Get Permission Kaarthiga S, Bhavana, Mahantesh, and Yadukul S: Study on prevalence of Vancomycin Resistant Enterococcus and high level Gentamicin resistance among Enterococcus isolates in a Pediatric tertiary care hospital


Introduction

Enterococcus spp are present as commensals mainly in the gastrointestinal tract in humans. They can also survive in environment, also in adverse environmental conditions like drying and high temperature to a certain extent. They are known to cause infections like urinary tract infections, wound infection and also blood stream infections primarily in debilitated patients. Enterococci are intrinsically resistant to many of the commonly used antibiotics, hence there are only a limited groups of antibiotics effective against Enterococci.1 Resistance to fluoroquinolones and high level Gentamicin(HLG) has become common among Enterococcus. So, Vancomycin is the main drug of choice for treating systemic infections. Emergence of Vancomycin Resistant Enterococcus (VRE) has possessed a greater threat in its treatment.2 VRE is also a potent nosocomial pathogen.1, 2 Surveillance for VRE becomes very important to prevent its cross infection.3

Objective of the study is to look for the prevalence of Vancomycin resistance and HLG resistance among Enterococcus isolates in our institute .

Materials and Methods

The study was conducted from Jan 2018- May 2020 in pediatric patients aged between 1 day- 18 years, in Department of Microbiology, in a Pediatric tertiary care hospital.

Non repetitive isolates of Enterococcus species from various samples were included in the study identified by Gram’s stain of the colonies which were Gram positive diplococci, grown on 5 % Sheep blood agar which were about 1 mm and non hemolytic or alpha hemolytic, and minute Lactose fermenting colonies from Mac Conkey agar, after 24- 48 hrs of incubation at 370C. Further identification was done by catalase test, where Enterococcus are catalase negative; Bile aesculin hydrolysis and heat tolerance test.4, 5 Further Antibiotic Susceptibility (AST) was tested for Penicillin (10 units), Ciprofloxacin (5μg), Levofloxacin (5μg), High level Gentamicin (120μg), Vancomycin (30μg) and Linezolid (30μg); Nitrofurantoin (300μg) was included for urine isolates. AST was done by Kirby Bauer Disk diffusion method on cation adjusted Muller Hinton Agar. CLSI guidelines were followed for interpretation of the zones.6 Vancomycin resistance was confirmed by Vitek 2 compact.

Results

A total of 310 Enterococcus spp was isolated between Jan 2018- May 2020 from pediatric patients aged between 1 day- 18 years and from various samples in Department of Microbiology, in a Pediatric tertiary care hospital. Among 310 isolates, 206 (66.5%) isolates were Enterococcus faecalis, 104(33.5%) isolates were Enterococcus spp including Enterococcus faecium. Most of the isolates were from urine (68%) followed by pus (16%) and blood (14%), 6(2%) isolates were from body fluids. 61.6% of isolates were from male and 39.4% were from female patients. 25% of the isolates were from Pediatric ICU, from Pediatric Surgery department 20%, Neonatal ICU (14%) and Pediatric Medicine department(13%), 9% of isolates were from Out patient Department. Antibiotic susceptibility, most of the isolates were resistant to Penicillin (90%), Ciprofloxacin (81%). High Level Gentamycin (HLG) resistance was seen in 69% of the isolates. 34% of the isolates were sensitive to Levofloxacin, 90.6 % of isolates were sensitive to Vancomycin, all the isolates were sensitive to Linezolid. 90.5% of the urine isolates were sensitive to Nitrofurantoin.

Vancomycin resistance was seen in 29(9.4%) isolates(VRE), most of the VRE isolates were resistant to Penicillin (100%), Ciprofloxacin (90%), Levofloxacin (86%) and HLG (79%), all of them were sensitive to Linezolid. 17 of the isolates were from urine sample (59%), and 15(88%) of the urine VRE isolates were sensitive to Nitrofurantoin. From Pus sample 7(25%) and from blood 5 (17%) VRE were isolated. 90% (26/29) of the VRE isolates were isolated from nosocomial infections. 14% (4/29) of VRE isolates were from Central line associated blood stream infection (CLABSI), all the urine VRE isolates were from Catheter associated urinary tract infections (CAUTI), 17% (5/29) of the VRE isolates were from Surgical site infections (SSI). Most of the VRE isolates were Enterococcus faecalis (58%), the rest were Enterococcus faecium and other Enterococcous spp.

Table 1

Sample wise distribution of Enterococcal isolates.

Sample E. faecalis E.faecium+ other Enterococcus spp Total
Urine 150 61 211 (68%)
Pus 27 24 51(16%)
Blood 26 16 42 (14%)
Body fluids 3 3 6 (2%)
Total 206(66.5%) 104 (33.5%) 310

Table 2

Antibiotic sensitivity of the Enterococcal isolates.

Antibiotic S R I
Penicillin 32 (10%) 278 (90%) 0
Ciprofloxacin 54 (17%) 252 (81%) 4(2%)
Levofloxacin 106 (34%) 203 (65.5%) 1(0.5%)
HLG 95(31%) 215 (69%) 0
Linezolid 310 (100%) 0 0
Vancomycin 281(90.6%) 29(9.4%) 0
Nitrofurantoin (urine isolates) 191(90.5%) 16 (7.5%) 4(2%)

Table 3

Percentage of VRE isolated out of 310 Enterococcus isolates from various samples

Sample VRE(E. faecalis) VRE(E.faecium+ other Enterococcus spp) Total VRE
Urine 11 6 17(5.4 %)
Pus 3 4 7 (3%)
Blood 3 2 5 (2%)
Total 17 (5.4%) 12 (4%) 29 (9.4%)

Table 4

Antibiotic sensitivity of VRE isolates

Antibiotic S R I
Penicillin 0 29 (100%) 0
Ciprofloxacin 2 (7%) 26 (90%) 1(3%)
Levofloxacin 4 (14%) 25 (86%) 0
HLG 6 (21%) 23 (79%) 0
Linezolid 29 (100%) 0 0
Nitrofurantoin (urine isolates) 15(88%) 2 (12%) 0

Table 5

VRE isolated from Nosocomical infections

VRE (n=29) NICU PICU Total
CLABSI 2(7%) 2(7%) 4(14%)
CAUTI 1(3%) 16(56%) 17(59%)
SSI 5(17%) 5(17%)
Total 7(24%) 18(62%) 26(90%)

Discussion

The prevalance of VRE in the present study was 9.4%. High Level Gentamycin (HLG) resistance among Enterococcus was 69%. Similar results were seen in many of the studies in India, Banerjee T et al in their study conducted from September 2010 to March 2014 in Varanasi, prevalance of VRE was 7.09%, HLG resistance was seen in 47.41% of the Enterococcus isolates.7 Sachan.S et.al, in their study in Uttarakhand during November 2013 to October 2015 observed High-level gentamicin (HLG) and vancomycin resistance among 55.57% and 6.01% of enterococcal isolates, respectively.2 Khanal LK et.al, in their study in Khanpur during November 2017 to May 2018 had 12% prevalence of VRE , and HLG resistance was seen in 60% of the Enterococcal isolates.3 Hathiwala R et.al, in their study in Chhattisgarh HLAR were seen in 58% and VRE in their study was only 1.6% and all were identified as E. faecium.1 Manimala E et al, in their study in Tirunelveli, Tamil Nadu from April 2017 to May 2018 had a prevalance of 4% of VRE in their center, HLG resistance was seen in 50% of their samples.8

The present result is comparable with the other similar studies taken up in India with few studies showing low prevalence, probable reasons being their location or shorter study duration.

VRE is challenging as a nosocomial pathogen because of its rapid spread, better survival in environment and limited option for treatment. It is also capable of transferring the resistance genes to other organisms. It has also been observed that there is high mortality associated with VRE infections. Hence surveillance and immediate hospital infection control measures on detecting VRE becomes more important for preventing its nosocomial infection.1, 2

Conclusion

Nosocomial infection with VRE has been increasing and treatment options for VRE is also limited. So, prompt detection, treatment and hospital infection control measures for VRE is utmost important to prevent it from causing HAI.

Further study of interest will be taken up; detection of Vancomycin resistance genes (Van A and Van B) in the VRE isolates.

Source of Funding

None.

Conflict of Interest

None.

References

1 

R Hathiwala A B Wankhade P Dhandale N J Bankar Antibiogram Study of Clinical Isolates of Enterococcus in a Tertiary Care Teaching HospitalNational J Lab Med201873MO015

2 

V Rawat S Sachan Umesh M Kumar T Kaur P Chaturvedi Susceptibility pattern of enterococci at tertiary care hospitalJ Global Infect Dis201792735

3 

L K Khanal A Bhatiani R Sujatha Prevalence of high level aminoglycoside and vancomycin resistance among Enterococci at a tertiary care hospital in Kanpur (India)Int J Health Sci Res201888625

4 

Streptococcus, Enterococcus, and Similar Organisms. In Catalase positive, gram positive cocci. Tille P.M. Bailey and Scott’s Diagnostic Microbiology13th Edn.St Louis, Missouri: Elsevier Mosby201424764

5 

W Winn S Allen W Janda Gram-Positive Cocci Part II: Streptococci, Enterococci, and the “Streptococcus- Like” BacteriaKoneman’s color atlas & textbook of microbiology7th Edn.Philadelphia: Lippincotts Williams & Wilkins2017733843

6 

CLSI. Performance standards for antimicrobial susceptibility testingCLSI supplement M10030th Edn.Wayne, PA: Clinical and Laboratory Standards Institute2020

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T Banerjee S Anupurba Prevalence of Virulence Factors and Drug Resistance in Clinical Isolates of Enterococci: A Study from North IndiaJ Pathogens2015201517

8 

E. Manimala I.M. Rejitha C. Revathy Detection of Vancomycin Resistant Enterococci in Various Clinical Sample Isolates from a Tertiary Care CentreInt J Curr Microbiol App Sci 201980291521



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