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Vol. 29. Issue. 4.August 2009
Pages 285-378
Vol. 29. Issue. 4.August 2009
Pages 285-378
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Peritonitis caused by Saccharomyces cerevisiae in an ambulatory peritoneal dialysis patient
PERITONITIS POR SACCHAROMYCES CEREVISIAE EN UN PACIENTE SOMETIDO A DIALISIS PERITONEAL AMBULATORIA
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Bárbara Gomila Sarda, Carlos José Téllez-Castilloa, Hector García Péreza, Rosario Moreno Muñoza
a Servicio de Microbiología y servicio de Nefrología, Hospital General de Castellón Castellón, Castellón, España,
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Dear Editor:

Saccharomyces cerevisiae (S. cerevisiae) is a yeast used habitually in breadmaking and alcoholic fermentation.1 Its isolation as a pathogen in humans is infrequent. This bears relation to its capacity to colonise the digestive tract and to its use as a probiotic in the treatment and prevention of diarrhoea associated with Clostridium difficile, and in other illnesses.2

We describe a case of peritonitis caused by S. cerevisiae in an ambulatory peritoneal dialysis patient. The case concerns a 59 year old male diagnosed 25 years ago with type 2 diabetes mellitus with photocoagulated retinopathy, arterial hypertension and asymptomatic nephrolithiasis in the lower pole of the left kidney which had evolved into advanced renal failure, for which the patient was included in a programme of peritoneal dialysis.

The patient attended the Emergency Unit presenting with retrosternal pain, nausea, vomiting, dysphagia with solid foods and diffuse abdominal pain. Fifteen days previously a diagnosis of peritonitis with negative cultures had been made by the nephrology department. This was treated empirically with vancomycin and ceftazidime. Cloudy liquid persisted over the following days. The patient was admitted and peritoneal liquid was sent to the biochemistry and microbiology departments, where it was cultured using the usual means. The cellular count was 350 leukocytes, 46% of which were polymorphonuclear.

After 24 hours the microbiology lab sent a preliminary report showing a result of Candida sp. with species pending; the nephrology department was also informed by telephone. The patient was initially treated with fluconazole and 5-fluorocytosine.

The following day the yeast was identified, using the VITEK 2 system, as S. cerevisiae. This identification was confirmed using the API ID 32C system (both from BioMerieux). In addition, an antimycogram was carried out using the SENSITITRE system, it being sensitive to all the tested antifungal drugs (amphotericin B, fluconazole, itraconazole, ketoconazole, 5-fluorocytosine, voriconazole and caspofungin), and this provided a definitive report. When we reported the isolation of this fungus to nephrology, they informed us that the patient was a baker.

Given this result, antifungal treatment was modified, suspending fluconazole and treating the infection with 5-fluorocytosine (500mg every 12 hours, following a loading dose of 2g on the first day) and lipsomal amphotericin B (70mg ev. on the first day, 150mg ev. on the second and 200mg ev. from the third day),. The patient showed a good level of tolerance to the treatment. After five days the liquid cell count was lower, and after fourteen days it was normal, with liquid showing as clear. Following twenty days of treatment the patient was healthy, and was discharged.

Although S. cerevisiae is not a common pathogen, it has been principally involved in various clinical processes such as fungaemia associated with catheters, arthritis, peritonitis, disseminated infection in advanced AIDS and in neutropaenia.3

We have found three published cases of peritonitis caused by this yeast in ambulatory peritoneal dialysis patients.4-6

Our patient could have been infected by this yeast, given that he and his wife were in daily contact with the fungus through being bakers. In the published cases, no reference is made as to what could have been the source of the infection.

Amphotericin B is the drug of choice in empirical treatment.7 Our strain was susceptible, in vitro, to all the tested antifungal drugs. According to the bibliography consulted, S. cerevisiae is usually susceptible in vitro to amphotericin B and 5-fluorocytosine, whereas there are some strains which are resistant or potentially resistant to the action of derived azoles.8 Therefore, when this yeast is isolated, it is advisable to modify treatment if it has been started with any derived azole, as was done in the case of our patient. The data referring to treatment of this fungus is scarce, since, as we have said, its isolation is uncommon.

Although fungal peritonitis in peritoneal dialysis patients at times requires the withdrawal of the peritoneal catheter, in our case this was not necessary, since following the treatment the patient developed well.

Bibliography
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Landinez Lagunero RJ, Alberte Castiñeiras A. Hongos productores de micosis oportunistas II. En García-Rodriguez JA, Picazo JJ. Microbiología médica. 1ª edición. Madrid: Harcourt-Brace, p 691-702, 1998.
[2]
Bouza E, Muñoz P. Saccharomyces cerevisiae: el fin de la inocencia. Rev Esp Quimioterapia 17 (3): 227-231, 2004.
[3]
Hazen KC, Howel SA. Candida, Cryptococcus, and other yeast of medical importance. In Murray PR, Baron EJ, Jorgensen JH, Landry ML, Pfaller MA. Manual of clinical Microbiology. Washingthon DC: ASM Press. p 1762-1788, 2007.
[4]
Mocan H, Murphy AV, Beattie TJ, McAllister TA. Fungal peritonitis in children on continuous ambulatory peritoneal dialysis. Scott Med J 34 (4): 494-496, 1989
[5]
Mydlik M, Tkacova E, Szovenyova K, Mizla P, Derzsiova K. Saccharomyces cerevisiae peritonitis complicating CAPD. Perit Dial Int 16 (2): 188, 1996
[6]
Snyder S. Peritonitis due to Saccaromyces cerevisise in a patient on CAPD. Perit Dial Int 12 (1): 77-78, 1992. [Pubmed]
[7]
Bouza E, Muñoz P. Saccharomyces cereviseae: un hongo causante de infección en el hombre. En Picazo J, Bouza E. Infección 2004. Fundación para el estudio de la infección. 1ª edición. Bilbao: Servisistem, p 69-81, 2004.
[8]
Salonen JH, Richardson MD, Gallacher K, Issakainen J, Elenius H, Lehtonen OP, Nikoskelainen J. Fungal colonization of haematological patients receiving cytotoxic chemotherapy: emergence of azole-resistant Saccharomyces cerevisiae. J Hosp Infect 45 (4): 293-301, 2000. [Pubmed]
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