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

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Cajethan O. Ezeamagu
Oluwafemi M. Adeogun
Toyosi F. Osisam

Resumé

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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Original Articles

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