Scientific Program

Conference Series Ltd invites all the participants across the globe to attend 13th World Congress on Infection Prevention and Control Rome, Italy.

Day 2 :

Keynote Forum

Waleed A. Mazi

Regional Directorate for Infection Prevention and Control
Directorate of Health Affairs, Taif
Kingdom of Saudi Arabia

Keynote: Application of high resolution melting to methicillin resistant Staphlococcus aureus and Shigella sonnei genotyping for epidemiological purposes

Time : 10:00AM- 10:40 AM

OMICS International Infection Prevention 2017 International Conference Keynote Speaker Waleed A. Mazi photo
Biography:

Waleed A. Mazi is a Regional Director for Infection Prevention and Control, Taif – Saudi Arabia, and also worked in Philosophy of Medical Science, Clinical Microbiology in Sweden. He also Became Infection Prevention and Control Director, King Abdul Aziz Specialist Hospital – Taif, Saudi Arabia, and published many International articles on prevention of central line –associated bloodstream infection, WHO- Hand Hygiene implementation program, prevention sharp injuries in healthcare settings and molecular genotyping for epidemiological purposes and also participated in the Poster and oral presentations in many international conferences

Abstract:

Introduction:

High resolution melting (HRM) analysis has been used in laboratory medicine as acurate, rapid and cost effective scheme method. Methicillin resistant Staphylococcus aureus (MRSA) infections impose huge risk to public health in healthcare and community settings worldwide. Shigella sonnei has been predominantly responsible for dysentary worldwide. The organism has only one serotype and is genetically homogeneous.

        We evaluated MRSA spa typing and introduced new tools for Shigella sonneil genotyping using HRM analysis for epidemiological purposes.

Methods:

Fifty clinical MRSA isolates were selected randomly from Scotland, Brazil, Sudan and Saudi Arabia. Methicillin-resistant phenotype was determined in accordance with BSAC standards using the Vitek 2system. Ten Shigella sonnei DNA samples were provided by Institut Pasteur, France. Primers for the polymorphic X region of the spa gene and the six single nucleotide polymorphisms (SNPs) within kduD, deoA, emrA, fdX and menF were amplified by colony PCR using the SensiMix HRM kit, and the melting temperature (Tm) and melting curves of the amplicons were analyzed in close tubes using a Rotor-Gene 6000 instrument.


Results

Fifteen spa types detected each had a distinct melting temperature (Tm) that unambiguously assigned 44 isolates. Both t008 and t2770, as well as t311 and t021 spa types, shared the same Tm .

         The first set run separated lineages I, II and III with distinctive melting curves and the Tm of each allele was at least a half degree away from that of other alleles. The second set run distinguished the sublineages IIIa, IIIb and IIIc with distinctive melting curves.

Conclusion:

HRM analysis is acurate, rapid and cost effective scheme method for identification of MRSA and Shigella sonnie for  epidemiological purposes