|Year : 2018 | Volume
| Issue : 1 | Page : 14-18
The emergence of Mupirocin resistance among the clinical isolates of Staphylococci in a rural tertiary health-care centre of South India
Vijaya Shivanna, R Nanda Kumar, D Venkatesha
Department of Microbiology, AIMS, B.G. Nagar, Karnataka, India
|Date of Web Publication||4-Jul-2018|
Dr. Vijaya Shivanna
Department of Microbiology, AIMS, B.G. Nagar - 571 448, Karnataka
Source of Support: None, Conflict of Interest: None
INTRODUCTION: Mupirocin is mainly used for decolonisation of Methicillin-resistant Staphylococcus aureus among patients and health-care workers. However resistance originates from coagulase negative staphylococci (CoNS) and spreads to S. aureus by horizontal gene transfer. Hence, the present study was done to determine the overall prevalence of high- and low-level Mupirocin resistance among S. aureus and CoNS and correlate with the occurrence of Methicillin and inducible Clindamycin resistance.
MATERIALS AND METHODS: A total of 100 consecutive, non-repetitive, clinical isolates of Staphylococci were obtained from various samples in a rural tertiary care hospital of Karnataka between August and September 2016. Antibiotic susceptibility testing was done according to the Clinical and Laboratory Standards Institute (M100-S25, 2015) guidelines. Low- and high-level Mupirocin resistance was screened using 5 μg and 200 μg discs, respectively.
RESULTS: Of 100 staphylococcal isolates, high-level Mupirocin resistance (MupRH) was detected in 13 isolates and low-level Mupirocin resistance (MupRL) was found in 4 isolates. Of 13 HLMR isolates, majority were CoNS (12 out of 13, 92.31%). Even in LLMR isolates, 75% (3 out of 4) were CoNS. All the HLMR and LLMR isolates were Methicillin resistant (P < 0.05).
CONCLUSION: High prevalence of Mupirocin resistance was found in the present study. Hence, screening for Mupirocin resistance should be routinely done and the drug must be used judiciously.
Keywords: High-level Mupirocin resistance, inducible Clindamycin resistance, low-level Mupirocin resistance, Methicillin resistance, Staphylococci
|How to cite this article:|
Shivanna V, Kumar R N, Venkatesha D. The emergence of Mupirocin resistance among the clinical isolates of Staphylococci in a rural tertiary health-care centre of South India. J Acad Clin Microbiol 2018;20:14-8
|How to cite this URL:|
Shivanna V, Kumar R N, Venkatesha D. The emergence of Mupirocin resistance among the clinical isolates of Staphylococci in a rural tertiary health-care centre of South India. J Acad Clin Microbiol [serial online] 2018 [cited 2019 Mar 26];20:14-8. Available from: http://www.jacmjournal.org/text.asp?2018/20/1/14/235917
| Introduction|| |
Mupirocin (pseudomonic acid A) is one of the structurally related antibiotics of pseudomonic acids A, B, C and D. It is an analogue of amino acid isoleucine and it is derived from Pseudomonas fluorescens. The mechanism of its action is by inhibition of protein synthesis by competing with isoleucine-transfer RNA (tRNA) synthetase (IleS). Thus, preventing the formation of isoleucyl tRNA halts the incorporation of isoleucine into the nascent polypeptide chain. As Mupirocin is preferentially active against Gram-positive organisms, it is widely used as a topical antibiotic to treat Staphylococcus aureus infection and for decolonisation. Irrational usage and over-the-counter availability has led to the development of resistance to this drug.
Mupirocin susceptibility is categorised into three types:
- Mupirocin susceptible with minimum inhibitory concentration (MIC) of <4 μg/ml [Mup S]
- Low-level Mupirocin resistance (Mup RL) with MIC of >8–256 μg/ml
- High-level Mupirocin resistance (Mup RH) with MIC of >512 μg/ml.
The resistance can be detected by Kirby–Bauer disc diffusion method, but dilution method is considered the gold standard for the determination of Mupirocin resistance levels.
The high-level Mupirocin resistance is associated with Methicillin-resistant S. aureus (MRSA) decolonisation failure. In low-level Mupirocin resistance, eradication occurs initially but recolonisation is frequent. Most isolates with high-level Mupirocin resistance have acquired plasmid-mediated mup A, which encodes a novel isoleucyl RNA synthetase. Isolates with low-level Mupirocin resistance usually have acquired base changes (point mutation) in the native isoleucyl RNA synthetase gene IleS.
Plasmids carrying mup A were detected in all major circulating MRSA clones, suggesting inter-clonal transfer of these plasmids. Intra-species transfer of mup A between Staphylococcus epidermidis and S. aureus occurs during Mupirocin prophylaxis. Hence, Mupirocin resistance in coagulase-negative Staphylococci (CoNS) may serve as a source for resistance in S. aureus. Studies regarding the overall prevalence of Mupirocin resistance among staphylococcal isolates are few globally. Hence, the present study was conducted to determine the overall prevalence of Mupirocin resistance among the clinical isolates of S. aureus and CoNS. And also, correlation of Mupirocin resistance with Methicillin and inducible Clindamycin resistance was evaluated.
| Materials and Methods|| |
Source of data
This prospective study was conducted at the Department of Microbiology, Adichunchanagiri Institute of Medical sciences, a 1000-bedded tertiary health-care centre, B. G. Nagara, Karnataka, for a period of 2 months in August and September 2016. The institutional ethical committee clearance was obtained to conduct the study (IEC reference number-AIMS/IEC/412/2016-17, dated 10/06/2016).
Collection of bacterial isolates
A total of 100 consecutive, non-repetitive, clinical isolates of S. aureus and CoNS obtained from various samples such as pus, urine and blood were included in the study. Of 100 patients, 64 were male and 36 were female. Majority of the isolates were from inpatients (65), and the rest were from outpatients (35). Of these 100 isolates, 8 were from neonates, 8 from infants, 14 from age group 2–20 years, 30 in age group 21–40 years, 25 from 41–60 years' age group and 15 were above 60 years. The isolates were identified as S. aureus and CoNS by the standard laboratory techniques. The pathogenic role of CoNS was established by repeated isolation of same species on two different occasions.
Antibiotic susceptibility testing
The antibiotic susceptibility testing was done by Clinical and Laboratory Standards Institute (CLSI, M100-S25, 2015) recommended Kirby-Bauer disc diffusion method. The test was done on Meuller Hinton agar with the following discs obtained from Himedia, Mumbai: Penicillin (10 units), Co-trimoxazole (1.25/23.75 μg), Gentamicin (10 μg), Ciprofloxacin (5 μg), Amoxicillin-Clavulanic acid (20/10 μg), Tetracycline (30 μg), Vancomycin (30 μg), Teicoplanin (30 μg), and Linezolid (30 μg). Quality control was achieved using S. aureus (ATCC 25923). Inducible and Constitutive Clindamycin resistance (iMLSB and cMLSB) was determined by placing Erythromycin (15 μg) and Clindamycin (2 μg) discs 15 mm apart. Methicillin resistance was detected by Cefoxitin disc (30 μg) along with routine sensitivity testing.
Detection of Mupirocin resistance by disc diffusion
Mupirocin discs (5 μg and 200 μg) were purchased from Himedia Laboratories Pvt., Ltd., (Mumbai, India). Both the discs were included in the routine sensitivity testing and plates were incubated for 24 h at 35°C + 2°C. The zone diameters were carefully examined with transmitted light for any light growth within the zone of inhibition. Isolates with no zone of inhibition were interpreted as Mupirocin resistant. Isolate resistant to 5 μg disc and any zone for 200 μg disc was considered Mup RL. Isolates resistant for both the discs were considered high-level Mupirocin resistant [Figure 1], [Figure 2], [Figure 3].
Statistical analysis was done using Microsoft excel. The data analysis involved transcription, preliminary data inspection, content analysis and interpretation. Percentages were used in this study to analyse variables. Chi-square test was done to determine the statistical significance. P < 0.05 was considered statistically significant.
| Results|| |
A total of 100 consecutive, non-duplicate Staphylococcus isolates (41 S. aureus and 59 CoNS) were included in the study. Among the 100 Staphylococcus clinical isolates, majority were obtained from pus (46), followed by blood (31), urine (15), high vaginal swab (3), body fluids (2), throat swab (3), sputum (1) and drain tip from abdominal mesh (1).
MRSA was found in 19 (46.34%) isolates. MRCoNS was detected in 52 (88.14%) isolates. Overall, the total Methicillin resistance was 71% among staphylococcal isolates.
Of 100 staphylococcal isolates, 26 showed constitutive Clindamycin resistance (cMLSB) and 7 isolates were inducible Clindamycin resistant (iMLSB).
High-level Mupirocin resistance (Mup RH) was detected in 13 isolates and low-level Mupirocin resistance (Mup RL) was seen in 4 isolates. Of the 13 Mup RH isolates, 9 (69.23%) were from blood and rest 4 were from pus (1), urine (1), and high vaginal swab (1). Among these three were from Neonatal Intensive Care Unit (NICU), eight from inpatient department (IPD) and two from outpatient department (OPD).
Among the four Mup RL, 2 (50%) from pus and 1 each (25% each) from blood and urine. Out of four Mup RL isolates, two were from IPD and two from OPD.
Mup RH was most commonly observed in age group <1 year (5, 38.46%) and 20–40 years age group (4, 30.77%). But, Mup RL was seen in all age groups except in 1–20 years.
[Table 1] shows the distribution of Mupirocin and Methicillin resistance among S. aureus and CoNS. All the 4 Mup RL and 13 Mup RH isolates were Methicillin resistant, which is statistically significant (P < 0.05).
|Table 1: Distribution of Mupirocin and Methicillin resistance among Staphylococcus aureus and coagulase-negative Staphylococci|
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None of the Mup R isolates were associated with inducible Clindamycin resistance (iMLSB).
[Table 2] shows the Comparison of antibiotic susceptibility with Mupirocin suceptibility. Out of 13 Mup RH, 11 were multidrug resistant (>3 non-β-lactam antibiotics). All the 4 Mup RL isolates were multidrug resistant.
|Table 2: Comparison of Mupirocin resistance from various studies from India|
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| Discussion|| |
Mupirocin use can increase resistance through enhanced antibiotic pressure, more effectively selecting Mupirocin-resistant strains, and through facilitating cross-transmission. Emergence of Mupirocin resistance following the increased use has been reported extensively, though not consistently and previous exposure has been identified as a risk factor for Mupirocin resistance in MRSA. Moreover, reducing Mupirocin use was associated with lower Mupirocin resistance levels over time.
In the present study, the prevalence of MRSA and MRCoNS was 46.34% and 88.14%, respectively. However, in other studies,, conducted in South India with similar study cohort, the prevalence rates were much lower. The prevalence of Methicillin resistance varies from place to place and also depends on local antibiotic policy, infection control strategies, duration of study, number of samples and biological characteristics of staphylococcal strains.
In this study, Mup RH was seen in 13 isolates, whereas Mup RL was seen in 4 isolates. This is higher than those observed in other studies.,,,, But, Rudresh et al. found a higher prevalence of Mup RL (14.7%). This is attributed to over-the-counter availability of Mupirocin in community settings and more frequent usage in general population for skin infections than for eradicating carriage or treating MRSA outbreaks. This increased usage of Mupirocin has led to the development of resistance.
We report an increase in the frequency of high-level Mupirocin resistance in Staphylococci compared to other studies done in India [Table 3].
|Table 3: Comparison of Mupirocin resistance from various studies from India|
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Majority of the Mup RH isolates (9 out of 13, i.e., 69.23%) were from blood which correlated with the report of Desroches et al. Among the overall Mupirocin-resistant isolates, majority were from IPD and NICU (13/17) than OPD, which was similar to other reports.,
In our setting, Mupirocin resistance was more common in CoNS (15/17) compared to S. aureus (2/17). There are not many studies documenting Mupirocin resistance in CoNS, which may be the reservoir of Mupirocin-resistant genes. The presence of comparatively higher rates of Mupirocin resistance in CoNS is also a cause for concern. Studies suggest that mupA gene which is known to code for mupirocin resistance can be transferred from S. epidermidis to MRSA during Mupirocin prophylaxis, which could be an important threat to the future use of Mupirocin against MRSA.
In our hospital, both high-level and low-level Mupirocin-resistant isolates were Methicillin resistant, which is statistically significant (P < 0.05). These results suggest that Mupirocin resistance may be linked to a MRSA epidemic in the hospital.
Our study showed no correlation between the existence of inducible Clindamycin resistance and Mupirocin resistance, as none of the Mupirocin-resistant isolates showed inducible Clindamycin resistance. This was in contrast to the observations of Abimanyu et al. and Rudresh et al.
High-level Mupirocin-resistant S. aureus were more likely to be susceptible to Cotrimoxazole, Gentamycin and Tetracycline. They were more likely to be resistant to Penicillin and Amoxicillin-Clavulanic acid. All the isolates were sensitive to Vancomycin, Teicoplanin and Linezolid. Hence, the judicial use of these antibiotics is a must.
The Mup RH CoNS showed decreased susceptibility to Penicillin, Amoxicillin-Clavulanic acid, Ciprofloxacin, Erythromycin and Clindamycin. The co-occurrence of Mupirocin resistance and resistance to other antibiotics may indicate the organism carrying plasmid with multiple resistance genes.
In the present study, a strong association of Mup RH with resistance to >3 non-β-lactam antimicrobial classes (multidrug resistance) in Staphylococci was observed, which was in agreement with the findings of Cadilla et al.
Our study defines the overall Mupirocin resistance rates among Staphylococcus species, while most of the previous studies have focused only on Mupirocin resistance in MRSA outbreaks. Since ours is a tertiary care hospital catering to the patients from different geographical areas, the information we report may also apply to other hospitals, where data are lacking.
The limitation of this study was relatively small sample size, since it is a short-term research project. Also, speciation of CoNS, MIC and gene detection for Mupirocin-resistant isolates were not done due to technical and financial constraints.
| Conclusion|| |
The increasing prevalence rates of Mupirocin resistance leads to loss of the major treatment option in MRSA carriers. Hence, Mupirocin must be used cautiously. Hence, a Mupirocin stewardship programme should be developed to monitor resistance in both S. aureus and CoNS, as CoNS is a huge reservoir of mupA gene capable of transferring resistance to other species of Staphylococci. Infection control and antibiotic policies have to be developed, audited and reviewed regularly. In addition, Mupirocin-resistant strains may be treated with other alternatives such as Chlorhexidine, Neomycin, Fusidic acid and newer agents such as Retapamulin.
Our sincere thanks to Indian Council of Medical Research (ICMR) for supporting this study as a short-term research project. We also thank Miss Manjula and Miss Anusha for their technical assistance.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2], [Table 3]