Skip to main content

Evaluation of efflux pump activity and biofilm formation in multidrug resistant clinical isolates of Pseudomonas aeruginosa isolated from a Federal Medical Center in Nigeria



Pseudomonas aeruginosa an opportunistic pathogen, is widely associated with nosocomial infections and exhibits resistance to multiple classes of antibiotics. The aim of this study was to determine the antibiotic resistance profile, biofilm formation and efflux pump activity of Pseudomonas strains isolated from clinical samples in Abeokuta Ogun state Nigeria.


Fifty suspected Pseudomonas isolates were characterized by standard biochemical tests and PCR using Pseudomonas species -specific primers. Antibiotic susceptibility testing was done by the disc diffusion method. Efflux pump activity screening was done by the ethidium bromide method and biofilm formation assay by the tissue plate method. Genes encoding biofilm formation (pslA & plsD) and efflux pump activity (mexA, mexB and oprM) were assayed by PCR.


Thirty-nine Pseudomonas spp. were identified of which 35 were Pseudomonas aeruginosa and 4 Pseudomonas spp. All 39 (100%) Pseudomonas isolates were resistant to ceftazidime, cefuroxime and amoxicillin-clavulanate. Thirty-six (92%), 10(25.6%), 20 (51.2%), 11(28%) and 9(23%) of the isolates were resistant to nitrofurantoin, imipenem, gentamicin, cefepime and aztreonam respectively. All the isolates had the ability to form biofilm and 11 (28%) of them were strong biofilm formers. They all (100%) harboured the pslA and pslD biofilm encoding genes. Varied relationships between biofilm formation and resistance to ciprofloxacin, ofloxacin, cefixime, gentamicin, imipenem, and aztreonam were observed. Only 23(59%) of the Pseudomonas isolates phenotypically exhibited efflux pump activity but mexA gene was detected in all 39 (100%) isolates while mexB and oprM genes were detected in 91%, 92%, and 88% of strong, moderate and weak biofilm formers respectively.


Multidrug resistance, biofilm and efflux pump capabilities in Pseudomonas aeruginosa have serious public health implications in the management of infections caused by this organism.


Treatment options available for mild and severe bacterial infections are now limited due to multidrug resistance making treatment difficult and expensive. Some bacteria possess intrinsic mechanisms that facilitate resistance to multiple antibiotics, while some acquire this capability through horizontal gene transfer. Pseudomonas species, most especially the opportunistic pathogen Pseudomonas aeruginosa are known to exhibit large intrinsic resistance to multiple antibiotics across most classes including aminoglycoside, fluoroquinolones and β-lactams (third and fourth generation cephalosporins, carbapenem, monobactam). Multidrug resistant (MDR) P. aeruginosa strains have been implicated in urinary tract infections, bacteremia, respiratory tract infections and wound infections [1,2,3,4]. Two prominent mechanisms, biofilm formation and efflux pump activity among other mechanisms play conspicuous role in persistence and antibiotic resistance of infecting Pseudomonas spp. Extruding action of bacteria efflux pumps prevent or limit antimicrobials from reaching their target site within the cell. About twelve resistance-nodulation-division (RND) family of efflux pumps have been identified in P. aeruginosa four of which mediate antibiotic resistance [5, 6]. The mexAB-oprM and mexXY-oprM multidrug efflux pump systems of P. aeruginosa are said to be involved in acquired and intrinsic resistance, while the other two systems only mediate acquired resistance [3]. The mexAB-oprM efflux pump system in particular have been reported to contribute to intrinsic resistance of P. aeruginosa to chloramphenicol, β-lactams, quinolones, macrolides, tetracycline and novobiocin [7]. Beyond resistance, these efflux pumps systems also have an interplay in stress response and virulence [8]. Adhesion of P. aeruginosa to host cell via the type IV pili coupled with the secretion of extracellular polysaccharide mediated by polysaccharide synthesis locus (psl) facilitates the formation of biofilm which promote antibiotic resistance and shields the pathogen from hosts’ immune system [9]. Biofilm formation by P. aeruginosa facilitate recalcitrant and severe clinical outcomes in patients with cystic fibrosis, wound infection and compromised immune system [10, 11]. There have been several reports on antibiotic resistant clinical P. aeruginosa isolates and associated resistance genes in Nigeria [12,13,14]. However there is a draught of information correlating biofilm formation and efflux pump activity with antibiotic resistance profile of P. aeruginosa. This present study evaluates efflux pump activity, biofilm forming potential and antibiotic resistance profile of Pseudomonas species isolated from clinical samples in Nigeria.


Bacterial strains

Fifty suspected Pseudomonas spp. that were isolated from various clinical samples and preserved in agar slants were obtained between April and September 2019 from the Federal Medical Center Abeokuta a tertiary medical health facility in Ogun state, South western Nigeria. Eleven suspected Pseudomonas isolates were of urine origin, 3 were from eye swab and 12 each were from wound and ear swabs respectively as shown in Table 1. To characterize Pseudomonas strains, isolates were inoculated into Brain Heart Infusion (BHI) (Oxoid, Basingstoke, UK) broth from agar slants and incubated at 37 °C for 18 h. Bacteria broth culture was then streaked onto nutrient agar (Oxoid, Basingstoke, UK) and cetrimide agar (Merck Darmstadt, Germany) and incubated at 37 °C for 24 h. This was followed by standard biochemical tests including Simmon’s citrate, oxidase, catalase, hydrogen sulphide production, sugar fermentation and gas production. Species- specific PCR using the primer pair PA-SSF and PA-SSR shown in Table 2 was used in characterizing Pseudomonas aeruginosa.

Table 1 Quantity of suspected Pseudomonas aeruginosa isolated from various clinical samples
Table 2 Lists primers for species specific (P. aeruginosa), efflux pumps and biofilm forming genes used in this study

Antimicrobial susceptibility testing

Antimicrobial susceptibility testing was done using the Kirby-Bauer disc diffusion method in accordance with the guideline of the European Committee on Antimicrobial Susceptibility Testing [15]. Bacterial isolates were inoculated into BHI broth and incubated for 18 h at 37 °C. Then broth culture was streaked on nutrient agar (Oxoid, Basingstoke, UK) and incubated for 24 h at 37 °C. One to two colonies were emulsified in sterile normal saline to make a suspension that was adjusted to 0.5 McFarland standard and then applied on the surface of Muller-Hinton agar (Oxoid, Basingstoke, UK) using sterile swab sticks. The following antibiotic discs comprising Ceftazidime (30 µg), Cefuroxime (30 µg), Gentamicin (10 µg), Cefixime (30 µg), Ofloxacin (30 µg), Augumentin (30 µg), Nitrofurantoin (30 µg), Ciprofloxacin (30 µg), Cefepime (30 µg), Aztreonam (30 µg) and Imipenem (10 µg) were then placed on the inoculated Muller-Hinton agar. Results were taken after 24 h incubation at 37 °C. Pseudomonas aeruginosa ATCC 27853 and Escherichia coli ATCC 25922 were used as quality control isolates for the antimicrobial susceptibility testing. Choice of antibiotics selected for this study was inferred from common antibiotics prescribed by physicians and generally consumed by individuals.

Phenotypic screening of isolates for efflux pump activity and biofilm formation assay

The Ethidium Bromide (EtBr)-agar cartwheel method as described by Anbazhagan et al. [16] was used to determine the efflux pump activity of isolates. Briefly, bacterial cell suspension of approximately 106 cells per mL was streaked on Mueller–Hinton agar plates containing 0 mg/L, 0.5 mg/L, 1 mg/L, 1.5 mg/L, and 2 mg/L concentrations of EtBr and incubated for 24 h at 37 °C. After incubation, the plates were examined under UV transilluminator (Cleaver Scientific Ltd) for fluorescence and isolates that fluoresced at minimum concentration of EtBr were recorded as not possessing active efflux pumps, while those that did not fluoresce possessed active efflux pumps.

Biofilm formation assay was performed using the tissue culture plate (TCP) method described by Mathur et al. [17]. Single colonies of each Pseudomonas isolate were inoculated into brain heart infusion (BHI) broth (Oxoid, Basingstoke, UK) supplemented with 2% sucrose and 200 µL of bacterial suspension was loaded into the individual wells of 96-well microtiter plate. Two hundred microlitres of sterile BHI broth was also loaded into a well as negative control. Plates were incubated at 37 °C for 24 h after which contents of each well was discarded and wells were washed three times with sterile deionized water to remove non-adherent bacteria. Wells were air-dried for 45 min and 200 µL of 0.1% (v/v) crystal violet solution was added to each well and incubated for 45 min at room temperature. Thereafter, the wells were again washed four times with sterile deionized water. Incorporated dye was solubilized by adding 200 µL of 33% (v/v) glacial acetic acid to each well and optical density (OD) was measured at 650 nm using the Emax® Plus Microplate Reader (Molecular Devices San Jose, CA). The assay was performed in triplicates and biofilm forming potential were recorded as mean OD values as described by Hassan et al. [18] to be strong (≥ 0.108), moderate (0.108–0.083) and weak (< 0.083).

Molecular characterization of isolates, efflux pump coding genes and biofilm coding genes

Genomic DNA of Pseudomonas isolates was extracted according to the method of Kpoda et al. [19]. Cell suspension was made from 3 to 5 colonies of overnight bacterial culture in 1 mL of sterile water and suspension was held for 10 min at 100 °C in a thermomixer (Eppendorf Hamburg Germany). Suspension was centrifuged at 13,000 rpm for 10 min at 4 °C and supernatant containing DNA was separated and stored at − 20 °C for subsequent use. PCR reaction targeting efflux pump genes (mexA, mexB and oprM), biofilm formation genes (pslA and pslD) and PA-SS gene (Pseudomonas aeruginosa specific) was done in a 20 µL reaction targeting specific primers listed in Table 2. A simplex PCR was used for amplification of mexA, oprM, pslA, pslD, mexB and PA-SS. PCR reaction mix contained 9.8 µL nuclease free water, 4 µL 5X FIREPOL Solis Biodyne (Tartu, Estonia) master mix, 0.6 µL each of both forward and reverse primers and 5 µL of DNA template. Template DNA sample from Pseudomonas aeruginosa ATCC 27853 was used as positive control, while nuclease free water was used as negative control. PCR cycling parameter was initial denaturation at 95 °C for 5 min and 30 cycles of denaturation at 95 °C for 30 s, annealing temperature at (Table 2) for 40 s, elongation at 72 °C for 1 min and final elongation at 72 °C for 10 min carried out in a thermal cycler (Eppendorf AG, Hamburg, Germany). PCR products were electrophoresed in 2% agarose gel at 100 V for 60 min and visualized under a trans-illuminator (Cleaver Scientific Ltd) and a Solis Biodyne 100 bp DNA ladder (Tartu, Estonia) was used as a molecular marker.

Statistical analysis

Statistical analysis and graphics were performed with IBM SPSS Statistics 20 and Microsoft Excel (Microsoft Cooperation, 2013 USA). Spearman rank correlation test was used to determine the association of biofilm formation and antibiotic susceptibility of isolates. Positive Spearman rank correlation coefficient (ρ) value of +1 was considered as perfectly positive correlation and negative ρ value of − 1 was considered as perfectly negative correlation. Also ρ value less than 0.3 or greater than − 0.3 was considered negligible [23].


Bacterial strains

Of the 50 suspected Pseudomonas isolates characterized, 39 were confirmed to be Pseudomonas species of which 35 were Pseudomonas aeruginosa as they were positive for the Pseudomonas species specific gene (PA-SS) as shown in Fig. 1.

Fig. 1

Electrophoretogram showing amplicons of Pseudomonas aeruginosa specific primers (PA-SS). Lane M: 100 bp molecular maker, P: positive control, N: negative control, Lane 1-17 positive for PA-SS

Antimicrobial Susceptibility

All the 39 (100%) Pseudomonas isolates were resistant to ceftazidime, cefuroxime and amoxicillin-clavulanate. Thirty-eight (97%) isolates were also resistant to cefixime, ofloxacin and ciprofloxacin. Thirty- six (92%) were resistant to nitrofurantoin, 10 (25.6%) were resistant to imipenem, 20 (51.2%) were resistant to gentamicin, 11 (28%) to cefepime and 9 (23%) to aztreonam as shown in Fig. 2.

Fig. 2

Antibiotic susceptibility profile of Pseudomonas isolates. CAZ: Ceftazidime; CRX: Cefuroxime; GEN: Gentamicin; CXM: Cefixime; OFL: Ofloxacin; AUG: Amoxicillin-clavulanate; NIT: Nitrofurantoin; CPR: Ciprofloxacin; IMI: Imipenem; FEP: Cefepime

Biofilm formation and antibiotic resistance

Pseudomonas isolates were categorized into strong, moderate and weak biofilm formers. Eleven (28%), 12 (31%) and 16 (41%) were strong, moderate and weak biofilm formers respectively. Irrespective of the isolates biofilm forming capabilities all isolates (100%) were resistant to ceftazidime, cefuroxime and amoxicillin + clavulanic acid. However, there was a positive correlation between biofilm formation and resistance to ciprofloxacin, ofloxacin and gentamicin as shown in Table 3. However, there was perfectly negative correlation between biofilm formation and resistance to imipenem and aztreonam. While the association between resistance to nitrofurantion and biofilm formation was negligible as correlation coefficient was − 0.25.

Table 3 Strong, moderate and weak biofilm formers and their percentage resistance to various antibiotics

All (100%) Strong biofilm formers (SBF) and moderate biofilm formers (MBF) were resistant to ofloxacin while 93.8% of weak biofilm formers (WBF) were resistant to the same antibiotic. Both SBF and WBF were 100% resistant to ciprofloxacin while 91.7% of MBF were resistant to ciprofloxacin. SBF displayed low level of resistance (9.1%) to cefepime, while 50% of both MBF and WBF were resistant to cefepime.

Efflux pump evaluation and biofilm capability

At 1 mg/L and 1.5 mg/L of EtBr, distinct efflux pump activity was observed as 23 (59%) of Pseudomonas isolates phenotypically exhibited efflux pump activity while 16(41%) did not. However, all (100%) Pseudomonas isolates possessed mexA gene a multidrug efflux pump gene that belong to the resistance-nodulation-division–division (RND) family. mexB and oprM genes members of the RND family as mexA were also detected in 91%, 92%, and 88% of strong, moderate and weak biofilm forming Pseudomonas isolates respectively as shown in Fig. 3 and all 23 Pseudomonas isolates that phenotypically exhibited efflux pump activity possessed both genes. Beyond phenotypic exhibition of biofilm formation, genotypic evaluation revealed that all SBF possessed the pslA and pslD genes while 83% and 92% of MBF harboured pslA and pslD respectively. Ninety-four percent of WBF possessed pslA and 88% had pslD genes.

Fig. 3

Percentage occurrence of efflux pump and biofilm formation encoding genes. SBF: Strong biofilm formers, MBF: Moderate biofilm formers, WBF: Weak biofilm formers


To our knowledge this study is the first in which the biofilm forming potential and efflux pump activity of multidrug resistant Pseudomonas species isolated from clinical samples were evaluated in Nigeria. Thirty- five (89.7%) of the 39 phenotypically identified Pseudomonas isolates were Pseudomonas aeruginosa indicating that it is wide spread in nosocomial infections as previously reported [24]. Managing infections caused by Pseudomonas strains are often challenging since they exhibit resistance to most classes of antibiotics [25]. In this study, all (100%) Pseudomonas isolates were resistant to ceftazidime, cefuroxime and amoxicillin-clavulanate, while 38 (97%) were resistant to cefixime, ofloxacin, ciprofloxacin and 36 (92%) were resistant to nitrofurantoin. Odumosu et al. [26] in their study in southwestern Nigeria also reported a 100% resistance of Pseudomonas isolates to amoxicillin-clavulanate, 87.1% resistance to ceftriaxone but a lower percentage (22.5) resistance to ceftazidime. The emergence of carbapenem and monobactam resistant Pseudomonas species have been reported by several workers [27,28,29]. Similarly, 9 (23%), 11 (28%) and 10 (25.6%) of Pseudomonas isolates in this study were resistant to aztreonam, cefepime and imipenem respectively.

Biofilm formation enhances antibiotic resistance and virulence in Pseudomonas aeruginosa resulting in persistence of lingering infections [30]. In this study all Pseudomonas isolates had the ability to form biofilm. However, 11 (28%) of them were strong biofilm former (SBF), while 12 (31%) and 16 (41%) were moderate (MBF) and weak (WBF) biofilm formers respectively. Furthermore, there was a positive correlation between observed resistance to ofloxacin, ciprofloxacin and gentamicin and biofilm formation. Although correlation factor for ofloxacin and ciprofloxacin were positive it would be difficult to ascertain the role of biofilm formation in the observed antibiotic resistance as majority (38) of the Pseudomonas isolates were resistant to both antibiotics. However, Cepas et al. [31] have reported a correlation between ciprofloxacin resistance and biofilm formation in P. aeruginosa. Similarly, Mohammed and Abd Alla [32] in Egypt reported the resistance of biofilm forming P. aeruginosa isolates to ciprofloxacin, tobramycin and gentamycin compared to their non-biofilm forming counterpart that were susceptible. In contrast we observed a positive relationship between resistance to gentamicin and biofilm formation. It has also been reported in P. aeruginosa that resistance to imipenem results in reduced biofilm formation [33]. This might explain the perfectly negative correlation between biofilm formation and resistance to imipenem observed in this study. A similar association was also observed with the antibiotic aztreonam. Adhesion and secretion of extracellular polysaccharide are requisites to initiate biofilm formation in bacteria. The pslA and pslD genes which are key components of the polysaccharide synthesis locus (psl) responsible for the secretion of extracellular polysaccharide in Pseudomonas aeruginosa were detected in majority of our Pseudomonas isolates. All (100%) SBF harboured both pslA and pslD genes while MBF and WBF possessed these genes in various proportions. In a similar study in Yaoundé Cameroon, Madaha et al. [34] reported the detection of pslA gene in 92% of antibiotic resistant Pseudomonas aeruginosa clinical isolates.

Apart from biofilm formation that contributes to antibiotic resistance, active efflux pump systems are prominent mechanisms that also mediate multidrug resistance in bacteria. The mexAB-OprM efflux pump identified to have a high level of expression in P. aeruginosa concomitantly driving resistance to multiple classes of antibiotics [35] was detected in this study. mexA gene was detected in all (100%) Pseudomonas isolates. This is similar to the report of Abbas et al. [24] who reported the detection of mexAB-R in all P. aeruginosa isolated from urinary tract infections in Egypt. Although the direct role of efflux pump in biofilm formation was not evaluated in this study, we observed that 91%, 92% and 88% strong, moderate and weak biofilm formers respectively were positive for mexB and oprM genes. Possession of these genes could have an interplay in the virulence of the pathogen. Alav et al. [36] in their study indicated the role of these efflux pump genes in biofilm formation in P. aeruginosa apart from extrusion of drug. Thus efflux pumps may be playing a dual role in this organism.


Pseudomonas aeruginosa isolates in this study were resistant to various antibiotics and had biofilm forming potential. The strains showed varied relationship between biofilm formation and resistance to some of the test antibiotics. These findings emphasize the health risks and difficulty that could be encountered in eradicating P. aeruginosa infections. Therefore scrupulous hygiene practice and antibiotic surveillance are important to prevent continuous spread of infection and mortality caused by this organism.

Availability of data and materials

Data sets used and analysed for this study are available from the corresponding author on reasonable request. All data generated or analysed during this study are also included in this published article.



Ethidium Bromide


European Committee on Antimicrobial Susceptibility Testing




Multidrug resistance


Optical density


Strong biofilm formers


Moderate biofilm formers


Weak biofilm formers


  1. 1.

    Odumosu BT, Adeniyi BA, Chandra R. First detection of OXA-10 extended spectrum beta-lactamases and the occurrence of mexR and nfxB in clinical isolates of Pseudomonas aeruginosa from Nigeria. Chemotherapy. 2015;16(61):87–92.

    Google Scholar 

  2. 2.

    Ferreiro JLL, Otero JA, Gonzalez LG, Lamazares LN, Blanco AA, Sanjurjo JRB, Conde IR, Soneira MF, de la Fuente Aguado J. Pseudomonas aeruginosa urinary tract infections in hospitalized patients: mortality and prognostic factors. PLoS ONE. 2017;12(5):e0178178.

    Article  Google Scholar 

  3. 3.

    Bassetti M, Vena A, Croxatto A, Righi E, Guery B. How to manage Pseudomonas aeruginosa infections. Drugs Context. 2018;7:212527.

    Article  PubMed  PubMed Central  Google Scholar 

  4. 4.

    Curran CS, Bolig T, Torabi-Parizi P. Mechanisms and targeted therapies for Pseudomonas aeruginosa lung infection. Am J Respir Crit Care Med. 2018;197(6):708–27.

    CAS  Article  Google Scholar 

  5. 5.

    Tenover FC. Mechanisms of antimicrobial resistance in bacteria. Am J Med. 2006;119(6A):S3–10.

    CAS  Article  Google Scholar 

  6. 6.

    Dreier J, Ruggerone P. Interaction of antibacterial compounds with RND efflux pumps in Pseudomonas aeruginosa. Front Microbiol. 2015;6:660–5.

    Article  Google Scholar 

  7. 7.

    Horna G, Lopez M, Guerra H, Saenz Y, Ruiz J. Interplay between MexAB-OprM and MexEF-OprN in clinical isolates of Pseudomonas aeruginosa. Sci Rep. 2018;8:16463.

    Article  Google Scholar 

  8. 8.

    Li XZ, Plésiat P. Antimicrobial drug efflux pumps in Pseudomonas aeruginosa. In: Li XZ, Elkins C, Zgurskaya H, editors. Efflux-mediated antimicrobial resistance in bacteria. Cham: Adis; 2016.

    Google Scholar 

  9. 9.

    Streeter K, Katouli M. Pseudomonas aeruginosa: a review of their pathogenesis and prevalence in clinical settings and the environment. Infect Epidemiol Med. 2016;2(1):25–32.

    Article  Google Scholar 

  10. 10.

    Lee K, Yoon SS. Pseudomonas aeruginosa biofilm, a programmed bacterial life for fitness. J Microbiol Biotechnol. 2017;27(6):1053–64.

    CAS  Article  Google Scholar 

  11. 11.

    Maurice NM, Bedi B, Sadikot RT. Pseudomonas aeruginosa biofilms: host response and clinical implications in lung infections. Am J Respir Cell Mol Biol. 2018;58(4):428–39.

    CAS  Article  Google Scholar 

  12. 12.

    Igbinosa EO, Odjadjare EE, Igbinosa IH, Orhue PO, Omoigberale MNO, Amhanre NI. Antibiotic synergy interaction against multidrug-resistant Pseudomonas aeruginosa isolated from an abattoir effluent environment. Sci World J. 2012.

    Article  Google Scholar 

  13. 13.

    Smith S, Ganiyu O, John R, Fowora M, Akinsinde K, Odeigah P. Antimicrobial resistance and molecular typing of Pseudomonas aeruginosa isolated from surgical wounds in Lagos, Nigeria. Acta Medica Iranica. 2012;50(6):433–8.

    PubMed  Google Scholar 

  14. 14.

    Walkty A, Gilmour M, Simner P, Embil JM, Boyd D, Mulvey M, Karlowsky J. Isolation of multiple carbapenemase-producing Gram-negative bacilli from a patient recently hospitalized in Nigeria. Diagn Microbiol Infect Dis. 2015.

    Article  PubMed  Google Scholar 

  15. 15.

    EUCAST. The European Committee on Antimicrobial Susceptibility Testing. Break point tables for interpretation of MICs and zone diameters version 9.0. 2019. Accessed 10 July 2019.

  16. 16.

    Anbazhagan PV, Thavitiki PR, Varra M, Annamalai L, Putturu R, Lakkineni VR, Pesingi PK. Evaluation of efflux pump activity of multidrug resistant Salmonella Typhimurium isolated from poultry wet markets in India. Infect Drug Resis. 2019;12:1081–8.

    CAS  Article  Google Scholar 

  17. 17.

    Mathur T, Singhal S, Khan S, Upadhyay DJ, Fatma T, Rathan A. Detection of biofilm formation among the clinical isolates of Staphylococci: an evaluation of three different screening methods. Indian J Med Microbiol. 2006;24(1):25–9.

    CAS  Article  Google Scholar 

  18. 18.

    Hassan A, Usman J, Kaleem F, Omair M, Khalid A, Iqbal M. Evaluation of different detection methods of biofilm formation in the clinical isolates. Braz J Infect Dis. 2011;15(4):305–11.

    Article  Google Scholar 

  19. 19.

    Kpoda DS, Ajayi A, Somda M, Traore O, Guessennd N, Ouattara AS, et al. Distribution of resistance genes encoding ESBLs in Enterobacteriaceae isolated from biological samples in health centers in Ouagadougou, Burkina Faso. BMC Res Notes. 2018;11:471.

    Article  Google Scholar 

  20. 20.

    Pourakbari B, Yaslianifard S, Yaslianifard S, Mahmoudi S, Keshavarz-Valian S, Mamishi S. Evaluation of efflux pumps gene expression in resistant Pseudomonas aeruginosa isolates in an Iranian referral hospital. Iran J Microbiol. 2016;8(4):249–56.

    PubMed  PubMed Central  Google Scholar 

  21. 21.

    Maita P, Boonbumrung K. Association between biofilm formation of Pseudomonas aeruginosa clinical isolates versus antibiotic resistance and genes involved with biofilm. J Chem Pharm Res. 2014;6(5):1022–8.

    Google Scholar 

  22. 22.

    Oluborode OB, Smith SI, Seriki TA, Fowora M, Ajayi A, Coker AO. Antibiotic susceptibility pattern and molecular typing by PCR-RAPD analysis of clinical and environmental isolates of Pseudomonas aeruginosa. Microbiol Biotechnol Lett. 2018;46(4):434–7.

    Article  Google Scholar 

  23. 23.

    Mukaka MM. Statistics corner: a guide to appropriate use of correlation coefficient in medical research. MMJ. 2012;24(3):69–71.

    CAS  Google Scholar 

  24. 24.

    Abbas HA, El-Ganiny A, Kamel HA. Phenotype and genotypic delection of antibiotic resistance of Pseudomonas aeruginosa isolated from urinary tract infections. Afri Health Sci. 2018;18(1):11–21.

    Article  Google Scholar 

  25. 25.

    Merchant S, Proudfoot EM, Quadri HN, McElroy HJ, Wright WR, Gupta A, Sarpong EM. Risk factors for Pseudomonas aeruginosa infections consequences of inappropriate initial antimicrobial therapy: a systematic literature review meta-analysis. J Glob Antibiot Resist. 2010.

    Article  Google Scholar 

  26. 26.

    Odumosu BT, Adeniyi BA, Chandra R. Analysis of integrons and associated gene cassettes in clinical isolates of multidrug resistant Pseudomonas aeruginosa from southwest Nigeria. Ann Clin Microbiol Antimicrob. 2013;12:29.

    Article  Google Scholar 

  27. 27.

    Bajpai V, Govindaswamy A, Khirana S, Batra P, Aravinda A, Katoch O, et al. Phenotypic and genotypic profile of antimicrobial resistance in Pseudomonas species in hospitalized patients. Indian J Med Res. 2019;149(2):216–21.

    CAS  Article  Google Scholar 

  28. 28.

    Dagher TN, Al-Bayssari C, Diene SM, Azar E, Rolain JM. Emergence of plasmid-encoded VIM-2 producing Pseudomonas aeruginosa isolated from clinical samples in Lebanon. New Microbe New Infect. 2019;29:100521.

    Article  Google Scholar 

  29. 29.

    Farhan SM, Ibrahim RA, Mahran KM, Hetta HF, Abd El-Baky RM. Antimicrobial resistance pattern and molecular genetic distribution of metallo-β-lactamases producing Pseudomonas aeruginosa isolated from hospital in Minia, Egypt. Infect Drug Resis. 2019;12:2125–33.

    CAS  Article  Google Scholar 

  30. 30.

    Kamali E, Jamali A, Ardebili A, Ezadi F, Mohebbi A. Evaluation of antimicrobial resistance, biofilm forming potential, and the presence of biofilm-related genes among clinical isolates of Pseudomonas aeruginosa. BMC Res Notes. 2020;13:27.

    CAS  Article  Google Scholar 

  31. 31.

    Cepas V, Lopez Y, Muno E, Rolo D, Ardanuy C, Martı S, et al. Relationship between biofilm formation and antimicrobial resistance in gram-negative bacteria. Microb Drug Resis. 2019;25(1):72–9.

    CAS  Article  Google Scholar 

  32. 32.

    Mohammed NA, Abd Alla IM. Antibiotic resistance and ndvb gene expression among biofilm producing Pseudomonas aeruoginosa isolates. Afri J Clin Exp Microbiol. 2016;17(4):222–8.

    Article  Google Scholar 

  33. 33.

    Musafer HK, Kuchma SL, Naimie AA, Schwartzman JD, Al-Mathkhury HJ, O’Toole GA. Investigating the link between imipenem resistance and biofilm formation by Pseudomonas aeruginosa. Microb Ecol. 2014;68:111–20.

    CAS  Article  Google Scholar 

  34. 34.

    Madaha EL, Gonsu HK, Bughe RN, Fonkoua MC, Ateba CN, Mbacham WF. Occurrence of blaTEM and blaCTX-M genes and biofilm forming ability among clinical isolates of Pseudomonas aeruginosa and Acinetobacter baumannii in Yaoundé Cameroon. Microorganism. 2020;8:708.

    CAS  Article  Google Scholar 

  35. 35.

    Pan Y, Xu Y, Wang Z, Fang Y, Shen J. Overexpression of MexAB-OprM efflux pump in carbapenem-resistant Pseudomonas aeruginosa. Arch Microbiol. 2016.

    Article  PubMed  Google Scholar 

  36. 36.

    Alva I, Sutton JM, Rahman KM. Role of bacterial efflux pumps in biofilm formation. J Antimicrob Chemother. 2018;73:2003–20.

    Article  Google Scholar 

Download references


Not applicable.


This study did not receive any funding.

Author information




UFC and ODA contributed to data collection, AA contributed to data analysis and preparation of draft, SSI and AAI contributed to conceptualization of study, supervision and correction of draft. All authors read and approved final manuscript.

Corresponding author

Correspondence to Stella Ifeanyi Smith.

Ethics declarations

Ethics approval and consent to participate

Ethical approval for this study was obtained from the Institutional Review Board, Nigerian Institute of Medical Research with code number IRBB/19/033.

Consent for publication

Not applicable.

Competing interests

There is no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Ugwuanyi, F.C., Ajayi, A., Ojo, D.A. et al. Evaluation of efflux pump activity and biofilm formation in multidrug resistant clinical isolates of Pseudomonas aeruginosa isolated from a Federal Medical Center in Nigeria. Ann Clin Microbiol Antimicrob 20, 11 (2021).

Download citation


  • Biofilm
  • Efflux pump
  • Pseudomonas aeruginosa
  • Antibiotic resistance