International Journal of Medical and Pharmaceutical Research
2026, Volume-7, Issue 3 : 1092-1097
Research Article
Aerobic Bacterial Profile and Antibiogram of Pus Isolates: A Six-Month Retrospective Study in a Tertiary Care Teaching Hospital, Krishnagiri, Tamil Nadu
 ,
 ,
 ,
Received
April 21, 2026
Accepted
May 1, 2026
Published
May 22, 2026
Abstract

Background: Wound infections contribute significantly to morbidity and involve diverse bacterial pathogens. Identification of causative organisms and their antimicrobial susceptibility patterns is essential for effective treatment and control of antimicrobial resistance.

Objective: To determine the aerobic bacterial profile and antibiogram of pus isolates in a tertiary care teaching hospital.

Materials and Methods: This retrospective study was conducted in the Department of Microbiology from January to June 2025. All pus and wound specimens received for aerobic culture were included. Bacterial identification was performed using standard microbiological methods, and antimicrobial susceptibility testing was carried out using the VITEK 2 Compact system. Results were interpreted according to Clinical and Laboratory Standards Institute (CLSI) 2025 guidelines.

Results: Out of 333 pus and wound specimens processed, 223 (67.0%) were culture positive. Among these, 198 (88.8%) were pathogenic isolates and 25 (11.2%) were commensals. Gram-negative bacilli predominated (162; 81.8%) over Gram-positive cocci (36; 18.2%). Among Gram-positive cocci, Staphylococcus aureus was the most common isolate (30; 15.2%), followed by Enterococcus spp. (6; 3.0%). Among Gram-negative bacilli, the predominant isolates were Escherichia coli (52; 26.3%), Klebsiella pneumoniae (30; 15.2%), Proteus spp. (17; 8.6%), Pseudomonas spp. (16; 8.1%), and Acinetobacter baumannii complex (15; 7.6%). Other Gram-negative isolates included Enterobacter cloacae complex (12; 6.1%), Morganella spp., Providencia spp., and Serratia spp. (8; 4.0%), Citrobacter spp. (5; 2.5%), and Burkholderia spp. (2; 1.0%). Resistance included methicillin-resistant Staphylococcus aureus (18/30; 60%), carbapenem-resistant E. coli (9/52; 17.3%), and multidrug-resistant K. pneumoniae (18/30; 60%). Gram-positive isolates showed high susceptibility to vancomycin, teicoplanin, linezolid, and tigecycline, while Gram-negative isolates were more susceptible to carbapenems, amikacin, and fosfomycin.

Conclusion: Gram-negative bacilli predominated, with a considerable burden of multidrug-resistant organisms. Continuous surveillance of local bacterial profiles and antibiogram patterns is essential to guide empirical therapy and strengthen antimicrobial stewardship.

Keywords
INTRODUCTION

Wound infections are a significant cause of morbidity and are associated with delayed healing and prolonged hospitalization, particularly in developing countries [1]. They commonly occur following surgical procedures, trauma, and burns, and are frequently influenced by underlying comorbid conditions. These infections are caused by a wide range of aerobic bacterial pathogens, including Gram-positive cocci and Gram-negative bacilli [2].

 

The increasing burden of antimicrobial resistance (AMR) among wound pathogens poses a major challenge to effective treatment and infection control [3]. Inappropriate and empirical antibiotic use has contributed to the emergence of multidrug-resistant (MDR) organisms, resulting in therapeutic failure, increased healthcare costs, and poor clinical outcomes [4]. Therefore, continuous surveillance of the local bacterial spectrum and antimicrobial susceptibility patterns is essential for guiding empirical therapy and improving patient care [5].

 

Studies from Tamil Nadu and other regions of South India have reported a predominance of Gram-negative bacilli in wound infections, with Escherichia coli and Klebsiella pneumoniae being frequently isolated [6,7]. In addition, the increasing prevalence of methicillin-resistant Staphylococcus aureus (MRSA) and carbapenem-resistant Enterobacteriaceae has further complicated the management of wound infections [8,11].

 

Hence, the present study was undertaken to determine the aerobic bacterial profile and antimicrobial susceptibility pattern of pus isolates in a tertiary care teaching hospital in Krishnagiri, Tamil Nadu.

 

MATERIALS AND METHODS

Study Design and Setting

This retrospective study was conducted in the Department of Microbiology of a tertiary care teaching hospital in Krishnagiri, Tamil Nadu, over a period of six- months (January to June 2025).

 

Study Population

All pus and wound specimens received for aerobic bacterial culture during the study period were included. Duplicate samples from the same patient and improperly collected specimens were excluded.

 

Figure 1: Workflow of Bacteriological Processing and Antimicrobial Susceptibility Testing of Pus/Wound Specimens

 

Data Analysis

Data were entered into Microsoft Excel and analyzed using descriptive statistics. Results were expressed as frequencies and percentages.

 

RESULTS

During the study period (January–June 2025), a total of 333 pus and wound swab specimens were received for aerobic culture and sensitivity testing. Out of these, 223 (67.0%) specimens yielded bacterial growth, while 110 (33.0%) showed no growth.

 

Figure 2: Distribution of Pathogenic and Commensal Isolates among Culture-Positive Samples (n=223)

 

Among the culture-positive specimens, 198 (88.8%) isolates were identified as pathogenic organisms, whereas 25 (11.2%) were reported as commensal isolates.

 

Table 1: Distribution of Aerobic Bacterial Pathogens Isolated from Pus/Wound Specimens (n = 198)

Gram Reaction

Organism

Number (n)

Percentage (%)

Gram-positive cocci (n = 36)

Staphylococcus aureus

30

15.2

 

Enterococcus spp.

6

3.0

 

Total GPC

36

18.2

Gram-negative bacilli (n = 162)

Escherichia coli

52

26.3

 

Klebsiella pneumoniae

30

15.2

 

Proteus spp.

17

8.6

 

Pseudomonas spp.

16

8.1

 

Acinetobacter baumannii complex

15

7.6

 

Enterobacter cloacae complex

12

6.1

 

Morganella spp./Providencia spp./Serratia spp.

8

4.0

 

Citrobacter spp.

5

2.5

 

Burkholderia spp.

2

1.0

 

Total GNB

162

81.8

Total pathogenic isolates

 

198

100

Note: Percentages are calculated out of total pathogenic isolates (n = 198).

 

A total of 198 pathogenic isolates were analyzed for bacterial distribution and antibiogram. Gram-negative bacilli (162; 81.8%) predominated over Gram-positive cocci (36; 18.2%).

 

Among Gram-positive cocci, Staphylococcus aureus was the most common isolate (30; 15.2%), followed by Enterococcus spp. (6; 3.0%).

 

Among Gram-negative bacilli, the most frequently isolated organism was Escherichia coli (52; 26.3%), followed by Klebsiella pneumoniae (30; 15.2%), Proteus spp. (17; 8.6%), Pseudomonas spp. (16; 8.1%), and Acinetobacter baumannii complex (15; 7.6%). Other isolates included Enterobacter cloacae complex (12; 6.1%), Morganella spp./Providencia spp./Serratia spp. (8; 4.0%), Citrobacter spp. (5; 2.5%), and Burkholderia spp. (2; 1.0%).

 

Table 2: Antibiotic susceptibility pattern of Gram-positive cocci isolates

Antibiotic

Staphylococcus spp. (n=30) Sensitive n (%)

Enterococcus spp. (n=6) Sensitive n (%)

Cefoxitin (MRSA marker)

11 (36.7)

Clindamycin

19 (63.3)

Erythromycin

13 (43.3)

1 (16.7)

Gentamicin / High-level Gentamicin

19 (63.3)

3 (50.0)

Ciprofloxacin

3 (10.0)

1 (16.7)

Levofloxacin

4 (13.3)

1 (16.7)

Linezolid

25 (83.3)

6 (100)

Vancomycin

30 (100)

6 (100)

Teicoplanin

30 (100)

6 (100)

Note: Data expressed as number sensitive (%). MRSA prevalence among Staphylococcus isolates = 18/30 (60%). (—) not tested / not applicable.

 

Table 3: Antibiotic susceptibility pattern of Gram-negative bacilli isolates

Antibiotic

E. coli (n=52)

K. pneumoniae (n=30)

Citrobacter spp. (n=5)

Enterobacter spp. (n=12)

Proteus spp. (n=17)

Morganella/Serratia/Providencia (n=8)

P. aeruginosa (n=16)

A. baumannii (n=15)

Amikacin

45 (87%)

10 (33%)

5 (100%)

10 (83%)

15 (88%)

8 (100%)

13 (81%)

1 (7%)

Gentamicin

29 (56%)

10 (33%)

4 (80%)

6 (50%)

13 (76%)

5 (63%)

11 (69%)

1 (7%)

Ciprofloxacin

0 (0%)

5 (17%)

3 (60%)

4 (33%)

2 (12%)

0 (0%)

2 (13%)

1 (7%)

Levofloxacin

42 (80%)

9 (30%)

3 (60%)

3 (25%)

4 (25%)

3 (60%)

13 (81%)

2 (13%)

Piperacillin/Tazobactam

24 (46%)

7 (23%)

0 (0%)

0 (0%)

15 (88%)

5 (63%)

8 (50%)

1 (7%)

Cefepime

9 (17%)

6 (20%)

5 (100%)

6 (50%)

10 (59%)

4 (50%)

12 (75%)

1 (7%)

Imipenem

43 (83%)

7 (23%)

5 (100%)

9 (75%)

3 (25%)

1 (13%)

8 (50%)

1 (7%)

Meropenem

29 (56%)

10 (33%)

5 (100%)

11 (92%)

4 (25%)

0 (0%)

12 (75%)

1 (7%)

Colistin

0 (0%)

0 (0%)

5 (100%)

0 (0%)

0 (0%)

0 (0%)

0 (0%)

0 (0%)

Tigecycline

51 (98%)

28 (93%)

0 (0%)

0 (0%)

0 (0%)

1 (13%)

0 (0%)

8 (100%)

 

Table 4: Major Resistance Patterns Observed among Common Pathogens

Organism

Resistance Pattern

Resistant isolates / Total isolates

Percentage (%)

Staphylococcus aureus

MRSA

18 / 30

60.0

Escherichia coli

Carbapenem-resistant (CRE)

9 / 52

17.3

Klebsiella pneumoniae

Multidrug-resistant (MDR)

18 / 30

60.0

Note: MRSA – Methicillin-resistant Staphylococcus aureus; CRE – Carbapenem-resistant Enterobacterales; MDR – Multidrug-resistant.

 

Regarding resistance patterns, methicillin-resistant Staphylococcus aureus (MRSA) accounted for 60% (18/30) of S. aureus isolates. Carbapenem resistance in E. coli was noted in 17.3% (9/52) isolates. Additionally, multidrug resistance in Klebsiella pneumoniae was observed in 60% (18/30) isolates. Gram-positive isolates showed high susceptibility to vancomycin, teicoplanin, linezolid, and tigecycline, whereas Gram-negative isolates demonstrated better susceptibility to carbapenems, amikacin, and fosfomycin.

 

DISCUSSION

In the present study, pus and wound infections were predominantly caused by Gram-negative bacilli, particularly the Enterobacterales, which is consistent with observations from Tamil Nadu and other Indian settings reporting a shift towards Gram-negative pathogens in wound infections [6,7]. The predominance of Escherichia coli and Klebsiella pneumoniae highlights their major contribution to wound and postoperative infections. This shift towards Gram-negative pathogens may be linked to increasing healthcare-associated infections and selective antibiotic pressure.

 

A notable finding was the high proportion of methicillin-resistant Staphylococcus aureus (MRSA) (60%). MRSA remains a major cause of skin and soft tissue infections globally and is associated with limited treatment options and increased morbidity [8]. In this study, vancomycin, teicoplanin, and linezolid retained excellent activity against Gram-positive cocci, supporting their continued usefulness in managing serious MRSA-associated infections [9].

 

The detection of carbapenem-resistant E. coli and multidrug-resistant K. pneumoniae is of significant concern, as these organisms severely restrict therapeutic choices and may contribute to treatment failure. Similar resistance trends have been reported in Indian surveillance data, reflecting the growing burden of resistant Enterobacterales [5]. The global rise of antimicrobial resistance, as highlighted by WHO, is strongly influenced by inappropriate antibiotic use and inadequate infection prevention measures [3,4].

 

Overall, the findings of this study emphasize the need for routine culture and susceptibility testing, continuous monitoring of local antibiogram patterns, and strict implementation of antimicrobial stewardship programs. Such measures are essential to guide appropriate empirical therapy, reduce the spread of multidrug-resistant organisms, and improve patient outcomes [3,5].

 

CONCLUSION

Gram-negative organisms, particularly Enterobacterales, were the most common isolates from pus and wound specimens, with a considerable proportion showing multidrug resistance. This reflects the increasing challenge in selecting effective empirical therapy for wound infections. Regular evaluation of local bacteriological trends and antibiogram data is essential to guide rational empirical treatment and to strengthen infection control and antimicrobial stewardship practices.

 

Limitations

This was a retrospective single-center study conducted over a limited duration, which may restrict generalizability. Only aerobic bacterial isolates were evaluated; anaerobic and fungal pathogens were not included, which may have led to underestimation of the true etiological agents. Clinical correlation with patient risk factors, prior antibiotic exposure, and outcomes could not be assessed. Molecular characterization of resistance mechanisms was not performed.

 

Conflict of Interest: None declared.

 

Funding: No external funding was received.

 

REFERENCES

  1. Bowler PG, Duerden BI, Armstrong DG. Wound microbiology and associated approaches to wound management. Clin Microbiol Rev. 2001;14(2):244-269.
  2. Cheesbrough M. District Laboratory Practice in Tropical Countries. 2nd ed. Cambridge: Cambridge University Press; 2006.
  3. World Health Organization. Global antimicrobial resistance and use surveillance system (GLASS) report 2023. Geneva: World Health Organization; 2023.
  4. Ventola CL. The antibiotic resistance crisis: causes and threats. P T. 2015;40(4):277-283.
  5. Indian Council of Medical Research. Antimicrobial Resistance Surveillance Network (AMRSN) annual report 2023. New Delhi: ICMR; 2023.
  6. Jalal SH, et al. Trends in antibiotic resistance among clinical isolates in rural Tamil Nadu: a prospective observational study. Open Forum Infect Dis. 2026;13(Suppl 1):P-2097.
  7. Vimala PB, et al. Clinical presentation and antibiotic resistance trends of Escherichia coli isolated from clinical samples in South India: a two-year study (2022–2023). Infect Dis Health. 2025;30(3):183-193.
  8. David MZ, Daum RS. Community-associated methicillin-resistant Staphylococcus aureus: epidemiology and clinical consequences of an emerging epidemic. Clin Microbiol Rev. 2010;23(3):616-687.
  9. Liu C, Bayer A, Cosgrove SE, et al. Clinical practice guidelines by the Infectious Diseases Society of America for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children. Clin Infect Dis. 2011;52(3):e18-e55.
  10. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing. 35th ed. Wayne (PA): CLSI; 2025.
  11. Karaiskos I, Giamarellou H. Multidrug-resistant and extensively drug-resistant Gram-negative pathogens: current and emerging therapeutic approaches. Clin Microbiol Infect. 2014;20(9):862-872.
  12. Falagas ME, Kastoris AC, Kapaskelis AM, Karageorgopoulos DE. Fosfomycin for the treatment of multidrug-resistant, including extended-spectrum β-lactamase producing, Enterobacteriaceae infections: a systematic review. Lancet Infect Dis. 2010;10(1):43-50.
Recommended Articles
Research Article Open Access
Validation Of the New Ballard Score in Term Neonates in South India– A Prospective Validational Study
2026, Volume-7, Issue 3 : 1080-1091
Research Article Open Access
Her2/Neu Immunoexpression in Primary Breast Carcinoma and its Correlation with Er/Pr Status and Various Clinicopathological Features
2026, Volume-7, Issue 3 : 1073-1079
Research Article Open Access
Ultrasonographic Comparative Study of Head Circumference In Fetuses of North Indian Women
2026, Volume-7, Issue 3 : 1058-1063
Research Article Open Access
Electrolyte Abnormalities in Diabetic Ketoacidosis and Their Clinical Implications: A Prospective Observational Study
2026, Volume-7, Issue 3 : 1064-1067
International Journal of Medical and Pharmaceutical Research journal thumbnail
Volume-7, Issue 3
Citations
6 Views
8 Downloads
Share this article
License
Copyright (c) International Journal of Medical and Pharmaceutical Research
Creative Commons Attribution License Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
All papers should be submitted electronically. All submitted manuscripts must be original work that is not under submission at another journal or under consideration for publication in another form, such as a monograph or chapter of a book. Authors of submitted papers are obligated not to submit their paper for publication elsewhere until an editorial decision is rendered on their submission. Further, authors of accepted papers are prohibited from publishing the results in other publications that appear before the paper is published in the Journal unless they receive approval for doing so from the Editor-In-Chief.
IJMPR open access articles are licensed under a Creative Commons Attribution-ShareAlike 4.0 International License. This license lets the audience to give appropriate credit, provide a link to the license, and indicate if changes were made and if they remix, transform, or build upon the material, they must distribute contributions under the same license as the original.
Logo
International Journal of Medical and Pharmaceutical Research
About Us
The International Journal of Medical and Pharmaceutical Research (IJMPR) is an EMBASE (Elsevier)–indexed, open-access journal for high-quality medical, pharmaceutical, and clinical research.
Follow Us
facebook twitter linkedin mendeley research-gate
© Copyright | International Journal of Medical and Pharmaceutical Research | All Rights Reserved