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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Microbiol.</journal-id>
<journal-title>Frontiers in Microbiology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Microbiol.</abbrev-journal-title>
<issn pub-type="epub">1664-302X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fmicb.2022.892485</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Microbiology</subject>
<subj-group>
<subject>Editorial</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Editorial: Microbial Siderophores: Biosynthesis, Regulation, and Physiological and Ecological Impacts</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Gao</surname> <given-names>Haichun</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/194782/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Bian</surname> <given-names>Xiaoying</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/480519/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Institute of Microbiology, College of Life Sciences, Zhejiang University</institution>, <addr-line>Hangzhou</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>Helmholtz International Lab for Anti-infectives, Shandong University-Helmholtz Institute of Biotechnology, State Key Laboratory of Microbial Technology, Shandong University</institution>, <addr-line>Qingdao</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited and reviewed by: Marc Strous, University of Calgary, Canada</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Haichun Gao <email>haichung&#x00040;zju.edu.cn</email></corresp>
<fn fn-type="other" id="fn001"><p>This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology</p></fn></author-notes>
<pub-date pub-type="epub">
<day>18</day>
<month>04</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="collection">
<year>2022</year>
</pub-date>
<volume>13</volume>
<elocation-id>892485</elocation-id>
<history>
<date date-type="received">
<day>09</day>
<month>03</month>
<year>2022</year>
</date>
<date date-type="accepted">
<day>29</day>
<month>03</month>
<year>2022</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2022 Gao and Bian.</copyright-statement>
<copyright-year>2022</copyright-year>
<copyright-holder>Gao and Bian</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license> </permissions>
<related-article id="RA1" related-article-type="commentary-article" xlink:href="https://www.frontiersin.org/research-topics/21160/microbial-siderophores-biosynthesis-regulation-and-physiological-and-ecological-impacts" ext-link-type="uri">Editorial on the Research Topic <article-title>Microbial siderophores: Biosynthesis, Regulation, and Physiological and Ecological Impacts</article-title></related-article>
<kwd-group>
<kwd>siderophore</kwd>
<kwd>siderophore biosynthesis</kwd>
<kwd>iron uptake</kwd>
<kwd>bacteria</kwd>
<kwd>iron homeostasis</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="9"/>
<page-count count="3"/>
<word-count count="1553"/>
</counts>
</article-meta>
</front>
<body>
<p>Iron is essential for virtually all living organisms because iron-dependent proteins are employed to perform a myriad of functions in diverse biological processes (Wandersman and Delepelaire, <xref ref-type="bibr" rid="B8">2004</xref>; Andrews et al., <xref ref-type="bibr" rid="B1">2013</xref>). Siderophore-dependent iron acquisition is the most efficient strategy for microorganisms to obtain iron from the low-iron environments (Wilson et al., <xref ref-type="bibr" rid="B9">2016</xref>). Siderophores are small molecules specifically chelating ferric ions and are categorized into several groups based on the iron-binding moiety. Siderophores are generally inducibly synthesized and secreted in response to iron starvation (Andrews et al., <xref ref-type="bibr" rid="B1">2013</xref>; Chareyre and Mandin, <xref ref-type="bibr" rid="B3">2018</xref>). While the diversity of the siderophore biosynthetic pathways is enormous, they either employ non-ribosomal peptide synthetases (NRPSs) or NRPS-independent enzymes (Barry and Challis, <xref ref-type="bibr" rid="B2">2009</xref>). Microorganisms usually produce multiple different siderophores, with one primarily responsible for iron acquisition and others implicated in a variety of physiological processes (R&#x000FC;tschlin et al., <xref ref-type="bibr" rid="B7">2018</xref>). Many siderophores possess beneficial and antimicrobial properties, playing an important role in directly shaping microbial community by mediating cooperative, exploitative and competitive interactions (Kramer et al., <xref ref-type="bibr" rid="B4">2020</xref>). Moreover, recently they show potential in medical and environmental applications (Kurth et al., <xref ref-type="bibr" rid="B5">2016</xref>; Ribeiro and Sim&#x000F5;es, <xref ref-type="bibr" rid="B6">2019</xref>).</p>
<p>This Research Topic contains four original research and one review articles. Two articles discuss the physiological function of siderophores produced by <italic>Yersinia pseudotuberculosis</italic> and <italic>Salmonella enteritidis</italic>. It has been well known that an <italic>iucABCD</italic>-<italic>iutA</italic> operon encodes a biosynthesis system for aerobactin in many bacteria. But this may not be the case in <italic>iucABCD</italic>-<italic>iutA</italic>-carrying pathogenic <italic>Yersinia</italic> spp. as aerobactin had never been detected before the study of <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2021.699913">Li et al.</ext-link> In their article, multiple lines of evidence were presented to show that <italic>Y. pseudotuberculosis</italic> YPIII is able to produce aerobactin, which is fully dependent on the operon. The operon appears to be under the direct repression of the ferric uptake regulator (Fur) in response to changes in iron concentrations. This aerobactin-mediated iron acquisition system not only plays an important role in supporting growth under low-iron conditions, but also is involved in biofilm formation, resistance to oxidative stress, removal of reactive oxygen species, and virulence. The work emphasizes the importance of aerobactin in the general physiology and the pathogenesis of <italic>Y. pseudotuberculosis</italic>. The investigations carried out by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.824052">Wellawa et al.</ext-link> focus on the role of the siderophore-mediated (enterobactin and salmochelin) Fe<sup>3&#x0002B;</sup> and the FeoABC-mediated Fe<sup>2&#x0002B;</sup> uptake systems in colonization of <italic>Salmonella enteritidis</italic> in chicken. The results clearly show that both systems contribute in cecal colonization, rapid systemic spread, and survival in extraintestinal sites in chickens. By using a bioluminescent reporter, the authors were able to visualize the changes in iron availability during gastrointestinal colonization of <italic>Salmonella via ex vivo</italic> imaging. They found that in the cecal compartment iron shortage becomes apparent to the bacterial cells even at early colonization stages. To overcome this, both iron acquisition systems are required although there is a redundancy. Overall, the work provides an invaluable insight into the impacts of iron acquisition on Salmonella colonization in chickens and stresses the need for an understanding of <italic>Salmonella</italic> iron homeostasis and its regulation.</p>
<p>A research article by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2021.783609">Zhang et al.</ext-link> aims at siderophore biosynthesis in fungi, in which these small molecular iron chelators participate in the multiple cellular processes. They discovered the siderophores and identified their biosynthetic pathway from <italic>Metarhizium robertsii</italic> ARSEF2575. This study highlights the method using differentially transcriptional expressions of biosynthetic genes under different iron concentration conditions. It was found that three genes from different NRPS gene clusters were upregulated under iron-deficient conditions, which leads to the identification of new coprogen metachelin C that was connected to a gene cluster by deletion of <italic>mrsidA</italic> and <italic>mrsidD</italic>. This work lays a foundation for further finding for new siderophores and studying the functions of siderophores. Apart from this, a research article by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2021.729032">Khan et al.</ext-link> discusses activity of catecholate siderophores released by <italic>E. coli</italic> against fungus <italic>Aspergillus nidulans</italic>. The study found that catecholate siderophore purified from an <italic>E. coli</italic> strain, presumably enterobactin, impacts the physiology of <italic>A. nidulans</italic> profoundly, evidenced by decreased colony size, increased filament length, and altered hyphal branching pattern. Interestingly, siderophore-treated cells show a reduction in the overall antioxidative enzyme activity but catalase appears to be different. Further analyses reveal that upon siderophore exposure, the fungal cells suffer from the membrane damage judged by changed malondialdehyde contents. Authors proposed that the oxidative stress caused by siderophore-mediated iron influx largely accounts for the inhibition and killing.</p>
<p>The only review article by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.823758">Liu et al.</ext-link> consider recent advances in the siderophore biology of <italic>Shewanella</italic>, a group of ubiquitously distributed &#x003B3;-proteobacteria that include animal/human pathogens and ones well-recognized for their potential in bioenergy. These bacteria encode and produce a large number of iron-containing proteins, cytochromes <italic>c</italic> in particular, and therefore, have a high demand for iron. To meet this, an array of novel features have been evolved, including a siderophore system that is able to synthesize a variety of siderophores, many siderophore receptors that recognize siderophores released by other bacteria, regulatory systems that coordinate iron uptake, storage, and assumption for maintaining homeostasis. They also review physiological impacts of siderophore in these bacteria, some of which are unusual, especially those on cytochrome <italic>c</italic> biosynthesis. Although to support growth the siderophore-mediated Fe<sup>3&#x0002B;</sup> uptake system is still secondary to the feo-mediated Fe<sup>2&#x0002B;</sup> uptake system, the former is closely linked to cytochrome <italic>c</italic> biosynthesis. Given cytochromes <italic>c</italic> endow <italic>Shewanella</italic> respiratory versatility and great potential for biotechnological applications, the biology of siderophore in these bacteria appears to be particularly important and needs to be explored further as the current understanding of the subject in <italic>Shewanlle</italic> is rather limited.</p>
<p>The articles in this Research Topic shed light on the diverse roles of siderophores for physiological adaptation to intra/extracellular environmental change. We hope that the findings presented in these topic articles will pave the way for future studies on the biochemistry, physiology, ecology, and medical and environmental applications of microbial siderophores.</p>
<sec id="s1">
<title>Author Contributions</title>
<p>Both authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.</p>
</sec>
<sec sec-type="funding-information" id="s2">
<title>Funding</title>
<p>This research was supported by National Natural Science Foundation of China, 41976087 and 31930003.</p>
</sec>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s3">
<title>Publisher&#x00027;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec> 
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