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Background <p>The rise in multidrug-resistant (MDR) bacteria has rendered common first- and last-line antibiotics ineffective, posing a serious threat to human health. Additionally, the global rise of wound infections caused by carbapenem-resistant <i>Acinetobacter baumannii</i> indicates that the “post-antibiotic” era has begun. Consequently, alternative antimicrobial therapies are urgently required, and the reuse of phages is a promising choice.</p> Methods <p>Twenty-six strains of <i>A. baumannii</i> were isolated from wound-infected patients, identified by the Vitek 2 automated system, and confirmed by 16&#xa0;S rDNA sequencing. The strains’ susceptibility to antibiotics and their ability to develop biofilms were then studied. <i>Acinetobacter</i> phage RM_A1 was isolated and characterized, and its lytic activity against <i>A. baumannii</i> was tested in vitro via time-killing curve and antibiofilm formation assays. The phage’s stability was also tested under various conditions. Genomic analysis was performed to characterize the phage and its virulence. Finally, the phage was assessed as a therapeutic and prophylactic agent against carbapenem-resistant <i>A. baumannii in vitro</i> by using human skin cells.</p> Results <p>The clinical strains of <i>A. baumannii</i> were found to be resistant to the carbapenem antibiotics, exhibiting high MAR index values and a strong ability to form biofilm. The isolated RM-A1 phage had a myoviral morphology and a 43,994&#xa0;bp double-stranded DNA genome encoding 84 open reading frames (ORFs), with no genes linked to antibiotic resistance or pathogenicity. This phage possesses a broad host range, with a lysis spectrum of 85% against clinical isolates. It also possesses a large burst size and a short adsorption rate. It was capable of withstanding temperatures as high as 90&#xa0;°C, was pH-stable, and remained viable for 45&#xa0;min when exposed to UV light. There was no significant drop in the vitality of HSF cells observed following phage treatment, proving that the phage is safe for use. In vitro results showed that the phage was able to inhibit and eliminate biofilm formation and significantly reduce bacterial growth.</p> Conclusion <p>Our research explores the potential use of RM_A1 phage as an alternative therapeutic agent for combating carbapenem-resistant <i>A. baumannii</i>.</p>

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Prophylactic and therapeutic efficacy of Acinetobacter phage RM_A1 against carbapenem-resistant Acinetobacter baumannii with no cytotoxicity to human skin cells

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月3日

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  • Rabab M. Soliman,
  • Ahmed B. Barakat,
  • Ayman El-Shibiny,
  • Iman Mohamed Amin Elkholy ,
  • Ahmed Askora,
  • Azza G. Kamel,
  • Hagar A. Elshibiny,
  • Marwa M. Gado

摘要

Background

The rise in multidrug-resistant (MDR) bacteria has rendered common first- and last-line antibiotics ineffective, posing a serious threat to human health. Additionally, the global rise of wound infections caused by carbapenem-resistant Acinetobacter baumannii indicates that the “post-antibiotic” era has begun. Consequently, alternative antimicrobial therapies are urgently required, and the reuse of phages is a promising choice.

Methods

Twenty-six strains of A. baumannii were isolated from wound-infected patients, identified by the Vitek 2 automated system, and confirmed by 16 S rDNA sequencing. The strains’ susceptibility to antibiotics and their ability to develop biofilms were then studied. Acinetobacter phage RM_A1 was isolated and characterized, and its lytic activity against A. baumannii was tested in vitro via time-killing curve and antibiofilm formation assays. The phage’s stability was also tested under various conditions. Genomic analysis was performed to characterize the phage and its virulence. Finally, the phage was assessed as a therapeutic and prophylactic agent against carbapenem-resistant A. baumannii in vitro by using human skin cells.

Results

The clinical strains of A. baumannii were found to be resistant to the carbapenem antibiotics, exhibiting high MAR index values and a strong ability to form biofilm. The isolated RM-A1 phage had a myoviral morphology and a 43,994 bp double-stranded DNA genome encoding 84 open reading frames (ORFs), with no genes linked to antibiotic resistance or pathogenicity. This phage possesses a broad host range, with a lysis spectrum of 85% against clinical isolates. It also possesses a large burst size and a short adsorption rate. It was capable of withstanding temperatures as high as 90 °C, was pH-stable, and remained viable for 45 min when exposed to UV light. There was no significant drop in the vitality of HSF cells observed following phage treatment, proving that the phage is safe for use. In vitro results showed that the phage was able to inhibit and eliminate biofilm formation and significantly reduce bacterial growth.

Conclusion

Our research explores the potential use of RM_A1 phage as an alternative therapeutic agent for combating carbapenem-resistant A. baumannii.