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Authors Kang J, Hossain MA, Park H, Kim Y, Park S, Kim TW
Received 26 December 2019
Accepted for publication 17 May 2020
Published 8 June 2020 Volume 2020:13 Pages 1601—1606
DOI https://doi.org/10.2147/IDR.S243826
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 2
Editor who approved publication: Dr Eric Nulens
Abstract: Rapid determination of antimicrobial
susceptibility/resistance is an important factor in selecting an appropriate
antimicrobial treatment and eradicating infections promptly. Conventional
antimicrobial susceptibility tests (ASTs) are very time consuming. Thus, we
developed a liquid chromatography-mass spectrometry (LC-MS/MS) method for
rapidly determining the resistance of Staphylococcus aureus to penicillin-G in an
animal-infection model. This technique will be able to detect those resistant
strains whose resistance mechanism specifically controlled by penicillinase.
The resistance status of S. aureus against penicillin-G was determined by
conventional AST. Cultured S. aureus cells were inoculated to chicken for
developing bacteraemia. The solution of penicillin-G was intravenously
administered (10 mg/kg b.w.) to chickens just after infection detection. Blood
samples were collected at different intervals after drug administration. The
concentration of active penicillin-G and its metabolites were determined from
the bacteria-free blood supernatant by utilizing the LC-MS/MS method. Evidence
of infection in chicken was observed within 5 h of bacterial inoculation. The
penicillinase enzyme generated by S. aureus transforms the active penicillin-G to
an inactive metabolite by hydrolysis, which is evident by the mass shift from
335.10600 to 353.11579 Da as quantified using liquid chromatography quadrupole
time-of-flight mass spectrometry (LC/Q-TOF/MS). The signal intensity of
inactive/hydrolysed penicillin-G is several-fold greater than that of the
active penicillin-G in the blood sample of chicken infected with resistant
strain and treated with penicillin-G. The antimicrobial resistance index (ARI)
value of resistant S. aureus strain was more than 1, demonstrating
the penicillin-G-resistance pattern of that strain. This method is able to
determine the extent of β-lactam antimicrobial resistance within 1.5 h from the
patient’s blood and is complementary with those existing AST methods which are usually
practicing in the evaluation of β-lactam antibiotic resistance.
Keywords: β-lactamase,
spectrometry, antibacterial susceptibility test, chicken infection model,
antibacterial resistance