Evidence map›Paper›PMID 28786013›Full record

ArticleJournal of industrial microbiology & biotechnology2017

Evaluation of metabolism of azo dyes and their effects on Staphylococcus aureus metabolome.

Jinchun Sun, Jinshan Jin, Richard D Beger, Carl E Cerniglia, Huizhong Chen

Open access · greenAbstract read
In one paragraph

Article in Journal of industrial microbiology & biotechnology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 36 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jinchun SunDivision of Systems Biology, National Center for Toxicological Research, US FDA, 3900 NCTR Rd, Jefferson, AR, 72079-9502, USA. Jinchun.Sun@fda.hhs.gov.
Jinshan JinDivision of Microbiology, National Center for Toxicological Research, US FDA, 3900 NCTR Rd, Jefferson, AR, 72079-9502, USA.
Richard D BegerDivision of Systems Biology, National Center for Toxicological Research, US FDA, 3900 NCTR Rd, Jefferson, AR, 72079-9502, USA.
Carl E CernigliaDivision of Microbiology, National Center for Toxicological Research, US FDA, 3900 NCTR Rd, Jefferson, AR, 72079-9502, USA.
Huizhong ChenDivision of Microbiology, National Center for Toxicological Research, US FDA, 3900 NCTR Rd, Jefferson, AR, 72079-9502, USA. Huizhong.Chen@fda.hhs.gov.
National Center for Toxicological Research · US

Funding

Intramural FDA HHS FD999999U.S. Food and Drug Administration E0729301U.S. Food and Drug Administration E0762101
6 · The paper itself

Abstract

Dyes containing one or more azo linkages are widely applied in cosmetics, tattooing, food and drinks, pharmaceuticals, printing inks, plastics, leather, as well as paper industries. Previously we reported that bacteria living on human skin have the ability to reduce some azo dyes to aromatic amines, which raises potential safety concerns regarding human dermal exposure to azo dyes such as those in tattoo ink and cosmetic colorant formulations. To comprehensively investigate azo dye-induced toxicity by skin bacteria activation, it is very critical to understand the mechanism of metabolism of the azo dyes at the systems biology level. In this study, an LC/MS-based metabolomics approach was employed to globally investigate metabolism of azo dyes by Staphylococcus aureus as well as their effects on the metabolome of the bacterium. Growth of S. aureus in the presence of Sudan III or Orange II was not affected during the incubation period. Metabolomics results showed that Sudan III was metabolized to 4-(phenyldiazenyl) aniline (48%), 1-[(4-aminophenyl) diazenyl]-2-naphthol (4%) and eicosenoic acid Sudan III (0.9%). These findings indicated that the azo bond close to naphthalene group of Sudan III was preferentially cleaved compared with the other azo bond. The metabolite from Orange II was identified as 4-aminobenzene sulfonic acid (35%). A much higher amount of Orange II (~90×) was detected in the cell pellets from the active viable cells compared with those from boiled cells incubated with the same concentration of Orange II. This finding suggests that Orange II was primarily transported into the S. aureus cells for metabolism, instead of the theory that the azo dye metabolism occurs extracellularly. In addition, the metabolomics results showed that Sudan III affected energy pathways of the S. aureus cells, while Orange II had less noticeable effects on the cells. In summary, this study provided novel information regarding azo dye metabolism by the skin bacterium, the effects of azo dyes on the bacterial cells and the important role on the toxicity and/or inactivation of these compounds due to microbial metabolism.

Indexed as

Aniline CompoundsAzo CompoundsBenzenesulfonatesColorMetabolomeNaphtholsStaphylococcus aureusSulfanilic AcidsTandem Mass Spectrometry2-naphthol2-naphthol orange4-sulfanilic acidanilineAniline CompoundsAzo CompoundsBenzenesulfonatesNaphtholssudan IIISulfanilic AcidsAzo dyesMetabolismMetabolomicsStaphylococcus aureus

Identifiers

PMID28786013
PMCPMC5863239
OpenAlexW2742743484

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.