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Journal of Clinical and Diagnostic Research : JCDR logoLink to Journal of Clinical and Diagnostic Research : JCDR
. 2017 Jun 1;11(6):DC19–DC22. doi: 10.7860/JCDR/2017/25140.10140

Revisiting Nitrofurantoin for Vancomycin Resistant Enterococci

Suneeta Meena 1, Sarita mohapatra 2,, Seema Sood 3, Benu Dhawan 4, Bimal Ku Das 5, Arti Kapil 6
PMCID: PMC5535353  PMID: 28764160

Abstract

Introduction

Enterococcal infection has emerged as a major therapeutic challenge. Emergence of High Level Aminoglycoside Resistance (HLAR) and Vancomycin-Resistant Enterococcus (VRE) has further limited the drug therapy in enterococcal infections. However, nitrofuratoin being an old drug reported to have less resistance in comparison to the other classes of antimicrobial agents.

Aim

To detect susceptibility of nitrofurantoin against VRE isolates from Urinary Tract Infection (UTI) of outdoor and indoor patient departments.

Materials and Methods

An observational study was carried out at a tertiary care hospital in New Delhi over a period of six months (from November 2015 to April 2016). A total of 14,714 urine samples were collected and processed from the patients symptomatic for UTI. The enterococcal isolates were identified and confirmed by standard phenotypic tests. The antimicrobial susceptibility tests of isolated organisms were performed by Kirby-Bauer Disc Diffusion Method as per Clinical and Laboratory Standards Institute (CLSI) 2015 guidelines. The Wilcoxon rank-sum (Mann-Whitney) test was used to compare continuous variables. Chi-square or Fisher’s exact tests were used to compare categorical variables. p<0.05 was considered as significant.

Results

A total of 70 enterococci species {Enterococcus faecalis (n=9), Enterococcus faecium, (n=61)} were isolated. Twenty six out of 70 isolates were observed resistant to vancomycin. Among 26 VRE, 21(80.76%) were susceptible to nitrofurantoin. Both the species {E. faecalis (80.32%) and E. faecium (88.8%)} were uniformly susceptible to nitrofurantoin.

Conclusion

Nitrofurantoin has retained antimicrobial efficacy against emerging VRE in vitro and can be used for treatment of enterococcal urinary tract infections.

Keywords: Enterococcus faecalis, Enterococcus faecium, Linezolid, Multiple drug resistance, Urinary tract infection

Introduction

Enterococcus species constitute normal intestinal flora of human and animals; also colonize the oral cavity, genitourinary tract and skin especially in the perineal area of healthy persons. The isolation of enterococci from clinical specimens usually denotes colonization rather than infection. Nonetheless, enterococci may also cause infection most commonly UTI followed by septicaemia, endocarditis, meningitis, wound infections etc., [1]. Emergence of Vancomycin-Resistant Enterococcus (VRE) from last two decades is a major concern worldwide due to limited option for treatment. VRE remains prevalent as a nosocomial pathogen especially targeting the chronically ill and debilitated patients [2]. The genus Enterococcus includes more than 49 species, although only a few cause clinical infections in human [2]. E. faecalis and E. faecium are the most prevalent species accounting for more than 90% of infection cultured from human [3].

Enterococcus spp. possesses a major therapeutic challenge because of having both intrinsic and acquired resistance to various antibiotics. Emergence of VRE has further limited the therapy leaving only handful drugs such as linezolid, quinopristin-dalfopristin, and nitrofurantoin. The prevalence of VRE in Europe and United Kingdom (UK) varies from 1% to 30% and 20% to 30%, respectively [4]. More ever, 30% of nosocomial enterococcal infections in the United States are reported as VRE [5]. The prevalence of VRE in India has been reported to be approximately 1%–23% in various infections [6-9]. Reports of linezolid resistance is the latest disturbing conquest of this organism, which would further limit the therapy in various life-threatening infections [10]. Above all, innovation of novel antibiotics is lagging far behind. In this scenario, the judicious use of older antibiotics could represent a solution to the treatment of multidrug resistant pathogens.

Nitrofurantoin (NF) is an age old drug, has been used for more than 50 years for treatment of uncomplicated UTIs. In comparison to the other classes of antimicrobial agents, acquired resistance to NF is quite infrequent because of its complex mechanism of action [11,12]. The drug uses the flavoproteins of bacterial cell to convert into multiple intermediate forms which damages the DNA. It also inhibits carbohydrate metabolism and interfere with the cell wall synthesis. But, there is very limited data on NF activity and the risk factors associated with VRE in India. Therefore, the following study was carried out to assess the role of NF against VRE isolates from UTI.

Materials and Methods

An observational study over a period of six months (November 2015 to April 2016) was carried out at the Department of Microbiology, All India Institute of Medical Science, New Delhi, India, to find out the in vitro action of NF against VRE isolates isolated from urinary tract infection. All the culture sensitivity testing was done as a part of routine diagnostics during the outdoor visit or indoor stay of the patient for which consent of the patient is not required. The urine samples from the symptomatic patients were processed within two hours of collection on Cystine Lactose Electrolyte-Deficient (CLED) agar. Enterococcus spp. were isolated from urine specimens and identified with standard biochemical tests (growth in media containing 6.5% sodium chloride and bile-esculin hydrolysis).

Colony forming units were counted by using standard semi-quantitative methods and speciation was performed by testing for carbohydrate fermentation (mannitol, arabinose). Consecutive same organism in two or more occasions within the duration of one week in same patient was considered as single isolate. The antibiotic sensitivity pattern was determined using Muller Hilton agar by Kirby-Bauer disc diffusion method as per CLSI 2015 guidelines[13]. The antibiotics (HiMedia, India) tested were Pencillin (10 Units), Ciprofloxacin (5 μg), Nitrofurantoin (300 μg), High level Gentamicin (120 μg), Erythromycin (15 μg), Teicoplanin (30 μg), Vancomycin (30 μg) and Linezolid (30 μg). Standard strains of Staphylococcus aureus ATCC® 25923TM and E. faecalis ATCC® 29212TM were used as controls for the antibiotic susceptibility testing. For the quality control of Mueller Hinton agar to determine the appropriate thymidine content, E. faecalis ATCC® 29212TM with trimethoprim/sulfamethoxazole discs were tested.

Statistical Analysis

The Wilcoxon rank-sum (Mann-Whitney) test was used to compare continuous variables such as age of patients and length of hospital stay. Chi-square or Fisher’s-exact tests were used to compare categorical variables like sex and distribution of inpatients in ICU and wards. The p-value <0.05 was considered significant.

Results

In total 14,714 urine samples were received over a period of six months out of which 942 (6.4%) samples were culture positive. The age of the patients ranged from three months to 88 years with mean age of 42.5 years. Female patients were predominant (54.2%, n=38) in comparison to male (45.7%, n=32). Majority (90%) of the patients were adults (≥ 18-year-old) [Table/Fig-1].

[Table/Fig-1]:

[Table/Fig-1]:

Age and sex distribution of patients positive for Enterococcus spp.

Eighty nine percent of the total samples were received from hospitalised patients. Only 1% (n=16) among the samples from outdoor patient department were found culture positive showing significant bacteriuria. However, all the Enterococcus spp. was isolated from admitted patients only. Gram Negative Bacilli (GNB) were isolated predominantly in comparison to Gram Positive Cocci (GPC). Most common bacterial isolate was Escherechia coli (45.8%) followed by Pseudomonas spp.(14.7%), Klebsiella spp.(13.5%) and Enterobacter spp.(9.5%). Seventy isolates (7.4%) were identified as Enterococcus spp [Table/Fig-2].

[Table/Fig-2]:

[Table/Fig-2]:

Bacterial spectrum of various urinary isolates. Other GNB: Acinetobacter spp. Other GPC: Coagulase negative Staphylococcus

Among the enterococcal isolates, 61 (87%) were identified as E. faecium and 9 (13%) were E. faecalis. Approximately 37% (n=26) of the total Enterococcus spp. were detected as VRE.

The mean age of VRE patients were observed to be higher than Vancomycin Susceptible Enterococci (VSE) by five years.

Prolonged hospitalisation and increased length of stay in intensive care unit were observed to be important risk factors for VRE bacteriuria (p-value<0.05) [Table/Fig-3].

[Table/Fig-3]:

Comparision of demographic profile of patients with VRE and non-VRE.

Variables VRE (n=26) NoN-VRE (n=44) p-value
Mean age 48.62 38.5 0.07
Median age 55 50
Sex
Male 7 25 0.648
Female 19 19 0.548
Urinary Catheter 22 34 -
Mean length of hospital stay 46.5 26.2 0.026
Ward 18 40 -
ICU 8 4 0.045

All the isolates of enterococci were observed susceptible to linezolid (100%) [Table/Fig-4]. However, nitrofurantoin (81.4%) susceptibility also had encouraging results. Among 26 VRE isolates, 21(80.76%) were susceptible to nitrofurantoin. High Level Aminoglycoside Resistance (HLAR) was detected in 81.4% of the isolates. Resistance to vancomycin was observed higher in E. faecium (96%) than E. faecalis (4%) while there was no significant difference between two species for susceptibility towards nitrofurantoin [Table/Fig-5].

[Table/Fig-4]:

Antibiotic susceptibility pattern of Enterococcus species Pencillin (10 U), Ciprofloxacin (5 μg), Nitrofurantoin (300 μg), HLG (High Level Gentamicin) (120 μg), Erythromycin (15 μg), Teicoplanin (30 μg), Vancomycin (30 μg), Linezolid (30 μg).

Antibiotic E. faecalis (n=9) E. faecium (n=61)
Vancomycin 88% 59%
Nitrofurantoin 80.32% 88.8%
Ciprofloxacin 11.4% 22.2%
Teicoplanin 59.01% 88.8%
Erythromycin 22.2% 8.1%
Pencillin 22.2% 14.7%
Linezolid 100% 100%
HLG 33.3% 13.1%

[Table/Fig-5]:

Comparison of sensitivity rate for vancomycin and nitrofurantoin.

Parameters NF resistant isolates NF sensitive isolates Total
E. faecium E. faecalis E. faecium E. faecalis
Vancomycin Resistant 5 0 20 1 26
Vancomycin Sensitive 7 1 29 7 44
Total 12 1 49 6 70

Nitrofurantoin found to have maximum susceptibility against VRE after linezolid.

Discussion

Enterococcus spp. are one of the most common nosocomial pathogens. It is the second most leading cause of nosocomial UTI and the third most common cause of nosocomial bacteraemia in the United States. The highest rate of Enterococcus spp. causing UTI was reported from Canada (16.8%), followed by the US (12.5%) and Europe (11.7%) [14]. Incidence of UTI due to Enterococcus spp. in India varies from 0.05%-13% among different population [7,15]. Enterococci were isolated from 7% of the patients in the current study which is in concordance with previous study by Mohanty S et al., [16]. However, the distribution of species is observed to be much different. All the enterococcal isolates in the earlier study from the same institute from urine sample were E. faecalis in comparison to a drastic increase in E. faecium in the current study. This extreme microbiological shift in the historical 10:1 ratio of E. faecalis and E. faecium is in concordance with another study from north India [7] but in contrast with studies reported from other parts of India [17,18].

The incidence of VRE is 2.7% in the current study which was not present in the previous published study. The mean age for VRE patients was 10 years more than non-VRE patients but the difference was not statistically significant (p-value>0.05). Still, this is in contrast to other long duration study in which mean age for VRE patients was 62 years. In our study there was no significant correlation with sex of the patients but other studies have found female sex as predisposing factor for VRE [18]. All the enterococcal isolates were obtained from inpatients as majority of the samples (99%) were from indoor patients only. This could be attributed to increased emergence of E. faecium in the present study. Prolonged hospitalisation and admission in intensive care unit were identified as significant (p-value<0.05) risk factors for VRE bacteriuria which have been identified in other studies as well [7,19].

Incidence of high level aminoglycoside resistance was detected in 81.4% (57) of the isolates. The rate is higher than the data published in previous study but in concordance with other studies [14,17]. E. faecalis isolates were observed to be more resistant than E. faecium as reported by others [19].

The antimicrobial susceptibility rate against nitrofurantoin was 81.4% which is in concordance with other studies [15,20,21]. It showed better susceptibility pattern in comparison to high dose of gentamycin, ciprofloxacin, teicoplanin, penicillin and erythromycin for both the species and the result was in concordance with other study results [22,23]. Though, the prevalence of VRE has increased over the years but susceptibility of NF has remained the same against Enterococcus spp. A total of 21 out of 26 (80.7%) among the VRE and eight out of 40 (18%) among the Vancomycin Susceptible Enterococcus (VSE) were susceptible to NF [Table/Fig-3].

The stupendous activity of linezolid and nitrofurantoin against VRE has been previously reported also [20,21]. Moreover, there was no difference in susceptibility pattern among the two common species of enterococci i.e. E. faecalis and E. faecium which is in concordance with other studies [17,18].

The advantage of NF is its action at multiple sites and multiple levels of the organism. This includes inhibition of bacterial enzymes involved in carbohydrate synthesis. In higher concentration, it inhibits nucleic acid and total protein synthesis by the nonspecific attack on bacterial ribosomal proteins [12]. Hence, clinical drug resistance emerges slowly. There is no cross resistance between nitrofurantoin and other antimicrobial agents also. Side effects such as anorexia, nausea and vomiting occur at rates <0.001% especially with macrocrystal formulations [24]. It is contraindicated in patients with renal failure with creatinine clearance rate of 60 ml/min. However, recent studies indicate that nitrofurantoin can be used among patients with creatinine clearance as low as 40 ml/min [25].

Our results indicate that susceptibility to penicillin, ciprofloxacin, aminoglycoside, teicoplanin, erythromycin has dropped to less than 20% for all enterococcal isolates. So, NF may be a reliable option for uncomplicated acute cystitis, which is in agreement with recommendations by other authors [26,27]. The complete susceptibility to linezolid is elicited in our study supports the recommendations of NF as a reserved drug to treat VRE in complicated cases of UTI such as pyelonephritis, urinary tract infection with bacteremia, or urosepsis etc., [21,24,28]. However, one must differentiate between colonisation and infection before the start of treatment.

Limitation

The current study included all positive urine cultures irrespective of symptomatic or asymptomatic bacteriuria. Catheter Associated UTI (CAUTI) could not be established due to lack of data.

Conclusion

Nitrofurantoin is effective even after 50 years with minimal resistance. It could serve as a useful therapeutic agent against rapidly emerging VRE especially in uncomplicated UTI. Linezolid could be used as reserve drug for complicated enterococcal UTI to prevent emergence of resistance.

Financial or Other Competing Interests

None.

References

  • [1].French GL. Enterococci and vancomycin resistance. Clin Infect Dis. 1998;27:S75–S83. doi: 10.1086/514910. [DOI] [PubMed] [Google Scholar]
  • [2].Facklam RR, Teixeira LM. Enterococcus. In: Lollier L, Balows A, Sussman M, editors. Topley & Wilson’s microbiology andmicrobial infections. 9th ed. New York: Oxford University Press; 1998. pp. 669–82. [Google Scholar]
  • [3].Mohanty S, Jose S, Singhal R, Sood S, Dhawan B, Das BK, et al. Species prevalence and antimicrobial susceptibility of enterococci isolated in a tertiary care hospital of north India. Southeast Asian J Trop Med Public Health. 2005;36:962–65. [PubMed] [Google Scholar]
  • [4].Werner G, Coque TM, Hammerum AM, Hope R, Hryniewicz W, Johnson A, et al. Emergence and spread of vancomycin resistance among enterococci in Europe. Euro Surveill. 2008;13:19046. [PubMed] [Google Scholar]
  • [5].Center for Disease Control and Prevention. Information for the public about VRE 2008. Atlanta (GA): Center for Disease Control and Prevention; 2016. [Last accessed on 27th May 2017]. Available from: http://www.cdc.gov/ncidod/dhqp/ar_VRE_publicFAQ.html . [Google Scholar]
  • [6].Kapoor L, Randhawa VS, Deb M. Antimicrobial resistance of enterococcal blood isolates at a pediatric care hospital in India. Jpn J Infect Dis. 2005;58:101–03. [PubMed] [Google Scholar]
  • [7].Taneja N, Rani P, Emmanuel R, Sharma M. Significance of vancomycin resistant enterococci from urinary specimens at a tertiary care centre in northern India. Indian J Med Res. 2004;119:72–74. [PubMed] [Google Scholar]
  • [8].Mathur P, Kapil A, Chandra R, Sharma P, Das B. Antimicrobial resistance in Enterococcus faecalis at a tertiary care centre of northern India. Indian J Med Res. 2003;118:25–28. [PubMed] [Google Scholar]
  • [9].Karmarkar MG, Gershom ES, Mehta PR. Enterococcal infections with special reference to phenotypic characterization & drug resistance. Indian J Med Res. 2004;119:22–25. [PubMed] [Google Scholar]
  • [10].Banora MG, Solbiati M, Stepan E, Zorzi A, Luzzani A, Catania MR, et al. Emergence of linezolid resistance in the vancomycin-resistant enterococcus faecium:multilocus sequence typing c1 epidemic lineage. J Clin Microbiol. 2006;44:1153–15. doi: 10.1128/JCM.44.3.1153-1155.2006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [11].Hooper CH. Urinary tract agents:Nitrofurantoin and methanamine. In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s Principles and Practice of Infectious Diseases. Philadelphia: Churchill Livingstone; 2005. pp. 473–lp78. [Google Scholar]
  • [12].Guay DR. An update on the role of nitrofurantoin in the management of urinary tract infections. Drugs. 2001;61:353–64. doi: 10.2165/00003495-200161030-00004. [DOI] [PubMed] [Google Scholar]
  • [13].Clinical and Laboratory Standards Institute. Twenty-fifth informational supplement M100-S25. Wayne PA: Clinical and Laboratory Standards Institute; 2015. Performance standards for antimicrobial susceptibility testing. [Google Scholar]
  • [14].Low DE, Keller N, Barth A, Jones RN. Clinical prevalence, antimicrobial susceptibility, and geographic resistance patterns of enterococci:results from the SENTRY Antimicrobial Surveillance Program 1997-1999. Clin Infect Dis. 2001;15:S133–45. doi: 10.1086/320185. [DOI] [PubMed] [Google Scholar]
  • [15].Kaur N, Sharma S, Malhotra S, Madan P, Hans C. Urinary tract infection:Aetiology and antimicrobial resistance pattern in infants from a tertiary care hospital in northern India. J Clin Diagn Res. 2014;8:DC01–03. doi: 10.7860/JCDR/2014/8772.4919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [16].Mohanty S, Kapil A, Das BK, et al. Antimicrobial resistance profile of nosocomial uropathogens in a tertiary care hospital. Indian J Med Sci. 2003;57:148–54. [PubMed] [Google Scholar]
  • [17].Shah L, Mulla S, Patel KG, Dhawan B. Prevalence of enterococci with higher resistance level in a tertiary care hospital:A matter of concern. Natl J Med Res. 2012;2:25–27. [Google Scholar]
  • [18].Praharaj I, Sujatha S, Parija SC. Phenotypic and genotypic characterization of vancomycin resistant Enterococcus isolates from clinical specimens. Indian J Med Res. 2013;138:549–56. [PMC free article] [PubMed] [Google Scholar]
  • [19].Toner L, Papa N, Aliyu SH, Dev H, Lawrentschuk N, Al-Hayek S. Vancomycin resistant enterococci in urine cultures:Antibiotic susceptibility trends over a decade at a tertiary hospital in the United Kingdom. IC Urology. 2016;57:129–34. doi: 10.4111/icu.2016.57.2.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [20].Sahni RD, Balaji V, Varghese R, John J, Tansarli GS, Falagas ME. Evaluation of fosfomycin activity against uropathogens in a fosfomycin-naive population in South India:A prospective study. Future Microbiol. 2013;8:675–80. doi: 10.2217/fmb.13.31. [DOI] [PubMed] [Google Scholar]
  • [21].Zhanel GG, Laing NM, Nichol KA, Palatnick LP, Noreddin A, Hisanaga T, et al. Antibiotic activity against urinary tract infection (UTI) isolates of vancomycin-resistant enterococci (VRE):results from the 2002 North American Vancomycin Resistant Enterococci Susceptibility Study (NAVRESS) J Antimicrob Chemother. 2003;52:382–88. doi: 10.1093/jac/dkg352. [DOI] [PubMed] [Google Scholar]
  • [22].Pulcini C, Bush K, Craig WA, Frimodt-Møller N, Grayson ML, Mouton JW, et al. ESCMID Study Group for Antibiotic Policies. Forgotten antibiotics:An inventory in Europe, the United States, Canada, and Australia. Clin Infect Dis. 2012;54:268–74. doi: 10.1093/cid/cir838. [DOI] [PubMed] [Google Scholar]
  • [23].Singh RM, Devi MU, Singh KL, Singh HL, Keisham C, Singh KH. Evaluation of nitrofurantoin activity against the urinary isolates in the current scenario of antimicrobial resistance. Ann Trop Med Public Health. 2015;8:280–85. [Google Scholar]
  • [24].Heintz BH, Halilovic J, Christensen CL. Vancomycin-resistant enterococcal urinary tract infections. Pharmacotherapy. 2010;30:1136–49. doi: 10.1592/phco.30.11.1136. [DOI] [PubMed] [Google Scholar]
  • [25].Oplinger M, Andrews CO. Nitrofurantoin contraindicationin patients with a creatinine clearance below 60 mL/min:Looking for the evidence. Ann Pharmacother. 2013;47:106–11. doi: 10.1345/aph.1R352. [DOI] [PubMed] [Google Scholar]
  • [26].Rivera AM, Boucher HW. Current concepts in antimicrobial therapy against select gram-positive organisms:methicillin resistant Staphylococcus aureus penicillin-resistant pneumococci, and vancomycin-resistant enterococci. Mayo Clin Proc. 2011;86:1230–43. doi: 10.4065/mcp.2011.0514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [27].Wang JL, Hsueh PR. Therapeutic options for infections due to vancomycin-resistant enterococci. Expert Opin Pharmacother. 2009;10:785–96. doi: 10.1517/14656560902811811. [DOI] [PubMed] [Google Scholar]
  • [28].Heintz BH, Cho S, Fujioka A, Li J, Halilovic J. Evaluation of the treatment of vancomycin-resistant enterococcal urinary tract infections in a large academic medical center. Ann Pharmacother. 2013;47:159–69. doi: 10.1345/aph.1R419. [DOI] [PubMed] [Google Scholar]

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