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. 2020 Jun 6;7(6):ofaa212. doi: 10.1093/ofid/ofaa212

Vibrio fluvialis Liver Abscess and Bacteremia in a Sashimi Lover: A Case Report and Review of the Literature

Satoshi Kitaura 1, Koh Okamoto 1,, Yoshitaka Wakabayashi 1, Yuta Okada 1, Aiko Okazaki 1, Mahoko Ikeda 1, Ryunosuke Hakuta 2, Yousuke Nakai 2, Shu Okugawa 1, Kazuhiko Koike 2, Kyoji Moriya 1
PMCID: PMC7305699  PMID: 32587879

Abstract

Vibrio fluvialis is a foodborne pathogen known to cause a cholera-like gastroenteritis syndrome. Here we report the first case of V. fluvialis liver abscess and bacteremia presumed to be from sashimi, a Japanese raw seafood delicacy. We also provide a literature review of reported cases of V. fluvialis extra-intestinal diseases including bacteremia.

Keywords: bacteremia, liver abscess, Vibrio fluvialis, Vibrio species


Vibrio fluvialis is commonly encountered [1], being the fifth commonest species (6%) among 1252 cases of Vibrio infection reported to the Centers for Disease Control and Prevention [2]. V. fluvialis is increasingly recognized as a foodborne pathogen associated with poor sanitation and increased seafood consumption [1]. Acute gastroenteritis is the most common presentation, although extra-intestinal infections have been reported infrequently [1]. Here, we report a case of V. fluvialis liver abscess with concomitant bacteremia and review the literature regarding extra-intestinal, including bacteremic, V. fluvialis infections.

CASE PRESENTATION

A 65-year-old man with a history of pancreatic head cancer and surgically resected bladder cancer presented to the outpatient clinic following 1 week of lethargy. He denied any abdominal pain, diarrhea, or other gastrointestinal symptoms. He was expected to receive chemotherapy for pancreatic cancer; however, he was admitted to the internal medicine ward because of profound hypotension and tachycardia. Twelve months before, pancreatic duct dilation was incidentally noted on follow-up computed tomography for bladder cancer. He was subsequently diagnosed with pancreatic head cancer following bile duct biopsy via endoscopic retrograde cholangiopancreatography. He underwent 2 biliary stent placements and 2 chemotherapy courses with gemcitabine and nab-paclitaxel 7 months before presentation. He gradually lost appetite and mainly consumed sashimi, a Japanese seafood delicacy, purchased at a nearby fish market on a daily basis.

Upon admission, he was alert and oriented with mild lethargy. Physical examination revealed moderate conjunctival pallor, but no focal findings, including abdominal tenderness or peritoneal signs. Complete blood count results were as follows: white blood cell count, 21.5×103/μL; hemoglobin, 7.7 mg/dL; and platelet count, 34.4×104/μL. Liver enzyme levels were as follows: aspartate transaminase, 34 U/L; alanine transaminase, 20 U/L; gamma-glutamyl transpeptidase, 132 U/L; alkaline phosphatase, 652 U/L; and total bilirubin, 0.5 mg/dL. Urinalysis and chest radiogram were unremarkable. Abdominal ultrasound revealed a low echoic lesion ~20 mm in size in segment 6 of the liver. This finding was confirmed with computed tomography with intravenous contrast, which showed a newly identified space-occupying lesion compatible with liver abscess in the corresponding location (Figure 1A). He subsequently underwent fluid resuscitation and percutaneous transhepatic abscess aspiration with empiric piperacillin-tazobactam. The following day, blood cultures and aspirate from the liver abscess were positive for gram-negative bacilli (Figures 1B and C). Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS; Bruker, Billerica, MA, USA) identified V. fluvialis (score of 2.129). Antimicrobial susceptibility testing revealed that the isolate was sensitive to ampicillin, ampicillin/sulbactam, piperacillin/tazobactam (minimal inhibitory concentration of 8 μg/mL), cefmetazole, ceftriaxone, ceftazidime, cefepime, aztreonam, meropenem, amikacin, minocycline, and levofloxacin. Because the abscess failed to decrease in size with the initial antibiotic treatment alone, minocycline and piperacillin/tazobactam were administered, along with additional biliary stent placement and percutaneous transhepatic abscess drainage.

Figure 1.

Figure 1.

A) A computed tomography scan depicting a low-density area compatible with liver abscess (white arrow). B) Vibrio fluvialis colony growing on thiosulfate-citrate-bile-sucrose agar plate. C) Gram stain of blood culture depicting curved gram-negative bacilli (black arrow).

After 3 weeks of parenteral antibiotic treatment, the regimen was switched to enteral clindamycin and minocycline. He was discharged and completed 6 weeks of treatment, achieving radiographic liver abscess resolution. The patient died from progression of pancreatic head cancer 6 months after this episode without any recurrence of V. fluvialis infection.

DISCUSSION

V. fluvialis is prevalent in aquatic environments and seafood, which are the main risk factors for acquiring the disease [1]. Gastroenteritis is the most common clinical manifestation [1], and only few extra-intestinal infections have been reported [1]. Here, we review clinically relevant reports of 7 extra-intestinal infection cases including 7 bacteremia cases (Table 1) [3–13]. Cases were mainly from island and peninsular regions [3–13]. Patients were typically middle-aged, with a 52-year median age, except for 1 infant [3–13]. There was no sex difference overall; however, 5 of 6 bacteremia cases occurred in male patients with ≥1 comorbidity, primarily diabetes mellitus [3–13]. Water or seafood exposure was noted in approximately half of cases [3–13]. Most bacteremia cases resulted from severe gastroenteritis, and 50% of patients died [3–13]. Extra-intestinal cases included 2 peritonitis cases, 1 hemorrhagic cellulitis, cerebritis, otitis externa, urinary tract infection, and cholangitis case; however, liver abscess has never been reported. Treatment was variable across cases, although combination therapy involving beta-lactams and agents, including aminoglycosides, quinolones, and tetracyclines, was used [3–12].

Table 1.

Literature Review of Extra-intestinal Infection Including Bacteremia by V. fluvialis

Case Age, y Sex Country Site of Disease Bacteremia Underlying Disease Route of Acquisition Treatment Outcome Reference
1 40 Female Taiwan Otitis externa No None Seawater exposure AMPC/CVA Survived 3
2 88 Female Taiwan Cholangitis No DM, ESRD, cirrhosis, intrahepatic ductal stones None PIPC/TAZ + trans-hepatic biliary drainage Survived 4
3 52 Female South Korea Peritonitis No None, postabdominal blunt injury from traffic accident None Cephamycin + netilmicin, PIPC/TAZ + MNZ, cefoperazone + prepenem + amikacin Died 5
4 40 Female USA Gastroenteritis catheter Yes DM, hypertension, ESRD (on HD) Seawater exposure CTRX + DOXY, gatifloxacin Survived 6
5 66 Male Korea Unknown Yes Gastric cancer NA NA Died 7
6 70 Male Korea Gastroenteritis Yes DM, hypertension, gastric cancer NA SBT/CPZ + ISP Survived 7
7 65 Male Taiwan Gastroenteritis Yes DM, chronic liver disease None CXM to ST Survived 8
8 55 Female New Zealand Peritonitis No ESRD (on CAPD), DM Seafood CTRX CPFX AMPC + GM ip Survived 9
9 45 Male Taiwan Hemorrhagic cellulitis cerebritis Yes Alcoholic liver disease Fire ant bites, brackish water exposure OXA + GM CAZ + oxytetracycline + fasciotomy + left transfemoral amputation Died 10
10 5 mo Male Bangladesh Gastroenteritis Yes Malnutrition NA ABPC + GM + amdinocillin pivoxil Died 11
11 52 Female Lebanon Urinary tract infection No Fibroid uterus, post–total abdominal hysterectomy and bilateral oophorectomy Home tap water CPFX Survived 13
12 65 Male Japan Liver abscess Yes Malnutrition, pancreatic cancer, bladder cancer (surgically resected) Seafood PIPC/TAZ + MINO, CLDM + MINO, biliary stent placement, PTAD Survived Our case

Abbreviations: ABPC, ampicillin; AMPC, amoxicillin; AMPC/CVA, amoxicillin/clavulanate; CAPD, continuous ambulatory peritoneal dialysis; CAZ, ceftazidime; CLDM, clindamycin; CPFX, ciprofloxacin; CTRX, ceftriaxone; CXM, cefuroxime; DM, diabetes mellitus; ESRD, end-stage renal disease; GM, gentamicin; HD, hemodialysis; ip, intraperitoneal; ISP, isepamicin; MINO, minocycline; NA, not available; OXA, oxacillin; PIPC/TAZ, piperacillin/tazobactam; PTAD, percutaneous transhepatic abscess drainage; SBT/CPZ, sulbactam-cefperazone; ST, trimethoprim-sulfamethoxazole.

The scarcity of extra-intestinal and bacteremia cases may partly be because of difficulty in identifying V. fluvialis [1]. Although classical thiosulfate-citrate-bile salts-sucrose agar medium and biochemical assays, including API20E and Vitek GNI+ systems, are often used for identification, different Vibrio species may show similar results [1]. V. fluvialis is closely related to V. furnissii, and differentiation may be difficult [12, 14]. Both species were originally classified as V. fluvialis; however, V. furnissii was later distinguished as separate owing to its gas-producing capability [14]. Besides biochemical identification methods, more reliable identification methods include polymerase chain reaction (PCR) DNA testing or MALDI-TOF MS [12, 14]. PCR results, using rpoB and the more conventional toxR gene segment, and MALDI-TOF MS results completely agreed in 1 study [14].

In line with reported cases, our patient was a middle-aged man with biliary tract disease owing to pancreatic cancer who was receiving chemotherapy. MALDI-TOF MS (Bruker, USA) reliably identified V. fluvialis. We presume that he acquired V. fluvialis from sashimi. Both the liver abscess and bacteremia were successfully treated with combination therapy and aggressive drainage.

In summary, while gastroenteritis is the most common presentation, extra-intestinal V. fluvialis infection is uncommon and exhibits high mortality. Heavy seafood consumption is a major risk factor [1]. As raw seafood consumption is getting more common than before worldwide, physicians should consider V. fluvialis infection alongside other Vibrio species in patients with heavy exposure to seafood, including sashimi.

Acknowledgments

We would like to thank Editage (www.editage.jp) for English language editing.

Potential conflicts of interest. All authors: no reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Author contributions. All authors cared for the patient, performed literature search, wrote the draft, and critically reviewed the draft.

References

  • 1. Ramamurthy T, Chowdhury G, Pazhani GP, Shinoda S. Vibrio fluvialis: an emerging human pathogen. Front Microbiol 2014; 5:91. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Centers for Disease Control and Prevention. National enteric disease surveillance: COVIS annual summary 2014. Available at https://www.cdc.gov/nationalsurveillance/pdfs/covis-annual-summary-2014-508c.pdf. Accessed 2 March 2020.
  • 3. Chen PJ, Tseng CC, Chan HT, Chao CM. Acute otitis due to Vibrio fluvialis after swimming. Case Rep Emerg Med 2012; 2012:838904. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Liu WL, Chiu YH, Chao CM, et al. Biliary tract infection caused by Vibrio fluvialis in an immunocompromised patient. Infection 2011; 39:495–6. [DOI] [PubMed] [Google Scholar]
  • 5. Lee JY, Park JS, Oh SH, et al. Acute infectious peritonitis caused by Vibrio fluvialis. Diagn Microbiol Infect Dis 2008; 62:216–8. [DOI] [PubMed] [Google Scholar]
  • 6. Nadkarni AS, Shah MK. Concomitant bacteremia caused by Vibrio fluvialis and Vibrio alginolyticus in a patient on hemodialysis: a first case report and review of literature. Infect Dis Clin Pract 2007; 15:129–31. [Google Scholar]
  • 7. Koh EM, Kim CK, Kim M, et al. Two cases of Vibrio fluvialis bacteremia in patients undergoing cancer chemotherapy. Korean J Clin Microbiol 2007; 10:4. [Google Scholar]
  • 8. Lai CH, Hwang CK, Chin C, et al. Severe watery diarrhoea and bacteraemia caused by Vibrio fluvialis. J Infect 2006; 52:e95–8. [DOI] [PubMed] [Google Scholar]
  • 9. Ratnaraja N, Blackmore T, Byrne J, Shi S. Vibrio fluvialis peritonitis in a patient receiving continuous ambulatory peritoneal dialysis. J Clin Microbiol 2005; 43:514–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Huang KC, Hsu RW. Vibrio fluvialis hemorrhagic cellulitis and cerebritis. Clin Infect Dis 2005; 40:e75–7. [DOI] [PubMed] [Google Scholar]
  • 11. Albert MJ, Hossain MA, Alam K, et al. A fatal case associated with shigellosis and Vibrio fluvialis bacteremia. Diagn Microbiol Infect Dis 1991; 14:509–10. [DOI] [PubMed] [Google Scholar]
  • 12. Hashimoto T, Takaya S, Kutsuna S, et al. A case report of Vibrio furnissii bacteremia and cellulitis in a malnourished patient without an apparent site of entry. J Infect Chemother 2018; 24:65–7. [DOI] [PubMed] [Google Scholar]
  • 13. Usta J, Araj G, Taleb R. An unusual urinary tract infection caused by Vibrio fluvialis. J Infect Dev Ctries 2018; 12:673–5. [DOI] [PubMed] [Google Scholar]
  • 14. Schirmeister F, Wieczorek A, Dieckmann R, et al. Evaluation of molecular methods to discriminate the closely related species Vibrio fluvialis and Vibrio furnissii. Int J Med Microbiol 2014; 304:851–7. [DOI] [PubMed] [Google Scholar]

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