Disruption of hmgA by DNA Duplication is Responsible for Hyperpigmentation in a Vibrio anguillarum Strain
Vibrio anguillarum 531A, isolated from a diseased fish in the Atlantic Ocean, is a mixture composed of about 95 and 5% of highly pigmented cells (strain 531Ad) and cells with normal levels of pigmentation (strain 531Ac), respectively. Analysis of the V . anguillarum 531Ad DNA region encompassing gen...
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Published in | Scientific reports Vol. 9; no. 1; pp. 14589 - 10 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
10.10.2019
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Vibrio anguillarum
531A, isolated from a diseased fish in the Atlantic Ocean, is a mixture composed of about 95 and 5% of highly pigmented cells (strain 531Ad) and cells with normal levels of pigmentation (strain 531Ac), respectively. Analysis of the
V
.
anguillarum
531Ad DNA region encompassing genes involved in the tyrosine metabolism showed a 410-bp duplication within the
hmgA
gene that results in a frameshift and early termination of translation of the homogentisate 1,2-dioxygenase. We hypothesized that this mutation results in accumulation of homogentisate that is oxidized and polymerized to produce pyomelanin. Introduction in
E
.
coli
of recombinant clones carrying the
V
.
anguillarum hppD
(4-hydroxyphenylpyruvate-dioxygenase), and a mutated
hmgA
produced brown colored colonies. Complementation with a recombinant clone harboring
hmgA
restored the original color to the colonies confirming that in the absence of homogentisate 1,2-dioxygenase the intermediary in tyrosine catabolism homogentisate accumulates and undergoes nonenzymatic oxidation and polymerization resulting in high amounts of the brown pigment. Whole-genome sequence analysis showed that
V
.
anguillarum
531 Ac and 531Ad differ in the
hmgA
gene mutation and 23 mutations, most of which locate to intergenic regions and insertion sequences. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-019-51126-8 |