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Norepinephrine Mediates Acquisition of Transferrin-Iron in Bordetella bronchiseptica
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ABSTRACT
Previous research demonstrated that the sympathoadrenal catecholamine norepinephrine could promote the growth of
Bordetella bronchiseptica
in iron-restricted medium containing serum. In this study, norepinephrine was demonstrated to stimulate growth of this organism in the presence of partially iron-saturated transferrin but not lactoferrin. Although norepinephrine is known to induce transcription of the
Bordetella bfeA
enterobactin catechol xenosiderophore receptor gene, neither a
bfeA
mutant nor a
bfeR
regulator mutant was defective in growth responsiveness to norepinephrine. However, growth of a
tonB
mutant strain was not enhanced by norepinephrine, indicating that the response to this catecholamine was the result of high-affinity outer membrane transport. The
B. bronchiseptica
genome encodes a total of 19 known and predicted iron transport receptor genes, none of which, when mutated individually, were found to confer a defect in norepinephrine-mediated growth stimulation in the presence of transferrin. Labeling experiments demonstrated a TonB-dependent increase in cell-associated iron levels when bacteria grown in the presence of
55
Fe-transferrin were exposed to norepinephrine. In addition, TonB was required for maximum levels of cell-associated norepinephrine. Together, these results demonstrate that norepinephrine facilitates
B. bronchiseptica
iron acquisition from the iron carrier protein transferrin and this process may represent a mechanism by which some bacterial pathogens obtain this essential nutrient in the host environment.
Title: Norepinephrine Mediates Acquisition of Transferrin-Iron in
Bordetella bronchiseptica
Description:
ABSTRACT
Previous research demonstrated that the sympathoadrenal catecholamine norepinephrine could promote the growth of
Bordetella bronchiseptica
in iron-restricted medium containing serum.
In this study, norepinephrine was demonstrated to stimulate growth of this organism in the presence of partially iron-saturated transferrin but not lactoferrin.
Although norepinephrine is known to induce transcription of the
Bordetella bfeA
enterobactin catechol xenosiderophore receptor gene, neither a
bfeA
mutant nor a
bfeR
regulator mutant was defective in growth responsiveness to norepinephrine.
However, growth of a
tonB
mutant strain was not enhanced by norepinephrine, indicating that the response to this catecholamine was the result of high-affinity outer membrane transport.
The
B.
bronchiseptica
genome encodes a total of 19 known and predicted iron transport receptor genes, none of which, when mutated individually, were found to confer a defect in norepinephrine-mediated growth stimulation in the presence of transferrin.
Labeling experiments demonstrated a TonB-dependent increase in cell-associated iron levels when bacteria grown in the presence of
55
Fe-transferrin were exposed to norepinephrine.
In addition, TonB was required for maximum levels of cell-associated norepinephrine.
Together, these results demonstrate that norepinephrine facilitates
B.
bronchiseptica
iron acquisition from the iron carrier protein transferrin and this process may represent a mechanism by which some bacterial pathogens obtain this essential nutrient in the host environment.
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