ABSTRACT
Antimicrobial resistance (AMR) has become one of the most pressing threats to public health worldwide. According to the Global Burden of Disease 2021 report, AMR was linked to 4.71 million deaths, of which 1.14 million were directly caused by bacterial resistance. The impact is not felt equally, with low‐ and middle‐income countries (LMICs) carrying the greatest burden due to weak health systems, limited diagnostics and widespread misuse of antibiotics in both healthcare and agriculture. Self‐medication and poor regulatory oversight further accelerate the crisis. This article explores these challenges and stresses the urgent need for a coordinated ‘One Health’ approach that connects human, animal and environmental health. Strengthening surveillance, investing in new antibiotics and promoting responsible use through stewardship programs and community awareness are critical steps forward. Without decisive global action, AMR could claim over 8 million lives each year by 2050; yet, with timely interventions, especially in LMICs, up to 92 million deaths could be prevented, protecting future generations from its devastating consequences.
Keywords: AMR surveillance systems, antimicrobial resistance (AMR), antimicrobial stewardship, Global Burden of Disease (GBD 2021), one health approach
Antimicrobial resistance remains a major global health threat, with the greatest burden concentrated in low‐ and middle‐income countries. Driven by antibiotic misuse, weak diagnostics, and human‐animal‐environmental transmission, the crisis demands a One Health response. Strengthened surveillance, stewardship, regulation, public awareness, and innovation are essential to reduce preventable deaths and slow the spread of resistance.

1. Introduction
Antimicrobial resistance (AMR) poses a severe threat to global public health. AMR poses substantial challenges to healthcare systems, economic stability and social welfare [1, 2]. If unaddressed, projections estimate that AMR could be associated with more than 8.2 million deaths annually by 2050, with a substantial proportion directly attributable to bacterial resistance, which would result in profound economic losses worldwide [3]. This commentary critically examines findings from the Global Burden of Disease (GBD) 2021 report, identifies current gaps in addressing AMR and proposes actionable strategies to mitigate its impact in line with global health initiatives like the World Health Organization's Global Action Plan on AMR.
1.1. Key Findings and Trends
This GBD report quantified AMR burden from 1990 to 2021 for 22 pathogens, 84 pathogen–drug combinations and 11 syndromes in 204 countries. It analysed all‐age and age‐specific deaths and disability‐adjusted life‐years attributable to and associated with AMR [3]. AMR‐related mortality varies notably by age and infection type. The report reveals significant regional disparities in AMR‐related mortality, as high burdens were observed in South Asia and sub‐Saharan Africa [3]. Although AMR mortality among children under 5 years has decreased by over 50% since 1990, the burden has shifted toward older adults, particularly those over 70, with an alarming 80% increase in deaths [3]. The increasing prevalence of multidrug‐resistant Gram‐negative organisms, particularly in low‐ and middle‐income countries (LMICs), signals an urgent need for targeted interventions [4].
1.2. Drivers of the AMR Crisis
AMR arises from a complex interplay of healthcare, agricultural, environmental and socio‐economic factors, with significant regional variation. Healthcare‐related drivers remain central to the AMR burden. Overprescription of antibiotics, frequent treatment of non‐bacterial infections and self‐medication are pervasive in LMICs, exacerbated by weak regulatory oversight and limited access to diagnostics [5, 6, 7]. For example, a study in Uganda reports that over 50% of the population engage in self‐medication, highlighting gaps in both community awareness and healthcare governance [6]. Although high‐income countries have established effective stewardship programmes, LMIC hospitals often face resource constraints that limit the implementation and monitoring of antimicrobial stewardship programs (ASPs) [8, 9].
Agricultural and environmental drivers further amplify AMR transmission. Extensive use of antibiotics for growth promotion and disease prevention in livestock and crop production contributes to the spread of resistant organisms from animals to humans through food chains, soil and water [10, 11]. Critically, most regional studies rely on cross‐sectional or modelling data with limited longitudinal validation, indicating a need for stronger empirical surveillance [12]. Environmental pathways, including contaminated wastewater, surface water and bioaerosols, facilitate horizontal gene transfer and cross‐species dissemination, yet remain underreported in LMIC research [13].
Surveillance and data limitations are another critical barrier to effective AMR control. Although global estimates, such as the GBD 2021 report, provide valuable insights, they rely heavily on modelling in regions with limited laboratory capacity, which may underestimate the true burden [3]. In many LMICs, surveillance systems are fragmented and lack standardization, restricting a timely detection of resistance trends and weakening evidence‐based policymaking [14].
Finally, governance and socio‐economic factors compound these challenges. Weak regulatory enforcement allows over‐the‐counter antibiotic sales, inconsistent agricultural controls and inequitable access to healthcare [7]. Urbanization, population growth and poverty intensify exposure risks and hinder adherence to recommended stewardship practices [15, 16].
1.3. Addressing Current Challenges and Opportunities for Interventions
Sustainable control of AMR requires a comprehensive One Health approach integrating human, animal and environmental health [17]. A key priority is strengthening surveillance systems through improved laboratory capacity, standardized antimicrobial susceptibility testing and coordinated data‐sharing platforms, particularly in resource‐limited settings [18]. Incentivizing the development of new antibiotics is also critical, especially for multidrug‐resistant Gram‐negative pathogens. Given the scientific and economic challenges facing the pharmaceutical industry, push–pull mechanisms, such as public–private partnerships and market entry rewards, are essential to stimulate innovation [19, 20].
Targeted interventions are needed across both community and healthcare settings [5, 6, 21]. At the community level, self‐medication and over‐the‐counter antibiotic sales remain major drivers of resistance, underscoring the need for stronger regulatory enforcement and public education [6]. Broad awareness campaigns through radio, television and social media can promote responsible antibiotic use [21], whereas behavioural strategies, such as pharmacy pledges, Short Message Service reminders and school‐based AMR education, can foster long‐term change [7, 21]. Governments and non‐governmental organizations should support outreach programs and farmer education to reduce non‐therapeutic antibiotic use in livestock under a One Health framework [10]. Improved hygiene, sanitation and safe disposal of unused antibiotics can further reduce community‐level risk.
Within healthcare settings, ASPs should be strengthened to optimize prescribing practices through monitoring, feedback and adherence to treatment guidelines [8, 9]. These efforts should be supported by improved infection prevention and control, access to rapid diagnostics and continued professional training to reduce inappropriate antibiotic use. Mandatory training and continuing medical education on AMR and stewardship are critical for healthcare professionals [22, 23]. The adoption of electronic prescription systems and expanded access to rapid diagnostics, including culture and sensitivity testing, can promote targeted therapy and reduce inappropriate antibiotic use [8]. Together, these coordinated actions provide a practical and scalable framework for mitigating AMR across sectors.
1.4. Future Directions and Recommendations
Expanding public awareness and strengthening national action plans should remain central to AMR control. Interventions must be context‐specific, particularly in LMICs, where regulatory enforcement, healthcare access and resource availability vary significantly [24, 25, 26, 27]. Integrated infection prevention and stewardship initiatives in Bangladesh and India demonstrate the importance of multisectoral approaches, whereas agricultural guidelines limiting non‐therapeutic antibiotic use in Kenya and Vietnam complement human health efforts under a One Health framework [28, 29].
Sweden's experience offers key lessons, including strict prescription regulations, robust stewardship and surveillance and active public engagement [30]. Although direct replication may be challenging, LMICs can adapt these principles through phased stewardship, sentinel surveillance and cost‐effective education, which integrates human, animal and environmental actions to achieve sustainable, scalable AMR control [31, 32].
Operationalizing a One Health approach requires coordinated implementation across sectors. Successful models from countries, such as Sweden, Thailand and South Africa, demonstrate the feasibility of combining surveillance, stewardship and public engagement into scalable AMR control strategies [33, 34]. Incentives for new antibiotic development combine push mechanisms (grants, partnerships like CARB‐X) and pull mechanisms (market entry rewards) [35]. Lastly, measurable outcomes, such as reporting coverage, data completeness and the number of antibiotics in development, provide a practical and adaptable roadmap for One Health AMR control [36, 37].
2. Conclusion
Addressing the AMR crisis necessitates immediate global collaboration. The GBD 2021 report reveals significant mortality rates, increasing regional inequalities and a growing burden on older populations in LMICs, jeopardizing healthcare and economic stability. A holistic One Health strategy must be implemented through enhanced surveillance, laboratory capabilities and data‐informed policies. Antimicrobial stewardship requires bolstering via electronic prescriptions, compulsory training, prescription audits and tighter regulations on over‐the‐counter antibiotics, along with improved infection control measures. Policies should also restrict non‐therapeutic antibiotic applications in agriculture, enhance farmer education and advocate for safer practices. Public awareness initiatives, educational programs in schools and digital outreach are crucial for diminishing self‐medication. Continued political dedication, investment in diagnostics and primary healthcare and renewed efforts in antibiotic innovation can profoundly influence the AMR trajectory and avert millions of preventable deaths in the future.
Author Contributions
Safayet Jamil conceptualized this topic. Safayet Jamil, Md. Golam Dostogir Harun and Hafiz T. A. Khan supervised this project. Safayet Jamil, Md. Golam Dostogir Harun, Mohammad Shahangir Biswas and Victor Abiola Adepoju conducted literature review. Safayet Jamil, Abdulrakib Abdulrahim and Neeru Chaudhary wrote the first draft. Mohammad Shahangir Biswas, Abdulrakib Abdulrahim, Victor Abiola Adepoju, Hafiz T. A. Khan and Uthman Okikiola Adebayo revised and edited this manuscript. All authors approved the final version of the manuscript.
Funding
The authors have nothing to report.
Conflicts of Interest
The authors declare no conflicts of interest.
Data Availability Statement
Data sharing is not applicable to this article as no datasets were generated or analysed during the current study.
References
- 1. Sharma S., Chauhan A., Ranjan A., et al., “Emerging Challenges in Antimicrobial Resistance: Implications for Pathogenic Microorganisms, Novel Antibiotics, and Their Impact on Sustainability,” Frontiers in Microbiology 15 (2024): 1403168, 10.3389/fmicb.2024.1403168. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. Aslam B., Asghar R., Muzammil S., et al., “AMR and Sustainable Development Goals: At a Crossroads,” Global Health 20 (2024): 73, 10.1186/s12992-024-01046-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Naghavi M., Vollset S. E., Ikuta K. S., et al., “Global Burden of Bacterial Antimicrobial Resistance 1990–2021: A Systematic Analysis With Forecasts to 2050,” Lancet 404 (2024): 1199–1226, 10.1016/S0140-6736(24)01867-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Salam M. A., Al‐Amin M. Y., Salam M. T., et al., “Antimicrobial Resistance: A Growing Serious Threat for Global Public Health,” Healthcare 11 (2023): 1946, 10.3390/healthcare11131946. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Gulumbe B. H., Sahal M. R., Abdulrahim A., et al., “Antibiotic Resistance and the COVID‐19 Pandemic: A Dual Crisis With Complex Challenges in LMICs,” Health Science Reports 6 (2023): e1566, 10.1002/hsr2.1566. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Makeri D., Dilli P. P., Pius T., et al., “The Nature of Self‐Medication in Uganda: A Systematic Review and Meta‐Analysis,” BMC Public Health [Electronic Resource] 25 (2025): 197, 10.1186/s12889-025-21380-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Sharma A., Singh A., Dar M. A., et al., “Menace of Antimicrobial Resistance in LMICs: Current Surveillance Practices and Control Measures to Tackle Hostility,” Journal of Infection and Public Health 15 (2022): 172–181, 10.1016/j.jiph.2021.12.008. [DOI] [PubMed] [Google Scholar]
- 8. Gulumbe B. H., Danlami M. B., and Abdulrahim A., “Closing the Antimicrobial Stewardship Gap—A Call for LMICs to Embrace the Global Antimicrobial Stewardship Accreditation Scheme,” Antimicrobial Resistance and Infection Control 13 (2024): 19, 10.1186/s13756-024-01371-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Harun M. G. D., Sumon S. A., Hasan I., Akther F. M., dS Islam M., and Anwar M. M. U., “Barriers, Facilitators, Perceptions and Impact of Interventions in Implementing Antimicrobial Stewardship Programs in Hospitals of Low‐Middle and Middle Countries: A Scoping Review,” Antimicrobial Resistance and Infection Control 13 (2024): 8, 10.1186/s13756-024-01369-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Arnold K. E., Laing G., McMahon B. J., et al., “The Need for One Health Systems‐Thinking Approaches to Understand Multiscale Dissemination of Antimicrobial Resistance,” Lancet Planetary Health 8 (2024): e124–e133, 10.1016/S2542-5196(23)00278-4. [DOI] [PubMed] [Google Scholar]
- 11. Enshaie E., Nigam S., Patel S., and Rai V., “Livestock Antibiotics Use and Antimicrobial Resistance,” Antibiotics 14 (2025): 621, 10.3390/antibiotics14060621. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Mothé D. A. C., Castro A. N., Novaes M. Z., et al., “Antimicrobial‐Resistant Bacteria in Environmental Samples from a Rural District Focused on Large‐Scale Agricultural Production,” Tropical Medicine & International Health: TM & IH 30 (2025): 1269–1282, 10.1111/tmi.70033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Larsson D. G. J. and Flach C.‐F., “Antibiotic Resistance in the Environment,” Nature Reviews Microbiology 20 (2022): 257–269, 10.1038/s41579-021-00649-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Matee M., Mshana S. E., Mtebe M., et al., “Mapping and Gap Analysis on Antimicrobial Resistance Surveillance Systems in Kenya, Tanzania, Uganda and Zambia,” Bulletin of the National Research Centre 47 (2023): 12, 10.1186/s42269-023-00986-2. [DOI] [Google Scholar]
- 15. Ljungqvist G., Van Kessel R., Mossialos E., et al., “Mapping Socioeconomic Factors Driving Antimicrobial Resistance in Humans: An Umbrella Review,” One Health 20 (2025): 100986, 10.1016/j.onehlt.2025.100986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16. Eke S. M. and Cua A., “Invisible Engines of Resistance: How Global Inequities Drive Antimicrobial Failure,” Antibiotics 14 (2025): 659, 10.3390/antibiotics14070659. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. Velazquez‐Meza M. E., Galarde‐López M., Carrillo‐Quiróz B., and Alpuche‐Aranda C. M., “Antimicrobial Resistance: One Health Approach,” Veterinary World 15 (2022): 743–749, 10.14202/vetworld.2022.743-749. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Do P. C., Assefa Y. A., Batikawai S. M., and Reid S. A., “Strengthening Antimicrobial Resistance Surveillance Systems: A Scoping Review,” BMC Infectious Diseases [Electronic Resource] 23 (2023): 593, 10.1186/s12879-023-08585-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Iskandar K., Molinier L., Hallit S., et al., “Surveillance of Antimicrobial Resistance in Low‐ and Middle‐Income Countries: A Scattered Picture,” Antimicrobial Resistance and Infection Control 10 (2021): 63, 10.1186/s13756-021-00931-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Lopez B. S., “Can Infectious Disease Control Be Achieved Without Antibiotics by Exploiting Mechanisms of Disease Tolerance?,” ImmunoHorizons 6 (2023): 730–740, 10.4049/immunohorizons.2200043. [DOI] [Google Scholar]
- 21. Acharya K. P. and Subedi D., “Use of Social Media as a Tool to Reduce Antibiotic Usage: A Neglected Approach to Combat Antimicrobial Resistance in Low and Middle Income Countries,” Front Public Health 8 (2020): 558576, 10.3389/fpubh.2020.558576. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. dG Harun M. D., Anwar M. M. U., Sumon S. A., et al., “Rationale and Guidance for Strengthening Infection Prevention and Control Measures and Antimicrobial Stewardship Programs in Bangladesh: A Study Protocol,” BMC Health Services Research [Electronic Resource] 22 (2022): 1239, 10.1186/s12913-022-08603-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Orok E., Ikpe F., Williams T., and Ekada I., “Impact of Educational Intervention on Knowledge of Antimicrobial Resistance and Antibiotic Use Patterns Among Healthcare Students: A Pre‐ and Post‐Intervention Study,” BMC Medical Education [Electronic Resource] 25 (2025): 283, 10.1186/s12909-025-06856-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Maduko W., Olamijuwon E., Kesby M., and Hale J. M., “Public‐Targeted Interventions Addressing Antimicrobial Resistance and Antibiotic Use in Sub‐Saharan Africa: A Scoping Review,” BMJ Global Health 10 (2025): e017455, 10.1136/bmjgh-2024-017455. [DOI] [Google Scholar]
- 25. Olagunju O. J., Ben E., Olagunju O., et al., “Poorly Regulated Antibiotic Use in Nigeria: A Critical Public Health Concern and Its Impact on Medical Practice,” Cureus 17 (2025): e85212, 10.7759/cureus.85212. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. Iregbu K. C., Nwajiobi‐Princewill P. I., Medugu N., et al., “Antimicrobial Stewardship Implementation in Nigerian Hospitals: Gaps and Challenges,” African Journal Of Clinical and Experimental Microbiology 22 (2021): 60–66, 10.4314/ajcem.v22i1.8. [DOI] [Google Scholar]
- 27. Kimbowa I. M., Ocan M., Eriksen J., et al., “Characteristics of Antimicrobial Stewardship Programmes in Hospitals of Uganda,” PLoS ONE 17 (2022): e0268032, 10.1371/journal.pone.0268032. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Rony M. K. K., Sharmi P. D., and Alamgir H. M., “Addressing Antimicrobial Resistance in Low and Middle‐Income Countries: Overcoming Challenges and Implementing Effective Strategies,” Environmental Science and Pollution Research 30 (2023): 101896–101902, 10.1007/s11356-023-29434-4. [DOI] [PubMed] [Google Scholar]
- 29. Ehsan H., “Antibiotic Resistance in Developing Countries: Emerging Threats and Policy Responses,” Public Health Challenges 4 (2025): e70034, 10.1002/puh2.70034. [DOI] [Google Scholar]
- 30. Sulis G., Sayood S., and Gandra S., “Antimicrobial Resistance in Low‐ and Middle‐Income Countries: Current Status and Future Directions,” Expert Review of Anti‐infective Therapy 20 (2022): 147–160, 10.1080/14787210.2021.1951705. [DOI] [PubMed] [Google Scholar]
- 31. Lewnard J. A., Charani E., Gleason A., et al., “Burden of Bacterial Antimicrobial Resistance in Low‐Income and Middle‐Income Countries Avertible by Existing Interventions: An Evidence Review and Modelling Analysis,” Lancet 403 (2024): 2439–2454, 10.1016/S0140-6736(24)00862-6. [DOI] [PubMed] [Google Scholar]
- 32. Zay Ya K., Lambiris M. J., Levine G. A., Tediosi F., and Fink G., “Coverage of Policies to Improve Antimicrobial Stewardship in human Medicine in Low and Middle Income Countries: Results From the Global Survey of Experts on Antimicrobial Resistance,” BMC Public Health [Electronic Resource] 24 (2024): 2297, 10.1186/s12889-024-19542-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33. Ahmad N., Joji R. M., and Shahid M., “Evolution and Implementation of One Health to Control the Dissemination of Antibiotic‐Resistant Bacteria and Resistance Genes: A Review,” Frontiers in Cellular and Infection Microbiology 12 (2023): 1065796, 10.3389/fcimb.2022.1065796. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34. Collignon P. J. and McEwen S. A., “One Health—Its Importance in Helping to Better Control Antimicrobial Resistance,” Tropical Medicine and Infectious Disease 4 (2019): 22, 10.3390/tropicalmed4010022. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35. Elbehiry A., Marzouk E., and Abalkhail A., “Antimicrobial Resistance at a Turning Point: Microbial Drivers, One Health, and Global Futures,” Frontiers in Microbiology 16 (2025): 1698809, 10.3389/fmicb.2025.1698809. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Ohia C. M. D., Falodun O. I., Adebudo L. I., and Bakarey A. S., “A One Health Perspective on Multidrug‐Resistant Bacterial Infections: Integrated Approaches for Surveillance, Policy and Innovation,” Frontiers in Cellular and Infection Microbiology 15 (2025): 1614232, 10.3389/fcimb.2025.1614232. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37. Muhammad Faheem A., “One Health, One World: Tackling Antimicrobial Resistance Through Integrated Action,” Annals of King Edward Medical University 31 (2025): 242–243, 10.21649/akemu.v31i3.6262. [DOI] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Data sharing is not applicable to this article as no datasets were generated or analysed during the current study.
