Saba Noor, Jamal Ahmad, Iqbal Parwez and Meher Rizvi
Aligarh Muslim University, India
Posters & Accepted Abstracts: J Diabetes Metab
Diabetic foot ulcerations (DFUs), a dreadful micro-vascular complication is responsible for substantial increase in morbidity and mortality. DFU is a complicated amalgam of neuropathy, peripheral arterial diseases, foot deformities and infection. Spanning the spectrum from superficial cellulitis, microbial flora leads to chronic osteomyelitis and gangrenous extremity requiring surgical interventions and lower limb amputations. Though expeditious and precise discerning of bacterial pathogens is a fundamental grail of clinical diagnostic microbiology, but when conventional methodologies are implemented in identifying bacteria, interpretation of test results requires substantial slanted judgment. Therefore, genotypic detection is budding as substitute to known phenotypic culture based processes. Typically, genotypic identification of bacteria involves the use of conserved sequences within phylogenetically informative genetic targets. Also, time required in conventional diagnosis delays the selection of antibiotic regime making and adversely affects the outcome. Therefore, we reported a comparative evaluation of biochemical and genomic based assays for exploring the common bacterial flora in infected DFU patients along with clinical variables of subjects enrolled. The pathogens selected were (i) Klebsiella pneumoniae, ii) Pseudomonas aeruginosa, iii) Escherichia coli and iv) Staphylococcus aureus , stood for the most frequent isolates of diabetic foot infection (DFIs) in previous studies from Northern India. Of 50 specimens obtained from infected DFUs, 74% of cases were affirmative by bacteriological assays and 95% showed positivity via PCR methodologies. Among processed samples 44 isolates were detectable through phenotypic analysis and 73 bacteria by species specific PCR. 13 samples and 19 isolates could not be scrutinized by phenotypic identification systems. The most prevalent pathogens identifiable by both assays were Klebsiella pneumonia, followed by Staphylococcus aureus, Pseudomonas aeruoginosa and Escherichia coli. We have shown that PCR based diagnostic methods improved the identification of common aerobic pathogens compared to conventional phenotypic methods. The outcome of this study expresses that polymerase chain reaction provides rapid, unambiguous identification of clinical bacterial isolates. The results highlighted the incorporation of PCR technique in bacterial identification due to shorten turnaround time and may translate into improve clinical outcomes by early use of appropriate antibiotic along with other principles followed in diabetic foot management.
Email: sabanooramu@gmail.com
