Diabetes, Vol 31, Issue 12 1109-1114, Copyright © 1982 by American Diabetes Association
A mechanism of susceptibility to mucormycosis in diabetic ketoacidosis: transferrin and iron availability
WM Artis, JA Fountain, HK Delcher and HE Jones
The defect in host defense that makes the diabetic ketoacidotic (DKA)
patient susceptible to mucormycosis has not been identified. Sera from 10
DKA patients and three normal volunteers were tested for their capacity to
support the in vitro growth of a common etiologic agent of mucormycosis,
Rhizopus oryzae. After equilibration with room air none of the normal or
DKA sera, each of which was now extremely alkaline, supported growth of R.
oryzae. When the sera were placed in a CO2 atmosphere that permitted
simulation of the in vivo clinical pH (normal 7.40 and DKA 7.3-6.6), four
of seven DKA sera supported profuse fungal growth. No growth occurred in
normal serum. The three DKA sera that did not support fungal growth at pH
less than or equal to 7.3 contained less iron (x = 13 micrograms/dl) than
the four sera that supported profuse fungal growth (x = 69 micrograms/dl).
Increasing the iron content of iron-poor DKA serum that did not support R.
oryzae growth allowed profuse growth at acidotic conditions but not at pH
greater than or equal to 7.4. Simulated acidotic conditions (pH 7.3-6.6)
also decreased the iron-binding capacity of normal serum stepwise from 266
micrograms/dl to 0. Our data indicate that acidosis temporarily disrupts
the capacity of transferrin to bind iron and suggest that this alteration
abolishes an important host defense mechanism that permits growth of R.
oryzae.