Targeted gene deletion in Candida parapsilosis demonstrates the role of secreted lipase in virulence
J. Clin. Invest. Attila Gácser, et al. 117:3049 doi:10.1172/JCI32294 [
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Figure 5Reconstituted human oral epithelium at 48 hours infected with
C. parapsilosis WT.
(
A and
B) Uninfected control tissues, (
C and
D) WT, (
E and
F) heterozygous mutant
CpLIP1-2/Δcplip1-2, (
G and
H) homozygous mutant
Δcplip1-2/ Δcplip1-2, and (
I and
J) reconstituted
Δcplip1-2/CpLIP2. Insets show histopathological alterations. Top insets in
C and
E show apoptotic cells; middle insets in
C and
E show intercellular edema; bottom inset in
C shows cleft formation and tissue separation; and bottom inset in
E shows vacuolization. Left panels demonstrate hematoxylin and eosin staining, and right panels periodic acid Schiff staining. Arrows indicate yeast cells, and arrowheads indicate pseudohyphae. Scale bars: 10 μm (
A–
J); 5 μm (all insets). (
K) Relative LDH measured in the tissue culture supernatant by reconstituted human oral epithelium after 48 hours of coculture with WT, heterozygous mutant
CpLIP1-2/Δcplip1-2, homozygous mutant
Δcplip1-2/ Δcplip1-2, and reconstituted mutant
Δcplip1-2/CpLIP2. Error bars indicate SD. The assay was repeated 3 times. *
P < 0.02 (ANOVA).