Volume 4, Issue 8 (Suppl)
J Infect Dis Ther 2016
ISSN: 2332-0877, JIDT an open access journal
Infection Control 2016
November 28-29, 2016
Page 23
Notes:
conference
series
.com
November 28-29, 2016 Valencia, Spain
4
th
World Congress on
Infection Prevention and Control
Polymerase chain reaction in the detection of the methicillin-resistant
staphylococci
Background:
Methicillin resistant strains of
Staphylococcus aureus
(MRSA) were identified shortly upon the introduction of
methicillin into the clinical practice. Rapid detection of MRSA is desirable.
Methods:
S. aureus
strains were isolated from hospitalized patients, including intensive care wards and other units. The
identification of the
S. aureus
strains was made by phenotypic methods and automated methods (Vitek2Compact BioMerieux).
The MecA gene of the clinical isolates detection has been unfold by PCR. The PBP2’ latex agglutination test, Cefoxitin E-test
and Oxacillin MIC as phenotypic methods of MRSA detection are evaluated and compared with the mecA detection by PCR,
as the standard method to identify the MRSA strains.
Results:
57.5% of the isolated strains from different pathological products were MRSA and 42.5% were MSSA. The PBP2’ latex
agglutination test detected PBP2a in 55.3% of the tested strains leading to a sensitivity of 96.3% using mec A gene detection.
Most of the MRSA isolates were multi-resistant to antibiotics, being resistant to -lactamins, Aminoglycosides, Macrolides and
Ciprofloxacin.
Conclusions:
Molecular methods which detect the mecA gene are replacing the Oxacillin MIC method as the reference one.
The comparison of the phenotypic methods with PCR reveals that among the first of them, PBP2a latex has a high sensitivity
(97.9%), being used as an alternative phenotypic method for the MRSA detection. Following the resistance profiles of the
strains, identified by these methods, we observe the existence among them of some different clones that reveal the importance
of the correct identification of the MRSA strains for the infection therapy and its prophylaxis.
Biography
Lia Monica Junie is an MD, Ph D, Professor, Head Microbiology Department, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj Napoca, Romania. She is a Co-
ordinator of resident doctor’s in the Laboratory Medicine specialty and Leadership PhD doctor’s thesis in Medicine field. She is a Board Member of European professional
Societies ESCMID (ESGCP Study Groups), Society of Chemotherapy, Scientia Parasitologica Pro Vita and is a Reviewer of international reviews, Member of International
organizations, Director/Coordinator in research projects. She has more than 63 papers published in full in international journals and is an editorial board member of national
reviews. She is an Organizer/President, Keynote, Invited Speaker and Chair of International and National Congresses.
mjunie@umfcluj.ro monicajunie@yahoo.comLia Monica Junie
University of Medicine and Pharmacy, Romania
Lia Monica Junie, J Infect Dis Ther 2016, 4:8 (Suppl)
http://dx.doi.org/10.4172/2332-0877.C1.019