Abstract

We investigated the incidence and antibiogram profile of <em>Serratia marcescens</em> among hospitalized individuals, hospital environments and halls of residence of Obafemi Awolowo University in Ile Ife, Osun state. These were with a view to provide key information at molecular level that are of epidemiological and therapeutic importance.

Highlights

  • The study concluded that occurrence of multidrug resistant S. marcescens pose a public health threat in the study area considering their carbapenemase production and carriage of various resistance genes

  • The susceptibility profile of the isolates against selected antibiotics were studied by the Kirby-baeur disc-diffusion technique and screened for extended spectrum betalactamase (ESBL) and carbapenemase enzymes using double disc synergy test (DDST) and modified carbapenem inactivation assay respectively

  • All samples were transferred to the laboratory for immediate cultures on freshly prepared sorbitol MacConkey agar infused with 200 U/ ml of colistin

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Summary

Introduction

The study concluded that occurrence of multidrug resistant S. marcescens pose a public health threat in the study area considering their carbapenemase production and carriage of various resistance genes. Introduction β-lactamases are hydrolytic enzymes that inactivate β-lactam antibiotics in the periplasmic membrane of Gram negative bacterial cell, effectively rendering it harmless to the cell [1]. Beta-lactam antibiotics induces ampC gene expression among Serratia sp. By a complex mechanism that involves cell wall recycling [2]. Strains with induced ampC expression were regarded as depressed mutants [5]. Upregulation and increased expression of ampC β-lactamase among S. marcescens occur due to mutation in processes involved in recycling the bacterial cell wall [6]. Such mutants are termed depressed mutants and are markedly resistant to carbapenems and cefoxitin [5]

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