Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Sep;161(3):441-447.e2.
doi: 10.1016/j.jpeds.2012.02.051. Epub 2012 Apr 14.

Candida virulence properties and adverse clinical outcomes in neonatal candidiasis

Affiliations

Candida virulence properties and adverse clinical outcomes in neonatal candidiasis

Joseph M Bliss et al. J Pediatr. 2012 Sep.

Abstract

Objective: To determine whether premature infants with invasive Candida infection caused by strains with increased virulence properties have worse clinical outcomes than those infected with less virulent strains.

Study design: Clinical isolates were studied from 2 populations of premature infants, those colonized with Candida spp (commensal; n = 27) and those with invasive candidiasis (n = 81). Individual isolates of C albicans and C parapsilosis were tested for virulence in 3 assays: phenotypic switching, adhesion, and cytotoxicity. Invasive isolates were considered to have enhanced virulence if detected at a level >1 SD above the mean for the commensal isolates in at least one assay. Outcomes of patients with invasive isolates with enhanced virulence were compared with those with invasive isolates lacking enhanced virulence characteristics.

Results: Enhanced virulence was detected in 61% of invasive isolates of C albicans and 42% of invasive isolates of C parapsilosis. All C albicans cerebrospinal fluid isolates (n = 6) and 90% of urine isolates (n = 10) had enhanced virulence, compared with 48% of blood isolates (n = 40). Infants with more virulent isolates were younger at the time of positive culture and had higher serum creatinine levels.

Conclusion: Individual isolates of Candida species vary in their virulence properties. Strains with higher virulence are associated with certain clinical outcomes.

PubMed Disclaimer

Conflict of interest statement

The authors have no conflicting financial interests.

Figures

Figure 1
Figure 1. Source of commensal and invasive isolates
Clinical isolates of C. albicans (C. alb) and C. parapsilosis (C. para) were obtained from two independent studies. In all cases the first isolate was included for any individual patient. Commensal isolates were from infants colonized orally, rectally, or on the skin, but without invasive infection.[8] One infant was colonized with both species. Thirteen C. albicans and fourteen C. parapsilosis isolates were available at the time of the current study. Invasive isolates came from blood, CSF, or urine.[14] One infant had a positive blood culture for both C. albicans and C. parapsilosis. Both isolates are reported, for a total of 82 positive cultures.
Figure 2
Figure 2. Rates of enhanced virulence by assay and species
Each isolate of C. albicans (C.a.) and C. parapsilosis (C.p.) obtained from cultures of blood, urine, or CSF was evaluated in each of three assays. The rate at which isolates from each source measured in the enhanced virulence range relative to the commensal strains in each assay is depicted.

Similar articles

Cited by

References

    1. Benjamin DK, Jr, Stoll BJ, Fanaroff AA, McDonald SA, Oh W, Higgins RD, et al. Neonatal candidiasis among extremely low birth weight infants: risk factors, mortality rates, and neurodevelopmental outcomes at 18 to 22 months. Pediatrics. 2006;117:84–92. - PubMed
    1. Stoll BJ, Hansen N, Fanaroff AA, Wright LL, Carlo WA, Ehrenkranz RA, et al. Late-onset sepsis in very low birth weight neonates: the experience of the NICHD Neonatal Research Network. Pediatrics. 2002;110:285–291. - PubMed
    1. Beck-Sague C, Jarvis WR. Secular trends in the epidemiology of nosocomial fungal infections in the United States, 1980–1990. National Nosocomial Infections Surveillance System. J Infect Dis. 1993;167:1247–1251. - PubMed
    1. Trofa D, Gacser A, Nosanchuk JD. Candida parapsilosis, an emerging fungal pathogen. Clin Microbiol Rev. 2008;21:606–625. - PMC - PubMed
    1. van Asbeck EC, Clemons KV, Stevens DA. Candida parapsilosis: a review of its epidemiology, pathogenesis, clinical aspects, typing and antimicrobial susceptibility. Crit Rev Microbiol. 2009;35:283–309. - PubMed

MeSH terms