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Searching for Bacterial Biofilm in Recurrent Cholangitis in Primary Sclerosing Cholangitis: A Case Presentation and Introduction of an Unexplored Disease Mechanism

  • Alyssa Y. Choi1,
  • Florencia Jalikis2,
  • Maria Westerhoff2,
  • Sarag Boukhar3,
  • Elinor Pulcini4,
  • Chris Damman5 and
  • Lei Yu*,5
Journal of Clinical and Translational Hepatology 2018;():-

DOI: 10.14218/JCTH.2017.00029

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Abstract

Inflammation and fibrosis of the bile ducts are the defining pathological characteristics of primary sclerosing cholangitis (PSC). A previously unexplored mechanism for recurrent cholangitis, one of PSC’s most common presentations, is bacterial colonization of the biliary epithelium in the form of biofilm, which may confer resistance to antibiotics and host phagocytic machinery. The aim of the current study was to assess whether bacteria could be seen on the liver explant and whether they organized in the form of biofilm. An explanted PSC liver from a 60-year-old male who suffered from recurrent cholangitis was formalin-fixed, paraffin-embedded and Gram stained. The specimens were observed under light microscopy. Neither bacteria nor biofilm were detected. We did not detect bacteria or biofilm in the liver explant of a single PSC patient with recurrent cholangitis using standard light microscopy. We suspect this may be in part due to techniques related to tissue preservation and microscopy.

Keywords

Primary sclerosing cholangitis, Recurrent cholangitis, Biofilm

Introduction

Primary sclerosing cholangitis (PSC) is a liver disease defined by inflammation, fibrosis and stricture of the intra- and extrahepatic bile ducts.1 It is a leading indication for liver transplantation in adults, despite its relatively low prevalence of 1–15 per 100,000 people.1 A subset of patients with PSC experience fever, right upper quadrant pain and jaundice.2 While these symptoms may resolve without specific treatment, a proportion of patients have repeated cholangitis with positive bacterial or fungal cultures from blood or bile, despite antibiotic therapy.3

In the context of liver transplant allocation, the most current definition of recurrent bacterial cholangitis includes the following criteria: 1. at least two episodes of culture-proven, non-iatrogenic cholangitis during a 6-month period; 2. cholangitis episodes that have occurred despite recent or active treatment with antibiotics; 3. single episode of cholangitis with severe sepsis-related complications.2 This unique syndrome of recurrent bacterial cholangitis in PSC is an accepted indication for liver transplantation, regardless of whether or not advanced liver failure is present.4

A previously unexplored explanation for the recurrent nature of cholangitis in PSC is chronic bacterial colonization of the biliary epithelium in the form of biofilms. It is now widely accepted that most bacteria in nature live in “sessile” communities surrounded by a glycocalyx matrix. Such arrangement, in contrast to the planktonic (single cell) form of existence, is associated with a distinctive bacterial phenotype that confers resistance to antibiotics and contributes to the host’s phagocytic machinery.5

We herein describe a case of a PSC patient with recurrent bacterial cholangitis who underwent successful liver transplantation. The primary aim was to assess whether bacteria could be “seen” on the liver explant and whether they organized in the form of biofilm.

Case report

A 60-year-old white male with PSC diagnosed 15 years ago presented with fever, chills, right upper quadrant abdominal pain and disorientation. In the past 2 years, he had been hospitalized with similar symptoms more than six times. His medical co-morbidities included Crohn’s disease managed by mesalamine, peptic ulcer disease and Type II diabetes. He had focal noncaseating granulomas on his ileum and colon biopsies without active inflammation. His cirrhosis was complicated by mild jaundice and encephalopathy. His cholangiogram showed diffuse biliary strictures and choledocholithiasis without a dominant stricture.

During episodes of abdominal pain, fevers and chills, carbapenem-resistant Eschericheria coli and Enterococcus faecium grew from blood cultures on multiple occasions. In contrast, growth from biliary cultures was always polymicrobial, including E, coli, Enterococcus faecalis and E. faecium, Stenotrophomonas maltophilia, Staphylococcus aureus, Corynebacterium amycolatum and yeast. In addition to antibiotics, treatment for his cholangitis included sphincterotomy, common bile duct dilation and stenting. Usually, his symptoms would improve temporarily after each ERCP. Despite having undergone internal-external biliary duct drainage several months before his transplant, he continued to experience culture-positive cholangitis and sepsis.

At the time of liver transplant, the patient’s model for end-stage liver disease (commonly known as MELD) score was 14 (total bilirubin: 2.5 mg/dL, creatinine: 0.56 mg/dL, international normalized ratio: 1.5), with additional points approved for recurrent cholangitis. According to the surgeon, pus was oozing from the liver at the time of hepatectomy. On postoperative day 4, the patient developed daptomycin-resistant enterococcus bacteremia, which was treated successfully with linezolid. The source was unknown. At the time of this writing (1 year after transplant), the patient was clinically well.

Pathological description

Gross examination of the explanted liver demonstrated nodular distortion of the parenchyma, consistent with cirrhosis. Thirteen representative sections of the liver explant (from segments 2, 4 and 8, the caudate lobe and the hilum) were submitted for histological evaluation. Microscopy was significant for patchy bile duct loss (Fig. 1A) and nodular formation (Fig. 1B), consistent with the patient’s history of PSC-associated cirrhosis. Some of the large bile ducts had large collections of neutrophils (Fig. 1C), and the bile duct epithelium showed active cholangitis (Fig. 1D). Light microscopy on Gram-stained, formalin-fixed and paraffin-embedded explant blocks did not show any bacteria, fungi or biofilm.

(A) Portal tract with preserved vascular structures, without accompanying bile duct, consistent with the patient’s diagnosis of PSC; H&E stain, 100×. (B) Trichrome stain highlights cirrhotic liver parenchyma; MT stain, 100×. (C) Bile duct with numerous intraepithelial neutrophils (arrows); H&E stain, 400×. (D) Large bile duct with intraluminal collections of neutrophils; H&E stain, 100×.
Fig. 1.  (A) Portal tract with preserved vascular structures, without accompanying bile duct, consistent with the patient’s diagnosis of PSC; H&E stain, 100×. (B) Trichrome stain highlights cirrhotic liver parenchyma; MT stain, 100×. (C) Bile duct with numerous intraepithelial neutrophils (arrows); H&E stain, 400×. (D) Large bile duct with intraluminal collections of neutrophils; H&E stain, 100×.

Discussion

Since Hoffman described the first official case of primary sclerosing cholangitis in 1867,6 its pathogenesis remains incompletely understood. While inflammation and fibrosis of the biliary tree are the defining pathological characteristics, the resulting biliary strictures are not always associated with true bacterial cholangitis. Among patients listed for liver transplantation for PSC, only one-fifth had two or more episodes of cholangitis.7,8 To our knowledge, no study has examined factors associated with recurrent bacterial cholangitis in PSC patients.

Based on physio-anatomical considerations and culture results, the gastrointestinal tract is the most likely source of infectious organisms in PSC-associated cholangitis. How exactly enteric organisms gain “entry” into bile, however, is unclear. The disease’s unique association with inflammatory bowel disease makes the portal vein a potential route, as bacteria translocate across an inflamed gastrointestinal tract. While animal studies have established portal vein as a route of bacteria entry into bile,9 in the most carefully performed human study to date, surgical sampling of colitis patients without PSC failed to show portal venous bacteremia.10 In Asian patients with recurrent pyogenic cholangitis commonly associated with hepatolithiasis and clonorchis infection, only 15% of patients had bacteria cultured from portal venous blood at the time of laparotomy.11 No similar study has been conducted in Caucasian patients with PSC.

Reflux of enteric organisms through the sphincter of Oddi was thought to be another route of bacterial entry into bile in non-PSC-associated cholangitis.1214 Supporting this concept, Olsson et al.15 reported that recent endoscopic instrumentation had the strongest association with positive bacterial culture in PSC liver explant specimens, regardless of whether fever, infection or dominant strictures were present or not. Identifying the exact route of bacteria entry into bile—translocation through the portal vein versus retrograde migration through the sphincter of Oddi—may be important to guide treatment and management strategies of recurrent cholangitis.

The presence of dominant strictures of the bile ducts (defined by Rudolph et al.16 as < 1.5 mm of the common bile duct and < 1.0 mm of the common hepatic duct within 2 cm of the bifurcation) is another logical etiologic suspect in recurrent cholangitis. This anatomical finding occurs in approximately 50% of PSC patients during their disease course.17 Elevated intrabiliary pressure from obstruction can distort tight junctions between hepatocytes, facilitating entry of bacteria into bile.18 In addition, biliary obstruction leads to a decrease in phagocytic activity of hepatic Kupffer cells.19 While dominant strictures are associated with liver disease progression and positive bacterial culture from bile, it is unclear whether they were associated with clinical evidence of cholangitis.17,20

In the study by Pohl et al.,20 in which a strong association was found between positive bacterial culture in bile and dominant strictures, the majority (36 of 37) of patients with dominant strictures had undergone multiple endoscopic instrumentation procedures prior to bile sample collection, implicating bacterial contamination. More importantly, experience from our case suggests that dilation of the biliary tree may not be effective, likely because of the diffuse nature of intrahepatic strictures, and that disruption of the sphincter of Oddi has the potential to promote additional enteric bacteria migration into the biliary system.

The current 2010 American Association for the Study of Liver Diseases (AASLD) practice guidelines do not recommend routine antibiotics in patients with recurrent cholangitis in PSC.21 While several antibiotics improve liver biochemistry in PSC patients without affecting liver histology or endoscopic features (Table 1), none of the studies to date have specifically investigated whether patients with or without bacterial cholangitis respond differently to treatment.23,24,3642 Occasionally, however, patients developed recurrent cholangitis later in their disease course without an initial presentation of cholangitis at the start of the study.23 Our case provides evidence (based on culture results) that standard oral antibiotics, even when given long-term, were not able to suppress cholangitis, although intravenous formulation did improve the acute presentations of fever and abdominal pain.

Table 1.

Reported series evaluating the role of antibiotics for treatment of PSC23,24,3642

StudyYearDesignSubjectsAntibioticsParametersResponse
Farkkila et al.2004RCT80Metronidazole, UCDAALP, ALT, AST, GGT, Mayo risk score, liver histologyPartial
Silveria et al.2009Pilot study16MinocyclineALP, AST, total bilirubin, direct bilirubin, PT, albumin, Mayo risk scorePartial
Tabibian et al.2013RCT35Vancomycin vs. MetronidazoleALP, total bilirubin, CRP, Mayo risk scorePartial
Davies et al.*2008Observational14Oral vancomycinALT, GGT, ESR, liver histologyPositive
Misitilis et al.1965Case report7TetracyclineALP, total bilirubin, liver histologyNegative
Boner et al.2007Case report1AzithromycinALP, ALT, AST, GGT, total bilirubinPositive
Rankin et al.1959Case report5TetracyclineALP, ALT, ALTPositive
Cox and Cox*1998Case report3Vancomycin (oral)ALT, GGT, ESR, liver histology, ERCPPositive
Mathew et al.1983Case report1MetronidazoleTotal bilirubin, clinical signs and symptomsPositive

Our interest in exploring biofilm formation in PSC patients with recurrent cholangitis was based on several lines of evidence. First, the presence of bacteria has been unequivocally demonstrated using traditional culture-based methods in PSC patients with advanced liver disease.15 Second, the recurrent nature of cholangitis suggests a unique bacterial ecology favoring its survival within a compromised host. Third, a molecular-based method for microbiota determination and imaging techniques for biofilm analysis have firmly established the role of bacterial colonization and infection in the pathogenesis of cystic fibrosis a disease complicated by recurrent pneumonia and having a phenotype similar to recurrent cholangitis.25 These methodological (and conceptual) advances may help define the role of bacteria in PSC as well. Fourth, the presence of biofilm presents itself as a novel therapeutic target in PSC with or without cholangitis. For example, rifampin, a second-line agent for the treatment of pruritis,26 penetrates biofilm in prosthetic hardware-associated methicillin-resistant S. aureus bacteremia.27 More recently, aspirin, an anti-biofilm agent, was found to be associated with a significantly lower risk of cholangiocarcinoma.28,29 Finally, formation of bacterial biofilm in vitro and bacterial membrane integrity are affected by the presence of bile.3032 It is possible that the higher mortality observed in the high-dose ursodeoxycholic acid arm of the recent PSC trial33 was related to excessive enrichment of bile with ursodeoxycholic acid, rendering it too hydrophilic to suppress biofilm formation from pathogenic enteric organisms.

Other than the possibility that biofilm does not exist in PSC-associated recurrent cholangitis, formalin fixation, which affects intestinal biofilm preservation in inflammatory bowel disease,34 may have hindered our ability to detect biliary biofilm. In addition, while standard light microscopy is an established method for detecting biofilm, scanning electron microscopy and fluorescence in situ hybridization have also been used.35 Even though no studies to date have directly compared the sensitivity and specificity of these microscopies, these more advanced methods, which were not available to us, may improve our ability to detect biliary biofilm. An effort to organize a larger study using proper tissue preservation technique, as well as more sophisticated microscopy, is currently underway.

Abbreviations

AASLD: 

American Association for the Study of Liver Diseases

EASL: 

European Association for the Study of the Liver

MELD: 

model for end-stage liver disease

PSC: 

primary sclerosing cholangitis

Declarations

Conflict of interest

The authors have no conflict of interests related to this publication.

Authors’ contributions

Study concept and design, interpretation of findings, drafting and revising the article (AC), reviewing pathology and interpretation of findings, revising the article (FJ), reviewing pathology and interpretation of findings, revising the article (MW), reviewing pathology and interpretation of findings, revising the article (SB), interpretation of findings, revising the article (EP), contributed to study concept and design, interpretation of findings, revising the article (CD), study concept, interpretation of findings, drafting and revising the article (LY).

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