Pertussis is an infectious bacterial disease caused by Bordetella pertussis; some human illness is also attributed to Bordetella parapertussis [1][2]. The organism is described as a Gram-negative, pleomorphic, aerobic coccobacillus [2]. Contemporary reviews characterize pertussis as both vaccine-preventable and epidemiologically complex, with questions remaining about natural immunity, vaccine-derived immunity, and transmission prevention [1].
Disease Profile
BacterialPertussis
百日咳
Pertussis is a vaccine-preventable cough illness caused primarily by Bordetella pertussis and is described as highly infectious [1][2]. It remains a significant cause of morbidity and mortality globally, with severe outcomes concentrated in very young infants and in unvaccinated persons [2][3]. Recent literature notes a resurgence in some countries despite high immunization coverage, underscoring the need to interpret surveillance data in the context of changing diagnostics, waning immunity, and possible organism evolution [1][2].
The source material characterizes pertussis as a cough illness that can produce serious and potentially fatal complications, particularly in very young infants [2][3]. Severe infection requiring hospitalization, including intensive care, is reported mainly in children under 3 months of age [2]. One review notes that the disease can be fatal in the unvaccinated, especially very young infants [1]. Source-backed detail on the full symptom sequence, duration, and specific complication spectrum is not yet available from the provided snippets [1][2][3].
Pertussis has been present in humans for at least 800 years and remains a worldwide public-health concern [1][2]. The introduction of whole-cell vaccines in the 1940s and 1950s was associated with a drastic decline in incidence, but some countries with high acellular vaccine coverage have since experienced a resurgence in reported cases [1]. The literature attributes this resurgence, at least in part, to molecular changes in the organism, waning immunity, lessened vaccine efficacy, and improved awareness or diagnostic capability [2]. Surveillance interpretation is complicated by incomplete case detection, limited genomic sequencing, heterogeneity in diagnostic methods, and the absence of a serologic marker of immunity [1].
Pertussis is described as highly contagious and highly infectious, but the provided sources do not give a detailed mechanism of spread [1][2][3]. In infants, the source of infection is usually a family member, indicating close-contact household exposure as an important epidemiologic pattern [2]. Source-backed detail on environmental persistence, specific infectious periods, or exposure settings is not yet available from the snippets [1][2].
The clearest high-risk group in the provided sources is very young infants, especially those under 3 months of age, who bear most severe disease and hospitalization burden and may be too young to benefit from immunization [1][2][3]. Unvaccinated persons are also identified as being at risk for fatal disease [1]. Infant exposure is often linked to a family member as the source of infection, highlighting household contacts as a relevant risk context [2].
Prevention is centered on vaccination, as pertussis is explicitly described as vaccine-preventable [2]. The source material notes that whole-cell vaccines reduced incidence substantially, while newer acellular vaccines were developed for improved tolerability and adopted mainly in high-income countries [1]. One cited public-health strategy is immunization during pregnancy, which was reported as favorable in cost-benefit analyses and expected to prevent more infant cases, hospitalizations, and deaths than cocooning strategies [2]. Source-backed detail on other exposure-control measures is not yet available from the snippets [1][2][3].
Pertussis surveillance should be interpreted cautiously because reported trends are influenced by incomplete case detection, variation in diagnostic methods, limited genome sequencing, and the absence of a serologic marker of immunity [1]. Apparent increases in case counts may reflect both true resurgence and improved awareness or diagnostic capability [2]. For monitoring purposes, severe disease in very young infants and household-linked infant infections are important contextual signals, but source-backed detail on standard case definitions or reporting intervals is not yet available [2].
- 1 Domenech de Cellès M et al. Pertussis vaccines, epidemiology and evolution. Nat Rev Microbiol. 2024 Nov. PMID: 38907021. doi: 10.1038/s41579-024-01064-8. PubMed: https://pubmed.ncbi.nlm.nih.gov/38907021/
- 2 Nieves DJ et al. Bordetella pertussis. Microbiol Spectr. 2016 Jun. PMID: 27337481. doi: 10.1128/microbiolspec.EI10-0008-2015. PubMed: https://pubmed.ncbi.nlm.nih.gov/27337481/
- 3 Nguyen VTN et al. Pertussis: The Whooping Cough. Prim Care. 2018 Sep. PMID: 30115332. doi: 10.1016/j.pop.2018.05.003. PubMed: https://pubmed.ncbi.nlm.nih.gov/30115332/
- 4 Pertussis toxin (Bordetella pertussis). Guidebook to Protein Toxins and Their Use in Cell Biology. 1997. doi: 10.1093/oso/9780198599555.003.0011. DOI: https://doi.org/10.1093/oso/9780198599555.003.0011
- 5 Pertussis and Pertussis Vaccine. JAMA. 1984. doi: 10.1001/jama.1984.03340470035022. DOI: https://doi.org/10.1001/jama.1984.03340470035022
- 6 Pertussis and Pertussis Syndrome. Introduction to Clinical Infectious Diseases. 2019. doi: 10.1007/978-3-319-91080-2_6. DOI: https://doi.org/10.1007/978-3-319-91080-2_6
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Figure 1 | Full historical trajectories across all reporting countries.
Figure 2 | Year-over-year monthly comparison for seasonality and structural shifts.
Dataset Archive
Supplementary Data | Multi-country disease dataset
Machine-readable multi-country disease dataset (JSON/CSV) with source metadata.
Source Register
Official sources and update cadences used to construct the downloadable dataset.
Australia
Australian national notifiable diseases surveillance dashboard.
Official sourceBrazil
Brazil Ministry of Health DATASUS/SINAN public DBC microdata aggregated to national monthly notification counts.
Official sourceChina
Monthly notifiable infectious disease reports published by China CDC.
Official sourceChina
Official China public health bulletin and query portal.
Official sourceChina
Biomedical literature discovery feed used as supplementary context.
Official sourceHong Kong, China
Hong Kong, China CHP annual notifiable infectious disease CSVs normalized to national monthly totals
Official sourceJapan
Japan weekly infectious disease surveillance via NIID/JIHS.
Official sourceSouth Korea
Korea KDCA notifiable infectious disease OpenAPI or portal/KOSIS downloads aggregated to national monthly notification counts.
Official sourceNew Zealand
PHF Science (formerly ESR) monthly notifiable disease surveillance data via internal globalID2 crawler
Official sourceTaiwan, China
Taiwan, China monthly notifiable infectious disease open-data CSV feed.
Official sourceUnited States
CDC National Notifiable Diseases Surveillance System provisional data.
Official source