ISSN: 0970-938X (Print) | 0976-1683 (Electronic)

Biomedical Research

An International Journal of Medical Sciences

- Biomedical Research (2016) Volume 27, Issue 1

The antibacterial effects of bilirubin on gram-negative bacterial agents of sepsis.
Huseyin Agah Terzi1, Hakan Kardes2, Ali Riza Atasoy1, Sadiye Berna Aykan3, Engin Karakece1, Gonca Handan Ustundag4, Bahri Ermis5, Ihsan Hakki Ciftci1
1Sakarya University, Training and Research Hospital, Department of Medical Microbiology, Sakarya.
2Akçaabat Haçkalı Baba State Hospital, Department of Pediatrics, Trabzon.
3Sakarya University, Health Care Vocational College, Sakarya.
4Bulent Ecevit University, School of Medicine, Department of Pediatrics, Zonguldak.
5Sakarya University, Training and Research Hospital, Department of Pediatrics, Sakarya.
Corresponding Author: Huseyin Agah Terzi, Department of Microbiology Sakarya University Training and Research Hospital Sakarya, Turkey
Accepted December 12, 2015
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Abstract

In this study, we investigated the antibacterial effects of bilirubin on certain Gram-negative bacteria using both agar dilution and liquid microdilution methods. Twenty-five strains each of Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii, and Pseudomonas aeruginosa strains, isolated from various clinical samples in the medical microbiology laboratory of our hospital, were evaluated. Stock solutions of bilirubin (5 mg, 10 mg, and 15 mg/dl) (AppliChem, GmbH, Darmstadt, Germany) were prepared for agar dilution method. Aliquots of bilirubin stock solutions were added to liquid brain heart infusion medium in sterile microplates for liquid dilution methods. The average bilirubin MICs were 61.44, 62.72, ≥ 64.00, and ≥ 64.00 μg/mL for E. coli, K. pneumoniae, A. baumannii, and P. aeruginosa. In agar and liquid dilution methods, all tested bacteria grew at all bilirubin concentrations used. Bilirubin had no in vitro antibacterial effect on E. coli, K. pneumoniae, A. baumannii, or P. aeruginosa.

Keywords
Bilirubin; Antibacterial effect; Newborn; Jaundice; Sepsis

Introduction
Bilirubin is an end product of heme metabolism which is released in association with the breakdown of hemoglobin. Previously, the products of heme metabolism considered negligible waste products. But unlike the other livings, only in mammals biliverdin undergoes additional metabolism that consumes the energy to produce bilirubin [1]. Elevated serum bilirubin levels are associated with the manifestation named as hyperbilirubinemi-jaundice in many newborn [2].
The natural antioxidant characteristics of bilirubin were first discovered by Stocker and colleagues [3]. Recent studies have suggested that bilirubin causes oxidative damage at pathological levels but exerts antioxidant effects at physiological levels [4]. Bilirubin can trigger apoptosis of cell cultures and stimulates the inflammatory response to lipopolysaccharide [5]. Bilirubin protected mice subjected to experimental sepsis [6]. Santangelo and colleagues found that bilirubin exhibited antiviral activity when added to infected cell cultures [7]. Bilirubin can be elevated in cases of sepsis, intra-abdominal abscesses from urological, gynecological or gastroenterological origins, and antiviral therapy [8].
Bilirubin has been suggested to be an effective antibacterial, but few data are available. Thus, we explored this topic by measuring the antibacterial effects of bilirubin on certain Gram-negative bacteria using both agar dilution and liquid microdilution methods.

Materials and Methods
Strains and bacterial identification
Gram-negative bacterial agents of sepsis were divided into four test groups according to their species. Twenty-five strains each of Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii, and Pseudomonas aeruginosa strains, isolated from various clinical samples in the medical microbiology laboratory of our hospital, were evaluated. Cultures were inoculated on blood agar, eosin methylene blue (EMB) agar, or chocolate agar, depending on the sample type and incubated by standard conventional microbiological methods [9]. Species identification was performed using the Vitek 2 automated system (bioMérieux, Marcy-l'Étoile, France), and evaluated based upon the recommendations of the Clinical Laboratory Standards Institute (CLSI) [10]. Patient laboratory records were examined retrospectively. If several isolates were obtained from the same patient, only one was included in the evaluation.
Medium preparation and dilution studies
Agar dilution: Stock solutions of bilirubin (5 mg, 10 mg, and 15 mg/dl) (AppliChem, GmbH, Darmstadt, Germany) containing EDTA and NaHCO3 were prepared and mixed in the appropriate amounts with Mueller-Hinton agar (Oxoid, Hampshire, England) at 50°C, which was used to prepare solid culture plates with 4-mm-thick agar. Bacterial suspensions of McFarland turbidity 0.5 were prepared, and 5-μl aliquots were spotted onto the agar plates within circles 5 mm in diameter (final bilirubin concentrations: 5, 10, and 15 mg/dl). Bacterial growth was evaluated after 18 h of incubation at 35°C. Control plates contained no bilirubin.
Microdilution Test: Bacterial suspensions of McFarland turbidity 0.5 were prepared from 24-h cultures using the Densi- Check 2 system (bioMerieux, Durham, NC, USA) and diluted 1/100 to 5 × 105 colony-forming units (cfu)/ml, as suggested by CLSI [11]. Growth, negative, and positive controls were included. Aliquots of bilirubin stock solutions were added to 120 μl liquid brain heart infusion medium in sterile microplates using an automatic pipette. Serial dilution yielded final bilirubin concentrations of 64, 32, 16, 8, 4, 2, 1, and 0.5 μg/ml. Bacterial suspensions were added to 5 × 105 cfu/ml, and initial optical densities (ODs) at 450 nm were recorded. After an 18-h incubation at 35°C, OD changes were recorded using an EPOC (Biotek, USA) device. The concentration of bilirubin that reduced the final OD value to 50% that of the growth control was defined as the MIC.
Statistical Analysis: E. coli ATCC 25922, K. pneumoniae ATCC 13883, A. baumannii ATCC 19606, and P. aeruginosa ATCC 27853 were used as control isolates. Agar and microdilution tests was carried out in triplicate using three samples for all isolates under the same conditions. Descriptive statistics are presented as mean ± standard deviation (SD). One Way ANOVA test was used for comparing the data. Statistical significance was assumed if p<0.05. All statistical evaluation was performed using SPSS (Version 17.0 for Windows; SPSS, Inc., Chicago, IL, USA).

Results
Liquid microdilution
The average bilirubin MICs were 61.44, 62.72, ≥ 64.00, and ≥ 64.00 μg/mL for E. coli, K. pneumoniae, A. baumannii, and P. aeruginosa respectively. Between E. coli and K. pneumoniae MIC values was found differences but there was no statistical significant (p>0.05). There was no difference between A. baumannii, and P. aeruginosa (Table 1). The detected MIC levels were found higher than the amount required that can be used in antibiotherapy.
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Table 1: Statistical analysis of MIC values.
Agar dilution
The E. coli isolates, which had different resistance profiles, and the control E. coli ATCC 25922 were resistant to bilirubin at all levels tested. This was also true of the K. pneumoniae isolates and ATCC 13883 control, the A. baumannii isolates and ATCC 19606 control, and the P. aeruginosa isolates and ATCC 27853 control. Moreover, there was no sensitive clinical isolate in the study at all levels tested.

Discussion
Despite extensive work, it remains unclear whether bilirubin, a heme catabolite, is a non-functional end-product or a biologically significant compound [4]. However, studies on the antioxidant properties of bilirubin have defined treatment threshold values [12]. Certain questions have arisen: “Are phototherapy and blood changes over-prescribed?”, “To what level should the plasma bilirubin level of a newborn be decreased?”, and “Are we interfering with a useful defense mechanism?”
Although advances in neonatal care have reduced complications in and increased the survival of preterm infants, neonatal sepsis is still associated with significant mortality and morbidity, particularly, of low birth-weight infants (<1,500 g) [13]. Such infants have high bilirubin levels. Maisels et al. found that jaundice in 306 newborns was neither the cause of nor a risk factor for bacteremia or sepsis [14]. However, a Nigerian study found that septicemia in preterm infants was associated with high bilirubin levels and high-level mortality [15]. In Turkey, Ergür et al. reported that 11% of infants with prolonged jaundice experienced sepsis and other infections [16].
Increased interest in the antioxidant effects of bilirubin has encouraged work on the antibacterial properties of biliverdin/ bilirubin, which are heme catabolites. Overhaus et al. found that intraperitoneal injection of biliverdin protected mice from sepsis-induced inflammation and intestinal dysmotility [12]. Biliverdin decreased intestinal morbidity by selectively decreasing inflammation. Wang et al. found that a single intravenous injection of bilirubin protected mice from mortality and liver dysfunction induced by injection of E. coli endotoxin [6]. Recently, Lanone et al. showed that mouse mortality caused by endotoxins decreased as the bilirubin level increased [17]. Supporting such data [18], the presence of high levels of oxidative metabolites of bilirubin in the urine of adult patients with sepsis suggests that bilirubin degradation parallels the oxidative stress of sepsis [19]. Goddard et al. inoculated group B streptococcus (GBS), coagulase-negative staphylococcus (CNS), and E. coli (all isolated from blood cultures) into media containing bilirubin at concentrations of 0-100 μmol/L [20]. E. coli was bilirubin-resistant, while GBS and CNS were not. It was suggested that physiological jaundice prevented the growth of Gram-positive bacteria such as GBS and CNS, thus protecting against sepsis in premature infants. In our study we evaluated the effects of bilirubin on Gram-negative agents of sepsis using both agar and liquid dilution methods. All tested bacteria grew at all bilirubin concentrations used; thus, bilirubin had no antibacterial effect.
Santangelo et al. investigated the antiviral effect of bilirubin in vivo conditions. Bilirubin at 1-10 μM concentrations significantly decreased the growth of human herpes virus type 1 (HSV-1) and enterovirus 71 (EV 71) in Hep-2 and Vero cells [7]. In our study the absence of any in vitro antibacterial effect of bilirubin may indicate that bilirubin is effective only in vivo. Furthermore, the antioxidant characteristic of bilirubin may have an in vivo antibacterial effect. Also in vivo detection of the any antibacterial effect of bilirubin may be useful for the regulation of treatment protocols in neonatal jaundice. In addition, we evaluated only low numbers of bacterial isolates. Device constraints rendered us unable to test bilirubin concentrations greater than 64 μg/ml (liquid culture) or 15 mg/dl (agar culture). Moreover, bilirubin at concentrations exceeding 15 mg/dl is toxic to newborns.

Conclusion
Bilirubin had no in vitro antibacterial effect on E. coli, K. pneumoniae, A. baumannii, or P. aeruginosa. As explained above, in vivo work using animal models is required. Also, different microorganisms should be tested.

References
  1. Sedlak TW, Snyder SH. Bilirubin benefits: cellular protection by a biliverdinreductase antioxidant cycle. Pediatrics 2004; 113: 1776-1782.
  2. Watchko JF, Maisels MJ. Neonatal jaundice. Semin Neonatal 2002; 7: 101-103.
  3. Stocker R, Yamamoto Y, McDonagh AF, Glazer AN, Ames BN. Bilirubin is an antioxidant of possible physiological importance. Science 1987; 235: 1043-1046.
  4. Brito MA, Brites D, Butterfield DA. A link between hyperbilirubinemia, oxidative stress and injury to neocortical synaptosomes. Brain Res 2004; 1026: 33-43.
  5. Fernandes A, Falcao AS, Silva RF, Gordo AC, Gama MJ, et al. Inflammatory signalling pathways involved in astroglial activation by unconjugated bilirubin. J Neurochem 2006; 96: 1667-1679.
  6. Wang WW, Smith DL, Zucker SD. Bilirubin inhibits iNOS expression and NO production in response to endotoxin in rats. Hepatology 2004; 40: 424-433.
  7. Santangelo R, Mancuso C, Marchetti S, Di Stasio E, Pani G, et al. Bilirubin: An Endogenous Molecule with Antiviral Activity in vitro. Front Pharmacol 2012; 3: 36.
  8. Buyukasik Y, Akman U, Buyukasik NS, Goker H, Kilicarslan A, et al. Evidence for higher red blood cell mass in persons with unconjugated hyperbilirubinemia and Gilbert’s syndrome. Am J Med Sci 2008; 335: 115-119.
  9. Koneman E, Winn W, Allen S, Janda W, Procop G, et al. Koneman’sColor Atlas and Textbook of Diagnostic Microbiology. Sixth edition, Lippincott Williams & Wilkins, USA, 2006.
  10. CLSI. Performance Standards for Antimicrobial Susceptibility Testing; Twenty-Fourth Informational Supplement. CLSI document M100-S24. Clinical and Laboratory Standards Institute. Wayne, PA, 2014.
  11. CLSI. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically; Approved Standard-Tenth Edition. CLSI document M07-A10. Clinical and Laboratory Standards Institute. Wayne, PA, 2015.
  12. Overhaus M, Moore AB, Barbato J, Behrendt F,Doering J, et al. Biliverdin protects against polymicrobial sepsis by modulating inflammatory mediators. Am J PhysiolGastrointest Liver Physiol 2006; 290: G695-703.
  13. Kaufman D, Fairchild KD. Clinical Microbiology of Bacterial and Fungal Sepsis in Very-Low-Birth-Weight Infants. ClinMicrobiol Rev 2004; 17: 638-680.
  14. Maisels MJ, Kring E. Risk of sepsis in newborns with sever hyperbilirubinemia. J Pediatr 1992; 90: 741-743.
  15. Owa J, Dawodu AH. Neonatal jaundice among Nigerian preterm infants. West Afr J Med 1990; 9: 252-257.
  16. Ergür AT, Murat M, Leylek OA, Cevit Ö, İçağasıoğlu D, et al. Evaluation Of Neonates Diagnosed As Prolonged Hyperbilirubinemia In The Our Neonatology Unit. TurkiyeKlinikleri J Pediatr 1997; 6: 167-172.
  17. Lanone S, Bloc S, Foresti R, Almolki A, Taillé C, et al. Bilirubin decreases nos2 expression via inhibition of NAD(P)H oxidase: implications for protection against endotoxic shock in rats. FASEB J 2005; 19: 1890-1892.
  18. Yamaguchi T, Horio F, Hashizume T, Tanaka M, Ikeda S, et al. Bilirubin is oxidized in rats treated with endotoxin and acts as a physiological antioxidant synergistically with ascorbic acid in vivo. BiochemBiophys Res Commun 1995; 214: 11-19.
  19. Otani K, Shimizu S, Chijiiwa K, Yamaguchi K, Kuroki S, et al. Increased urinary excretion of bilirubin oxidative metabolites in septic patients: a new marker for oxidative stress in vivo. J Surg Res 2001; 96: 44-49.
  20. Goddard M, Hansen R, Karcher AM, Munro MJ, Berry SH, et al. Bilirubin has anti-bacterial properties against gram-positive bacteria: A potential benefit of physiological jaundice? Gastroenterology 2011; 140: S-941.