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Bioactive Products From Plant-Endophytic Gram-Positive Bacteria

Identifieur interne : 000552 ( Pmc/Corpus ); précédent : 000551; suivant : 000553

Bioactive Products From Plant-Endophytic Gram-Positive Bacteria

Auteurs : María J. Ek-Ramos ; Ricardo Gomez-Flores ; Alonso A. Orozco-Flores ; Cristina Rodríguez-Padilla ; Guadalupe González-Ochoa ; Patricia Tamez-Guerra

Source :

RBID : PMC:6449470

Abstract

Endophytes constitute plant-colonizing microorganisms in a mutualistic symbiosis relationship. They are found in most ecosystems reducing plant crops’ biotic and abiotic stressors by stimulating immune responses, excluding plant pathogens by niche competition, and participating in antioxidant activities and phenylpropanoid metabolism, whose activation produces plant defense, structural support, and survival molecules. In fact, metabolomic studies have demonstrated that endophyte genes associated to specific metabolites are involved in plant growth promotion (PGP) by stimulating plant hormones production such as auxins and gibberellins or as plant protective agents against microbial pathogens, cancer, and insect pests, but eco-friendly and eco-safe. A number of metabolites of Gram-positive endophytes isolated from agriculture, forest, mangrove, and medicinal plants, mainly related to the Firmicutes phyla, possess distinctive biocontrol and plant growth-promoting activities. In general, Actinobacteria and Bacillus endophytes produce aromatic compounds, lipopeptides, plant hormones, polysaccharides, and several enzymes linked to phenylpropanoid metabolism, thus representing high potential for PGP and crop management strategies. Furthermore, Actinobacteria have been shown to produce metabolites with antimicrobial and antitumor activities, useful in agriculture, medicine, and veterinary areas. The great endophytes diversity, their metabolites production, and their adaptation to stress conditions make them a suitable and unlimited source of novel metabolites, whose application could reduce agrochemicals usage in food and drugs production.


Url:
DOI: 10.3389/fmicb.2019.00463
PubMed: 30984118
PubMed Central: 6449470

Links to Exploration step

PMC:6449470

Le document en format XML

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<p>Endophytes constitute plant-colonizing microorganisms in a mutualistic symbiosis relationship. They are found in most ecosystems reducing plant crops’ biotic and abiotic stressors by stimulating immune responses, excluding plant pathogens by niche competition, and participating in antioxidant activities and phenylpropanoid metabolism, whose activation produces plant defense, structural support, and survival molecules. In fact, metabolomic studies have demonstrated that endophyte genes associated to specific metabolites are involved in plant growth promotion (PGP) by stimulating plant hormones production such as auxins and gibberellins or as plant protective agents against microbial pathogens, cancer, and insect pests, but eco-friendly and eco-safe. A number of metabolites of Gram-positive endophytes isolated from agriculture, forest, mangrove, and medicinal plants, mainly related to the Firmicutes phyla, possess distinctive biocontrol and plant growth-promoting activities. In general, Actinobacteria and
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endophytes produce aromatic compounds, lipopeptides, plant hormones, polysaccharides, and several enzymes linked to phenylpropanoid metabolism, thus representing high potential for PGP and crop management strategies. Furthermore, Actinobacteria have been shown to produce metabolites with antimicrobial and antitumor activities, useful in agriculture, medicine, and veterinary areas. The great endophytes diversity, their metabolites production, and their adaptation to stress conditions make them a suitable and unlimited source of novel metabolites, whose application could reduce agrochemicals usage in food and drugs production.</p>
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<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Front Microbiol</journal-id>
<journal-id journal-id-type="iso-abbrev">Front Microbiol</journal-id>
<journal-id journal-id-type="publisher-id">Front. Microbiol.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Microbiology</journal-title>
</journal-title-group>
<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="pmid">30984118</article-id>
<article-id pub-id-type="pmc">6449470</article-id>
<article-id pub-id-type="doi">10.3389/fmicb.2019.00463</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Microbiology</subject>
<subj-group>
<subject>Mini Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Bioactive Products From Plant-Endophytic Gram-Positive Bacteria</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Ek-Ramos</surname>
<given-names>María J.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/359805/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gomez-Flores</surname>
<given-names>Ricardo</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Orozco-Flores</surname>
<given-names>Alonso A.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/695806/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rodríguez-Padilla</surname>
<given-names>Cristina</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>González-Ochoa</surname>
<given-names>Guadalupe</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/695794/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tamez-Guerra</surname>
<given-names>Patricia</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">
<sup>*</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/534040/overview"></uri>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Departamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León</institution>
,
<addr-line>San Nicolás de los Garza</addr-line>
,
<country>Mexico</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Departamento de Ciencias Químico Biológicas, División de Ciencias e Ingeniería, Universidad de Sonora</institution>
,
<addr-line>Navojoa</addr-line>
,
<country>Mexico</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: José E. Barboza-Corona, Universidad de Guanajuato, Mexico</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Ashutosh Sharma, Tecnologico de Monterrey, Mexico; Tapan Kumar Adhya, KIIT University, India</p>
</fn>
<corresp id="c001">*Correspondence: Patricia Tamez-Guerra,
<email>patamez@hotmail.com</email>
;
<email>patricia.tamezgr@uanl.edu.mx</email>
</corresp>
<fn fn-type="other" id="fn001">
<p>This article was submitted to Microbiotechnology, Ecotoxicology and Bioremediation, a section of the journal Frontiers in Microbiology</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>29</day>
<month>3</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="collection">
<year>2019</year>
</pub-date>
<volume>10</volume>
<elocation-id>463</elocation-id>
<history>
<date date-type="received">
<day>29</day>
<month>10</month>
<year>2018</year>
</date>
<date date-type="accepted">
<day>21</day>
<month>2</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2019 Ek-Ramos, Gomez-Flores, Orozco-Flores, Rodríguez-Padilla, González-Ochoa and Tamez-Guerra.</copyright-statement>
<copyright-year>2019</copyright-year>
<copyright-holder>Ek-Ramos, Gomez-Flores, Orozco-Flores, Rodríguez-Padilla, González-Ochoa and Tamez-Guerra</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-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.</license-p>
</license>
</permissions>
<abstract>
<p>Endophytes constitute plant-colonizing microorganisms in a mutualistic symbiosis relationship. They are found in most ecosystems reducing plant crops’ biotic and abiotic stressors by stimulating immune responses, excluding plant pathogens by niche competition, and participating in antioxidant activities and phenylpropanoid metabolism, whose activation produces plant defense, structural support, and survival molecules. In fact, metabolomic studies have demonstrated that endophyte genes associated to specific metabolites are involved in plant growth promotion (PGP) by stimulating plant hormones production such as auxins and gibberellins or as plant protective agents against microbial pathogens, cancer, and insect pests, but eco-friendly and eco-safe. A number of metabolites of Gram-positive endophytes isolated from agriculture, forest, mangrove, and medicinal plants, mainly related to the Firmicutes phyla, possess distinctive biocontrol and plant growth-promoting activities. In general, Actinobacteria and
<italic>Bacillus</italic>
endophytes produce aromatic compounds, lipopeptides, plant hormones, polysaccharides, and several enzymes linked to phenylpropanoid metabolism, thus representing high potential for PGP and crop management strategies. Furthermore, Actinobacteria have been shown to produce metabolites with antimicrobial and antitumor activities, useful in agriculture, medicine, and veterinary areas. The great endophytes diversity, their metabolites production, and their adaptation to stress conditions make them a suitable and unlimited source of novel metabolites, whose application could reduce agrochemicals usage in food and drugs production.</p>
</abstract>
<kwd-group>
<kwd>metabolites</kwd>
<kwd>amylases</kwd>
<kwd>chitinases</kwd>
<kwd>endoglucanases</kwd>
<kwd>esterases</kwd>
<kwd>proteases</kwd>
<kwd>plant hormones</kwd>
<kwd>toxins</kwd>
</kwd-group>
<funding-group>
<award-group>
<funding-source id="cn001">Consejo Nacional de Ciencia y Tecnología
<named-content content-type="fundref-id">10.13039/501100007350</named-content>
</funding-source>
</award-group>
</funding-group>
<counts>
<fig-count count="3"></fig-count>
<table-count count="0"></table-count>
<equation-count count="0"></equation-count>
<ref-count count="128"></ref-count>
<page-count count="12"></page-count>
<word-count count="0"></word-count>
</counts>
</article-meta>
</front>
<body>
<sec>
<title>Introduction to Endophytes</title>
<p>Endophytes are facultative or obligate symbiotic microorganisms, mainly bacterial and fungal species, that live in apparently healthy internal plant tissues, without causing disease (
<xref rid="B102" ref-type="bibr">Schulz and Boyle</xref>
,
<xref rid="B102" ref-type="bibr">2006</xref>
). The most studied ones are bacterial and fungal species.</p>
<p>The purpose of this minireview is to highlight the importance of previously reported endophytic Gram-positive bacteria bioactive products. The International Union for Conservation of Nature and Natural Resources estimates that there are about 297,326 species of plants (Monocotyledons, Dicotyledons, Gymnosperms, Ferns and allies and Mosses), but only a few of them have been studied for their endophyte microbiota (
<xref rid="B108" ref-type="bibr">Strobel and Daisy, 2003</xref>
;
<xref rid="B1" ref-type="bibr">Aitken, 2004</xref>
). Endophytic microorganisms are known to influence plant physiology and development, among which, Gram-positive bacteria are important in such activities as bioremediation, biocontrol, plant growth, symbiotic-mutualistic, commensalistic, trophobiotic interactions, control of soil-borne pathogens, and support of host plant defense against environmental stress (
<xref rid="B98" ref-type="bibr">Ryan et al., 2008</xref>
). An endophytic community is complex and several factors may affect its structure, such as plant-microbe and microbe-microbe interactions and environmental conditions (
<xref rid="B98" ref-type="bibr">Ryan et al., 2008</xref>
). For bacterial endophytes diversity analysis, cultivation-based and culture-independent methods are used. In regard to cultivation studies, a great number of bacteria, mostly Proteobacteria, have been reported as endophytes, being the most frequent from Actinobacteria, Bacteroidetes, and Firmicutes phyla (
<xref rid="B97" ref-type="bibr">Rosenblueth and Martínez-Romero, 2006</xref>
).</p>
<p>The most abundant metabolite producing Gram-positive bacteria endophytes found within diverse environments are
<italic>Bacillus</italic>
and
<italic>Streptomyces</italic>
species (
<xref rid="B95" ref-type="bibr">Reinhold-Hurek and Hurek, 2011</xref>
;
<xref rid="B42" ref-type="bibr">Frank et al., 2017</xref>
;
<xref ref-type="fig" rid="F1">Figure 1</xref>
<xref ref-type="fig" rid="F3">3</xref>
).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Production of metabolites by endophytes among plant tissues.
<sup>1</sup>
The “ESKAPE” bacterial pathogens (
<italic>Acinetobacter baumannii, Enterobacter</italic>
spp.,
<italic>Enterococcus faecium, Klebsiella pneumoniae, Pseudomonas aeruginosa</italic>
, and
<italic>Staphylococcus aureus</italic>
) are the leading nosocomial infectious agents throughout the world.
<sup>2</sup>
Metabolites synthesized by non-ribosomal peptide synthetases (NRPS) or polyketide synthase (PKS). Detailed information on antimicrobial metabolites against animal/human pathogens are in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>
, against plant pathogens and insect pests in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S2</xref>
, as plant growth stimulant in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S3</xref>
and as anti-cancer agent in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S4</xref>
.</p>
</caption>
<graphic xlink:href="fmicb-10-00463-g001"></graphic>
</fig>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Production of metabolites by
<italic>Bacillus</italic>
spp. and strains as plant endophytes. (a)
<italic>Bacillus amyloliquefaciens</italic>
; (b)
<italic>Bacillus subtilis</italic>
.
<sup>1</sup>
PGP, plant growth promoting.
<sup>2</sup>
Metabolites synthesized by NRPS or PKS.
<sup>3</sup>
IAA, indol acetic acid. Detailed information on antimicrobial metabolites against animal/human pathogens are in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>
, against plant pathogens and insect pests in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S2</xref>
, as plant growth stimulant in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S3</xref>
and as anti-cancer agent in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S4</xref>
.</p>
</caption>
<graphic xlink:href="fmicb-10-00463-g002"></graphic>
</fig>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>Production of metabolites by
<italic>Streptomyces</italic>
spp. and strains as plant endophytes. (a) Antimicrobial metabolites against human pathogens; (b) metabolites showing antimicrobial and cytotoxic activity; (c) cytotoxic metabolites against several tumor cell lines.
<sup>1</sup>
PGP, plant growth promote. Detailed information on antimicrobial metabolites against animal/human pathogens are in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>
, against plant pathogens and insect pests in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S2</xref>
, as plant growth stimulant in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S3</xref>
and as anti-cancer agent in
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S4</xref>
.</p>
</caption>
<graphic xlink:href="fmicb-10-00463-g003"></graphic>
</fig>
<p>Endophytes are found in plants of most ecosystems and are of agricultural importance since they help to improve crops yields, by stimulating plants growth and immune response, excluding plant pathogens by niche competition, as well as actively participating in phenylpropanoid metabolism and antioxidant activities (
<xref rid="B85" ref-type="bibr">Pandey et al., 2018</xref>
). Among plant microbiota, endophytic bacteria can be found in most plant species and be recovered from roots, leaves, stems, and a few from flowers, fruits, and seeds (
<xref rid="B74" ref-type="bibr">Lodewyckx et al., 2002</xref>
); they have the potential to produce a variety of secondary metabolites with application in agriculture and pharmaceutical and industrial biotechnology (
<xref rid="B74" ref-type="bibr">Lodewyckx et al., 2002</xref>
;
<xref rid="B108" ref-type="bibr">Strobel and Daisy, 2003</xref>
;
<xref rid="B98" ref-type="bibr">Ryan et al., 2008</xref>
). Bacterial endophytes live within cell walls and xylem vessels intercellular regions and they may colonize seeds (
<xref rid="B13" ref-type="bibr">Cankar et al., 2005</xref>
;
<xref rid="B64" ref-type="bibr">Johnston-Monje and Raizada, 2011</xref>
), fruits (
<xref rid="B30" ref-type="bibr">de Melo-Pereira et al., 2012</xref>
), and flowers (
<xref rid="B27" ref-type="bibr">Compant et al., 2011</xref>
), among other tissues. It is known that endophytic bacteria are located in the apoplast (
<xref rid="B70" ref-type="bibr">Koskimäki et al., 2015</xref>
), and plant roots are proposed to be the entry point (
<xref rid="B86" ref-type="bibr">Paungfoo-Lonhienne et al., 2010</xref>
). It is also suggested that they are transmitted using an alternative vertical strategy due to their presence in flowers and seeds (
<xref rid="B113" ref-type="bibr">Tamosiune et al., 2017</xref>
). The potential explanation for their ubiquitous presence into plant tissues is the diversity of positive effects on plant growth and fitness they have shown, by stimulating the host phenylpropanoid pathway or by producing several linked-metabolites to the plants’ metabolism (
<xref rid="B11" ref-type="bibr">Brader et al., 2014</xref>
;
<xref rid="B54" ref-type="bibr">Haidar et al., 2016</xref>
;
<xref rid="B75" ref-type="bibr">Lòpez-Fernàndez et al., 2016</xref>
;
<xref rid="B3" ref-type="bibr">Alaimo et al., 2018</xref>
). Many reports indicate that bacterial endophytes help to provide nutrients as plant growth-promoters, and induce tolerance/resistance against biotic and abiotic stress conditions (
<xref rid="B98" ref-type="bibr">Ryan et al., 2008</xref>
).</p>
<p>In addition, several metabolites produced by microbial endophytes act as antimicrobial agents against human, animal, and plant pathogens. Whereas the antimicrobial effect against phytopathogens will have the positive effect on the host plant, the efficacies of endophyte metabolites may show a great clinical potential for medical and veterinary treatments. Indeed, nature-occurring antibiotics are low-molecular-weight products made by microbes that inhibit the growth or kill phytopathogens, bacteria, fungi, viruses, and protozoans, that cause human and animal diseases (
<xref rid="B31" ref-type="bibr">Demain, 1981</xref>
;
<xref rid="B62" ref-type="bibr">Jakubiec-Krzesniak et al., 2018</xref>
;
<xref rid="B115" ref-type="bibr">Tripathi et al., 2018</xref>
). Some important antibiotics producers have been recently found as endophytes in different plant species (
<xref rid="B37" ref-type="bibr">Eljounaidi et al., 2016</xref>
).</p>
<p>It is known that immunocompromised individuals (AIDS, cancer, and organ transplant patients) are at high risk for developing opportunistic microbial infections by
<italic>Aspergillus</italic>
sp.,
<italic>Candida albicans, Clostridium difficile, Coccidioides immitis, Cryptococcus neoformans, Cryptosporidium, Mycobacterium avium</italic>
complex,
<italic>M. tuberculosis, Pneumocystis jirovecii, Pseudomonas aeruginosa, Salmonella</italic>
sp.,
<italic>Staphylococcus aureus, Streptococcus pneumoniae</italic>
, and
<italic>S. pyogenes</italic>
, as well as parasitic infections caused by
<italic>Cryptosporidium</italic>
spp.,
<italic>Encephalitozoon</italic>
spp.,
<italic>Isospora belli, Leishmania</italic>
spp.,
<italic>Plasmodium falciparum, Toxoplasma gondii</italic>
, and
<italic>Trypanosoma cruzi</italic>
. The urgent need for human diseases prevention and treatment, has promoted the discovery and development of novel and efficient therapeutic agents to which resistance has not been produced (
<xref rid="B108" ref-type="bibr">Strobel and Daisy, 2003</xref>
;
<xref rid="B25" ref-type="bibr">Chinedum, 2005</xref>
). For instance, drug resistance is a recognized phenomenon that disease-causing microbial agents develop against pharmaceutical therapy. Infectious diseases and cancer share similarities in the mechanisms of resistance to drugs, such as drug efflux, which is evolutionarily conserved (
<xref rid="B55" ref-type="bibr">Housman et al., 2014</xref>
). Therefore, in this review, the antibacterial, antifungal, antiviral, and antitumor activities of metabolites produced by specific Gram-positive bacteria endophytes are highlighted, as well as their potential use as plant growth promoters (PGP).</p>
</sec>
<sec>
<title>Gram-Positive Endophytes Against Human/Animal Pathogens</title>
<p>Among Actinobacteria, Actinomycetes are Gram-positive, filamentous bacteria with great potential as biocontrol agents, which produce approximately two-thirds of natural antibiotics, where 75% derived from
<italic>Streptomyces</italic>
species (
<xref rid="B29" ref-type="bibr">de Lima Procópio et al., 2012</xref>
;
<xref ref-type="fig" rid="F1">Figure 1</xref>
,
<xref ref-type="fig" rid="F3">3</xref>
). Actinomycetes, including the
<italic>Actinomyces, Actinoplanes, Amycolatopsis, Micromonospora, Saccharopolyspora</italic>
, and
<italic>Streptomyces</italic>
genera, are recognized as bioactive secondary metabolites producers, not only showing antimicrobial, but also insecticidal and antitumoral activities (
<xref rid="B96" ref-type="bibr">Renu et al., 2008</xref>
;
<xref rid="B67" ref-type="bibr">Kekuda et al., 2010</xref>
).</p>
<p>Lipopeptides are among the most important classes of secondary metabolites produced by endophytic bacteria, which are formed by cyclic or short linear peptides linked to a lipid tail or lipophilic molecules. Lipopeptides may show antimicrobial, cytotoxic and surfactant activities; they are synthesized by non-ribosomal peptide synthetases (NRPS), or polyketide synthase (PKS) and have great structural diversity based on a hydrophobic fatty acid acyl chain of 13 to 17 carbons, linked to a hydrophilic peptide of 7–25 aminoacids. Lipopeptides are important for both, their antibiotic activity and for inducing plant defense mechanisms (
<xref rid="B107" ref-type="bibr">Stein, 2005</xref>
;
<xref rid="B92" ref-type="bibr">Raaijmakers et al., 2010</xref>
). One bacterial strain may synthesize several polypeptide isoforms.
<italic>Bacillus</italic>
and
<italic>Paenibacillus</italic>
-related lipopeptides are the most studied ones (
<xref rid="B119" ref-type="bibr">Villarreal-Delgado et al., 2018</xref>
), whereas several
<italic>Bacillus amyloliquefaciens</italic>
strains have been recognized as higher lipopeptides producers (
<xref ref-type="fig" rid="F2">Figure 2A</xref>
;
<xref rid="B84" ref-type="bibr">Ongena and Jacques, 2008</xref>
). In addition to lipopeptides,
<italic>B. subtilis</italic>
produces NRPS lantibiotics (lanthionine-containing antibiotics) (
<xref rid="B107" ref-type="bibr">Stein, 2005</xref>
); lipopeptides are responsible for biofilm and swarming development, whereas lantibiotics play as pheromones in quorum-sensing (
<xref rid="B107" ref-type="bibr">Stein, 2005</xref>
).
<italic>B. subtilis</italic>
also produces compounds such as polyketides, an aminosugar, and a phospholipid; polyketides include bacillomycin, fengycin, iturin, lichenysin, mycosubtilin, plipastatin, pumilacidin, and surfactin (
<xref ref-type="fig" rid="F2">Figure 2B</xref>
); whereas
<italic>Paenibacillus polymyxa</italic>
synthesizes polymyxins (cyclic cationic lipopeptides) (
<xref rid="B107" ref-type="bibr">Stein, 2005</xref>
;
<xref rid="B51" ref-type="bibr">Grady et al., 2016</xref>
;
<xref ref-type="supplementary-material" rid="SM1">Supplementary Tables S1</xref>
<xref ref-type="supplementary-material" rid="SM1">S4</xref>
).</p>
<p>In addition to biologically active secondary metabolites, bacterial endophytes also produce important antimicrobial enzymes, mainly by Bacilli class members (
<xref ref-type="fig" rid="F2">Figure 2</xref>
). In a study looking for highly producing enzymes endophytes, in the mangrove in Thailand,
<xref rid="B68" ref-type="bibr">Khianngam et al. (2013)</xref>
found that Gram-positive bacteria showed more hydrolytic activity compared with that of Gram-negative ones. Testing endophytes in hosts from the Rhizophoraceae family, results showed amylase, cellulase, and lipase activity by
<italic>B. infantis</italic>
and
<italic>B. granadenis</italic>
; and amylase, cellulase, lipase, lipolytic and proteinase activity by
<italic>B. safensis</italic>
. Similarly, cellulase, lipase, and proteinase activities by
<italic>Paenibacillus</italic>
sp. and
<italic>S. warneri</italic>
were detected in Acanthaceae family endophytes. Endophytes isolated from Brazilian mangrove plants showed high enzymatic activity; among these isolates,
<italic>Bacillus</italic>
sp. (MCR2.56) was reported to show particularly high amylase and esterasic activities; six
<italic>Bacillus</italic>
isolates (MCR2.51, MCA2.42, MCA2.51, MBR2.4, MBA2.33, and MBA2.4) high endocellulolytic activity, whereas the actinobacteria
<italic>Microbacterium</italic>
sp. (MCA2.54) and
<italic>Curtobacterium</italic>
sp. (MBR2.20) showed high endoglucanase and protease activity, respectively (
<xref rid="B19" ref-type="bibr">Castro et al., 2014</xref>
;
<xref ref-type="fig" rid="F2">Figure 2</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Tables S1</xref>
<xref ref-type="supplementary-material" rid="SM1">S3</xref>
).</p>
<p>Bioactive endophytic Streptomycetes can be isolated from plants worldwide (
<xref rid="B16" ref-type="bibr">Castillo et al., 2007</xref>
;
<xref ref-type="fig" rid="F3">Figure 3</xref>
). Medicinal plants have been used for centuries as an alternative therapy for disease treatment. Interestingly, Chinese medicinal plants-endophytic actinomycetes were reported to have antibacterial activity against
<italic>E. coli</italic>
and
<italic>S. aureus</italic>
(
<xref rid="B127" ref-type="bibr">Zhao et al., 2011</xref>
;
<xref ref-type="fig" rid="F1">Figure 1</xref>
). Recently, endophytic actinomycetes were reported in several Chinese mangrove plants to exhibit antibacterial activity against
<italic>Acinetobacter baumannii, Enterococcus faecali</italic>
s,
<italic>E. coli, Klebsiella pneumoniae, P. aeruginosa</italic>
, and
<italic>S. aureus</italic>
, some of which are resistant to the vancomycin, methicillin, and carbapenem antibiotics (
<xref rid="B63" ref-type="bibr">Jiang et al., 2018</xref>
;
<xref ref-type="fig" rid="F1">Figure 1</xref>
,
<xref ref-type="fig" rid="F3">3</xref>
). Several metabolites from endophytic
<italic>Streptomyces</italic>
species have been characterized and associated with antibiotic activity, including kakadumycins, munumbicins,
<italic>p</italic>
-aminoacetophenonic acids, and xiamycins (
<xref rid="B17" ref-type="bibr">Castillo et al., 2002</xref>
,
<xref rid="B15" ref-type="bibr">2003</xref>
;
<xref rid="B52" ref-type="bibr">Guan et al., 2005</xref>
); antimalarial (coronamycin, munumbicin D) (
<xref rid="B17" ref-type="bibr">Castillo et al., 2002</xref>
;
<xref rid="B39" ref-type="bibr">Ezra et al., 2004</xref>
); and antifungal (munumbicin D) (
<xref rid="B106" ref-type="bibr">Shimizu et al., 2000</xref>
;
<xref rid="B39" ref-type="bibr">Ezra et al., 2004</xref>
) activities (
<xref ref-type="fig" rid="F3">Figure 3</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>
). Similarly, Iranian medicinal plants-endophytic actinomyctes exhibited antimicrobial activity against the pathogenic bacteria
<italic>B. cereus, B. subtilis, E. coli, Citrobacter freundii, K</italic>
.
<italic>pneumoniae, Proteus mirabilis, Shigella flexneri</italic>
, and
<italic>S. aureus</italic>
(
<xref rid="B8" ref-type="bibr">Beiranvand et al., 2017</xref>
;
<xref ref-type="fig" rid="F1">Figure 1</xref>
,
<xref ref-type="fig" rid="F3">3</xref>
), whereas Malaysian plants-endophytic
<italic>B. subtilis</italic>
possessed antibacterial activity against
<italic>S. aureus</italic>
, methicillin resistant
<italic>S. aureus</italic>
, and
<italic>P. aeruginosa</italic>
(
<xref rid="B41" ref-type="bibr">Fikri et al., 2018</xref>
;
<xref ref-type="fig" rid="F2">Figure 2B</xref>
). The African
<italic>Combretum molle</italic>
-endophytic
<italic>Bacillus</italic>
and
<italic>Lysinibacillus</italic>
species exhibited antibacterial activity against
<italic>B. cereus, E. coli, P. aeruginosa</italic>
, and
<italic>S. aureus</italic>
(
<xref rid="B33" ref-type="bibr">Diale et al., 2018</xref>
;
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>
).</p>
<p>
<italic>Kennedia nigriscans</italic>
-endophytic
<italic>Streptomyces</italic>
sp. strain NRRL 30562 produces munumbicins A, B, C, and D, active against growth of
<italic>B. anthracis, E. faecalis</italic>
, vancomycin-resistant
<italic>E. faecalis</italic>
, multiple-drug-resistant (MDR)
<italic>M. tuberculosis, S. pneumoniae, S. aureus</italic>
, and methicillin-resistant
<italic>S. aureus</italic>
; furthermore, munumbicins have been shown to be more effective than chloroquine to kill the malaria-causing agent
<italic>P. falciparum</italic>
(
<xref rid="B17" ref-type="bibr">Castillo et al., 2002</xref>
,
<xref rid="B18" ref-type="bibr">2006</xref>
;
<xref rid="B26" ref-type="bibr">Christina et al., 2013</xref>
;
<xref ref-type="fig" rid="F3">Figure 3A</xref>
). Similarly, kakadumycins have antibacterial and antimalarial activities comparable with those of munumbicins (
<xref rid="B121" ref-type="bibr">Waring and Wakelin, 1974</xref>
;
<xref rid="B66" ref-type="bibr">Katagiri et al., 1975</xref>
;
<xref rid="B15" ref-type="bibr">Castillo et al., 2003</xref>
;
<xref ref-type="fig" rid="F3">Figure 3A</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>
).</p>
<p>
<italic>Streptomyces</italic>
sp. strain SUK06, isolated from the Malasian medicinal plant
<italic>Thottea grandiflora</italic>
, commonly used as an alternative mean to heal wounds and treat skin infections and fever, produces secondary antimicrobial metabolites against
<italic>B. cereus, B. subtilis, Plesiomonas shigelloides, P. aeruginosa</italic>
, and methicillin-resistant
<italic>S. aureus</italic>
(
<xref rid="B46" ref-type="bibr">Ghadin et al., 2008</xref>
). Similarly, metabolites and cell wall-degrading enzymes from
<italic>Panax ginseng</italic>
- and
<italic>Plectranthus tenuiflorus</italic>
-endophytic
<italic>Bacillus</italic>
sp.,
<italic>Micrococcus</italic>
sp., and
<italic>P. polymyxa</italic>
, were reported to possess antibacterial activity against
<italic>E. coli, K. pneumoniae, P. mirabilis, Salmonella enterica</italic>
subsp.
<italic>enterica</italic>
serovar Typhi,
<italic>S. aureus</italic>
, and
<italic>S. agalactiae</italic>
(
<xref rid="B36" ref-type="bibr">El-Deeb et al., 2013</xref>
;
<xref ref-type="fig" rid="F2">Figure 2</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>
).</p>
<p>Secondary metabolites spinosyn A and D, are produced by the soil actinomycete
<italic>Saccharopolyspora spinosa</italic>
, highly effective against lepidopteran and dipteran pests, among others, which commercial product named spinosad, has been commercialized for ∼250 countries and adopted in integrated pest management programs worldwide. Furthermore, there are reports of endophytic
<italic>Saccharopolyspora</italic>
species, although their potential as bioinsecticide has not yet been elucidated (
<xref rid="B91" ref-type="bibr">Qin et al., 2011</xref>
).</p>
<p>There are many medical and agricultural applications for the
<italic>Azadirachta indica</italic>
(known as neem) produced compounds (
<xref ref-type="fig" rid="F1">Figure 1</xref>
).
<italic>Macrococcus caseolyticus</italic>
(ALS-1), a member of the Firmicutes, has been reported to produce free radical scavenging compounds. This strain was isolated from
<italic>Aloe vera</italic>
in an effort to cultivate bacterial endophytes that could be related to this plant curative and therapeutic uses (
<xref rid="B2" ref-type="bibr">Akinsanya et al., 2015</xref>
). In fact, 80% of the
<italic>A. vera</italic>
bacterial endophytes produced 1,1-diphenyl-2-picrylhydrazyl, showing over 75% scavenging properties. The
<italic>Raphanus sativus</italic>
(young radish) leaf and root endophytic
<italic>B. subtilis, Sphingobacterium siyangensis</italic>
, and
<italic>P. polymyxa</italic>
were shown to inhibit the growth of
<italic>B. cereus, E. coli, P. aeruginosa</italic>
, and
<italic>S. aureus</italic>
, in addition to
<italic>Salmonella, Shigella</italic>
, and
<italic>Listeria</italic>
species (
<xref rid="B72" ref-type="bibr">Liu et al., 2010</xref>
).
<italic>Zingiber officinale</italic>
roots-endophytic
<italic>Streptomyces</italic>
sp. was shown to possess antimicrobial activity against
<italic>B. cereus, B. subtilis</italic>
, and
<italic>S. aureus</italic>
(
<xref rid="B111" ref-type="bibr">Taechowisan et al., 2013</xref>
;
<xref ref-type="fig" rid="F3">Figure 3B</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>
).</p>
</sec>
<sec>
<title>Gram-Positive Endophytes Against Plant Pathogens</title>
<p>Endophytes found in grapevine (
<italic>Vitis vinifera</italic>
) may represent one interesting example of a widely studied crop system. Metatranscriptoma analysis of vineyards prokaryotic microbiome confirmed that two out of three main bacterial phyla detected (Actinobacteria and Firmicutes) belonged to the Gram-positive group, thus reflecting bacterial metabolic assessments to become symbionts (either epiphytes or endophytes) and be distributed along plant tissues. This study demonstrated that the abundance and richness balance between beneficial microorganisms was critical for phytopathogens biocontrol and grapevine management, where the microbiota stability relied on environmental physicochemical conditions; being the soil type, geography and climate crucial factors to favor this crop. Moreover, detection of a specific strain reflected its ability to be established under the host microclimatic conditions, where
<italic>Bacillus</italic>
spp. were widely spread in flowers, leaves and grapes (
<xref rid="B3" ref-type="bibr">Alaimo et al., 2018</xref>
). In addition,
<xref rid="B54" ref-type="bibr">Haidar et al. (2016)</xref>
found that
<italic>B. pumilus</italic>
conferred systemic resistance against this pathogen, after studying the antagonistic bacteria modes of action for the phytopathogen
<italic>Phaeomoniella chlamydospora</italic>
biocontrol in grapevine.</p>
<p>The biological control of plant phytopathogens by endophytes was reported in late 50s where, a
<italic>Micromonospora</italic>
isolate from tomato showed antagonistic activity against
<italic>Fusarium oxysporum</italic>
f.sp.
<italic>lycopersici</italic>
(
<xref rid="B78" ref-type="bibr">Manikprabhu and Li, 2016</xref>
). As previously stated, the most abundant Gram-positive bacterial endophytes found within diverse environments are
<italic>Bacillus</italic>
and
<italic>Streptomyces</italic>
species (
<xref rid="B95" ref-type="bibr">Reinhold-Hurek and Hurek, 2011</xref>
;
<xref rid="B42" ref-type="bibr">Frank et al., 2017</xref>
), both exhibiting secondary metabolites showing antimicrobial activity also against plant pathogens. In fact, there have been proposed
<italic>Bacillus</italic>
spp. endophytes for crop management (
<xref rid="B4" ref-type="bibr">Aloo et al., 2018</xref>
;
<xref ref-type="fig" rid="F2">Figure 2</xref>
). Similarly,
<italic>Streptomyces</italic>
spp. endophytes are widely reported as phytopathogens biocontrol agents (
<xref ref-type="fig" rid="F1">Figure 1</xref>
,
<xref ref-type="fig" rid="F3">3</xref>
). For example,
<italic>K. nigriscans</italic>
-endophytic
<italic>Streptomyces</italic>
sp. strain NRRL 30562 were recently reported to produce antibiotics as munumbicins A, B, C, and D, active against plant pathogenic bacteria and fungi (
<xref rid="B17" ref-type="bibr">Castillo et al., 2002</xref>
). Leguminose plants-endophytic
<italic>Streptomyces caeruleatus</italic>
was reported to be effective against the soybean pathogen
<italic>X. campestris</italic>
pv.
<italic>glycine</italic>
(
<xref rid="B80" ref-type="bibr">Mingma et al., 2014</xref>
;
<xref ref-type="fig" rid="F3">Figure 3B</xref>
); whereas metabolites from
<italic>A. indica</italic>
- and
<italic>Nothofagus</italic>
spp.-endophytic actinomyctes inhibited the plant pathogenic fungi
<italic>Mycosphaerella fijiensis, Sclerotinia sclerotiorum</italic>
, and
<italic>Rhizoctonia solani</italic>
, and
<italic>Pythium</italic>
and
<italic>Phytophthora</italic>
species (
<xref rid="B16" ref-type="bibr">Castillo et al., 2007</xref>
;
<xref rid="B118" ref-type="bibr">Verma et al., 2009</xref>
;
<xref ref-type="fig" rid="F1">Figure 1</xref>
,
<xref ref-type="fig" rid="F3">3B</xref>
). Indeed,
<xref rid="B16" ref-type="bibr">Castillo et al. (2007)</xref>
reported
<italic>Streptomyces</italic>
spp. endophytic of
<italic>Nothofagus</italic>
spp. in southern Patagonia, where the same strain characterized as
<italic>Streptomyces seoulensis</italic>
(based on molecular sequenciation and biological activity) was isolated from two different plants (strains coded C2 and C4, respectively); their antifungal activity was then proposed to elucidate the native plants survival mechanisms against plant pathogens within that area (
<xref ref-type="fig" rid="F1">Figure 1</xref>
,
<xref ref-type="fig" rid="F3">3B</xref>
). Similarly, metabolites produced by roots’ endophytic actinomycetes previously described (
<xref rid="B79" ref-type="bibr">Matsumoto and Takahashi, 2017</xref>
), inhibited
<italic>Kocuria rhizophila</italic>
strain KB-212,
<italic>Mucor racemosus</italic>
strain KF-223, and
<italic>Xanthomonas campestris</italic>
pv.
<italic>oryzae</italic>
strain KB-88 growth (
<xref ref-type="fig" rid="F1">Figure 1</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S2</xref>
).</p>
<p>
<italic>Zea mays</italic>
seeds-endophytic
<italic>B. amyloliquefaciens</italic>
and
<italic>B. subtilis</italic>
were observed to inhibit
<italic>F. moniliforme</italic>
fungus growth by producing lipopeptides (
<xref rid="B49" ref-type="bibr">Gond et al., 2015</xref>
); similarly,
<italic>Bruguiera gymnorrhiza</italic>
(L.) Lam-endophytic
<italic>B. amyloliquefaciens</italic>
was shown to be antagonistic to various bacterial (
<italic>Ralstonia solanacearum, P. syringae</italic>
, and
<italic>X. campestris</italic>
), and fungal (
<italic>Colletotrichum musae, F. oxysporum, Phytophthora capsici</italic>
, and
<italic>R. solani</italic>
) pathogens of plants and to be effective in the biocontrol of
<italic>Capsicum</italic>
bacterial wilt in pot and field trials (
<xref rid="B56" ref-type="bibr">Hu et al., 2010</xref>
).</p>
<p>
<italic>Oryza sativa</italic>
-endophytic
<italic>B. cereus</italic>
and
<italic>B. mojavensis</italic>
were observed to exhibit antimicrobial activity against the fungal rice pathogens
<italic>F. fujikuroi, F. proliferum, F. verticillioides, Magnaporthe grisea</italic>
, and
<italic>M. salvinii</italic>
(
<xref rid="B38" ref-type="bibr">Etesami and Alikhani, 2017</xref>
;
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S2</xref>
).</p>
<p>Young radish-endophytic
<italic>B. subtilis, Brachybacterium</italic>
, and
<italic>P. polymyxa</italic>
were reported to possess antifungal activity against
<italic>F. oxysporum, Pythium ultimum, Phytophthora capsici</italic>
, and
<italic>R. solani</italic>
(
<xref rid="B104" ref-type="bibr">Seo et al., 2010</xref>
). An antifungal protein from the wheat-endophytic
<italic>B. subtilis</italic>
strain EDR4 inhibited
<italic>B. cinerea, F. graminearum, F. oxysporum</italic>
f.sp.
<italic>vasinfectum, G. graminis</italic>
var.
<italic>tritici, Macrophoma kuwatsukai</italic>
, and
<italic>R. cerealis</italic>
growth (
<xref rid="B72" ref-type="bibr">Liu et al., 2010</xref>
;
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S2</xref>
).</p>
</sec>
<sec>
<title>Metabolites From Gram-Positive Endophytes as Plant Growth-Promoters</title>
<p>Endophytic bacteria use to protect crops from microbial diseases is relevant, for their potential to promote host growth and antimicrobial activity (
<xref rid="B100" ref-type="bibr">Safiyazov et al., 1995</xref>
;
<xref rid="B9" ref-type="bibr">Berg et al., 2005</xref>
). Plant growth promotion (PGP) and, in most cases, abiotic stress tolerance and disease protection properties induction, are associated with endophytic bacteria potential to produce different compounds. Plants acclimate to environmental stresses by altering their physiology to be able to overcome stress factors such as dehydration, mechanical injury, nutrient deficiency, high solar radiation, or biotic/abiotic factors. It has been observed that plant inoculation with endophytic bacteria leads to accumulation of “protective” compounds, such as proline, carbohydrates, and antioxidants, in addition to antibiotics and fungal cell-wall lytic enzymes, which can inhibit growth of plant pathogens (
<xref rid="B11" ref-type="bibr">Brader et al., 2014</xref>
) or prime plant response to pathogens by induced systemic resistance (ISR) mechanisms (
<xref rid="B88" ref-type="bibr">Pieterse et al., 2014</xref>
).</p>
<p>Bacterial endophytes PGP potential is explained through several proposed mechanisms. Several of which help to increase accessibility to nutrients, e.g., nitrogen and phosphorus or metals, or produce metabolites that could regulate plant growth, development and defense responses, such as the well-known phytohormones abscisic acid, auxins, brassinosteroids, cytokinins, ethylene, gibberellins, jasmonates, and strigolactones (
<xref rid="B95" ref-type="bibr">Reinhold-Hurek and Hurek, 2011</xref>
;
<xref rid="B11" ref-type="bibr">Brader et al., 2014</xref>
;
<xref rid="B101" ref-type="bibr">Santoyo et al., 2016</xref>
;
<xref rid="B105" ref-type="bibr">Shahzad et al., 2016</xref>
;
<xref ref-type="fig" rid="F1">Figure 1</xref>
<xref ref-type="fig" rid="F3">3</xref>
).</p>
<p>Some examples of Gram-positive PGP bacterial endophytes are
<italic>B. pumilus</italic>
strain E2S2, whose treatment increased roots and shoots length and fresh and dry biomass, as compared with untreated sorghum plants, and helped to augment cadmium uptake (
<xref rid="B77" ref-type="bibr">Luo et al., 2012</xref>
).
<italic>B. amyloliquefaciens</italic>
strain NBRI-SN13 (SN13) isolated from an alkaline soil of Banthara, Lucknow, India, showed several PGP attributes and to induce solubilization of tricalcium phosphate more efficiently, when inoculated as endophyte (
<xref rid="B82" ref-type="bibr">Nautiyal et al., 2013</xref>
;
<xref ref-type="fig" rid="F2">Figure 2A</xref>
). Plants treated with
<italic>B. atrophaeus</italic>
strain EY6,
<italic>B. sphaericus</italic>
GC subgroup B EY30,
<italic>B. subtilis</italic>
strain EY2,
<italic>S. kloosii</italic>
strain EY37 and
<italic>K. erythromyxa</italic>
strain EY43 as endophytes, have been shown to increase strawberry fruit growth and yield (
<xref rid="B65" ref-type="bibr">Karlidag et al., 2011</xref>
;
<xref ref-type="fig" rid="F2">Figure 2</xref>
).</p>
<p>Interestingly,
<italic>C. botulinum</italic>
strain 2301 has been shown to have a significant PGP effect on clover in field experiments (
<xref rid="B125" ref-type="bibr">Zeiller et al., 2015</xref>
); whereas
<italic>Exiguobacterium acetylicum</italic>
1P strain MTCC 8707, a cold tolerant bacterial strain from the Uttarakhand Himalayas, promotes wheat seedlings growth (
<xref rid="B103" ref-type="bibr">Selvakumar et al., 2010</xref>
;
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S3</xref>
).</p>
<p>
<italic>Brevibacillus</italic>
brevis strain SVC(II)14 exerted beneficial PGP on cotton crop (
<xref rid="B83" ref-type="bibr">Nehra et al., 2016</xref>
).
<italic>Bacillus</italic>
spp. strains CPMO6 and BM17, actinobacteria isolates ACT01 and ACT07, and lactic acid bacteria strain BL06 induce phosphate solubilization more efficiently when present as endophytes in citrus (
<xref rid="B47" ref-type="bibr">Giassi et al., 2016</xref>
).</p>
<p>In recent years, it has also been demonstrated that the entomopathogenic bacteria
<italic>B. thuringiensis</italic>
can have PGP attributes.
<xref rid="B5" ref-type="bibr">Armada et al. (2016)</xref>
tested an autochthonous isolate in interaction with native arbuscular mycorrhizal fungi (single or mixture) and found stimulating plant growth, nutrition and drought tolerance responses.</p>
<p>Siderophores production by endophytes improves plant growth by binding to available iron, competing for this element with phytopathogens and protecting the host plant from their infection (
<xref ref-type="fig" rid="F2">Figure 2</xref>
,
<xref ref-type="fig" rid="F3">3</xref>
;
<xref rid="B99" ref-type="bibr">Sabaté et al., 2018</xref>
).
<italic>B. subtilis</italic>
strain B26 has been shown to induce drought tolerance in
<italic>Brachypodium distachyon</italic>
grass. This was correlated to augmentation of starch, fructose, glucose and total soluble carbohydrates content. However, increase of raffinose-related family carbohydrates (well-known stress response metabolites) was not observed in control and treated plants (
<xref rid="B43" ref-type="bibr">Gagné-Bourque et al., 2015</xref>
). A proline accumulation stimulating effect by endophytic strains of the actinobacteria
<italic>Arthrobacter</italic>
sp. and the Firmicutes
<italic>Bacillus</italic>
spp. were reported in pepper (
<italic>Capsicum annuum</italic>
L., Solanales: Solanaceae) plants
<italic>in vitro</italic>
, where their synthesis was related to osmotic stress responses (
<xref rid="B109" ref-type="bibr">Sziderics et al., 2007</xref>
). In addition, plants inoculated with bacterial endophytes, could tolerate abiotic stresses by increasing enzymatic activity.
<italic>B. cereus</italic>
strain CSR-B-1,
<italic>B. marisflavi</italic>
strain CSR-G-4,
<italic>B. pumilus</italic>
strain CSR-B-2,
<italic>B. saffensis</italic>
strain CSR-G-5,
<italic>B. subtilis</italic>
strain CSR-G-1, and
<italic>B. thuringiensis</italic>
strain CSRB-3, induced increment of superoxide dismutase, phenylalanine lyase, catalase, and peroxidase enzymes activity in gladiolus plants under sodium high concentration conditions (
<xref rid="B28" ref-type="bibr">Damodaran et al., 2014</xref>
;
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S3</xref>
).</p>
<p>Tolerance to low temperatures and growth promotion by endophytic activity has been reported as well.
<xref rid="B117" ref-type="bibr">Verma et al. (2015)</xref>
, found
<italic>Bacillus</italic>
and
<italic>Bacillus</italic>
derived genera as wheat (
<italic>Triticum aestivum</italic>
) endophytes from the northern hills zone of India, among others. Phosphate and potassium are major essential macronutrients, but soluble phosphate and potassium concentrations in soil for plant intake are usually very low. Plants need zinc at low concentration since it is toxic at high concentration, thus zinc solubilization by endophytes dosifies the plant intake amount in response to plant and microbial nutritional requests. The most efficient phosphate solubilizing Gram-positive bacteria (PSB) belong to the genera
<italic>Bacillus</italic>
. Besides, it has been reported that
<italic>B. amyloliquefasciens, B. megaterium</italic>
, and
<italic>Bacillus</italic>
sp., exhibit phosphorus, potassium, and zinc solubilization (
<xref ref-type="fig" rid="F2">Figure 2</xref>
;
<xref rid="B117" ref-type="bibr">Verma et al., 2015</xref>
).</p>
</sec>
<sec>
<title>Anticancer Activity of Gram-Positive Endophytic Bacteria</title>
<p>Cancer prevails as one of the leading causes of death worldwide, in spite of therapy advances (
<xref rid="B48" ref-type="bibr">Global Cancer Observatory [GLOBOCAN], 2008</xref>
;
<xref rid="B24" ref-type="bibr">Chen et al., 2013</xref>
). Conventional chemotherapy and radiotherapy have important disadvantages including drug resistance and serious side effects, which has prompted the search for new antitumor agents with high therapeutic efficacy and marginal or null detrimental effects.</p>
<p>Many endophytic actinomycete compounds were isolated and have found application not only as antimicrobial agents but also as cytotoxic agents against tumor cells (
<xref ref-type="fig" rid="F1">Figure 1</xref>
,
<xref ref-type="fig" rid="F3">3</xref>
). Some members of the Gram-positive bacteria group have been recently found as endophytes in different plant species (
<xref rid="B37" ref-type="bibr">Eljounaidi et al., 2016</xref>
). Endophyte extracts have demonstrated to be a better choice versus chemotherapy agents due to their antitumor activity efficacy and lower side-effects, since they are less toxic to normal cells and more effective against several drug resistant microorganisms. As a consequence, the natural endophyte-derived metabolites have attracted peculiar attention with the purpose of being human cancer-chemopreventive compounds and anticancer chemotherapeutic drugs (
<xref rid="B14" ref-type="bibr">Cardoso-Filho, 2018</xref>
;
<xref ref-type="fig" rid="F3">Figure 3B,C</xref>
). Endophytic Gram-positive bacterial natural products have emerged as one of the most reliable alternative treatment sources (
<xref rid="B53" ref-type="bibr">Gutierrez et al., 2012</xref>
;
<xref rid="B24" ref-type="bibr">Chen et al., 2013</xref>
), including antitumor agents such as anthracyclines, anthraquinones, aureolic acids, β-glucans, carzinophilin, coumarins, enediynes, flavonoids, glycopeptides, macrotetrolides, mitomycins, naphthoquinones, polysaccharides, and quinoxalines (
<xref rid="B121" ref-type="bibr">Waring and Wakelin, 1974</xref>
;
<xref rid="B58" ref-type="bibr">Igarashi et al., 2007</xref>
;
<xref rid="B112" ref-type="bibr">Taechowisan et al., 2007</xref>
;
<xref rid="B24" ref-type="bibr">Chen et al., 2013</xref>
;
<xref rid="B14" ref-type="bibr">Cardoso-Filho, 2018</xref>
;
<xref ref-type="fig" rid="F3">Figure 3B,C</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S4</xref>
).</p>
<p>Actinomycetes, including the genera
<italic>Actinomyces, Actinoplanes, Amycolatopsis, Micromonospora, Saccharopo-lyspora</italic>
, and
<italic>Streptomyces</italic>
are recognized as producers of bioactive metabolites with not only antimicrobial, but also antitumor potential (
<xref rid="B96" ref-type="bibr">Renu et al., 2008</xref>
;
<xref rid="B67" ref-type="bibr">Kekuda et al., 2010</xref>
;
<xref ref-type="fig" rid="F3">Figure 3C</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S4</xref>
). In this concern,
<italic>Ophiopogon japonicus</italic>
-endophytic
<italic>B. amyloliquefaciens</italic>
sp. exopolysaccharides were reported to possess antitumor activity against the human gastric carcinoma cell lines MC-4 and SGC-7901 (
<xref rid="B24" ref-type="bibr">Chen et al., 2013</xref>
;
<xref ref-type="fig" rid="F2">Figure 2A</xref>
). Furthermore,
<italic>Maytenus hookeri</italic>
-maytansine-producing endophytic
<italic>Streptomyces</italic>
sp. strain Is9131 inhibited human SGC7901 gastric, HL60 leukemia, BEL7402 liver, and A-549 lung tumor cell lines growth (
<xref rid="B76" ref-type="bibr">Lu and Shen, 2003</xref>
;
<xref rid="B128" ref-type="bibr">Zhao et al., 2005</xref>
;
<xref ref-type="fig" rid="F3">Figure 3B</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S4</xref>
).
<italic>Alnus glutinosa</italic>
-endophytic
<italic>Streptomyces</italic>
alnumycin was reported to inhibit the growth of K562 human leukemia cells (
<xref rid="B10" ref-type="bibr">Bieber et al., 1998</xref>
;
<xref ref-type="fig" rid="F3">Figure 3C</xref>
), whereas
<italic>Ricinus communis</italic>
-endophytic salaceyins-producing
<italic>Streptomyces laceyi</italic>
strain MS53 was observed to be cytotoxic against the human breast cancer cell line SKBR3 (
<xref rid="B69" ref-type="bibr">Kim et al., 2006</xref>
;
<xref ref-type="fig" rid="F3">Figure 3B</xref>
). In addition, herbaceous and arbor plants-pterocidin-producing endophytic
<italic>Streptomyces hygroscopicus</italic>
strain TP-A0451 was reported to inhibit human cancer cell lines NCI-H522, OVCAR-3, SF539, and LOX-IMVI growth (
<xref rid="B57" ref-type="bibr">Igarashi et al., 2006</xref>
;
<xref rid="B91" ref-type="bibr">Qin et al., 2011</xref>
), and
<italic>Z. officinale</italic>
4-arylcoumarins-producing-endophytic
<italic>Streptomyces aureofaciens</italic>
strain CMUAc130 was shown to be cytotoxic against murine Lewis lung carcinoma (
<xref rid="B112" ref-type="bibr">Taechowisan et al., 2007</xref>
;
<xref rid="B91" ref-type="bibr">Qin et al., 2011</xref>
;
<xref ref-type="fig" rid="F3">Figure 3C</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S4</xref>
).</p>
<p>Many plant growth promoter compounds have shown cytotoxicity against tumor cells. Nodules of
<italic>Lupinus angustifolius</italic>
-endophytic anthraquinones-producing
<italic>Micromo-nospora</italic>
sp. actinomycete significantly inhibited invasion of murine colon 26-L5 carcinoma cells (
<xref rid="B58" ref-type="bibr">Igarashi et al., 2007</xref>
;
<xref rid="B91" ref-type="bibr">Qin et al., 2011</xref>
). Recently,
<xref rid="B110" ref-type="bibr">Taechowisan et al. (2017)</xref>
reported anticancer activity of
<italic>Boesenbergia rotunda</italic>
-endophytic biphenyls-producing
<italic>Streptomyces</italic>
sp. strain BO-07 against human HepG2 and Huh7 liver, and HeLa cervical tumor cell lines (
<xref ref-type="fig" rid="F3">Figure 3B</xref>
). Furthermore,
<italic>Cinnamomum cassia</italic>
-endophytic
<italic>Streptomyces cavourensis</italic>
strain YBQ59 was shown to inhibit human lung adenocarcinoma EGFR-TKI-resistant cells A549 and H1299 growth (
<xref rid="B120" ref-type="bibr">Vu et al., 2018</xref>
;
<xref ref-type="fig" rid="F3">Figure 3C</xref>
and
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S4</xref>
).</p>
</sec>
<sec>
<title>Conclusion and Perspectives</title>
<p>Since the first reports of the industrial potential use of secondary metabolites produced by endophytes, there is more evidence that endophytic Gram-positive bacteria are one of the most important sources of novel compounds that have proven potential for either agriculture, medical and/or pharmaceutical application, thanks to their PGP, antimicrobial and anticancer activities. Indeed, endophytic Gram-positive bacteria help plants to better survive under biotic and abiotic stress conditions. It is not random that many endophytic Gram-positive have been isolated from medicinal plants from all over the world. In fact, many reports of endophytic Gram-positive bacteria showing such activities have been isolated from mangrove and under extreme environment conditions growing plants, like crops from salty soils and crops and trees from cold areas, where phylogenic analysis of native strains demonstrate they contain genes to produce different metabolites that, all together, are helping the host plant, not just to survive, but also to improve the plant adaptation to these extreme environmental conditions. In general,
<italic>Bacillus</italic>
class endophytes have been reported to produce aromatic compounds, lipopeptides, plant hormones, polysaccharides, and several enzymes, thus representing higher potential in agriculture for PGP and crop management strategies (
<xref rid="B119" ref-type="bibr">Villarreal-Delgado et al., 2018</xref>
). Similarly, Actinobacteria class endophytes are being found to produce antimicrobial- and antitumor-like activity metabolites, thus representing high potential for agriculture, medical, and veterinary application. In this minireview, we presented sources and specific isolated strains information, with the aim to provide current research highlights and perspectives for their future applications. These fascinating microorganisms are diverse and greatly adaptable to extreme stress conditions, making them excellent novel metabolites sources, whose application would be important for environmentally friendly and sustainable food and drugs production.</p>
</sec>
<sec>
<title>Author Contributions</title>
<p>All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.</p>
</sec>
<sec>
<title>Conflict of Interest Statement</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>
</body>
<back>
<fn-group>
<fn fn-type="financial-disclosure">
<p>
<bold>Funding.</bold>
This work was supported by Consejo Nacional de Ciencia y Tecnología, Grant No. 5109 to PTG and by Laboratorio de Inmunología y Virología del Departamento de Microbiología e Inmunologia (LIV-DEMI) de la FCB-UANL.</p>
</fn>
</fn-group>
<sec sec-type="supplementary material">
<title>Supplementary Material</title>
<p>The Supplementary Material for this article can be found online at:
<ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fmicb.2019.00463/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fmicb.2019.00463/full#supplementary-material</ext-link>
</p>
<supplementary-material content-type="local-data" id="SM1">
<media xlink:href="Data_Sheet_1.pdf">
<caption>
<p>Click here for additional data file.</p>
</caption>
</media>
</supplementary-material>
</sec>
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