Detection of biofilm genes in multi-drug resistance Staphylococcus species and its relevance in drug resistance
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Keywords

Biofilm
Multi-drug resistance
PCR
Resistance genes
Staphylococcus species

Abstract

Objectives: Staphylococcus species are notorious

pathogens associated with significant morbidity and

mortality in healthcare institutions. Studies have

shown that biofilm-producing Staphylococci are more

difficult to control with higher resistance to

antibacterial agents than those not embedded in

biofilm. The study was aimed to evaluate the

prevalence of biofilm genes in multidrug resistance

Staphylococcus species and its effect on drug

resistance.

Methods: A total of 53 Staphylococcal isolates were

obtained from two teaching hospitals (include name

of the hospitals), with the sources comprising of urine

[6] and feaces [1]; hospital door handles [31], hospital

walls [5], and hospital bed [10]. Identity of

Staphylococcus species were confirmed by

sequencing its tuf gene. Antibiotic susceptibility was

performed using the diffusion method. Biofilm genes

(fnbA, cna, icaA, icaD and fnbB) were assayed by

multiplex polymerase chain reaction. The data were

analyzed by descriptive statistics and effect on

resistance by Chi square at pd”0.05.

Results: Staphylococcus species identified were

Staphylococcus epidermidis [38], Staphylococcus

scuiri [7], Staphylococcus xylosus [5],

Staphylococcus saprophyticus

[2] and

Staphylococcus arlettae [1]. The isolates were

highly resistant to all the antibiotics tested except

ofloxacin, ciprofloxacin and levofloxacin. The biofilm

genes (fnbA, icaD and icaA) were found in 35%,

17% and 1% isolates respectively and had no effect

on antibiotic resistance (p>0.05).

Conclusion: This study revealed that some

Staphylococcus species irrespective of the sources

produced biofilms and were highly resistant to

different antibiotic classes regardless of the biofilm

status. Therefore, regular surveillance system is

important to monitor and mitigate the spread of

antimicrobial resistance in our community.

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