Published December 22, 2025
| Version v1
Journal article
Complex multiannual cycles of Mycoplasma pneumoniae: Persistence and the role of stochasticity
Creators
- 1. Princeton University
- 2. University of Chicago
- 3. Canal Pointe
- 4. University of Copenhagen
Description
The epidemiological dynamics of Mycoplasma pneumoniae is characterized by poorly understood complex multiannual cycles. The origins of these cycles have long been debated, and multiple explanations of varying complexity have been suggested. Using Bayesian methods, we fit a dynamical model to half a century of M. pneumoniae surveillance data from Denmark (1958 to 1995, 2010 to 2025) and uncover a parsimonious explanation for the persistent cycles, based on the theory of quasicycles. The period of the multiannual cycle (approx. 5 y in Denmark) is explained by susceptible replenishment due, primarily, to loss of immunity. While an excellent fit to shorter time series (a few decades), the deterministic model eventually settles into an annual cycle, unable to reproduce the persistent cycles. We find that environmental stochasticity (e.g., varying contact rates) stabilizes the multiannual cycles and so does demographic noise, at least in smaller or incompletely mixing populations. The temporary disappearance of cycles during 1979 to 1985 is explained as a consequence of stochastic mode-hopping. The circulation of M. pneumoniae was recently disrupted by COVID-19 nonpharmaceutical interventions (NPIs), providing a natural experiment on the effects of large perturbations. Consequently, the effects of NPIs are included in the model and medium-term predictions are explored. Our findings highlight the intrinsic sensitivity of M. pneumoniae dynamics to perturbations and interventions, underscoring the limitations for long-term prediction. More generally, our findings provide further evidence for the role of stochasticity as a driver of complex cycles across endemic and recurring pathogens.
Data availability
All code and data used in this manuscript have been deposited in Zenodo (https://doi.org/10.5281/zenodo.15232137) (85). Previously published data were used for this work (2).Additional details
Identifiers
- DOI
- 10.1073/pnas.2509184122
- Other
- oai:uchicago.tind.io:16788
Funding
- Carlsberg Foundation
- CF23-0173
- Life Sciences Research Foundation
- The Peter and Carmen Lucia Buck Foundation
- Novo Nordisk Foundation
- NNF20OC0064978
- Novo Nordisk Foundation
- NNF24OC0089788
- Princeton University
- Princeton Catalysis Initiative
- Princeton University
- Princeton Precision Health
- Carlsberg Foundation
- CF24-1337