Elimination of multidrug-resistant Proteus mirabilis biofilms using bacteriophages

Salwa Gomaa1, Fathy Serry2, Hemmat Abdellatif2

  • 1Department of Microbiology and Immunology, Faculty of Pharmacy, Zagazig University, Zagazig, 44519, Egypt. salwaesmat@zu.edu.eg.

Archives of Virology
|June 15, 2019
PubMed

Insights

Bacteriophages effectively controlled multidrug-resistant Proteus mirabilis biofilms, reducing viable cells by up to 99.9%. This offers a promising new strategy against challenging bacterial infections.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Biotechnology

Background:

  • Proteus mirabilis causes diverse infections and exhibits high antimicrobial resistance.
  • Multidrug-resistant (MDR) Proteus mirabilis poses a significant therapeutic challenge, particularly in biofilm-based infections.

Purpose of the Study:

  • To investigate the efficacy of bacteriophages in controlling biofilms formed by MDR Proteus mirabilis.

Main Methods:

  • Proteus mirabilis isolates were identified and their antimicrobial resistance and biofilm-forming capacity were assessed.
  • Bacteriophages targeting Proteus mirabilis were isolated from sewage.
  • The impact of bacteriophages on pre-formed biofilms was evaluated using the viable count method.

Main Results:

  • A high prevalence of antimicrobial resistance (87.2%) was observed in Proteus mirabilis isolates.
  • The majority of isolates (80.5%) demonstrated strong biofilm formation.
  • Five isolated bacteriophages significantly disrupted pre-formed biofilms, reducing viable cells by up to 99.9%.

Conclusions:

  • Bacteriophages demonstrate significant potential as a therapeutic strategy against MDR Proteus mirabilis biofilm infections.
  • Phage therapy offers a promising alternative for combating challenging bacterial infections where conventional antibiotics are ineffective.

Related Concept Videos

Lysogenic Cycle of Bacteriophages00:43

Lysogenic Cycle of Bacteriophages

In contrast to the lytic cycle, phages infecting bacteria via the lysogenic cycle do not immediately kill their host cell. Instead, they combine their genome with the host genome, allowing the bacteria to replicate the phage DNA along with the bacterial genome. The incorporated copy of the phage genome is called the prophage. Some prophages can re-activate and enter the lytic cycle. This often occurs in response to a perturbation, such as DNA damage, but can also transpire in the absence of...
67.4K
Lytic Cycle of Bacteriophages01:30

Lytic Cycle of Bacteriophages

Bacteriophages, also known as phages, are specialized viruses that infect bacteria. A key characteristic of phages is their distinctive “head-tail” morphology. A phage begins the infection process (i.e., lytic cycle) by attaching to the outside of a bacterial cell. Attachment is accomplished via proteins in the phage tail that bind to specific receptor proteins on the outer surface of the bacterium. The tail injects the phage’s DNA genome into the bacterial cytoplasm. In the...
77.6K
DNA Bacteriophages01:26

DNA Bacteriophages

Bacteriophages, or phages, are viruses that specifically infect bacteria, utilizing their genetic material to hijack host cellular machinery for replication. DNA bacteriophages employ single-stranded DNA (ssDNA) or double-stranded DNA (dsDNA) genomes. These phages exhibit diverse replication strategies and host interactions, influencing their ecological roles and applications in biotechnology and medicine.ssDNA BacteriophagesssDNA phages, with their small genomes, utilize unique strategies to...
867
Kinetics of Drug Elimination01:17

Kinetics of Drug Elimination

Eliminating drugs from the body is a vital process that occurs through excretion or metabolism. Understanding the kinetics of drug elimination is crucial for drug development, dosage determination, and optimizing patient outcomes.
Drug clearance depends on the rate of drug elimination and its plasma concentration. Another important parameter is the half-life of a drug, which is the time required for its concentration to decrease by half. In most cases, drug clearance follows first-order...
4.1K
Enhanced Elimination of Poison01:26

Enhanced Elimination of Poison

Poison can be effectively removed from the gastrointestinal (GI) tract through various decontamination procedures.
Antidotes serve a crucial role in counteracting the effects of poison by inhibiting enzymes responsible for producing harmful drug metabolites. In some cases, these toxic metabolites can be neutralized by endogenous cosubstrates, which are maintained at specific concentrations to prevent interaction with cellular macromolecules and subsequent cell death.
Renal excretion is the...
878
Radical Formation: Elimination00:51

Radical Formation: Elimination

Another method of radical formation is the elimination process. It is the opposite of the addition route and is driven by the instability of the radical. For example, as depicted in Figure 1, dibenzoyl peroxide yields a pair of unstable radicals upon homolysis. Given its instability, this radical spontaneously undergoes elimination via a C–C bond cleavage to form a relatively more stable phenyl radical. The mechanism involves cleavage of the bond between the α and β positions with respect...
2.3K