A strain of Listeria monocytogenes recovered from blood and cerebrospinal fluid had no detectable catalase activity, a characteristic used for primary identification. The sporadic occurrence of pathogenic catalasenegative strains highlights the need for a reconsideration of diagnostic criteria and questions the role of catalase in the pathogenesis of listeria infection.
CASE REPORTA 28-year-old Caucasian male receiving immunosuppressive therapy with cyclosporine and prednisolone following renal transplantation developed a sudden onset of rigors, high fever (38.9°C), vomiting, and progressive confusion after routine hemodialysis. On arrival in the emergency room, he sustained a generalized tonic-clonic seizure requiring anticonvulsants. Physical examination revealed no obvious source of infection or skin rash, mild photophobia but no other signs of meningeal irritation, and generalized hyperreflexia consistent with a postictal state. A lumbar puncture was performed, and a full septic screen was obtained before the patient was started on intravenous ceftriaxone therapy (2 g every 12 h). Cerebrospinal fluid (CSF) revealed a lymphocyte count of 1,008 cells/mm 3 ; therefore, intravenous acyclovir (10 mg/kg of body weight every 8 h) and ampicillin (2 g every 4 h) were added as per local protocol. The patient's general condition rapidly deteriorated, and he required respiratory and hemodynamic support in the intensive care unit.Two days later, blood cultures in four bottles became positive for a gram-positive, rod-shaped organism suggestive of a Listeria sp., but catalase testing (performed by observing the generation of bubbles of oxygen formed when a colony was suspended in a drop of hydrogen peroxide on a glass slide) showed consistently negative results. Biochemical identification (esculin positive, glucose positive, and maltose positive) using an API Coryne system (bioMerieux, Basingstoke, United Kingdom) repeatedly failed to identify the organism as Listeria monocytogenes due to negative catalase and xylose reactions. On the following day, an additional set of blood cultures and a CSF sample grew the same organism.Initial sensitivity testing using the British Society of Antimicrobial Chemotherapy disk diffusion method showed that the sizes of the zones with ampicillin were inconsistent between the blood and CFS isolates. Ampicillin was therefore discontinued, and co-trimoxazole (10 mg/kg every 12 h) commenced. Subsequent susceptibility testing of both isolates by agar dilution at the Health Protection Agency antibiotic reference laboratory confirmed the organism's susceptibility to ampicillin and co-trimoxazole, with MICs of 0.5 mg/liter and 0.064 mg/ liter, respectively.The patient made a slow but progressive recovery, regained consciousness, and experienced no further seizures. The antibiotic therapy with co-trimoxazole was continued for a total of 4 weeks.The organism was identified as L. monocytogenes by PCR amplification and sequence analysis of 1,156 base pairs of the 16S rRNA genes and confirmed by the Foo...