Premanath R, Suresh S, Alva P. P, Akash S. K. Biofilm Forming Abilities of Microorganisms Associated with Diabetic Wound Infection: A Study from A Tertiary Care Hospital. Biomed Pharmacol J 2019;12(2).

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Manuscript received on :15-Jan-2019
Manuscript accepted on :15-April-2019
Published online on: 09-05-2019

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Ramya Premanath*¹, Sarika Suresh¹, Prathiksha P. Alva¹ and Akash S. K²

¹Infectious Diseases, Nitte University Centre for Science Education and Research, Paneer Campus, Deralakatte, Mangaluru-575018, India.

²Kasturba Medical College, Hampankatta, Mangaluru-575001, India.

Corresponding Author E-mail: ramya@nitte.edu.in

DOI : https://dx.doi.org/10.13005/bpj/1687

Abstract

Diabetes mellitus, a chronic metabolic disease is increasing worldwide. Diabetic foot infections are one of the most feared and bothersome complications of diabetes caused by different genera of bacteria. There is an increasing evidence which demonstrates the presence of biofilm former's in chronic diabetic foot ulcers which contribute to the development of antibiotic-resistant strains and treatment failure. The present study aimed at isolating bacteria from diabetic wounds, to check for its antibiotic susceptibility and biofilm forming ability. From the diabetic wounds, isolates belonging to the genera of Staphylococcus, Pseudomonas, Klebsiella, Esherichia, Vibrio, Acinetobacter and Citrobacter were recovered. To the best of our knowledge, Vibrio parahaemolyticus was isolated for the first time from diabetic ulcer. Antibiotic sensitivity profile of the organisms infers the presence of multidrug-resistant strains. Majority of bacteria isolated were found to be biofilm formers. High biofilm former's were observed in strains of P. aeruginosa, S. aureus and Klebsiella spp. There was significant association between incubation time and intensity of biofilm formation in P. aeruginosa [ᵡ² (p< 0.05) = 0.001)], Staphylococcus spp. [ᵡ² (p< 0.05) = 0.023)] and Acinetobacter spp. [ᵡ² (p< 0.05) = 0.018)]. The presence of biofilm forming multidrug-resistant bacteria infers the chronic nature of diabetic wounds.

Keywords

Biofilm; Diabetic Wound; Multidrug-Resistant Bacteria; Poly Microbial Infection

Introduction

Diabetes mellitus (DM), a metabolic disorder is increasing at an alarming rate all over the world. India has nearly 33 million diabetic subjects today and tops the list of countries with the highest number of diabetics and considered the “diabetic capital of the world” (1). The number of diabetics in India is expected to rise to a whopping 79.4 million by 2030 (2). Diabetics are more susceptible to infections due to increased glucose levels and suppressed immune response as well as decreased blood flow to extremities that lead to slow healing wounds (3). Diabetic foot infections caused by different genera of bacteria are the most feared complications of diabetes associated with high morbidity which can end up with gangrene and amputation. High incidence of diabetic foot infection in India can be attributed to practices such as bare foot walking, inadequate facilities for diabetic care, illiteracy and low socioeconomic status (4). As bacteria that cause diabetic foot infection have become resistant to number of available antibiotics, the most successful strategies to manage infection is the frequent debridement of foot ulcer (5). Many of the organisms that cause infection have acquired resistance to the available antibiotics making treatment regimen complicated.

The polymicrobial community that cause infection can produce extracellular polymeric substances called biofilms. Biofilm formed performs a dual function in acting as a physical barrier for biological and antimicrobial substances and also facilitate adhesion to surfaces (6). In recent years, biofilms have gained as an important means of survival of microorganisms in hostile environment. Bacteria in biofilm exchange genetic material, communicate with each other, which often result in altered phenotype of bacteria which influences the wound healing process (7). Chronic diabetic foot infection due to biofilm formers contribute to the development of antibiotic resistant strains and treatment failure. Though there are many studies worldwide on this topic, hardly few studies have been conducted in Mangaluru region focusing on the biofilm forming abilities of the organisms isolated from foot wounds. Against this background, our study focused on isolating bacteria from diabetic wound infection, checking for its antibiotic susceptibility and also biofilm forming abilities of these pathogens.

Materials and methods

Sample collection

Clinical samples (wound swab) from patients with a history of diabetes was collected from Justice K.S Hegde hospital, Deralakatte, Mangaluru, by taking clearance from the institutional ethics committee (INST.EC/2017-18/003) before commencement of this work. Patient consent was taken before sample collection and was anonymized. Sample collection was carried for a period of 3 months between January and March, 2018. Collected swabs were enriched in brain heart infusion broth for the period of 8 hours.

Selective Isolation

Culture from the enrichment media was streaked onto nutrient agar and colonies that developed were inoculated onto different selective media viz. cetrimide agar, mannitol salt agar, MacConkey agar, Leeds Acinetobacter agar and thiosulphate citrate bile salt sucrose agar.

Identification of bacteria

Phenotypic identification was done by performing Gram staining and an array of biochemical tests. Genotypic identification was carried out by polymerase chain reaction using genus and species specific primers. The list of primers used in the study is given in Table 1.

Table 1: Name and sequence of primers used for identification of different bacteria.

Antibiotic susceptibility testing

All the confirmed isolates were subjected to antibiotic susceptibility test by employing Kirby Bauer disc diffusion method (17). Antibiotics norfloxacin, imipenem, tetracycline, gentamicin, amoxyclav, ampicillin, amoxicillin, ciprofloxacin, cefoxitin, cefotaxime were used for Gram negative bacteria, vancomycin, penicillin G, amoxyclav, azithromycin, tetracycline, trimethoprim, and oxacillin were used for Gram positive bacteria and cefoperazone, piperacillin, levofloxacin, gentamicin, amikacin, imipenem, aztreonam, cefoperazone/sulbactam, piperacillin/tazobactam, ceftazidime, netillin, ciprofloxacin, tobramycin were used for P. aeruginosa. The zones of inhibition (mm) that developed after an incubation period of 24 h were measured.

Qualitative and quantitative assay for biofilm

Congo red Method

Qualitative detection of biofilm formation was carried out by Congo red method (18) Biofilm formers formed black colonies with a dry crystalline consistency.

Microtitre Plate Method

Biofilm quantification was carried out according to the method of O’Toole and Kolter with slight modification. In a microtitre plate, 100 µl of the diluted culture was taken and incubated for 24 h at 37ºC. Using PBS of pH 7.4, the adherent cells were washed thrice. 125 µl of 0.1% freshly prepared crystal violet was added to the dried pellet, and incubated for 10 min. 200 µl of 30% acetic acid was added to the stained and washed pellet, and incubated for 15 min for stain solubilisation. To a fresh plate, 100 µl from the well was transferred and optical density was measured at 600 nm in an ELISA reader (Biorad, USA). Reduction in the biofilm formation was measured in terms of per cent inhibition as [(OD of control – OD of treated)/OD of control] x100. The biofilm formed by the confirmed isolates was compared with positive culture of different organisms. The biofilm formers were grouped as weak biofilm formers (OD₆₀₀ 0.071 – 0.142), moderate biofilm formers (OD₆₀₀ 0.142 – 0.284) and high biofilm formers (OD₆₀₀ ≥ 0.284) (42). Biofilm formation was quantified at different time intervals (24, 48 and 72 h).

Results

Isolation and Identification of Bacteria

Out of 133 colonies found growing on the selective media, 36 developed on Mac Conkey agar, 26 on thiosulphate citrate bile salt sucrose agar, 27 on cetrimide agar, 36 on mannitol salt agar and 8 on Acinetobacter agar. The development of bacteria was predominantly more on mannitol salt agar and cetrimide agar indicating the presence of large number of Staphylococcus spp. and P. aeruginosa respectively. The isolates were identified after performing an array of biochemical tests in addition to molecular confirmation. Staphylococcus spp. and P. aeruginosa were found to be the predominating organisms isolated from diabetic wounds. The number of organisms isolated is given in (Graph.1). The most important observation from the study is the isolation of V. parahaemolyticus from diabetic wounds. To the best of our knowledge, this is the first report in India to encounter V. parahaemolyticus in diabetic wounds.

Graph 1: Number of isolates recovered from diabetic wound.   Click here to view figure

Antibiotic Susceptibility Test

Antibiotic susceptibility test was performed for the confirmed 107 isolates. Susceptibility of bacterial isolates to the different antibiotics used is shown in (Graph. 2). Among the Gram positive isolates, resistance for oxacillin was significantly high. Bacteria were found to be sensitive for tetracycline followed by vancomycin (Graph.2A). Among the Gram negative isolates other than P. aeruginosa, resistance was significantly more to ampicillin and amoxicillin when compared to other antibiotics used (Graph.2B). Around 60% of the isolates were sensitive to imipenem. In general, more number of isolates was found to be resistant to the antibiotics used. All isolates of E. coli were completely resistant to the antibiotics used other than tetracycline. Klebsiella spp. (94% isolates) showed highest resistance to amoxicillin. Acientobacter spp. were highly sensitive to imipenem and resistant towards ampicillin and amoxyclav. Complete resistance was found to cefocitin/cloxacillin among the Vibrio spp. P. aeruginosa isolates were generally sensitive to all the antibiotics used (Graph.2C). Nearly 40% of the isolates showed resistance to cefperazone/sulbectum combination. Around 85% of isolates showed least resistance to ciprofloxacin.

Graph 2: Antibiotic susceptibility of bacteria isolated from diabetic wounds.   Click here to view figure

2A: Susceptibility of Gram positive bacterial isolates; 2B: Susceptibility of Gram negative bacterial isolates other than P.aeruginosa; 2C: Susceptibility of P. aeruginosa.

Biofilm Assay

Out of 107 isolates checked for their biofilm forming abilities, 80 isolates formed black colonies with a dry crystalline consistency indicating a positive result. Staphylococcus spp. (88%) and P. aeruginosa (88%) were the predominant biofilm formers. In Klebsiella spp. 53% of isolates, in Vibrio spp. 80% of isolates, in Acinetobacter spp. 37% of isolates formed biofilm. Both the E. coli isolates were biofilm formers. In the microtitre plate assay, biofilm formation varied at different time intervals. High biofilm formers were found in Staphylococcus spp., Klebsiella spp. and P. aeruginosa isolates. Majority of the Staphylococcus spp. and E. coli isolates were moderate biofilm formers (92%). The numbers of high biofilm formers (9%) were more in P. aeruginosa when compared to other bacteria. High biofilm formers were not found in E. coli, Vibrio spp. and Acinetobacter spp. Majority of the isolates formed weak and moderate biofilms at 24 h. P. aeruginosa isolates showed moderate biofilm formation at 24 h. But, at 48 h around 27% of them showed high biofilm formation. At 72 h, around 7% of Klebsiella spp. showed high biofilm formation. In P. aeruginosa the number of isolates forming weak biofilm increased at 72 h. In E. coli, Acientobacter spp. and Vibrio spp. the number of isolates forming moderate biofilm increased at 48 and 72 h. There was significant association between incubation time and intensity of biofilm formation in P. aeruginosa [ᵡ² (p< 0.05) = 0.001)], Staphylococcus spp. [ᵡ² (p< 0.05) = 0.023)] and Acinetobacter spp. [ᵡ² (p< 0.05) = 0.018)]. There was no significant association in Klebsiella spp., E. coli and Vibrio spp. The percentage of biofilm formed at different time intervals is shown in (Graph 3).

Graph 3: Biofilm formation in the bacterial isolates at different time intervals (24,48 & 72 h).   Click here to view figure

Discussion

Diabetic foot infections are a major problem worldwide. In India, more than 62 million people have been diagnosed with diabetes. Foot ulcer is the major problem in diabetes which if left untreated, results in limb amputation (19). In the present study, isolation and identification of bacteria causing foot ulcers along their antibiotic susceptibility profile and biofilm forming ability were attempted. As reported from the present study, the percent prevalence of Gram negative bacteria was more than Gram positive bacteria. The result is not in agreement with studies which have exhibited higher proportions of Gram positive bacteria isolated form diabetic wounds (20 , 21). A study from Malaysia has reported Proteus spp. to be the predominating organism in diabetic wound (22). However, Proteus spp. was hardly encountered in this study. S. aureus and P. aeruginosa were the predominant organisms isolated and identified in this study. Contradicting results have been observed in a study which has shown the prevalence of E. coli in diabetic wounds (21). The present study highlights presence of multidrug-resistant bacteria in diabetic wounds as depicted by its resistance to more than one drug used. Gram positive isolates showed resistance to vancomycin in our study. Contradictory results have been seen in a study which has shown 100% sensitivity of S. aureus to vancomycin (22). Gram negative bacteria in the current study have shown significant resistance to amoxicillin+clavulanic acid. The results are in agreement with a study which has shown similar result (21). Resistance to imepenam was around 30%. The results does not correspond with a study has shown 100% sensitivity of Gram negative bacteria towards imepenam (23). Infections with bacteria forming biofilms are difficult to eradicate. These biofilms are not only less susceptible to host cell immune responses but also have a high tolerance to antibiotics than the planktonic cells (24). The resistance of biofilm forming bacteria towards antibiotics is due to obstruction in the permeability of the drug by the polysaccharide matrix (25) and alteration of the drug efficacy in the biofilm environment (3). Not only biofilm effect antimicrobial agents, but also they give protection against host defenses. Biofilms have anti-phagocytic activity and also inactivates complement and antibodies (26). In the present study, 75 per cent of drug resistant bacteria were biofilm formers. The percent of biofilm formers in our study is significantly larger in comparison to a previous study (21) and corresponds to studies by Swarna et al. and James et al. (27, 28). The higher percentage of biofilm formers in diabetic wounds could be due to ineffective debridement procedure or longer duration of ulcer in patients (29). P. aeruginosa was a predominant biofilm former with 89 per cent of the isolates being positive for biofilm formation. This was an expected result as studies have reported biofilm formation by P. aeruginosa more readily in diabetic wound environment (30).

Conclusion

It is clear from the present study that, majority of bacteria isolated from diabetic wounds are multi-drug resistant and moderate-high biofilm formers which resist antibiotic therapy. In order to decrease the undesirable consequences associated with diabetic wounds, it is essential to recognize the biofilm forming abilities of the organism in addition to their antibiotic susceptibility profile. Decline in the morbidity due to diabetic foot ulcers caused by multidrug resistant biofilm producing bacteria is possible by adopting alternative therapies which prevent bacterial attachment, disrupt biofilm and act as quorum sensing inhibitors. Developing new tools to reduce the suffering of diabetic patients with foot ulcers should be taken as a challenging research.

Acknowledgements

We thank Nitte (Deemed to be University) for all the facilities provided.

Ethical Approval

The study was approved by the Institutional Ethics Committee of the Nitte University Centre of Science Education & Research (INST. EC/2017-18/003), Mangaluru, India.

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