Volume 24, Number 3—March 2018
Invasive Infections Caused by Nannizziopsis spp. Molds in Immunocompromised Patients
Views: Views equals page views plus PDF downloadsMetric Details
Highlight and copy the desired format.
|EID||Nourrisson C, Vidal-Roux M, Cayot S, Jacomet C, Bothorel C, Ledoux-Pilon A, et al. Invasive Infections Caused by Nannizziopsis spp. Molds in Immunocompromised Patients. Emerg Infect Dis. 2018;24(3):549-552. https://dx.doi.org/10.3201/eid2403.170772|
|AMA||Nourrisson C, Vidal-Roux M, Cayot S, et al. Invasive Infections Caused by Nannizziopsis spp. Molds in Immunocompromised Patients. Emerging Infectious Diseases. 2018;24(3):549-552. doi:10.3201/eid2403.170772.|
|APA||Nourrisson, C., Vidal-Roux, M., Cayot, S., Jacomet, C., Bothorel, C., Ledoux-Pilon, A....Poirier, P. (2018). Invasive Infections Caused by Nannizziopsis spp. Molds in Immunocompromised Patients. Emerging Infectious Diseases, 24(3), 549-552. https://dx.doi.org/10.3201/eid2403.170772.|
We report 2 new cases of invasive infections caused by Nannizziopsis spp. molds in France. Both patients had cerebral abscesses and were immunocompromised. Both patients had recently spent time in Africa.
Nannizziopsis spp. molds have been reported in extremely rare cerebral and disseminated infections (1,2), (Table). We describe 2 cases of Nannizziopsis infection diagnosed in France during the past 2 years. Both case-patients were immunocompromised and had recently returned from Africa.
Case-patient 1 was a 63-year-old woman from France who had been treated for T-cell prolymphocytic leukemia diagnosed in December 2014. She initially received alemtuzumab, switching to bendamustine in March 2015 after tumor progression. That treatment failed, and idelalisib was started on July 11, 2015. The patient was hospitalized 2 days later for acute renal failure with mild fever. She became confused and drowsy, and cerebral computed tomography (CT) scan showed systematized subcortical hypodense areas. Lumbar puncture showed neoplastic cells in the cerebrospinal fluid (CSF) and glucose concentration within reference range. Bacteriological and fungal cultures were sterile. A large volume of ascites fluid remained, despite iterative punctures with negative bacteriological cultures. We initiated intrathecal chemotherapy with methotrexate/cytarabine/methylprednisolone. However, the patient’s condition worsened, with heart failure and loss of consciousness. On July 18, we took new specimens of CSF, bronchial wash, ascites fluid, and blood cultures and sent them for bacteriological investigation. We started empiric treatment with imipenem/aminoglycosides, but the patient died on July 19 of septic shock. No autopsy was performed. Extended-spectrum β-lactamase–producing Escherichia coli sensitive to imipenem grew quickly in 1 pair of blood cultures. A second pair was positive 4 days later, with the presence of large septate fungal hyphae and arthroconidia. White and thin cottony mold colonies grew on Sabouraud media incubated at 35°C (Technical Appendix [PDF - 405 KB - 2 pages] Figure 1). We performed best model determination and phylogenetic analyses in MEGA6 (http://www.megasoftware.net). We identified N. obscura by sequencing the 18S-internal transcribed spacer (ITS) 1–5.8S-ITS2 region (Technical Appendix [PDF - 405 KB - 2 pages] Figure 2). The strain had low MICs for antifungals as defined by the European Committee on Antimicrobial Susceptibility Testing (http://www.eucast.org/): amphotericin B 0.06 µg/mL, itraconazole 0.25 µg/mL, voriconazole 0.03 µg/mL, posaconazole 0.06 µg/mL, caspofungin 0.5 µg/mL, and micafungin 0.015 µg/mL. We performed mycologic investigations of CSF and ascites fluid a posteriori on frozen aliquots and conducted PCR assays targeting the ITS region on CSF sampled on July 15 and July 19 and on ascites fluid sampled on July 19. We observed positive amplifications in all samples; subsequent sequencing confirmed the presence of DNA from N. obscura. We investigated the origin of the patient’s contamination. She had made several trips to Senegal, the latest in January 2015, during which an ulcerative inflammatory lesion developed on her left little finger. However, Grocott stain and PCR on paraffin-embedded tissue of skin biopsy were negative, and we attributed the lesion to the hematological malignancy.
Case-patient 2 was a 52-year-old woman from France living in Mali, who was hospitalized in Bamako in November 2016 for cough, fever, alteration of general state, and headache. She tested seropositive for HIV (CD4 3/µL; HIV-1 viral load 45.300 copies/mL). Chest radiograph showed bilateral pneumonia, and cerebral CT scan showed a single process on the left temporal lobe. Antiretroviral therapy was initiated with a combination of efavirenz/lamivudine/tenofovir associated with isoniazid, metronidazole, amoxicillin/clavulanate, and trimethoprime/sulfamethoxazole. Because of worsening of her neurologic status, she was repatriated to France. At hospital admission on January 12, 2017, she had a lesion on the left middle fingernail suggestive of onychomycosis, hemiparesis, and paralysis of the right side of the face associated with Broca’s aphasia. A thoracic-abdominal-pelvic scan revealed a nodular lesion in the right lung (Figure, panel A) and multiple partly calcified pleural lesions. Bacteriological assays, including investigation for mycobacteria on bronchoalveolar lavage (BAL) fluid, showed negative results. A Penicillium grew rapidly on mycological medium, and Pneumocystis jiroveci PCR was slightly positive. Cranial tomodensitometry showed multiple gadolinium-enhancing nodules surrounded by edema (Figure, panel B). We initiated fluconazole and pyrimethamine/sulfadiazine and switched antiretroviral therapy to raltegravir/abacavir/lamivudine after the onset of acute renal insufficiency. Hemiplegia developed 15 days later. A new CT scan showed stable cerebral lesions but an increase in surrounding edema. We performed a lumbar puncture and started intravenous corticotherapy. CSF contained 127 leukocytes (61% lymphocytes) and showed hypoglycorrhachia. Investigations for toxoplasmosis, cryptococcosis, histoplasmosis, tuberculosis, and CMV showed negative results, but ITS-targeting PCR results were positive on CSF. The sequence was closely related to N. obscura, but mycological cultures were sterile (Technical Appendix [PDF - 405 KB - 2 pages] Figure 2). The result of a β-
The molds of the N. vriesii complex (Chrysosporium-like anamorph, CANV) are members of the Nannizziopsis genus (Onygenales, Eurotiomycetidae, Eurotiomycetes, Ascomycota). CANV includes the keratinophilic species, which causes skin and fatal disseminated infections in reptiles (3,4). There is no documented evidence of zoophilic species involvement in human infections, but 3 other CANV species have been recovered from human samples (Table). Of the 5 previous cases of Nannizziopsis infections, 3 involved HIV patients. One of our patients was seropositive for HIV and the other had a T-cell prolymphocytic leukemia, which suggests that lymphopenia could be a key risk factor. All patients with reported N. obscura infection had recently traveled in Africa. Results for case-patient 1 showed that the fungus grows in blood cultures and thus has high potential for dissemination. Case-patient 2 had pulmonary lesions, but BAL cultures were rapidly invaded by a Penicillium fungus. Although we could not detect Nannizziopsis in BAL, the lesion evolved favorably after antifungal therapy. Because Nannizziopsis spp. are keratinophilic molds, we looked for cutaneous lesions. Both case-patients had recently developed cutaneous or nail lesions during their time in Africa, but we did not detect Nannizziopsis from these lesions. These molds have not been isolated in our laboratory in other kinds of samples (clinical or environmental).
CSF cultures from both our case-patients and ascites cultures from case-patient 1 were negative, but panfungal PCR successfully detected molds (6). Data on biomarkers are scarce. N. infrequens cross-reacts with the Histoplasma AccuProbe test and N. hominis with the Blastomyces AccuProbe test (Hologic, San Diego, CA, USA) (5). In case-patient 2, β-
These observations show how difficult this infection is to detect, which could explain why so few cases of human infections have been reported. However, the diagnosis of these 2 cases since 2015 suggests that the prevalence of Nannizziopsis infections may be underestimated.
The authors thank all the members of the Centre National de Référence des Mycoses et Antifongiques (CNRMA, Institut Pasteur de Paris, France) for their invaluable help in the antifungal susceptibility testing.
- Stillwell WT, Rubin BD, Axelrod JL. Chrysosporium, a new causative agent in osteomyelitis. A case report. Clin Orthop Relat Res. 1984; (
- Steininger C, van Lunzen J, Sobottka I, Rohde H, Horstkotte MA, Stellbrink HJ. Mycotic brain abscess caused by opportunistic reptile pathogen. Emerg Infect Dis. 2005;11:349–50.
- Sigler L, Hambleton S, Paré JA. Molecular characterization of reptile pathogens currently known as members of the chrysosporium anamorph of Nannizziopsis vriesii complex and relationship with some human-associated isolates. J Clin Microbiol. 2013;51:3338–57.
- Stchigel AM, Sutton DA, Cano-Lira JF, Cabañes FJ, Abarca L, Tintelnot K, et al. Phylogeny of chrysosporia infecting reptiles: proposal of the new family Nannizziopsiaceae and five new species. Persoonia. 2013;31:86–100.
- Brandt ME, Gaunt D, Iqbal N, McClinton S, Hambleton S, Sigler L. False-positive Histoplasma capsulatum Gen-Probe chemiluminescent test result caused by a Chrysosporium species. J Clin Microbiol. 2005;43:1456–8.
- Ihrmark K, Bödeker ITM, Cruz-Martinez K, Friberg H, Kubartova A, Schenck J, et al. New primers to amplify the fungal ITS2 region—evaluation by 454-sequencing of artificial and natural communities. FEMS Microbiol Ecol. 2012;82:666–77.
Technical AppendixCite This Article
- Page created: February 16, 2018
- Page last updated: February 16, 2018
- Page last reviewed: February 16, 2018
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)