scholarly journals Serum Stimulates Growth of and Proteinase Secretion by Aspergillus fumigatus

2002 ◽  
Vol 70 (1) ◽  
pp. 19-26 ◽  
Author(s):  
Anna H. T. Gifford ◽  
Jodine R. Klippenstein ◽  
Margo M. Moore

ABSTRACT Serum contains iron-binding proteins, which inhibit the growth of most pathogenic microorganisms, including fungi. The purpose of this research was to investigate the effect of serum on growth of the opportunistic fungal pathogen Aspergillus fumigatus. Supplementing minimal essential medium (MEM) with up to 80% human serum or up to 80% fetal bovine serum (FBS) stimulated growth and increased the amount of A. fumigatus dry biomass approximately fourfold. In addition, a 100-fold increase in proteinase secretion, as measured by azocasein hydrolysis, was observed when 10% human serum or 10% FBS was added to MEM. The fungal proteinases secreted in serum-containing media were shown to degrade 3H-labeled basal lamina proteins. The factor in serum that stimulated proteinase secretion was larger than 10 kDa and was 85% inactivated when the serum was heated for 30 min at 66°C. The proportions of proteinases of each catalytic class secreted by A. fumigatus in the presence of serum were different from the proportions secreted in media containing single proteins. Proteinase secretion did not result from increased protein concentration in the medium per se because bovine serum albumin (BSA) at a concentration equivalent to the concentration of serum produced only 20% of the proteinase activity per milligram (dry weight) that was produced by FBS. Addition of BSA plus 100 μM FeCl3 to MEM resulted in the same level of growth as addition of serum, indicating that a combination of nutritional factors in serum may stimulate growth. However, the level of proteinase secretion was still only 30% of the level observed with FBS. These data indicate that serum does not inhibit the growth of A. fumigatus and that the nutrients in serum result in high levels of proteinase secretion, potentially increasing the invasiveness of this species.

2003 ◽  
Vol 53 (1) ◽  
pp. 89-90 ◽  
Author(s):  
Gianluca Tognon ◽  
Roberta Frapolli ◽  
Marco Zaffaroni ◽  
Eugenio Erba ◽  
Massimo Zucchetti ◽  
...  

1992 ◽  
Vol 175 (6) ◽  
pp. 1643-1651 ◽  
Author(s):  
M A Moors ◽  
T L Stull ◽  
K J Blank ◽  
H R Buckley ◽  
D M Mosser

Candida albicans, an opportunistic fungal pathogen of humans, is dependent upon iron for growth. Consequently, human serum inhibits C. albicans growth due to the presence of high affinity iron-binding proteins that sequester serum iron, making it unavailable for use by the organism. We report that in the inhibitory environment of human serum, the growth of C. albicans can be restored by the addition of exogenous hemoglobin or heme, but not by protoporphyrin IX, the heme precursor that does not contain iron. We further report that C. albicans can utilize cell surface proteins that are homologues of the mammalian complement receptors (CR) to rosette complement-coated red blood cells (RBC) and obtain RBC-derived iron for growth. The ability of Candida to acquire RBC-derived iron under these conditions is dependent upon Candida-RBC rosetting mediated by CR-like molecules. Unopsonized RBC do not support Candida growth in serum, and restoration of Candida growth in serum by complement-opsonized RBC is inhibited by monoclonal antibodies to the human CR type 3 (CR3). In addition, activation of the human alternative pathway of complement by Candida leads to "bystander" deposition of C3 fragments on the surface of autologous, unopsonized RBC, generating the ligands necessary for Candida-RBC rosetting. These results suggest that C. albicans has evolved a unique strategy for acquiring iron from the host, which exploits the host complement system, and which may contribute to the pathogenic potential of the organism.


2008 ◽  
Vol 17 (5) ◽  
pp. 549-557 ◽  
Author(s):  
K. Tateishi ◽  
W. Ando ◽  
C. Higuchi ◽  
D. A. Hart ◽  
J. Hashimoto ◽  
...  

2015 ◽  
Vol 48 (3) ◽  
pp. 170 ◽  
Author(s):  
Elham Younesi ◽  
Vahid Bayati ◽  
Mahmoud Hashemitabar ◽  
Seyyed Saeed Azandeh ◽  
Dariush Bijannejad ◽  
...  

2011 ◽  
Vol 7 (4) ◽  
pp. 860-868 ◽  
Author(s):  
Abdullah Aldahmash ◽  
Mandana Haack-Sørensen ◽  
May Al-Nbaheen ◽  
Linda Harkness ◽  
Basem M. Abdallah ◽  
...  

1974 ◽  
Vol 18 (1) ◽  
pp. 86 ◽  
Author(s):  
J. LESLIE GLICK ◽  
CLARA LOCKWOOD ◽  
JETHON WILLIAMS ◽  
BEN W. PAPERMASTER ◽  
ALEX A. BURNS ◽  
...  

2015 ◽  
Vol 40 (6) ◽  
Author(s):  
Ayşe Mine Yılmaz ◽  
Ergül Mutlu Altundağ ◽  
Gülşah Gedik ◽  
Semra Koçtürk ◽  
A. Süha Yalçın ◽  
...  

AbstractObjective: Dendritic cells (DCs) are members of the mammalian immune system and are considered to be the most powerful antigen presenting cells. They are responsible for the induction of T-cells or T-cell dependent immunity and tolerance. In this study we have investigated the effect of different serum supplements on generation and yield of mature dendritic cells isolated from peripheral blood mononuclear cells.Methods: Three different serum supplements (10% Fetal Bovine Serum, 1% Human Serum Albumin and 1% autologous serum) were compared with serum-free media to identify the role and importance of serum supplements on DC cultivation. Effect of different media on maturation signs (CD40, CD80, CD86, CD209a) and cytokine release (TNF-α, IL-10, IL-12, IL-6) was examined.Results: DCs generated in serum-free media was similar to those of cells in medium with autologous serum. Few dendritic-like cells were observed in fetal bovine serum and human serum albumin. The effect of different media on maturation of DCs was compared phenotypically and increased expression of CD80, CD86 and CD209a identified maturation and yield of DCs.Conclusion: Our results suggest that serum free media can be used to overcome potential drawbacks associated with different serum containing supplements.


2008 ◽  
Vol 58 (2) ◽  
pp. 501-510 ◽  
Author(s):  
Akimoto Nimura ◽  
Takeshi Muneta ◽  
Hideyuki Koga ◽  
Tomoyuki Mochizuki ◽  
Koji Suzuki ◽  
...  

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