The Relationship between Biofilm Production and Antimicrobial Resistance in Methicillin-sensitive and Methicillin-resistant Staphylococcus aureus Isolates: In vitro Evaluation
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作者:
Dalgic, Bahise Cagla Taskin
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Turhal State Hosp, Med Microbiol Lab, Tokat, TurkeyTurhal State Hosp, Med Microbiol Lab, Tokat, Turkey
Dalgic, Bahise Cagla Taskin
[1
]
Yenisehirli, Gulgun
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机构:
Tokat Gaziosmanpasa Univ, Dept Med Microbiol, Fac Med, Tokat, TurkeyTurhal State Hosp, Med Microbiol Lab, Tokat, Turkey
Yenisehirli, Gulgun
[2
]
Otlu, Baris
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机构:
Inonu Univ, Dept Med Microbiol, Fac Med, Malatya, TurkeyTurhal State Hosp, Med Microbiol Lab, Tokat, Turkey
Otlu, Baris
[3
]
Tanriverdi, Elif Seren
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机构:
Inonu Univ, Dept Med Microbiol, Fac Med, Malatya, TurkeyTurhal State Hosp, Med Microbiol Lab, Tokat, Turkey
Tanriverdi, Elif Seren
[3
]
Yenisehirli, Aydan
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机构:
Tokat Gaziosmanpasa Univ, Dept Med Pharmacol, Fac Med, Tokat, TurkeyTurhal State Hosp, Med Microbiol Lab, Tokat, Turkey
Yenisehirli, Aydan
[4
]
Bulut, Yunus
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Tokat Gaziosmanpasa Univ, Dept Med Microbiol, Fac Med, Tokat, TurkeyTurhal State Hosp, Med Microbiol Lab, Tokat, Turkey
Bulut, Yunus
[2
]
机构:
[1] Turhal State Hosp, Med Microbiol Lab, Tokat, Turkey
[2] Tokat Gaziosmanpasa Univ, Dept Med Microbiol, Fac Med, Tokat, Turkey
[3] Inonu Univ, Dept Med Microbiol, Fac Med, Malatya, Turkey
[4] Tokat Gaziosmanpasa Univ, Dept Med Pharmacol, Fac Med, Tokat, Turkey
Methicillin-resistant S. aureus;
methicillin-sensitive S. aureus;
antimicrobial susceptibility;
biofilm formation;
ANTIBIOTIC-RESISTANCE;
STRAINS;
SUSCEPTIBILITY;
VANCOMYCIN;
IS256;
GENES;
D O I:
10.4274/mjima.galenos.2022.2021.14
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Introduction: The biofilm formation ability plays an important role in the pathogenesis of Staphylococcus aureus infections. This study aimed to investigate the biofilm production ability of methicillin-resistant S. aureus (MRSA) and methicillin-sensitive S. aureus (MSSA) isolates and evaluate the relationship between their antimicrobial resistance profile and biofilm formation ability. Materials and Methods: A total of 50 MRSA and 50 MSSA isolates were examined. The antimicrobial susceptibility testing of isolates was performed using the disk diffusion method. The broth microdilution method was used to determine the minimum inhibitor concentrations (MICs) of vancomycin and teicoplanin. The biofilm formation ability of isolates was tested on Congo Red Agar. The presence of icaA, icaD, IS256, and eno genes was investigated by polymerase chain reaction. Results: Both MRSA and MSSA isolates were found susceptible to vancomycin, teicoplanin, chloramphenicol, and linezolid. Two MRSA and 2 MSSA isolates were determined as heterogeneous vancomycin-intermediate S. aureus. No significant difference was observed between the biofilm formation ability of MRSA and MSSA isolates. The eno and icaD genes were detected in 100% of both MSSA and MRSA isolates. The icaA gen was detected in all MRSA and 49 MSSA isolates. The IS256 was detected in 35 of the 50 MRSA isolates. None of the MSSA isolates were positive for the IS256. The amikacin, gentamicin, ciprofloxacin, levofloxacin, rifampin, clindamycin, and tetracycline resistance rates in IS256-positive MRSA isolates were significantly higher than those IS256-negative MRSA isolates. The mean MIC values of vancomycin and teicoplanin in IS256-positive MRSA isolates were significantly higher than those in IS256-negative MRSA isolates. Conclusion: This study revealed that the presence of the IS256 sequence was correlated with antimicrobial resistance, especially MRSA isolates.
机构:
AUSTRALIAN NATL UNIV, FAC SCI, DIV BIOCHEM & MOLEC BIOL, CANBERRA, ACT 2601, AUSTRALIAAUSTRALIAN NATL UNIV, FAC SCI, DIV BIOCHEM & MOLEC BIOL, CANBERRA, ACT 2601, AUSTRALIA
INGLIS, B
ELADHAMI, W
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AUSTRALIAN NATL UNIV, FAC SCI, DIV BIOCHEM & MOLEC BIOL, CANBERRA, ACT 2601, AUSTRALIAAUSTRALIAN NATL UNIV, FAC SCI, DIV BIOCHEM & MOLEC BIOL, CANBERRA, ACT 2601, AUSTRALIA
ELADHAMI, W
STEWART, PR
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机构:
AUSTRALIAN NATL UNIV, FAC SCI, DIV BIOCHEM & MOLEC BIOL, CANBERRA, ACT 2601, AUSTRALIAAUSTRALIAN NATL UNIV, FAC SCI, DIV BIOCHEM & MOLEC BIOL, CANBERRA, ACT 2601, AUSTRALIA
机构:
King Fahad Armed Forces Hosp, Dept Cardiac Surg, Jeddah, Saudi ArabiaKing Fahad Armed Forces Hosp, Dept Cardiac Surg, Jeddah, Saudi Arabia
Alghamdi, Bandar Ali
Al-Johani, Intisar
论文数: 0引用数: 0
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机构:
Taif Univ, Dept Biotechnol, Taif City, Saudi ArabiaKing Fahad Armed Forces Hosp, Dept Cardiac Surg, Jeddah, Saudi Arabia
Al-Johani, Intisar
Al-Shamrani, Jawhra M.
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机构:
Taif Univ, Dept Biotechnol, Taif City, Saudi ArabiaKing Fahad Armed Forces Hosp, Dept Cardiac Surg, Jeddah, Saudi Arabia
Al-Shamrani, Jawhra M.
Alshamrani, Hussein Musamed
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机构:
Namerah Primary Hlth care, Pharm Dept, Directorate Hlth Affairs Qunfudah Ctr, Halaba, Saudi ArabiaKing Fahad Armed Forces Hosp, Dept Cardiac Surg, Jeddah, Saudi Arabia
Alshamrani, Hussein Musamed
Al-Otaibi, Bandar G.
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机构:
Albandr Clin, Taif, Saudi ArabiaKing Fahad Armed Forces Hosp, Dept Cardiac Surg, Jeddah, Saudi Arabia
Al-Otaibi, Bandar G.
Master, Kholod Almazmomi
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机构:
Taif Univ, Dept Biotechnol, Taif City, Saudi ArabiaKing Fahad Armed Forces Hosp, Dept Cardiac Surg, Jeddah, Saudi Arabia
Master, Kholod Almazmomi
Yusof, Nik Yusnoraini
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机构:
Univ Sains Malaysia, Inst Res Mol Med INFORMM, Hlth Campus, Kubang Kerian 16150, Kelantan, Malaysia
Univ Sains Malaysia, Inst Res Mol Med INFORMM, Kubang Kerian 16150, Kelantan, MalaysiaKing Fahad Armed Forces Hosp, Dept Cardiac Surg, Jeddah, Saudi Arabia
机构:
Western Sydney Univ, Sch Med, Locked Bag 1797, Penrith, NSW 2751, AustraliaWestern Sydney Univ, Sch Med, Locked Bag 1797, Penrith, NSW 2751, Australia
Mudgil, Poonam
Harman, David G.
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机构:
Western Sydney Univ, Sch Med, Locked Bag 1797, Penrith, NSW 2751, AustraliaWestern Sydney Univ, Sch Med, Locked Bag 1797, Penrith, NSW 2751, Australia
Harman, David G.
Whitehall, John
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机构:
Western Sydney Univ, Sch Med, Locked Bag 1797, Penrith, NSW 2751, AustraliaWestern Sydney Univ, Sch Med, Locked Bag 1797, Penrith, NSW 2751, Australia