnoses had to fall between 6,500–29,900 (i.e.10–46% of 65,000 NCNGU diagnoses). The parameter-selection process was run until 200 accepted parameter sets were obtained (from ~40,000 candidate sets), which comprise the posterior distribution. Sensitivity analysis was then performed to determine the most influential parameters, by calculating partial rank correlation coefficients (PRCCs)53.
After selection of parameter sets to represent uncertainty in transmission dynamics, the model was used to examine the impact of NAAT testing of (i) symptomatic individuals of both sexes in both genitourinary medicine (GUM) and general practice (GP) clinics (plus the 5% of asymptomatic patients in GUM who were being tested by microscopy because those clinics would be unlikely to stop testing that patient group), and (ii) all symptomatic patients of both sexes in both GUM and GP clinics plus asymptomatic patients attending GUM. In addition to higher diagnosis rates, it was assumed that NAAT testing would allow for more effective treatment, so that treatment failure rates would be lower. In scenario analysis, we varied the progression rate parameter, \(\psi \), using values of 0.022, 0.044, and 0.09, which correspond to percentages of M. genitalium infections in women progressing to PID of 2.1%, 4.5%, and 8.5%6,11.
Model code (available on request) was implemented using Matlab version 2016b.
Model sensitivity analysis and calibration
The model was able to reproduce the observed epidemiological data (diagnosis rates in men and prevalence in women). In the univariate sensitivity analysis that was performed to determine which parameters would be varied in the model calibration step, the most influential parameters associated with uncertainty in the model output were proportion of infections that are symptomatic; proportion of symptomatics abstaining from sex; the proportion of those patients who seek care; time from onset to care-seeking; per-capita rate of care-seeking; proportion of patients who go to GUM, directly or via GP; sexual mixing pattern (assortativeness coefficient); transmission probabilities; proportion of partners traced; treatment failure rate; and natural recovery rates. (Table 1, parameters with prior and posterior ranges, Tables 2, 3 for post-fitting PRCC calculations as described below).
For parameters that were varied in probabilistic sampling, the prior ranges are reported in Table 1, with the distribution of model prevalence in females and annual diagnoses in males amongst the posterior parameter sets shown in Fig. 2. Posterior parameter distributions are reported in Table 1 and plotted in Fig. 3. For some of the parameters, the prior and posterior ranges and mean values were similar (Fig. 3), indicating that the priors were in agreement with the other available data that we synthesised, but also that those data provided only limited additional information on these parameter values, indicated by the limited reduction in the range of uncertainty. For other parameters, related to sexual behaviour (ε, σ(m)), natural history of infection (ϕ(f), ϕ(m), z(f), z(m), γ(f), γ(m)), use of and performance of the health service (ρ(f), d seek , f GUM , f GP ), and the treatment failure proportion (ζ), prior and posterior mean values were different, indicating that the surveillance data were informative, although in most cases the prior and posterior ranges were similar.
There is uncertainty in the baseline number of PID cases due to M. genitalium, with estimates of 155,700 (95% range 69,000–273,000), 306,000 (134,000–545,000), and 605,000 (256,000–1,120,000) over 20 years, corresponding to proportions of untreated infections in women progressing to PID of 2.1%, 4.5%, and 8.5%, respectively (Table 4 and Supplementary Tables 1 & 2), which are generated by using ψ values of 0.022, 0.044, and 0.09, respectively. Price et al.30 estimated the incidence of all-cause PID to be 1.8% p.a., which equates to 192,000 cases annually in a population of the size used in the model, and corresponds to 3,843,000 cases over 20 years. This means that the proportion of all-cause PID that is estimated to be due to M. genitalium is 4.1%, 8.0%, or 15.7%, corresponding to proportions of untreated infections in women progressing to PID of 2.1%, 4.5%, and 8.5%, respectively. For comparison, Price et al.30 estimated that 14.8% of chlamydia infections progress to PID, and that 19.7% of all-cause PID is due to chlamydia.
Impact of NAAT testing
Introduction of NAAT testing leads to an increase in diagnosis and treatment, leading to a reduction in the incidence of infection, which declines over a sustained period, with uncertainty in natural history and behaviour parameters leading to uncertainty in the magnitude of the reduction (Figs 4 and 5). The impact on PID of NAAT testing is marked (Fig. 5, Table 4), particularly in the scenario where asymptomatic patients are screened because this identifies many more of the infections that occur compared with only testing symptomatic patients. NAAT testing enables detection of infection in women as well as men, detection of asymptomatic infection, and improved care of symptomatic patients because M. genitalium is treated specifically, rather than syndromic management being given for NCNGU/mucopurulent cervicitis.
Whereas introducing NAAT testing results in an immediate reduction in incidence which increases over time in both sexes, the effect on the rate of diagnoses is different. Initially there is an increase in diagnoses, due to the increase in testing, followed by a decline in diagnoses, due to the consequent reduction in prevalence and incidence of infection. The long-term effect on the diagnosis rate depends upon the testing scenario and differs for each sex. When NAAT testing is used for symptomatic patients (Figs 4a and 5a), the diagnosis rate in women increases by a relatively small amount and in the long-term falls below the baseline diagnosis rate prior to the intervention, whereas in men the initial increase in the diagnosis rate is proportionately larger, and in the long term, the diagnosis rate remains above baseline. When NAAT testing is used for symptomatic patients and asymptomatic patients in GUM (Figs 4b and 5b), the diagnosis rate in women increases by a relatively large amount and in the long-term remains slightly above the baseline diagnosis rate, whereas in men the initial increase in the diagnosis rate is proportionately smaller, and in the long term, the diagnosis rate remains slightly below baseline. The scenario presented in Figs (4b and 5b) is perhaps the one more likely to occur in practice, with the advent of multiplex NAAT tests meaning that asymptomatic patients tested for C. trachomatis and/or N. gonorrhoeae will often be tested automatically for M. genitalium as well.
Whilst in all cases NAAT testing reduced the incidence of M. genitalium infection and reduced the incidence of PID and other sequelae, it is important to note that uncertainty in M. genitalium’s natural history parameters leads to substantial uncertainty in the magnitude of these changes. In the case of the rate of diagnosis of M. genitalium infection there was uncertainty not only in the magnitude of the change but also in whether in the long term the diagnosis rate would be higher or lower (and it could be different for each sex). We calculated PRCCs for each parameter with respect to symptomatic male cases, epidemiologically treated male cases, and female prevalence, as well as for reductions in female and male incidence and PID prevalence (Tables 2, 3). The most influential parameters for each were rate of asymptomatic males seeking care, proportion of females who are symptomatic and female to male transmission probability. This analysis indicates that getting better estimates for these parameters will be key for maximally accurate assessment of the impact of NAAT testing roll-out.
We find that screening for M. genitalium using NAATs could lead to significant reductions in rates of PID in women due to M. genitalium, with cumulative incidence over 20 years reduced by 31.1% (95% range: 13.0–52.0%). This will reduce incidence of other serious sequelae arising from PID such as ectopic pregnancy and tubal factor infertility. Using NAAT testing for M. genitalium in general practice/community and specialist settings, instead of urethral smear microscopy testing of symptomatic men in GUM and syndromic management of both sexes, greatly reduces the incidence of infection and PID, particularly when symptomatic and asymptomatic patients are tested. This is for several reasons. Firstly, coverage of testing can be greater, as it can be offered to more patients (in community settings as well as GUM), and will likely be more acceptable to men than urethral smear microscopy. Secondly, women can be tested by NAAT, meaning that treatment of infection in women is not dependent upon either having symptomatic infection or being a notified partner of a man diagnosed with infection. Thirdly, detecting infection in women then enables contact tracing to find their male partners, further-reducing infection in the population. Moreover, with antibiotic resistance in M. genitalium causing increasing concern2,27,54, an important benefit of NAAT diagnosis of M. genitalium infection rather than syndromic management of NCNGU is that it allows use of a more-appropriate treatment regimen; NAATs can detect genetic determinants of drug resistance.
Importantly, our modelling shows that patterns observed in rates of diagnosis differ from patterns in underlying incidence, which needs to be taken into account when assessing surveillance data, as has previously been highlighted for gonorrhoea55: specifically, incidence falls immediately and remains lower than prior to intervention, whilst the diagnosis rate initially increases and then falls, and in the long-term the diagnosis rate may be lower or higher than prior to the intervention. A diagnosis rate that remains elevated may be interpreted wrongly as indicating a failure of the intervention or even a higher incidence of infection than prior to intervention.
To our knowledge, we are the first to use a transmission-dynamic model to synthesise evidence on the natural history and epidemiology of M. genitalium, and the impact of screening and treatment. We have identified key natural history parameters whose values are uncertain, which leads to considerable uncertainty in the magnitude of the effect of screening. Further research is required to obtain better estimates of these parameters before it can be determined how effective NAAT-based screening for M. genitalium is likely to be. Natural history studies of sexually-transmitted infections typically concentrate on women, due to concern about serious sequelae, but since most infected women become infected from men it is important to know parameter values for both sexes, to inform effective control policies. We note that results are not always as expected: in the case of C. trachomatis, established infections clear more slowly in men than women, which is the opposite of what is typically assumed31.
Our analysis shows that particularly important for M. genitalium transmission are the proportion of infections that are symptomatic (and proportion of those that are treated), duration of untreated infection, and infectivity, in both sexes. Measurement of these parameters will involve a variety of studies56, including analysis of surveillance data; it is possible to calculate population prevalence of infection based on rates of screening and diagnosis57. To maximise the value of surveillance data it is important to have a good understanding of the processes that lead to patients being tested and diagnosed to be able to make more-precise inferences57, e.g. what proportion of diagnosed infections are in symptomatic vs asymptomatic individuals, and what is each patient’s reason for testing, e.g. due to symptoms, being a notified partner of a diagnosed case, having been at perceived risk of infection and sought a test, or having been offered screening by a healthcare provider.
Combining data from contact tracing with whole-genome sequencing of isolates allows estimation of the timing of transmission from person to person, which provides lower-bound information on the duration of infection; this has been done for gonorrhoea and could be applied to M. genitalium 58. Estimates of the duration of untreated infection are best obtained from cohort studies in which individuals are followed over months or years without infections being treated, which have been performed for M. genitalium in women11,59 (see Smieszek & White 201660 for a synthesis of those studies) but not men. Such studies are only possible where testing for and treating M. genitalium is not the standard of care. It is therefore vital to conduct studies urgently before screening and treating M. genitalium becomes common due to adoption of multiplex NAAT testing.
Multiplex NAATs that test for both C. trachomatis and M. genitalium provide an opportunity for large-scale surveillance, of M. genitalium, at minimal cost, through unlinked anonymous testing for M. genitalium of samples from patients who are screened for C. trachomatis, in order to identify risk groups in whom screening for M. genitalium would be justified. Additionally, diagnosis of NCNGU requires ruling-out of C. trachomatis and N. gonorrhoeae, so using a multiplex test that detects those organisms plus M. genitalium would be a simple way to monitor the proportion of NCNGU that is associated with M. genitalium and examine associations with age, sex, and location. Such studies are important since the positive predictive value (PPV) of the test depends upon the prevalence of infection in those screened, as well as test sensitivity and specificity, and only in groups where prevalence is sufficiently high is the PPV high enough to justify screening for treatment. It might be appropriate to target M. genitalium testing by age, or according to patient characteristics (e.g. those with symptoms, and/or with greater numbers of recent sexual partners)11,61,62,63. Geographic targeting may be appropriate, since it is likely that prevalence will vary geographically, as it does for C. trachomatis 57.
In conclusion, it is unclear at present whether screening for M. genitalium should be recommended, due to uncertainty in key natural history parameters identified in our analysis. The ongoing uncertainty in the impact of chlamydia screening highlights the need for caution. We hope that this work will enable empirical research activity to be focused where it will be most effective in informing public-health decision-making.
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We thank Geraldine Leong, Public Health England, for supplying surveillance data; Jorgen Skov Jensen, Mycoplasma Laboratory, Statens Serum Institut, Copenhagen S, Denmark for advice on parameter values, and Lorna Sutcliffe, Barts and The London School of Medicine & Dentistry, Queen Mary University of London, Barts Sexual Health Centre. We thank the two anonymous reviewers for their helpful comments. This paper presents independent research commissioned by the National Institute for Health Research (NIHR) under its Programme Grants for Applied Research scheme (RP-PG-0707-10208). PJW also thanks the UK Medical Research Council for Centre funding (MR/K010174/1) and the UK National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Modelling Methodology at Imperial College London in partnership with Public Health England (PHE) for funding (HPRU-2012-10080). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The views expressed in this paper are those of the authors and not necessarily those of the Department of Health, the NHS, the NIHR, or Public Health England.
The authors declare that they have no competing interests.
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Birger, R., Saunders, J., Estcourt, C. et al. Should we screen for the sexually-transmitted infection Mycoplasma genitalium? Evidence synthesis using a transmission-dynamic model. Sci Rep 7, 16162 (2017). https://doi.org/10.1038/s41598-017-16302-8