Get Permission Wadekar, Sathish J V, Jayashree, and Pooja C: Bacteriological profile of pus samples and their antibiotic susceptibility pattern


Introduction

Pyogenic infections refer to infection that causes pus formation and are characterized by several local inflammations, usually multiplication of microorganism.1 Pus is a collection of thick, white or yellow fluid, formed at the site of inflammation during infection. It is made up of dead tissue, white blood cells, and damaged cells.2 The occurrence of wound infections depends on various factors like condition of wound, microbial load and the host defense mechanisms.3 The overall incidence of wound sepsis in India is from 10% to 33%.4 The infecting pathogens not only differ from country to country, but also vary from one hospital to another within the same country.5 It is caused by bacteria, virus, fungi and protozoa and in many cases there is a mixed infection with more than one bacterial species.6

The most common causative agent includes Staphylococcus aureus which account for 20-40%. Infection with Pseudomonas aeruginosa occurs mainly following surgery and burns which account for 5-15%. Escherichia coli, Klebsiella sp., Proteus sp. and Enterococci sp. are commonly associated with pyogenic infections.8, 7

Selection of an effective antimicrobial agent for a microbial infection depends on the causative agent, pathophysiology of the infectious process and on pharmacodynamics and pharmacokinetics of the antimicrobial agents. Also, antibiotic resistance to the commonly used antibiotics is now emerging as a result of misuse and abuse of particular antibiotics.9 The routine use of antibiotics has resulted in wide spread antibiotic resistance especially within the gram negative organisms.10 Bacteria have the ability to acquire resistance and can transfer the resistance from one bacteria to another.11 Earlier, such multidrug resistant organisms were common in immunosuppressed patients but now, reports are showing such infections in normal healthy individuals. Also, such drug-resistant infections may complicate the newly emerging infectious diseases.12 The emergence of high anti-microbial resistance among bacterial pathogens has made the management and treatment difficult.13 It is ideal to give proper antibiotic after culture and sensitivity of the wound swab or pus.14 The present study aimed to detect common bacteriological profile and their antibiotic susceptibility profile from wound infection.

Materials and Methods

A retrospective study was conducted at Chamarajanagar Institute of medical sciences, Chamarajanagar from January to June 2019. All pus samples collected during the study period were included. Socio-demographic and laboratory results were collected from Hospital Microbiology Laboratory registration books by using a standard data collection format. Pus samples were aseptically collected using sterile swab in a test tube and inoculated on to blood agar and MacConkey agar. Plates were incubated at 37°C for 24 hours. Organisms were identified by series of biochemical reactions standard following standard procedures.

Antimicrobial susceptibility testing was performed using Muller-Hinton agar plates by disc diffusion method following Clinical and Laboratory Standards Institute (CLSI) guidelines.15 The isolates were tested against ampicillin (10 μg), amoxyclav (20/10µg), gentamicin (10 μg), amikacin (30 μg), ciprofloxacin (5 μg), ceftazidime (30 μg), Cefotaxime (30 μg), Meropenem (10 μg) and Piperacillin – Tazobactum (100/10µg). For gram-positive isolates, Cotrimoxazole (1.25μg /23.75μg), Erythromycin (5µg), Clindamycin (2µg), Chloramphenicol (30μg), Tetracycline (30μg), Linezolid (30µg), Vancomycin(30µg). For Enterococci high level gentamicin (HLG) was used.

ESBL was detected by combined disk test. This was performed by phenotypic confirmatory test as per the recommendations of CLSI. The ceftazidime (30 μg) discs alone and in combination with clavulanic acid (ceftazidime + clavulanic acid, 30/10 μg discs) were used. An increase of ≥ 5mm in zone of inhibition of the combination discs in comparison to the ceftazidime disc alone was considered to be ESBL producer.

Methicillin resistant Staphylococcus aureus (MRSA) was detected by Cefoxitin disc diffusion test. Lawn culture was done onto Mueller– Hinton agar plate. A 30 μg cefoxitin disc was placed and incubated at 37°C for 24 hrs. The zone of inhibition of S. aureus ≤ 21 mm was considered as methicillin resistant.

Statistical analysis

Analysis was done using MS Excel.

Ethical considerations

Ethical clearance was obtained from the Institutional Ethical clearance committee of Chamarajanagar Institute of medical sciences, Chamarajanagar.

Results

Of 118 pus samples collected, 101(85.5%) were positive cultures, which included 62 (52.5%) Gram negative and 39(33.1%) Gram positive bacteria. Mixed growth was seen in 5(4.2%) samples and no growth in 17(14.4%) samples. Middle age group of 19-45 years 51 (43.2%) was most commonly affected age group. Males 75(63.6%) were commonly affected than females 43(36.4%). S. aureus 27(22.9%) was most common isolate followed by Pseudomonas spp. 17(14.4%), E. coli 16(13.6%), CONS 10(8.5%), Citrobacter spp. 9(7.6%), Klebsiella pneumoniae and Enterobacter spp. 6(05.1%) each, Proteus spp. 5(04.2%), Acinetobacter spp. 3(02.5%) and Enterococcus spp. 2(1.7%). ESBL positivity was seen in 38(61.2%) Gram negative isolates and most were susceptible to piperacillin / tazobactum 55(88.7%) and meropenem 53(85.4%). MRSA was detected in 13(48.1%) S. aureus isolates and were susceptible vancomycin 27(100%) and linezolid 25(92.5%).

Table 1

Age and gender wise distribution

Age (years) No. of isolates No. (%) Gender
M No. (%) F NO. (%)
1 – 18 27 (22.9) 17 (14.4) 10 (08.5)
19 -45 51 (43.2) 31 (26.3) 20 (16.9)
> 45 40 (33.9) 27 (22.9) 13 (11.0)
Total 118 (100) 75 (63.6) 43 (36.4)
Table 2

Organisms isolated from pus culture

Organisms No. of organisms Percentage (%)
Staphylococcus aureus 27 22.9
CONS 10 08.5
Enterococcus spp. 02 01.7
Escherichia coli 16 13.6
Klebsiella pneumoniae 06 05.1
Proteus spp. 05 04.2
Citrobacter spp. 09 07.6
Acinetobacter spp. 03 02.5
Enterobacter spp. 06 05.1
Pseudomonas spp. 17 14.4
No growth 17 14.4
Total 118 100
Table 3

Antibiotic susceptibilitypattern of Gram negative isolates

Organisms AMP AMC G AK CIP CAZ CTX MRP PIT
Escherichia coli (n=16) 06 (37.5) 10 (62.5) 08 (50.0) 10 (62.5) 12 (75.0) 07 (43.7) 07 (43.7) 12 (75.0) 13 (81.2)
Klebsiella spp. (n=06) 02 (33.3) 03 (50.0) 05 (83.3) 04 (66.6) 04 (66.6) 03 (50.0) 03 (50.0) 05 (83.3) 04 (66.6)
Proteus spp. (n=05) 04 (80.0) 05 (100) 04 (80.0) 04 (80.0) 05 (100) 04 (80.0) 04 (80.0) 05 (100) 05 (100)
Citrobacter spp. (n=09) 05 (55.5) 05 (55.5) 06 (66.6) 06 (66.6) 08 (88.8) 05 (55.5) 05 (55.5) 09 (100) 09 (100)
Acinetobacter spp. (n=03) 02 (66.6) 02 (66.6) 02 (66.6) 02 (66.6) 02 (66.6) 02 (66.6) 02 (66.6) 01 (33.3) 02 (66.6)
Enterobacter spp. (n=06) 03 (50.00) 03 (50.00) 04 (66.6) 05 (83.3) 04 (66.6) 03 (50.00) 03 (50.00) 06 (100) 05 (83.3)
Pseudomonas spp. (n=17) 05 (29.4) 11 (64.7) 11 (64.7) 13 (76.5) 09 (52.9) 09 (52.9) 09 (52.9) 15 (88.2) 16 (94.1)
Total (n=62) 27 (43.5) 39 (62.9) 40 (64.5) 44 (70.9) 44 (70.9) 33 (53.2) 33 (53.2) 53 (85.4) 55 (88.7)

[i] AMP – Ampicillin, AMC – Amoxyclav, G – Gentamycin, AK – Amikacin, CIP – Ciprofloxacin, CAZ – Ceftazidime, CTX – Cefotaxime, MRP – Meropenem, PIT – Piperacillin-Tazobactum

Table 4

Antibiotic susceptibility pattern of Gram positive isolates

Organisms AMP No. (%) G No. (%) AK No. (%) CIP No. (%) COT No. (%) E No. (%) CD No. (%) C No. (%) TE No. (%) LZ No. (%) VA No. (%)
Staphylococcus aureus (n=27) MRSA 13 MSSA 14 00 (00) 05 (35.7) 05 (38.5) 11 (78.5) 07 (53.8) 12 (85.7) 03 (23.1) 07 (50.0) 04 (30.7) 12 (85.7) 08 (61.5) 07 (50.0) 06 (46.1) 08 (57.1) 07 (53.8) 12 (85.7) 08 (61.5) 12 (85.7) 12 (92.3) 13 (92.8) 13 (100) 14 (100)
Total (n=27) 05 (18.5) 16 (59.2) 19 (70.3) 10 (37.0) 16 (59.2) 15 (55.5) 14 (51.8) 19 (70.3) 20 (74.1) 25 (92.5) 27 (100)
CONS (n=10) 00 (00) 06 (60.0) 08 (80.0) 04 (40.0) 04 (40.0) 03 (30.0) 06 (60.0) 06 (60.0) 05 (50.0) 09 (90.0) 10 (100)
Enterococcus (n=02) 01 (50.0) 01 (50.0) - 01 (50.0) - - - - 01 (50.0) 02 (100) 02 (100)

[i] AMP – Ampicillin, G – Gentamycin, AK – Amikacin, CIP – Ciprofloxacin, COT- Cotrimoxozole, E – Erythromycin, CD – Clindamycin, C- Chloramphenicol, TE- Tetracycline, LZ- Linezolid, VA- Vancomycin

Table 5

Number of ESBL producers

No. of Gram negative isolates ESBL producers No. (%)
62 38(61.2)

Discussion

Pyogenic infections are characterized by local and systemic inflammation usually with pus formation. It may be either monomicrobial or polymicrobial. Gram negative bacteria such as Pseudomonas, Escherichia coli, Klebsiella spp., Proteus spp., and Gram positive cocci such as Staphylococcus aureus and Enterococci are the common causative agents.16

 In this study, both gram positive and gram negative pathogens were isolated from samples. The predominant pathogens were gram negative bacteria (52.5%). It was agreed with studies done by Swati Duggal et al.17 and Shama et al.18 which showed dominance pathogens as Gram negative bacteria. The most common gram negative being Pseudomonas spp. 17(14.4%), followed by E. coli 16(13.6%), Citrobacter spp. 9(7.6%), Klebsiella pneumoniae and Enterobacter spp. 6(05.1%) each, Proteus spp. 5(04.2%) and Acinetobacter spp. 3(02.5%). These organisms are commonly found in hospital environment. They tend to be resistant to common antiseptics and are also multidrug resistant. Among gram positive pathogens, Staphylococcus aureus was commonly isolated followed by CONS and Enterococci which correlates with the study done by Kumari PH et al.19 Staphylococcus aureus being normal flora of the skin, is usually associated with pyogenic infections.20

ß-lactamases, which are responsible for resistance of ß-lactam group of antibiotics, hydrolyse the amide bond of the four-membered characteristic ß-lactam ring, thus rendering the antimicrobial ineffective.21 Present study showed ESBL positivity in 38(61.2%) Gram negative isolates.

Methicillin-resistant Staphylococcus aureus (MRSA) strains are resistant to a large group of antibiotics called beta-lactams, including penicillins and cephalosporins. Methicillin resistance is caused by the acquisition of a mecA gene. This produces an alternative penicillin-binding pro­tein 2a (PBP2a), which has lower affinity for β-lactam antibiotics.23, 22 In present study, MRSA was detected in 13(48.1%) S. aureus isolates. Most of Gram negative isolates were susceptible to piperacillin / tazobactum 55(88.7%) and meropenem 53(85.4%) which is similar to study done by Rameshkannan S. et al. which showed maximum susceptibility to these antibiotics.24 Most of Gram positive isolates were sensitive to vancomycin 27(100%) and linezolid 25(92.5%) which is same as the results of studies conducted by Verma P25 and Shittu AO et al.26

As antibiotic resistance among microorganisms is increasing, it has become mandatory to select antibiotics properly and to administer it at appropriate dosage and duration. Our study also showed existence of high drug resistance to multiple antibiotics in E. coli, S. aureus, K.pneumoniae, and P. aeruginosa isolates from pus samples. Hence formulation of antibiotic policies and infection control measures suitable has to be considered essential.27

Conclusion

The spread of beta-lactamase producing organisms has been increasing. Present study showed increased resistance to beta-lactam antibiotics which is a serious problem. To combat resistance irrational use of antibiotics should be avoided. Also regular surveillance helps in implementing better therapeutic strategies to reduce morbidity and mortality.

Source of Funding

None.

Conflict of Interest

None.

References

1 

Kulandhaivel Murugesan Rekha Sivankutty Radha Hridhya Vijayan Study on Antibiotic Susceptibility Testing against Pyogenic Organisms from Wound InfectionsInt J Pharm Sci Rev Res20174512625

2 

D Bindu Chitralekhasaikumar M Kiran R Praveena V Illamani Bacterial Profile and Antibiotic Resistance Pattern of Aerobic Gram Positive Bacteria Isolated From Pus SampleRes J Pharm, Biol Chem Sci2014556436

3 

S. Nithya Gomatheswari T. Jeyamurugan Bacteriological Profile and the Antibiotic Susceptibility Pattern of Microorganisms Isolated from Pus/Wound Swab Isolates in Patients Attending a Tertiary Care Hospital in South IndiaInt J Curr Microbiol Appl Sci2017610140513

4 

Hima Mantravadi Mallikarjuna Chinthaparthi V Shravani Aerobic isolates in pus and their antibiotic sensitivity pattern: a study conducted in a teaching hospital in Andhra PradeshInt J Med Sci Public Health20154810769

5 

Dagnachew Muluye Yitayih Wondimeneh Getachew Ferede Tesfaye Nega Kasaw Adane Belete Biadgo Bacterial isolates and their antibiotic susceptibility patterns among patients with pus and/or wound discharge at Gondar university hospitalBMC Res Notes201471619

6 

Nandkishor Bankar Bacteriological Profile of pus/ wound swab and antimicrobial susceptibility of Staphylococcus aureus isolated from pus & wound swab of Indoor Patients of Tertiary Care HospitalInt J Innov Res Med Sci20183424558737

7 

H Sida P Pethani H Dalal N Shah Shaikh Current Microbial Isolates From Wound Samples And Their Susceptibility Pattern In A Tertiary Care HospitalNatl J Integr Res Med2018921721

8 

Namita A., Raytekar, Meghna R. Choudhari Sonali Das Antibiotic profiling of Pseudomonas aeruginosa isolates from pus sample of rural tertiary care hospital of Western Maharashtra, Loni, IndiaInt J Res Med Sci201757307681

9 

Poonam Verma A study on isolation of different type of bacteria from pusInt J Pharm Life Sci2012311210710

10 

Poonam Verma Antibiotic Sensitivity Treatment for Gram Positive Bacteria Isolated from Pus SampleBull. Environ. Pharmacol. Life Sci2012110306

11 

S Krishnamurthy A C Sajjan G Swetha Shalini Characterization and resistance pattern of bacterial isolates from pus samples in a tertiary care hospital KarimnagarJ Path Micro2016224954

12 

Rudrajit Paul Jayanti Ray Sourav Sinha Jayati Mondal Antibiotic resistance pattern of bacteria isolated from various clinical specimens: an eastern Indian studyInt J Community Med Public Health201744136771

13 

Ananthi M Ramakumar V Kalpanadevi R. Sopia Abigail L. Karthiga H. Kalavathy Victor Aerobic Bacteriological Profile and Antimicrobial Susceptibility Pattern in Postoperative Wound Infections at a Tertiary Care HospitalInt J Med Sci Clin Inventions20174227026

14 

Mustafa Sofiur Rahman Surendra Prasad Chauhan Smita Bawankar Bacteriological profile and antibiotic susceptibility profile of wound infection in a tertiary care hospital ChattisgarhIndian J Appl Res2018862931

15 

Performance Standards for antimicrobial susceptibility testing, XXI International Supplement (M100-S27)Clinical Laboratory Standards Institutes (CLSI)2017Wayne, Pennsylvania, USA

16 

Sundararajan Thangavel Gomathi Maniyan S Vijaya C Venkateswaran A study on aerobic bacteriological profile and antimicrobial susceptibility pattern of isolates from pus samples in a tertiary care hospitalInt J Bioassays2017603531720

17 

Swati Duggal P K Khatri R S Parihar Rajat Arora Antibiogram of Various Bacterial Isolates from Pus Samples in a Tertiary Care Centre in RajasthanInt J Sci Res201545158084

18 

Mary Shama Kulandhaivel Murugesan Hridhya Vijayan Isolation Identification and Antibiotic Sensitivity Pattern of Pyogens from Pyogenic PathogensBiomed Pharmacol20181114638

19 

P H Kumari Purimitla Usha Rani Payala Vijayalakshmi Evaluation of microbiological profile and antibiogram of aerobic bacteria isolated from pus samplesJ Med Allied Sci2018812635

20 

Shahin Sultana Nurunnahar Mawla Shamima Kawser Nayareen Akhtar Md Khoybar Ali Current Microbial Isolates from Wound Swab and Their Susceptibility Pattern in a Private Medical College Hospital in Dhaka cityDelta Med Col J2015312530

21 

Prashant Durwas Peshattiwar and Basavaraj Virupaksappa Peerapur. ESBL and MBL Mediated Resistance in Pseudomonas aeruginosaJ Clin Diagnostic Res20115815524

22 

Seyed Mohsen Mahdiyoun Hossein Kazemian Mohammad Ahanjan Hamidreza Houri Mehdi Goudarzi Frequency of Aminoglycoside-Resistance Genes in Methicillin-Resistant Staphylococcus aureus (MRSA) Isolates from Hospitalized PatientsJundishapur J Microbiol20169827800135

23 

E A Ihsan Alsaimary Antibiogram and multidrug resistance patterns of Staphylococcus aureus (MDRSA) associated with post operative wound infections in Basrah - IraqMed J Islamic World Acad Sci20122025766

24 

S Rameshkannan G Nileshraj S Rameshprabu A Mangaiarkkarasi Meher Ali R. Pattern of pathogens and their sensitivity isolated from pus culture reports in a tertiary care hospital PuducherryIndian J Basic Appl Med Res2014412438

25 

P Verma Antibiotic Sensitivity Treatment for Gram Positive Bacteria Isolated from Pus SampleBull Environ Pharmacol Life Sci201211036

26 

A O Shittu D O Kolawole Ear Oyedepo A study of wound infections in two health institutions in ile-ife NigeriaAfr J Biomed Res2002597102

27 

Sukumar Nirmala Rajesh Sengodan Aerobic Bacterial Isolates and their Antibiotic Susceptibility Pattern from Pus Samples in a Tertiary Care Government Hospital in Tamilnadu, IndiaInt J Curr Microbiol App Sci20176642342



jats-html.xsl


This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

  • Article highlights
  • Article tables
  • Article images

View Article

PDF File   Full Text Article


Copyright permission

Get article permission for commercial use

Downlaod

PDF File   XML File  


Digital Object Identifier (DOI)

Article DOI

https://doi.org/10.18231/j.ijmr.2020.010


Article Metrics






Article Access statistics

Viewed: 15786

PDF Downloaded: 2970