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Ascending cholangitis presenting with Lactococcus lactis cremoris bacteraemia: a case report

  • Jane Davies1Email author,
  • Michael David Burkitt2 and
  • Alastair Watson2
Contributed equally
Journal of Medical Case Reports20093:3

DOI: 10.1186/1752-1947-3-3

Received: 18 February 2008

Accepted: 06 January 2009

Published: 06 January 2009

Abstract

Introduction

A case of Lactococcus lactis cremoris causing cholangitis is described. This Gram-positive organism is not routinely considered to be pathogenic in immunocompetent individuals. To our knowledge, this is the thirteenth report of invasive infection and the first of cholangitis to be reported in association with this organism.

Case presentation

A 72-year-old patient presented with Charcot's triad and was demonstrated to have cholangitis with Lactococcus lactis cremoris bacteraemia. Biliary drainage was achieved through endoscopic retrograde cholangiography. Antibiotic therapy with multiple agents was necessary.

Conclusion

This report provides corroboration of evidence that Lactococcus lactis cremoris is a potential pathogen in immunocompetent adults. There remains a debate about the most appropriate empirical antibiotic therapy in this condition. In the light of this case, it is important to keep an open mind to potential pathogens.

Introduction

Lactococcus lactis cremoris is commonly considered to be a non-pathogenic organism in humans. It is recognized as a commensal organism of mucocutaneous surfaces, however, over the past 50 years, there have been a number of case reports [111] demonstrating the potential for this organism to cause infection. We report the first case of cholangitis associated with septicaemia caused by Lactococcus lactis cremoris.

Case presentation

A 72-year-old lady, normally fit and well, presented with a 5-day history of jaundice and abdominal pain. She was nauseated and had dark urine. On initial assessment, she was deeply icteric and her temperature was 38.2°C but she was haemodynamically stable. Systemic examination did not reveal any other abnormalities, specifically there were no stigmata of chronic liver disease. No organs or lymph nodes were palpable and the abdomen was soft and non-tender.

Biochemical analyses demonstrated a leukocytosis and neutrophilia; haemoglobin (Hb) 11.9 g/dL, white blood cell count (WCC) 13.9 × 109/L, neutrophils 11.4 × 109/L. An acute phase response was evident with C-reactive protein (CRP) 131 mg/L. A mixed cholestatic and hepatic picture of hepatic enzymes with alkaline phosphatase (ALP) 340 U/L, alanine aminotransferase (ALT) 240 U/L and gamma-glutamyl-transferase (γGT) 381 U/L was demonstrated; total bilirubin was 351 μmol/L. Hepatic synthetic function was preserved with albumin 30 g/L and prothrombin time (PT) of 13.8 seconds. A clinical diagnosis of cholangitis was made on the basis of Charcot's triad (abdominal pain, fever and jaundice), and empirical antibiotic therapy (oral ciprofloxacin 500 mg bd) was commenced.

An ultrasound of the biliary tree was performed demonstrating dilatation of the common bile duct to 1.5 cm with visualization of at least one stone in the lumen of the duct. Intrahepatic duct dilatation was also noted. Blood cultures confirmed a Lactococcus lactis cremoris septicaemia. The organism was sensitive to tazobactam/piperacillin and co-amoxiclav. In light of these results, antibiotic therapy was changed to intravenous tazobactam/piperacillin 4.5 g tds.

The patient proceeded to endoscopic retrograde cholangiopancreatogram (ERCP) where an impacted common bile duct stone was identified. Unfortunately, this was not amenable to endoscopic removal despite sphincterotomy; however two biliary stents were inserted with good drainage.

The patient recovered rapidly with resolution of her symptoms and signs and was discharged home 48 hours post-ERCP. Treatment was completed with 2 weeks of oral co-amoxiclav 625 mg tds.

Discussion

The Tokyo Consensus guidelines of 2007 have now established definitive diagnostic criteria and severity assessment of cholangitis [12]. The diagnosis of cholangitis is made either by the presence of Charcot's triad or by the presence of two of these features backed up by abnormal liver function tests, raised inflammatory markers and imaging demonstrating a dilated biliary tree. Severity is assessed by the presence or absence of organ failure once a diagnosis has been made and response to initial therapy. As our patient had no signs of organ failure but failed to respond to the primary treatment, she constitutes cholangitis of moderate severity.

Empirical antibiotic therapy for cholangitis is targeted towards gut organisms, particularly Gram-negative organisms. Commonly (including in our unit), ciprofloxacin is considered to be an appropriate empirical therapy. This is backed up by reports of an 85% clinical cure rate in trials [13]. The Tokyo Consensus group [13] failed to recommend a single specific empirical treatment, therefore local antibiotic guidelines will continue to direct empirical therapy. In the presence of positive microbiological investigations, there is a clear consensus that agents should be changed for more appropriate treatment according to sensitivity.

Biliary drainage reduces mortality and speeds recovery from cholangitis and is therefore a vital part of management [14]. The Tokyo guidelines recognize that this must be done in an emergency setting for patients with severe cholangitis and as promptly as practical in other patients. Endoscopic drainage is the preferred modality [15].

Lactococcus lactis cremoris is a Gram-positive coccus, formerly classified as Streptococcus cremoris but now recognized as a member of the genus Lactococcus [3]. This species is commonly regarded as non-pathogenic in immunocompetent adults, however we report the thirteenth case to our knowledge of this pathogen causing clinically significant infection. Previously, four cases of bacterial endocarditis [4, 6, 9, 11], one of septicaemia [7], two liver abscesses [3, 5] and one each of necrotizing pneumonitis [10], septic arthritis [8], deep neck infection [2], cerebellar abscess [4] and canaliculitis [1] have been reported. Of these, it appears that nine were immunocompetent patients. All bar one of the case reports were in adults (Table 1).
Table 1

Previously reported cases of Lactococcus lactis cremoris associated infections

Year

Age

Sex

Site of infection

Exposure to unpasteurized milk products

Treatment

Outcome

Immune status

2006 [1]

80

F

Canaliculitis

None

Oral ampicillin and topical chloramphenicol

Complete resolution

Normal

2005 [2]

68

M

Deep neck infection

Cow breeder and consumed unpasteurized milk

Ceftriaxone and metronidazole for 6 weeks

Resolution on discharge

Previous malignancy

2004 [3]

79

F

Liver abscess

None

Percutaneous drainage, Imipenem Cilastatin for 5 weeks

Complete resolution

Normal

2002 [4]

45

F

Cerebellar abscess

Not commented

Ceftriaxone 8 weeks, gentamicin 2 weeks, Metronidazole

No residual deficit and no recurrence at 9 months

Normal

2002 [3]

67

M

Endocarditis

History of drinking unpasteurized milk

Co-amoxiclav and gentamicin 15 days

Well 6 months post discharge

Normal

     

Penicillin for 6 weeks

  

2000 [5]

14

F

Liver abscess

None

Percutaneous drainage

Discharged from hospital on day 48

Normal

     

Cefotiam, Amikacin and Clindamycin for 8 days

  
     

Panipenem for 8 days

  
     

Piperacillin 15 days and amikacin 10 days

  

1996 [6]

56

M

Endocarditis

None

Penicillin G for 12 days and Clarithromycin for 18 days

Well 18 months post discharge

Normal

1995 [7]

69

M

Septicaemia

Yoghurt ingested

Cefotaxime and Amikacin

No comment

Chronic lymphocytic leukaemia

1993 [8]

57

F

Septic arthritis

Unpasteurized milk

Penicillin for 6 weeks

Deformity 8 months post discharge, but no ongoing infection

Normal

1990 [9]

65

F

Endocarditis

Not commented

Benzylpenicillin and gentamicin

No ongoing infection

Normal

1990 [10]

24

M

Necrotizing pneumonitis and empyema

Unpasteurized milk and cheese eaten

Thoracocentesis (*3)

Penicillin and clindamycin 15 days

Well 1 month post discharge

HIV positive

1955 [11]

21

M

Endocarditis

Sour cream known to contain S. Lactis

Penicillin and Dihydrostreptomycin for 22 days

Well 4 months post discharge

Normal

Lactococcus lactis cremoris is a recognized skin commensal of cattle and is also used in the dairy industry for milk fermentation. It may therefore be present in unpasteurized dairy products. Of the previously reported cases, six have been associated with a clear history of exposure to unpasteurized dairy products; in one of these cases, the organism was isolated from the milk product (Table 1). Our patient is not aware of having had any such exposure.

Conclusion

This report provides corroboration of evidence that Lactococcus lactis cremoris is a potential pathogen in immunocompetent adults. Lactococcus lactis cremoris has now been reported as a pathogen in many different systems, both acutely and subacutely. This may well represent an underreporting of the true incidence of invasive infection related to this organism.

Diagnosis and assessment of the clinical severity of cholangitis are now the subject of consensus guidelines. These guidelines also extend to the appropriate timing and method of biliary drainage. However, there remains a debate about the most appropriate empirical antibiotic therapy in this condition. In the light of this case, it is important to consider other potential pathogens causing ascending cholangitis.

Consent

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Notes

Abbreviations

Hb: 

haemoglobin

WCC: 

white cell count

CRP: 

C-reactive protein

ALT: 

alanine aminotransferase

ALP: 

alkaline phosphatase

γGT: 

gamma-glutamyl-transferase

PT: 

prothrombin time

bd: 

twice daily

tds: 

three times daily

ERCP: 

endoscopic retrograde cholangiopancreatogram

Declarations

Authors’ Affiliations

(1)
Tropical and Infectious Diseases Unit, Royal Liverpool and Broadgreen University Hospitals Trust
(2)
The Henry Wellcome Laboratories, Unit of Gastroenterology, School of Clinical Science, The University of Liverpool

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Copyright

© Davies et al; licensee BioMed Central Ltd. 2009

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.