Topic Editors

1. UCIBIO—Applied Molecular Biosciences Unit, Translational Toxicology Research Laboratory, University Institute of Health Sciences (1H-TOXRUN, IUCS-CESPU), 4585-116 Gandra, PRD, Portugal
2. LEPABE, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, s/n, 4200-465 Porto, Portugal
LEPABE, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, s/n, 4200-465 Porto, Portugal

Multidrug Resistance Across Pathogens: Fungi, Bacteria, Parasites, and Viruses

Abstract submission deadline
31 October 2026
Manuscript submission deadline
31 December 2026
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1142

Topic Information

Dear Colleagues,

The global emergence of multidrug resistance (MDR) across diverse pathogen types represents one of the most pressing challenges in modern medicine and public health. The challenge of multidrug resistance transcends traditional pathogen boundaries, requiring coordinated responses that recognize both the unique and shared mechanisms across fungi, bacteria, parasites, and viruses. AMR affects many of the gains of modern medicine, making infections harder to treat and making other medical procedures and treatments much riskier. Success in combating this global threat demands unprecedented collaboration between clinicians, researchers, public health officials, and policymakers.

This Topic examines the multifaceted nature of antimicrobial resistance (AMR), which affects countries in all regions and at all income levels, with its drivers and consequences being exacerbated by poverty and inequality. The scope encompasses bacterial superbugs, emerging fungal threats, parasitic drug resistance, and viral escape mechanisms, highlighting both shared resistance mechanisms and pathogen-specific challenges. The articles in this topics will provide critical insights into current resistance patterns, emerging mechanisms, and innovative solutions that collectively chart a path forward in our ongoing battle against multidrug-resistant pathogens.

Dr. Célia F. Rodrigues
Dr. Andreia S. Azevedo
Topic Editors

Keywords

  • antimicrobial resistance
  • bacteria
  • fungi
  • virus
  • parasitic
  • novel treatments
  • diagnosis
  • prevention

Participating Journals

Journal Name Impact Factor CiteScore Launched Year First Decision (median) APC
Antibiotics
antibiotics
4.6 8.7 2012 15 Days CHF 2900 Submit
Bacteria
bacteria
- 2.8 2022 25.4 Days CHF 1000 Submit
Microbiology Research
microbiolres
2.2 2.8 2010 20.7 Days CHF 1600 Submit
Microorganisms
microorganisms
4.2 7.7 2013 15.2 Days CHF 2700 Submit
Pathogens
pathogens
3.3 6.8 2012 13.5 Days CHF 2200 Submit
Parasitologia
parasitologia
1.5 2.4 2021 18.5 Days CHF 1200 Submit

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Published Papers (2 papers)

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12 pages, 1373 KB  
Article
Genomic Surveillance of Plasmodium falciparum Drug Resistance Markers Between October 2021 and June 2023 in Kigali, Rwanda
by Sandra Noukimi Fankem, Jean-Bosco Mbonimpa, Edgar Mutebwa Kalimba, Mariama Telly Diallo, Mary Efeti Teke and Jacob Souopgui
Pathogens 2025, 14(11), 1092; https://doi.org/10.3390/pathogens14111092 - 27 Oct 2025
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Abstract
Artemisinin-based combination therapies (ACTs) remain the cornerstone of malaria treatment in Rwanda, but the emergence of drug resistance threatens their efficacy. This study conducted genomic surveillance of Plasmodium falciparum isolates collected in Kigali between October 2021 and June 2023 to assess resistance markers. [...] Read more.
Artemisinin-based combination therapies (ACTs) remain the cornerstone of malaria treatment in Rwanda, but the emergence of drug resistance threatens their efficacy. This study conducted genomic surveillance of Plasmodium falciparum isolates collected in Kigali between October 2021 and June 2023 to assess resistance markers. Using Oxford Nanopore Technology and Sanger sequencing methods, we analyzed 250 clinical isolates focusing on mutations in the pfcrt, pfmdr1, pfdhfr, pfdhps, and Pfkelch13 genes. Resistance-associated mutations were highly prevalent: pfcrt 76T (26%) and pfmdr1 184F (72.8%) were common, indicating continued lumefantrine pressure. All isolates carried mutations in pfdhfr and pfdhps, with the IRNI-SAEAA and IRNI-SAEGA haplotypes found in 45.6% and 24.8% of samples, respectively, suggesting sustained antifolate resistance. Pfkelch13 mutations were present in 50.4% of isolates, including validated R561H (25.6%), A675V and candidate P441L mutations. Novel haplotypes, including K189T + R561H (24.8%), were identified for the first time in Rwanda. The BTB/POZ domain mutation H384R was observed in 6.4% of isolates, raising questions about its potential functional role. These findings highlight complex and evolving resistance patterns and emphasize the urgent need for continued molecular surveillance and functional validation to inform malaria control strategies in Rwanda. Full article
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Article
Molecular Epidemiology of Different Bacterial Pathogens and Their Antimicrobial Resistance Genes Among Patients Suffering from Surgical Site Infections in Lebanon
by Inass Kawtharani, Ghassan Ghssein, Ola Srour, Abdul Amir Chaaban and Pascale Salameh
Microbiol. Res. 2025, 16(10), 216; https://doi.org/10.3390/microbiolres16100216 - 1 Oct 2025
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Abstract
Background: Antimicrobial resistance (AMR) is a major global health threat, particularly in surgical site infections (SSIs), where multidrug-resistant (MDR) pathogens complicate treatment. Objective: This study aimed to identify antimicrobial resistance genes and assess their prevalence in bacterial species causing SSIs in Lebanon. Materials [...] Read more.
Background: Antimicrobial resistance (AMR) is a major global health threat, particularly in surgical site infections (SSIs), where multidrug-resistant (MDR) pathogens complicate treatment. Objective: This study aimed to identify antimicrobial resistance genes and assess their prevalence in bacterial species causing SSIs in Lebanon. Materials and Methods: The present research is a multicenter and prospective study that included patients who developed SSIs after surgery in seven hospitals, within the period of January 2024–September 2024. Bacterial isolates from wound swabs or tissue samples were identified using standard microbiological methods. Antimicrobial susceptibility was tested by disk diffusion, and resistance genes were detected by PCR. Data were analyzed using Statistical Package for the Social Sciences (SPSS). Results: Among 6933 surgical patients, 63 developed SSIs (0.91%; 95% CI [0.70–1.15]). Gram-negative bacteria predominated (73%), mainly Escherichia coli and Pseudomonas aeruginosa, while Gram-positive isolates accounted for 27%, mostly Staphylococcus aureus. MDR was observed in 71% of Gram-positive and 61% of Gram-negative isolates. The most frequent genes were mecA in S. aureus (100%) and coagulase-negative staphylococci (83.3%); blaCTX-M in E. coli, Klebsiella pneumoniae, and Enterobacter cloacae (100%); and blaNDM in E. cloacae (100%) and Acinetobacter baumannii (60%). blaKPC was less common, and no isolates carried Imipenemase (IMP), Verona integron-encoded metallo-β-lactamase (VIM), and Oxacillinase-48-like β-lactamase (OXA-48). Conclusions: This study highlights the high prevalence of antibiotic resistance in agents causing SSIs in Lebanese hospitals. Resistance genes, particularly mecA, blaCTX-M, and blaNDM, were highly prevalent in SSI pathogens, underscoring the urgent need for surveillance and judicious antibiotic use in Lebanese hospitals. Full article
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