Volume 17, Number 7—July 2011
Catabacter hongkongensis Bacteremia with Fatal Septic Shock
Highlight and copy the desired format.
|EID||Elsendoorn A, Robert R, Culos A, Roblot F, Burucoa C. Catabacter hongkongensis Bacteremia with Fatal Septic Shock. Emerg Infect Dis. 2011;17(7):1330-1331. https://dx.doi.org/10.3201/eid1707.101773|
|AMA||Elsendoorn A, Robert R, Culos A, et al. Catabacter hongkongensis Bacteremia with Fatal Septic Shock. Emerging Infectious Diseases. 2011;17(7):1330-1331. doi:10.3201/eid1707.101773.|
|APA||Elsendoorn, A., Robert, R., Culos, A., Roblot, F., & Burucoa, C. (2011). Catabacter hongkongensis Bacteremia with Fatal Septic Shock. Emerging Infectious Diseases, 17(7), 1330-1331. https://dx.doi.org/10.3201/eid1707.101773.|
To the Editor: Catabacter hongkongensis is a newly described anaerobic agent that is likely an intrinsic component of normal gut flora; it was first reported by Lau et al. in 2007 (1). We report a fatal case of infection caused by C. hongkongensis that was identified by 16S rRNA sequence.
A man 52 years of age was admitted to an intensive care unit in France for septic shock. He was a retired service member, smoker, and alcohol drinker. He had a history of hypertension but no previously known gastrointestinal disease. He sought treatment for acute abdominal pain and diarrhea of several hours’ duration. On admission, he had persistent abdominal pain with generalized abdominal distension, arterial hypotension, and hypoxemia but was not febrile. Two sets of anaerobic and aerobic blood cultures were performed at a 1-hour interval, and empiric treatment with amoxicillin/clavulanic acid and gentamicin was started. Biochemical screening showed severe metabolic acidosis, acute renal insufficiency, and systemic inflammatory response syndrome. An abdominal radiograph revealed massive pneumoperitonitis. Laparotomy showed multiple lesions and intestinal perforation at the ascending and first part of the transverse colon, with a large amount of purulent fluid in the peritoneal cavity. A complete colectomy was performed, with rectum closure and end ileostomy. Despite fluid resuscitation and catecholamine infusions, hemodynamic instability worsened rapidly and led to the patient’s death.
Microbiological analysis of abdominal fluid revealed the presence of Pseudomonas aeruginosa, Escherichia coli, and Enterococcus spp., but no anaerobic agent. On day 3 postincubation, 1 of the 2 anaerobic blood cultures grew a motile gram-positive bacillus, which grew only in strictly anaerobic conditions. Phenotypic analysis showed catalase production but not indole positivity or nitrate reduction. Standard phenotypic tests were performed with the rapid ID 32A and api20A strips (bioMérieux, Marcy l’Etoile, France). The numeric profiles obtained were 0002000010 and 4030121, respectively. The bacteria produced acid from arabinose, glucose, mannose, and xylose, was negative for glycerol fermentation and leucine arylamidase and positive for rhamnose fermentation. Despite these results, phenotypic tests failed to identify the isolate. Antimicrobial drug susceptibility was determined by disk diffusion method and Etest for MICs. The isolate showed susceptibility to metronidazole (MIC <0.016 µg/mL), vancomycin, and colistin (MIC <0.016 µg/mL) and resistance to penicillin (MIC 2 µg/mL), gentamicin, netilmycin, kanamycin, amikacin, and cefotaxime (MIC >32 µg/mL) according to Eucast clinical breakpoints (www.eucast.org). No other bacteria were isolated in the blood cultures.
Genetic analysis was performed by 16S rRNA gene sequencing of a 1,265-bp fragment by using DG74 and RDRO80 primers (2). The nucleotide sequence obtained was compared with known sequences in GenBank by multiple sequence alignment using the ClustalW program (3). It was 100% identical to C. hongkongensis (GenBank accession no. AY574991).
The first 4 case-patients with C. hongkongensis infection were described by Lau et al. in 2007 (1). Two of these patients lived in Hong Kong and the 2 others in Canada. As in our case, only 1 patient died. Since there was a high degree of phenotypic and genetic difference with other anaerobic agents, the authors proposed a new genus and species and affiliation with a new family, Catabacteriacae. The 2 isolates from Canada differed from the 2 others by being negative for glycerol fermentation and positive for rhamnose fermentation and leucine arylamidase, similar to our case, except for leucine arylamidase, which in our case was negative. In the previously reported cases, C. hongkongensis was susceptible to metronidazole, vancomycin, and kanamycin; variably susceptible to penicillin (MICs 0.5–4.0 µg/mL); and resistant to colistin and cefotaxime (1).
Whether C. hongkongensis belongs to the intestinal flora, as do Bifidobacterium, Eggerthella, Eubacterium, and Lactobacillus spp., remains undetermined. Codony et al. recently investigated by real-time PCR the presence of Catabacteriaceae in 29 water samples in the vicinity of Barcelona, Spain. Four samples were positive, demonstrating presence of this organism in the European environment and its probable enteric origin (4).
Because our patient sought treatment with severe infection associated with isolation of other pathogenic bacteria, whether blood infection by C. hongkongensis may be responsible for such a fatal outcome is unknown. Nevertheless, we can exclude sample contamination by this anaerobic bacteria for the 2 following reasons. First, anaerobic contaminants are rare in blood cultures and generally involve Propionibacterium acnes. Furthermore, the rapid growth of the present isolate in blood cultures within 3 days suggested a relatively high bacterial load in the blood sample.
Our report confirms that C. hongkongensis can be found in blood culture associated with gastrointestinal disease and may reflect intestinal perforation. Identification may be difficult. Isolation of motile gram-positive anaerobic bacillus together with catalase positivity should lead to suspicion of C. hongkongensis in clinical laboratories. Full identification of this pathogen requires 16S sequencing. Environmental reports have demonstrated the presence of this organism in human wastewater in Europe, which suggests that it may be universally present as part of the normal human gastrointestinal flora.
- Lau SKP, McNabb A, Woo GKS, Hoang L, Fung AMY, Chung LMW, Catabacter hongkongensis gen. nov., sp. nov., isolated from blood cultures of patients from Hong Kong and Canada. J Clin Microbiol. 2007;45:395–401.
- Lane DJ. 16S/23S rRNA sequencing. In: Stackebrandt E, Goodfellow M, editors. Nucleic acid techniques in bacterial systematics. New York: John Wiley and Sons; 1991. p. 115–75.
- Thompson JD, Higgins DG, Gibson TJ. CLUSTALW: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994;22:4673–80.
- Codony F, Adrados B, Pérez LM, Fittipaldi M, Morató J. Detection of Catabacter hongkongensis in polluted European water samples. J Zhejiang Univ Sci B. 2009;10:867–9.
Please use the form below to submit correspondence to the authors or contact them at the following address:
Antoine Elsendoorn, CHU de Poitiers, 2, Rue de la Milétrie 86021 Poitiers CEDEX, France
Comment submitted successfully, thank you for your feedback.
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
- Page created: August 18, 2011
- Page last updated: August 18, 2011
- Page last reviewed: August 18, 2011
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)