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Case Reports in Infectious Diseases
Volume 2019, Article ID 2148654, 3 pages
https://doi.org/10.1155/2019/2148654
Case Report

Scombroid Poisoning with Concurrent Brevundimonas Septicemia: A Unique Case Report and Brief Literature Review

1Division of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA
2Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA

Correspondence should be addressed to Caroline C. Eskind; gro.cmuv@nehoc.r.enilorac

Received 24 January 2019; Accepted 26 October 2019; Published 11 November 2019

Academic Editor: Peter Olumese

Copyright © 2019 Caroline C. Eskind et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Scombroid poisoning is a predominantly self-limited illness associated with ingestion of poorly handled fish. It is not frequently associated with bacteremia and has never been described with Brevundimonas septicemia. We describe a case of a man who presented in shock with histamine poisoning after ingesting sushi. Blood cultures grew an uncommon pathogen, Brevundimonas vesicularis. This case demonstrates systemic bacterial infection in the setting of histamine poisoning, which is an atypical presentation for a well-known foodborne illness.

1. Background

Scombroid poisoning is a relatively infrequent cause of foodborne toxicity that is usually attributable to ingestion of improperly handled fish. While most commonly identified in association with fish of the Scombridae family, such as mackerel, albacore, and bonito, poisoning has been attributed to ingestion of other fish as well, including mahi-mahi, salmon, and sardines. Symptoms are due to ingestion of histamine which is produced on the surface of improperly stored fish. Symptoms include flushing, vomiting, diarrhea, urticaria, and occasionally more severe symptoms such as cardiopulmonary distress and shock. A variety of bacteria have been implicated in the reaction to convert histidine to histamine through the enzyme histidine decarboxylase, including Proteus, Enterobacter, Serratia, Pseudomonas, and Vibrio. Treatment primarily consists of antihistamines and supportive care, and symptoms usually self-resolve in under 12 hours [1, 2]. Bacteremia has not been routinely described as a complication of scombroid poisoning, though affected patients can be severely ill with shock, myocardial infarction, or respiratory distress with bronchospasm [1].

Brevundimonas vesicularis is a motile Gram-negative bacillus, previously identified as a member of the Pseudomonas family. It is commonly found in soil, as well as a variety of aqueous environments including bottled and filtered water, pools, and deep-sea water [35]. By 2017, only 35 cases of human infection with B. vesicularis had been described in the literature, including cases of bacteremia, endocarditis, peritonitis, and urinary tract infections [4]. Infected patients are usually immunocompromised with malignancy, autoimmune disease, or multiple comorbid conditions, such as diabetes and end-stage renal disease. Isolates have variable sensitivity profiles, but regularly are resistant to ampicillin and fluoroquinolones and occasionally to 1st and 2nd generation cephalosporins [35]. Cases are described as community-acquired or hospital-acquired, but the original source of the bacteria is rarely identified and has never been associated with fish consumption [6].

We report a case of an immunocompetent man who was admitted to an acute care hospital in shock, with presumed scombroid poisoning, who was later found to have concurrent bacteremia with B. vesicularis.

2. Case Presentation

A 76-year-old man with chronic diastolic heart failure, well-controlled bipolar disorder on lithium, and atrial fibrillation was admitted to the hospital with gastrointestinal distress that developed just six hours prior to admission. He had been briefly hospitalized less than two weeks prior due to a heart failure exacerbation requiring intravenous (IV) diuretics, but was feeling well in the days leading up to presentation. For dinner that evening, he and his wife consumed prepared sushi containing imitation crab meat that had been purchased the day before from a national grocery store chain. Within 45 minutes of consumption, he developed sudden nausea, violent emesis, and nonbloody diarrhea. He developed diffuse pruritus and discovered an urticarial rash covering the majority of his skin. He took two tablets of Benadryl and retired to his bedroom, where he eventually fell onto the floor and was overwhelmingly weak, unable to stand or walk. Per EMS report, he was hypotensive to 50 s/30 s and was given 1 liter of IV fluids en route to the hospital. Upon arrival to the hospital, he remained hypotensive to 70 s/40 s and tachycardic to 120 s, but his gastrointestinal symptoms and rash had already resolved. He required admission to the intensive care unit due to persistent hypotension despite fluid resuscitation, and he was given intravenous norephinephrine. He was given 1000 mg IV vancomycin every 12 hours and 3.375 grams IV piperacillin-tazobactam every 6 hours for presumed septic shock and was also given IV Benadryl and subsequently switched to oral cetirizine for presumed histamine fish toxicity. His shock resolved by the next day after receiving 5 L of IV fluids, and the vasopressor was weaned off.

Initial lab tests were significant for a leukocyte count of 24,000 cells/μL, potassium of 6.4 mEq/L, serum creatinine of 2.3 mg/dL, lactic acid of 4.1 mmol/L, troponin of 0.05 ng/L, and brain-type natriuretic peptide of 3730 pg/mL. Of note, a noncontrasted computerized tomography (CT) scan obtained on admission was concerning for sigmoid colitis. The aerobic bottle of his blood cultures (BD Bactec) obtained upon admission eventually grew a Gram-negative bacillus, which was later identified as B. vesicularis using Vitek 2 identification with the VITEK 2 GN ID card. Antibiotic susceptibilities were determined using the Vitek 2 system with AST-GN69 and AST-XN06 cards to determine mean inhibitory concentration (MIC) based on the Clinical and Laboratory Standards Institute (CLSI) guidelines. The isolate was sensitive to piperacillin-tazobactam, amikacin, tobramycin, gentamicin, imipenem, and tetracycline and was resistant to fluoroquinolones, aztreonam, and ceftazidime. The public health department was notified and, unfortunately, the sushi had already been consumed and disposed of, so it was not available for testing. A urine methylhistamine level was ordered, but ultimately, the testing was never performed by the lab.

He remained on renally dosed IV piperacillin-tazobactam at 2.25 grams every 6 hours and initially improved with antibiotics and supportive care, and subsequent blood culture bottles did not grow any further bacteria. Later in his hospital course, he decompensated with progressive renal failure, acute liver injury, and persistent leukocytosis. He underwent repeat CT scanning, which demonstrated a small amount of pericholecystic fluid and small dependent gallbladder calculi. His previously described sigmoid colitis had improved radiographically. These findings were thought to represent acute cholecystitis or secondary liver disease in the setting of worsening abdominal ascites. He was transferred back to the ICU due to tachycardia to the 160–170 s and hypotension.

Cardiology was consulted and attributed his clinical decompensation to heart failure with congestive hepatopathy. Despite broad-spectrum antibiotics, vasopressor support, and diuretics, his clinical status did not improve and his family elected to pursue comfort measures. He passed away in the ICU on hospital day 10.

3. Discussion

Brevundimonas vesicularis is infrequently described in cases of human infection, most often affecting patients with underlying immunocompromising conditions. The source of bacterial infection is thought to be community-derived in most cases; however, the organism itself is frequently isolated from water sources [6]. Cases have been reported in the bloodstream of patients acutely postoperative from cardiac surgery and in meningeal infection after surgical resection of a brain tumor. Patients have also been diagnosed with B. vesicularis peritonitis in the setting of peritoneal dialysis [4]. These infections raise the possibility of the bacteria being introduced into patients by contaminated fluid. Notably, Brevundimonas species are very small and can pass through sterilizing filters and have been identified in bottled water and in cases of pseudooutbreaks that truly represented contamination of laboratory media [4]. This did not appear to be the case in our laboratory, as the isolate was not identified in any other specimens.

We hypothesize that our patient may have acquired infection with Brevundimonas from consumption of improperly stored fish that lead to simultaneous histamine poisoning and bacteremia. Unfortunately, the food source was not kept and, therefore, confirmatory testing was not possible. Brevundimonas spp. have been isolated from the surface and intestine of various fish [7]; however, they have not frequently been identified as causative agents of histamine poisoning. One study has demonstrated that Brevundimonas vesicularis isolated from Spanish mackerel was histamine-forming [8]. Pseudomonas species have frequently been associated with histamine production [2]; given the taxonomic relatedness of the two species, it is plausible that Brevundimonas spp. share this trait. While no human infection with Brevundimonas has been described in relation to seafood consumption, other cases of bloodstream infection with water-associated bacteria, such as Edwardsiella tarda and Raoultella planticola, have been documented in relation to the consumption of fish [9, 10]. Two cases of septicemia with Raoultella spp. have been described with concurrent symptoms of histamine poisoning, but in both cases, definitive testing for histamine toxicity was not performed [11, 12]. Our patient’s multidrug resistant isolate is consistent with the existing reports of Brevundimonas infections [4, 5]. Our lab was able to identify the bacteria using the advanced colorimetry technique of VITEK 2; however, given the slow-growing nature and infrequent incidence of infection, 16S rRNA sequencing may aid in identification of more cases of B. vesicularis infection.

Future cases of Brevundimonas infection should be investigated for association with seafood consumption. Similarly, patients with severe manifestations of scombroid poisoning should have blood cultures obtained to identify possible concurrent bacteremia with waterborne pathogens.

Abbreviations

CT:Computed tomography
EMS:Emergency medical services
ICU:Intensive care unit
IV:Intravenous
rRNA:Ribosomal ribonucleic acid.

Consent

Verbal consent for use of the patients’ medical history and details in a publication was given by the patient to the authors during his hospitalization. Unfortunately, the patient died prior to documentation of written consent. Many attempts were made to contact the patient’s wife; however, she remains unable to be reached, but was aware of our intent to potentially write about the patient’s medical course. The authors believe that our manuscript sufficiently anonymizes the patient and does not violate the patient’s right to privacy. If change need to be made to maintain anonymity of our patient, the authors are happy to make any recommended changes.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this article.

Acknowledgments

All authors have contributed significantly to this work. CCE receives support from an academic training grant (Vanderbilt Infection Pathogenesis and Epidemiology Research Training Program T32 grant- 5T32AI007474-23). The publication of this manuscript was supported by the training grant.

References

  1. C. Feng, S. Teuber, and M. E. Gershwin, “Histamine (scombroid) fish poisoning: a comprehensive review,” Clinical Reviews in Allergy & Immunology, vol. 50, no. 1, pp. 64–69, 2016. View at Publisher · View at Google Scholar · View at Scopus
  2. Y. Hu, Z. Huang, and X. Chen, “Histamine-producing bacteria in blue scad (Decapterus maruadsi) and their abilities to produce histamine and other biogenic amines,” World Journal of Microbiology and Biotechnology, vol. 30, no. 8, pp. 2213–2221, 2014. View at Publisher · View at Google Scholar · View at Scopus
  3. J. Gilad, A. Borer, N. Peled et al., “Hospital-acquired brevundimonas vesicularis septicaemia following open-heart surgery: case report and literature review,” Scandinavian Journal of Infectious Diseases, vol. 32, no. 1, pp. 90-91, 2000. View at Publisher · View at Google Scholar
  4. M. P. Ryan and J. T. Pembroke, “Brevundimonas spp: emerging global opportunistic pathogens,” Virulence, vol. 9, no. 1, pp. 480–493, 2018. View at Publisher · View at Google Scholar · View at Scopus
  5. S.-T. Shang, S.-K. Chiu, M.-C. Chan et al., “Invasive Brevundimonas vesicularis bacteremia: two case reports and review of the literature,” Journal of Microbiology, Immunology and Infection, vol. 45, no. 6, pp. 468–472, 2012. View at Publisher · View at Google Scholar · View at Scopus
  6. C.-C. Zhang, H.-J. Hsu, and C.-M. Li, “Brevundimonas vesicularis bacteremia resistant to trimethoprim-sulfamethoxazole and ceftazidime in a tertiary hospital in southern Taiwan,” Journal of Microbiology, Immunology and Infection, vol. 45, no. 6, pp. 448–452, 2012. View at Publisher · View at Google Scholar · View at Scopus
  7. T. Ozaktas, B. Taskin, and A. G. Gozen, “High level multiple antibiotic resistance among fish surface associated bacterial populations in non-aquaculture freshwater environment,” Water Research, vol. 46, no. 19, pp. 6382–6390, 2012. View at Publisher · View at Google Scholar · View at Scopus
  8. Z.-h Zhao, H. Lin, and Z.-x Li, “Isolation and identification of histamine-forming bacteria from Spanish mackerel meat,” Food Science, vol. 32, no. 7, pp. 194–197, 2011. View at Google Scholar
  9. P. W. Lam and I. E. Salit, “Raoultella Planticola Bacteremia following consumption of seafood,” Canadian Journal of Infectious Diseases and Medical Microbiology, vol. 25, no. 4, pp. e83–e84, 2014. View at Publisher · View at Google Scholar · View at Scopus
  10. K. Suzuki, M. Yanai, Y. Hayashi, H. Otsuka, K. Kato, and M. Soma, “Edwardsiella tarda bacteremia with psoas and epidural abscess as a food-borne infection: a case report and literature review,” Internal Medicine, vol. 57, no. 6, pp. 893–897, 2018. View at Publisher · View at Google Scholar · View at Scopus
  11. N. Mau and L. A. Ross, “Raoultella ornithinolytica bacteremia in an infant with visceral heterotaxy,” The Pediatric Infectious Disease Journal, vol. 29, no. 5, pp. 477-478, 2010. View at Publisher · View at Google Scholar · View at Scopus
  12. S. Puerta-Fernandez, F. Miralles-Linares, M. V. Sanchez-Simonet, M. R. Bernal-Lopez, and R. Gomez-Huelgas, “Raoultella planticola bacteraemia secondary to gastroenteritis,” Clinical Microbiology and Infection, vol. 19, no. 5, pp. E236–E237, 2013. View at Publisher · View at Google Scholar · View at Scopus