Meliani, Amina

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EXCLI Journal 2020;19:813-816 – ISSN 1611-2156 Received: March 28, 2020, accepted:June 10 2020, published: June 17, 2020   813 Letter to the editor: THE MULTIFACTORIAL RESISTANCE OF  PSEUDOMONAS AERUGINOSA  Amina Meliani  Department of Biology, Faculty of Nature and Life Sciences, University Mustapha  Stambouli of Mascara, 29000, Algeria, Tel: 213770509024; 213551805873,  E-mail: ameliani2003@yahoo.fr  ORCID ID: 0000-0003-2355-5933   http://dx.doi.org/10.17179/excli2020-2197  This is an Open Access article distributed under the terms of the Creative Commons Attribution License  (http://creativecommons.org/licenses/by/4.0/).   Dear Editor, It was with great interest that we have read the review article entitled “Antibiotic re-sistance in Pseudomonas aeruginosa: mechanisms and alternative therapeutic strategies”. We truly thank Pang and colleagues for this successful research review (Pang et al., 2019). A myriad of factors involved in the P. aeruginosa resistance are provided in this over-view. Interestingly, these multidrug resistant (MDR) bacteria have engaged an intrinsic, ac-quired and adaptive antibiotic resistance. In the present contribution, we are highlighting how biofilm-mediated resistance comes into play.  Biofilm formation is often thought to represent a protective mode of growth which may enhance bacterial survival under conditions of environmental stress (Webb et al., 2003). Bio-films are clusters of microbial cells that are attached to a number of different surfaces such as natural aquatic and soil environments, living tissues, medical devices or industrial or portable water piping systems (Flemming, 1995). Unsurprisingly, biofilm antibiotic susceptibility has been the subject of intense research and has been the focus of several excellent reviews (Harrison et al., 2007). Biofilms render re-sistance to the harboring microbial cells and they are several times resistant to antimicrobials than their free living planktonic counterparts (Mah, 2012). This formation is of great concern owing to it nonspecific resistance toward antibiotics, metal ions (Meliani and Bensoltane, 2016), biocidal agents, protozoan grazers, desiccation and other hostile environmental condi-tions (Flemming and Wingender, 2010). The attached communities of microorganisms act as a protective barrier preventing the penetration of drug molecules. They secrete various inactivating and modifying enzymes which nullify the effects exerted by antimicrobials (Flemming and Wingender, 2010). The in-creased resistance of biofilms to antibiotics allows biofilm-based infections to persist chroni-cally in spite of antibiotic therapy (Costerton et al., 1999). Bowler et al. (2012) reported that the basis for biofilm-specific antibiotic resistance and tolerance is multifactorial.  Being highly resistant within biofilm, P. aeruginosa has served as the prototypic model organisms for the study of antibiotics and biocides resistance. It is becoming increasingly clear that the particular antimicrobial agent, the bacterial strain, the developmental stage of EXCLI Journal 2020;19:813-816 – ISSN 1611-2156 Received: March 28, 2020, accepted:June 10 2020, published: June 17, 2020   814 the biofilm, and the biofilm growth conditions orchestrate mechanisms of resistance and tol-erance. This letter provides a proposed hypothesis focused on understanding the Pseudomonas aeruginosa resistance to optimize new approaches that may challenge the medical practice to fight these multidrug-resistant (MDR) bacteria. For example, the recent advances in nano-technology can offer new prospects to develop novel formulations based on distinct types of nanoparticles (NPs) with flexible antimicrobial properties. It is also interesting to note that the structure dependent metabolic heterogeneity may also explain in part the tolerance of bacterial biofilms to these NPs. We felt that several aspects of this resistance warrant need further dis-cussion.  Consistent with biofilm culture studies, it has been shown that in Pseudomonas aerugino-sa biofilms that are less than 100 µm thick, the cells that are nearest to the substratum are in anoxic zones and are slow growing. This induces an intrinsic tolerance to killing by antibiot-ics relative to the aerobic fast growers in the outer-biofilm layers (Walters et al., 2003). To date, extended-spectrum β lactamases (ESBLs) have the ability to hydrolyze and cause resistance to various types of β-lactam antibiotics. As an ESKAPE organism, Pseudomonas aeruginosa is one of the most concerning pathogens involved in antibiotic resistance.  The primary outcome of a comparative study done in 2018 (Ps1…Ps16) and 2016 (Ps17…Ps29) is the increased resistance to Cefazolin (KZ30) and Penicillin (P10) (Figure 1). Many P. aeruginosa strains can produce different classes of ESBLs and are resistant to nearly all antibiotics, including carbapenems.   Figure 1: Resistance pattern of P. aeruginosa isolates for Cefazolin (KZ) and Penicillin (P10). Of note, an increased resistance in 2018 compared to 2016 using the frequently prescribed antibiotics of the β-lactams.  In other study, a total of 80 clinical isolates of P. aeruginosa were collected from different samples (March to June 2015-2016). Out of these isolates, 20 % were from urine, 30 % were from coproculture and 30 % were from cervicovaginal fluid. Generally, the isolates were found resistant following Clinical and Laboratory Standards Institute (CLSI) standards for performance and interpretation for disk diffusion susceptibility tests (NCCLS, 2004). Our re-sults clearly showed that the highest resistance levels occurred with IMP-ATM (Imipenem, 00,511,522,533,54Ps 1 Ps 2 Ps 3 Ps 4 Ps 5 Ps 6 Ps 7 Ps 8 Ps 9 Ps 10Ps 11Ps 12Ps 13Ps 14 Ps15 Ps 16 Ps17 Ps18 Ps19 Ps20 Ps21 Ps22 Ps23 Ps24 Ps25 Ps26 Ps28 Ps29DO 590nmP.aeruginosa isolatesKZ 30 P 10 Control20162018EXCLI Journal 2020;19:813-816 – ISSN 1611-2156 Received: March 28, 2020, accepted:June 10 2020, published: June 17, 2020   815 Aztreonam) (60 %) while the remaining at 40 % was shown to be P-AX (Penicillin, Amoxi-cillin) resistant. Likewise, 30 % of isolates were resistant to AMC (Augmentin: Amoxicillin-Clavulanate), this level of resistance is relatively higher. These results are likely similar to Jones (2001) study.  The potential for P. aeruginosa strains to evolve antimicrobials' resistance are incomplete-ly explored. Furthermore, the biofilm mode of growth contributes to increase this resistance. Our previous data (Amina and Ahmed, 2017) were consistent with Giwercman et al. (1991) reports, in which the exposure of biofilm cells to beta-lactamase inducers triggers the production of the β-lactamase enzyme that remains associated with the biofilm. The highlighted resistance was discussed in many scientific reports. So, the major obstacle for treatment of P. aeruginosa infections is the formation of biofilm and sometimes the for-mation of bacterial persister cells, phenotypic variants that are not genetically resistant to an-tibiotics but are tolerant to high concentrations of antibiotics.  It has previously been reported that P. aeruginosa is thought to have acquired a resistance for other antimicrobials. In another study, we found that P. aeruginosa biofilms were marked-ly also resistant to the essential oil (Es) of Costus sp. The chemical composition of this oil was investigated by GC-MS (Hewlett-Packard GC-MS system (GC: 5890 séries II, MSD 5972)), it led to the identification of 45 among the 121 constituents. Linolenic acid 12, 15-Octadecatrien-1-ol, (Z,Z,Z)-) (25.03 %) and Eugenol (23.99 %) were the main components. The second major group was Bicyclo [5.2.0] nonane (6.40 %), Isogenyl acetate (4.89 %), ox-ide of Caryophyllene (3.02 %), α-Ionone (2.49 %) and β-Eudesmol (1.15 %) (unpublished). Consequently, in vitro studies have shown that the mentioned phenylpropanoid compounds did not display antibiofilm activity vis a vis P. aeruginosa.  Nevertheless, these findings have challenged the longstanding theory of essential oil-bacteria interaction since the biofilm formation was significantly correlated to oil concentra-tions. Additional researches are required to elucidate the direct or indirect interaction. High levels of essential oil resistance arose readily during our in vitro study, carried out in 2018. A significant correlation between biofilm formation and Es concentrations were obtained from both P. aeruginosa and P. fluorescens (R2 = 0,89, R2 = 0,79, respectively). Based on the data published so far, this study reveals inherent mechanisms of essential oil resistance. The key question we ask in this breakthrough study is: why the Costus oil did not inhibit biofilm for-mation? Is it because it is unable to penetrate the biofilm or it is metabolized within other pathways.  The development of new antimicrobials is a long and winding road. Regardless of the im-portance of the above-mentioned results for a rewarding research area, it remains crucial to maintain a conclusion that the biofilm-mediated resistance is far more complex than initially thought.    Conflict of interest The author received no financial support and declares no potential conflicts of interest with respect to the authorship and/or publica-tion of this article.  REFERENCES Amina M, Ahmed B. Pseudomonas motility and anti-biotics resistance. J Bioeng Biomed Sci. 2017;7:220.  Bowler LL, Zhanel GG, Ball TB, Saward LL. Mature Pseudomonas aeruginosa biofilms prevail compared to young biofilms in the presence of ceftazidime. An-timicrob Agents Chemother. 2012;56:4976-9. Costerton JW, Stewart PS, Greenberg EP. Bacterial biofilms: a common cause of persistent infections. Science.1999;284:1318-22. Flemming HC. Sorption sites in biofilms. Water Sci Technol. 1995;32:27-33. EXCLI Journal 2020;19:813-816 – ISSN 1611-2156 Received: March 28, 2020, accepted:June 10 2020, published: June 17, 2020   816 Flemming HC, Wingender J. The biofilm matrix. Nat Rev Microbiol. 2010;8:623-33. Giwercman B, Jensen ET, Hoiby N, Kharazmi A, Costerton JW. Induction of beta-lactamase production in Pseudomonas aeruginosa biofilm. Antimicrob Agents Chemother. 1991;35:1008-10. Harrison JJ, Turner RJ, Ceri H. Multimetal resistance and tolerance in microbial biofilms. Nat Rev Micro-biol. 2007;5:928-38.  Jones RN. Resistance patterns among nosocomial pathogens: trends over the past few years. Chest.2001;119(2 Suppl):397S-404S.  Mah TF. Biofilm-specific antibiotic resistance. Future Microbiol. 2012;7:1061-72. Meliani A, Bensoltane A. Biofilm-mediated heavy metals bioremediation in PGPR Pseudomonas. J Bio-remediat Biodegrad. 2016;7:370.  NCCLS, National Committee for Clinical Laboratory Standards. Performance standards for antimicrobial susceptibility testing; 14th informational supplement M100-S14. Wayne, PA: National Committee for Clin-ical Laboratory Standards, 2004. Pang Z, Raudonis R, Glick BR, Lin TJ, Cheng Z. An-tibiotic resistance in Pseudomonas aeruginosa: mech-anisms and alternative therapeutic strategies. Biotech-nol Adv. 2019;37:177-92. Walters MC III, Roe F, Bugnicourt A, Franklin MJ, Stewart PS. Contributions of antibiotic penetration, oxygen limitation, and low metabolic activity to toler-ance of Pseudomonas aeruginosa biofilms to ciprof-loxacin and tobramycin. Antimicrob Agents Chemother.2003; 47:317-23. Webb JS, Thompson LS, James S, Charlton T, Tolker-Nielsen T, Koch B, et al. Cell death in Pseu-domonas aeruginosa biofilm development. J Bacteri-ol. 2003;185:4585-92.   

The multifactorial resistance of Pseudomonas aeruginosa

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The multifactorial resistance of Pseudomonas aeruginosa

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