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Peer-reviewedCC BY-NC-NDBiosafety and health

Evolving priorities in the WHO Bacterial Priority Pathogens List

  1. 1Center for Microbiome Research of Med-X Institute, Department of Critical Care Medicine, Shaanxi Provincial Key Laboratory of Sepsis in Critical Care Medicine, The First Affiliated Hospital, Xi’an Jiaotong University, Xi’an 710061, China
  2. 2The Key Laboratory of Environment and Genes Related to Disease of Ministry of Education Health Science Center, Xi’an Jiaotong University, Xi’an 710061, China
  3. 3Key Laboratory of Multiple Organ Failure (Ministry of Education), Departments of Microbiology and General Intensive Care Unit of the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China

Abstract

The 2024 World Health Organization (WHO) Bacterial Priority Pathogens List (BPPL) updates the 2017 framework by expanding to 24 pathogens across 15 bacterial families, addressing the growing antimicrobial resistance (AMR) crisis, which was estimated to have caused 1.27 million deaths in 2019. The revised list introduces four new pathogen-antibiotic combinations—rifampicin-resistant Mycobacterium tuberculosis, macrolide-resistant Group A Streptococci, macrolide-resistant Streptococcus pneumoniae, and penicillin-resistant Group B Streptococci—while removing five, including clarithromycin-resistant Helicobacter pylori, reflecting evolving resistance patterns, regional disparities, and therapeutic advancements. Notably, third-generation cephalosporin-resistant Enterobacterales is now a standalone critical-priority pathogen due to its high burden in low- and middle-income countries. This review examines these updates, driven by complex resistance mechanisms, surveillance gaps, and the impact of coronavirus disease 2019 (COVID-19)-related antibiotic misuse. It highlights trends such as the dominance of Gram-negative bacteria, rising rates of community-acquired infections, and the urgent need for innovative therapies, including phage therapy, phenazine-based antimicrobials, and metal-based strategies. Enhanced global surveillance, equitable access to treatments, and collaborative efforts are critical to combating AMR effectively.

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BibTeX
@article{ouyang2026evolving,
  title = {{Evolving priorities in the WHO Bacterial Priority Pathogens List}},
  author = {Zhenlin Ouyang and Wenbo He and Xiaoyu He and Min Jiao and Youjun Feng and Yurong Wen},
  journal = {Biosafety and health},
  year = {2026},
  month = jul,
  doi = {10.1016/j.bsheal.2026.07.004},
  url = {https://europepmc.org/article/PMC/PMC13729071},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Evolving priorities in the WHO Bacterial Priority Pathogens List
AU  - Zhenlin Ouyang
AU  - Wenbo He
AU  - Xiaoyu He
AU  - Min Jiao
AU  - Youjun Feng
AU  - Yurong Wen
PY  - 2026
DA  - 2026/07/21
JO  - Biosafety and health
DO  - 10.1016/j.bsheal.2026.07.004
UR  - https://europepmc.org/article/PMC/PMC13729071
AB  - The 2024 World Health Organization (WHO) Bacterial Priority Pathogens List (BPPL) updates the 2017 framework by expanding to 24 pathogens across 15 bacterial families, addressing the growing antimicrobial resistance (AMR) crisis, which was estimated to have caused 1.27 million deaths in 2019. The revised list introduces four new pathogen-antibiotic combinations—rifampicin-resistant Mycobacterium tuberculosis, macrolide-resistant Group A Streptococci, macrolide-resistant Streptococcus pneumoniae, and penicillin-resistant Group B Streptococci—while removing five, including clarithromycin-resistant Helicobacter pylori, reflecting evolving resistance patterns, regional disparities, and therapeutic advancements. Notably, third-generation cephalosporin-resistant Enterobacterales is now a standalone critical-priority pathogen due to its high burden in low- and middle-income countries. This review examines these updates, driven by complex resistance mechanisms, surveillance gaps, and the impact of coronavirus disease 2019 (COVID-19)-related antibiotic misuse. It highlights trends such as the dominance of Gram-negative bacteria, rising rates of community-acquired infections, and the urgent need for innovative therapies, including phage therapy, phenazine-based antimicrobials, and metal-based strategies. Enhanced global surveillance, equitable access to treatments, and collaborative efforts are critical to combating AMR effectively.
SN  - 2590-0536
SN  - 2096-6962
ER  -