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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.2023.1256275</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 associates of blood-sucking arthropods and other animals: relevance to their physiology, ecology and evolution</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Fukatsu</surname> <given-names>Takema</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/753738/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Gottlieb</surname> <given-names>Yuval</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/268497/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Duron</surname> <given-names>Olivier</given-names></name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Graf</surname> <given-names>Joerg</given-names></name>
<xref ref-type="aff" rid="aff6"><sup>6</sup></xref>
<xref ref-type="aff" rid="aff7"><sup>7</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/108490/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology</institution>, <addr-line>Tsukuba</addr-line>, <country>Japan</country></aff>
<aff id="aff2"><sup>2</sup><institution>Department of Biological Sciences, Graduate School of Science, The University of Tokyo</institution>, <addr-line>Tokyo</addr-line>, <country>Japan</country></aff>
<aff id="aff3"><sup>3</sup><institution>Graduate School of Life and Environmental Sciences, University of Tsukuba</institution>, <addr-line>Tsukuba</addr-line>, <country>Japan</country></aff>
<aff id="aff4"><sup>4</sup><institution>The Robert H. Smith Faculty of Agriculture, Food and Environment, Koret School of Veterinary Medicine, The Hebrew University of Jerusalem</institution>, <addr-line>Rehovot</addr-line>, <country>Israel</country></aff>
<aff id="aff5"><sup>5</sup><institution>MIVEGEC, CNRS, IRD, University of Montpellier</institution>, <addr-line>Montpellier</addr-line>, <country>France</country></aff>
<aff id="aff6"><sup>6</sup><institution>Department of Molecular and Cell Biology, University of Connecticut</institution>, <addr-line>Storrs, CT</addr-line>, <country>United States</country></aff>
<aff id="aff7"><sup>7</sup><institution>Pacific Biosciences Research Center, University of Hawai&#x00027;i at M&#x00101;noa</institution>, <addr-line>Honolulu, HI</addr-line>, <country>United States</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited and reviewed by: M. Pilar Francino, Fundaci&#x000F3;n para el Fomento de la Investigaci&#x000F3;n Sanitaria y Biom&#x000E9;dica de la Comunitat Valenciana (FISABIO), Spain</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Takema Fukatsu <email>t-fukatsu&#x00040;aist.go.jp</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>26</day>
<month>07</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>14</volume>
<elocation-id>1256275</elocation-id>
<history>
<date date-type="received">
<day>10</day>
<month>07</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>17</day>
<month>07</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2023 Fukatsu, Gottlieb, Duron and Graf.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Fukatsu, Gottlieb, Duron and Graf</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/18330/microbial-associates-of-blood-sucking-arthropods-and-other-animals-relevance-to-their-physiology-ecology-and-evolution" ext-link-type="uri">Editorial on the Research Topic <article-title>Microbial associates of blood-sucking arthropods and other animals: relevance to their physiology, ecology and evolution</article-title></related-article>
<kwd-group>
<kwd>blood-feeding</kwd>
<kwd>insect</kwd>
<kwd>tick</kwd>
<kwd>mite</kwd>
<kwd>crustacean</kwd>
<kwd>leech</kwd>
<kwd>microbiome</kwd>
<kwd>B vitamin</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="19"/>
<page-count count="3"/>
<word-count count="2122"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Microbial Symbioses</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>Lice, bed bugs, ticks, leeches, and other tiny blood-sucking crawling creatures are regarded as nasty vampires, causing itches, eliciting disgusting feeling, vectoring human and animal diseases, and thereby bringing about medical, health, hygienic and mental problems in human societies (Lehane, <xref ref-type="bibr" rid="B15">2005</xref>). Besides the microbial pathogens they carry and transmit, unique microorganisms are associated with them and affect their physiology, ecology, and other biological aspects in a variety of ways (Rio et al., <xref ref-type="bibr" rid="B17">2016</xref>; Husnik, <xref ref-type="bibr" rid="B12">2018</xref>). For example, their food, vertebrate blood, is certainly nutrition-rich, but devoid of some important nutrients like B vitamins. Hence, many blood feeders possess specialized organs called bacteriomes for hosting vitamin-provisioning symbionts (Buchner, <xref ref-type="bibr" rid="B6">1965</xref>), which enable them to thrive only on the blood meal (Duron and Gottlieb, <xref ref-type="bibr" rid="B9">2020</xref>). Fully engorged blood feeders exhibit a challenging gut environment with plenty of proteins, iron, heme and antimicrobial components such as antibodies and complements, which may foster unique gut microbiome (Sterkel et al., <xref ref-type="bibr" rid="B19">2017</xref>).</p>
<p>Owing to recent development of high-throughput DNA sequencing technologies, our knowledge of the microbiomes associated with these blood-sucking invertebrates, which must be connected to their unique feeding habit and physiology, has been growing rapidly. Hence, this Research Topic &#x0201C;<italic>Microbial Associates of Blood-Sucking Arthropods and Other Animals: Relevance to Their Physiology, Ecology and Evolution</italic>&#x0201D; is aimed to provide a forum for new findings emerging in this research field. In total, nine articles and two reviews are compiled, which showcase the microbial associates of a diverse array of blood-feeding invertebrates including lice (Insecta: Psocodea), tsetse flies (Insecta: Diptera), fleas (Insecta: Siphonaptera), ticks (Arachnida: Ixodida) and mites (Arachnida: Mesostigmata) from the terrestrial ecosystem, and <italic>Elthusa</italic> and <italic>Nerocila</italic> (Crustacea: Isopoda), <italic>Lernanthropus</italic> (Crustacea: Copepoda) and fish leeches (Hirudinea: Piscicolidae) from the marine ecosystem.</p>
<p>Sucking lice (Psocodea: Anoplura) live on vertebrate blood as the sole food source throughout their life cycle (Durden and Musser, <xref ref-type="bibr" rid="B8">1994</xref>), many of which possess specialized symbiotic organs for harboring specific symbiotic bacteria (Ries, <xref ref-type="bibr" rid="B16">1931</xref>; Buchner, <xref ref-type="bibr" rid="B6">1965</xref>). Both histological inspection and molecular phylogenetic survey revealed that their symbiotic organs and associated bacterial symbionts are strikingly diverse among different lice lineages and likely of independent evolutionary origins (Hyp&#x00161;a and Kri&#x0017D;ek, <xref ref-type="bibr" rid="B13">2007</xref>; Boyd and Reed, <xref ref-type="bibr" rid="B5">2012</xref>). In this Research Topic, three articles dealt with louse-associated symbiotic bacteria. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.962252">Nishide, Oguchi, et al.</ext-link>, investigated the endosymbiotic microbiota of the boar louse <italic>Haematopinus apri</italic>, identified a primary endosymbiont clade associated with the boar, swine and cattle lice, and designated it as &#x0201C;<italic>Candidatus</italic> Haematopinicola symbiotica&#x0201D;. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.900312">&#x00158;&#x000ED;hov&#x000E1; et al.</ext-link> screened and assembled the metagenomic data of the chipmunk lice <italic>Neohaematopinus</italic> spp. and identified a genome-reduced endosymbiont designated as &#x0201C;<italic>Candidatus</italic> Lightella neohaematopini&#x0201D;. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2021.642543">Do&#x000F1;a et al.</ext-link> surveyed the microbiota associated with the seal louse <italic>Echinophthirius horridus</italic>, which uncovered diverse bacterial associates but failed to identify principal symbiotic bacteria. These reports highlight the dynamic evolutionary trajectories of the louse-microbe endosymbiotic associations entailing multiple and independent gains and losses.</p>
<p>Tsetse flies (Diptera: Glossinidae) are obligatory blood feeders distributed in sub-Saharan Africa, where they vector devastating human and animal pathogens <italic>Trypanosoma</italic> spp. (Krafsur, <xref ref-type="bibr" rid="B14">2009</xref>). Tsetse flies are associated with a vitamin-provisioning primary symbiont <italic>Wigglesworthia glossinidia</italic>, a commensal bacterial associate <italic>Sodalis glossinidius</italic>, and a facultative endosymbiont <italic>Wolbachia pipientis</italic> (Aksoy, <xref ref-type="bibr" rid="B1">2000</xref>). In the Research Topic, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.905826">Lee et al.</ext-link> reviewed the current understanding of tsetse-microbe molecular interactions, with particular focus on recently accumulating knowledge about possible involvement of DNA methylation and microRNAs.</p>
<p>Fleas (Siphonaptera) are obligatory blood feeders of mammals and birds as adults, and notorious for vectoring <italic>Yersinia pestis</italic> and other pathogens (Bitam et al., <xref ref-type="bibr" rid="B3">2010</xref>). Probably because their larvae live on organic debris without blood feeding, no obligatory microbial symbionts have been known from fleas, whereas diverse facultative bacterial associates have been detected, as <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2023.1188155">Dong et al.</ext-link> identified <italic>Wolbachia, Rickettsia</italic> and <italic>Bartonella</italic> as the major bacterial associates of the fleas <italic>Oropsylla silantiewi</italic> and <italic>Callopsylla dolabris</italic> from Himalayan marmots. In the flea <italic>Synosternus cleopatrae</italic> from desert rodents, it was reported that, interestingly, <italic>Wolbachia</italic> infection is fixed in females but lacking or partial in males (Flatau et al., <xref ref-type="bibr" rid="B10">2018</xref>). In this Research Topic, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2021.649248">Flatau et al.</ext-link> treated <italic>S. cleopatrae</italic> with tetracycline and compared the life history parameters of <italic>Wolbachia</italic>-infected fleas with those of <italic>Wolbachia</italic>-free fleas, but no significant differences were detected between them.</p>
<p>Ticks (Ixodida: Ixodea) are obligatory blood feeders of terrestrial vertebrates including mammals, birds, reptiles and amphibians (Anderson and Magnarelli, <xref ref-type="bibr" rid="B2">2008</xref>). Conventionally, ticks have been regarded as vectors of <italic>Rickettsia, Coxiella</italic> and other pathogens causing human and animal diseases (de la Fuente et al., <xref ref-type="bibr" rid="B7">2008</xref>), but now it is widely recognized that ticks commonly host non-pathogenic, either commensalistic or mutualistic, microbial associates allied to <italic>Coxiella, Rickettsia, Francisella, Midichloria, Wolbachia</italic> and others (Bonnet et al., <xref ref-type="bibr" rid="B4">2017</xref>). In this Research Topic, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.854803">Hussain et al.</ext-link> reviewed such tick-microbe symbiotic continuum spanning from pathogens through commensals to mutualists. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2023.1188155">Dong et al.</ext-link> detected <italic>Anaplasma, Wolbachia</italic> and <italic>Ehrlichia</italic> as the major bacterial associates of the tick <italic>Haemaphysalis qinghaiensis</italic> from Himalayan marmots. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.1050063">Militzer et al.</ext-link> analyzed the effects of artificial feeding and antibiotic treatment on microbiome composition and fecundity of the tick <italic>Ixodes ricinus</italic> associated with <italic>Midichloria, Rickettsia</italic> and <italic>Spiroplasma</italic>.</p>
<p>The poultry red mite <italic>Dermanyssus gallinae</italic> (Mesostigmata: Dermanyssidae) is a blood sucking avian ectoparasite that often causes significant economic damage on poultry production (Sparagano et al., <xref ref-type="bibr" rid="B18">2014</xref>). A previous study identified <italic>Bartonella, Cardinium, Wolbachia</italic> and <italic>Rickettsiella</italic> in European populations of <italic>D. gallinae</italic> (Hubert et al., <xref ref-type="bibr" rid="B11">2017</xref>). In this Research Topic, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2021.695346">Price et al.</ext-link> detected <italic>Rickettsiella</italic> from all 63 samples of <italic>D. gallinae</italic> derived from 63 localities across 15 European countries, and determined the 1.9 Mbp <italic>Rickettsiella</italic> genome that retains the synthetic pathways for thiamine (= vitamin B1), riboflavin (= vitamin B2) and pyridoxine (= vitamin B6). By contrast, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.1031535">Nishide, Sugimoto, et al.</ext-link>, reported that, from 144 samples of <italic>D. gallinae</italic> collected from 18 poultry farms in Japan, <italic>Bartonella, Cardinium, Wolbachia</italic> and <italic>Tsukamurella</italic> were detected as major bacterial components, but <italic>Rickettsiella</italic> was not detected at all. These reports uncovered strikingly different microbiota across European and Japanese populations of <italic>D. gallinae</italic>. At present, whether <italic>Rickettsiella</italic> is the vitamin-provisioning primary symbiont of <italic>D. gallinae</italic> or not is elusive and to be established in future studies.</p>
<p>Finally, as the highlight of this Research Topic, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2022.1113237">Goffredi et al.</ext-link> reported the microbiomes of marine obligatory blood feeders that have been little investigated previously: fish ectoparasitic isopods <italic>Elthusa vulgaris</italic> and <italic>Nerocila californica</italic> (Isopoda: Cymothoidae); a fish ectoparasitic copepod <italic>Lernanthropus latis</italic> (Copepoda: Lernanthropidae); and fish leeches <italic>Pterobdella occidentalis, Ostreobdella californiana</italic>, and <italic>Branchellion lobata</italic> (Hirudinea: Piscicolidae). Interestingly, all the marine blood suckers exhibited peculiar gut microbiomes characterized by relatively low diversity dominated by <italic>Vibrio</italic> species.</p>
<p>In conclusion, the Research Topic presents an impressive overview of the current research coverage on the diversity of microbial symbioses among blood-sucking arthropods and other invertebrates. These reports significantly broaden our knowledge as to what types of microbiomes are associated with the obligatory blood feeders, and highlight the untouched research fields represented by, for example, marine obligatory blood feeders and their biological and functional aspects, as promising targets for future studies. It has been widely accepted that symbiotic interactions with microorganisms are essential for the ecology of insects, ticks, leeches and other invertebrates with obligatory blood feeding habit. Diverse bacterial lineages have independently evolved functional interactions with the obligatory blood feeders, but, notably, all converge to an analogous biochemical feature of vitamin provisioning.</p>
<sec sec-type="author-contributions" id="s1">
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<p>All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.</p></sec>
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<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>
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