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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.2018.00483</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Microbiology</subject>
<subj-group>
<subject>General Commentary</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Commentary: A Novel and Validated Protocol for Performing MIC Tests to Determine the Susceptibility of <italic>Piscirickettsia salmonis</italic> Isolates to Florfenicol and Oxytetracycline</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Mancilla</surname> <given-names>Marcos</given-names></name>
<xref ref-type="author-notes" rid="fn001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/282987/overview"/>
</contrib>
</contrib-group>
<aff><institution>Research and Development Laboratory, ADL Diagnostic Chile</institution>, <addr-line>Puerto Montt</addr-line>, <country>Chile</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Hongyue Dang, Xiamen University, China</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Kevin R. Maisey, Universidad de Santiago de Chile, Chile; Zhe Zhao, Hohai University, China</p></fn>
<fn fn-type="corresp" id="fn001"><p>&#x0002A;Correspondence: Marcos Mancilla <email>mmancilla&#x00040;adldiagnostic.cl</email></p></fn>
<fn fn-type="other" id="fn002"><p>This article was submitted to Aquatic Microbiology, a section of the journal Frontiers in Microbiology</p></fn></author-notes>
<pub-date pub-type="epub">
<day>14</day>
<month>03</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="collection">
<year>2018</year>
</pub-date>
<volume>9</volume>
<elocation-id>483</elocation-id>
<history>
<date date-type="received">
<day>08</day>
<month>09</month>
<year>2017</year>
</date>
<date date-type="accepted">
<day>28</day>
<month>02</month>
<year>2018</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2018 Mancilla.</copyright-statement>
<copyright-year>2018</copyright-year>
<copyright-holder>Mancilla</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 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" journal-id="Front Microbiol" journal-id-type="nlm-ta" vol="8" page="1255" xlink:href="28729865" ext-link-type="pubmed">A commentary on <article-title>A Novel and Validated Protocol for Performing MIC Tests to Determine the Susceptibility of <italic>Piscirickettsia salmonis</italic> Isolates to Florfenicol and Oxytetracycline</article-title> by Contreras-Lynch, S., Smith, P., Olmos, P., Loy, M. E., Finnegan, W., and Miranda, C. D. (2017). Front. Microbiol. 8:1255. doi: <object-id>10.3389/fmicb.2017.01255</object-id></related-article>
<kwd-group>
<kwd><italic>Piscirickettsia salmonis</italic></kwd>
<kwd>minimum inhibitory concentration (MIC)</kwd>
<kwd>antimicrobial susceptibility testing</kwd>
<kwd>epidemiological cut-off value</kwd>
<kwd>florfenicol</kwd>
</kwd-group>
<contract-num rid="cn001">14IDl2-30005</contract-num>
<contract-sponsor id="cn001">Corporaci&#x000F3;n de Fomento de la Producci&#x000F3;n<named-content content-type="fundref-id">10.13039/100009465</named-content></contract-sponsor>
<counts>
<fig-count count="1"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="5"/>
<page-count count="3"/>
<word-count count="1168"/>
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</article-meta>
</front>
<body>
<p>Contreras-Lynch et al. (<xref ref-type="bibr" rid="B2">2017</xref>) recently published <italic>Piscirickettsia salmonis</italic> epidemiological cut-off values (ECOFF) for florfenicol and oxytetracycline, and we note that the overall results of their study closely resemble those reported by us previously (Henr&#x000ED;quez et al., <xref ref-type="bibr" rid="B3">2015</xref>). The authors claim that their protocol yielded more accurate ECOFF values under the chosen experimental conditions for minimum inhibitory concentration (MIC) assessment, despite basing their findings on a considerably lower number of isolates (58 vs. 292, respectively). They also concluded that the <italic>P. salmonis</italic> population has experienced minor reductions in susceptibility to antibiotics. Although we are thankful for any constructive criticism regarding the precision of our study, as it enriches the discussion on this relevant research topic, we only partially agree with these statements. Indeed, we pointed out the markedly reduced susceptibility to oxytetracycline exhibited by a set of isolates analyzed in our study and warned on the potential consequences of the dissemination of such a resistant phenotype.</p>
<p>Notwithstanding the differences, an overlapped bimodal distribution of florfenicol susceptibility was obtained in both studies. This finding resulted intriguing because the acquisition of a resistance mechanism is generally accompanied by a notorious shift of MIC to a reduced susceptibility zone. This observation and subsequent studies that accounted for obvious phenotypic (Brevik &#x000D8; et al., <xref ref-type="bibr" rid="B4">2016</xref>) and genotypic (Bravo and Martinez, <xref ref-type="bibr" rid="B1">2016</xref>) differences among <italic>P. salmonis</italic> isolates, encouraged us to further investigate the topic considering the epidemiology of the disease. In fact, we later demonstrated that piscirickettsiosis is caused by two strains showing a degree of consistent phenotypic diversity that may justify the distinction of two subspecies (Saavedra et al., <xref ref-type="bibr" rid="B5">2016</xref>). In the mentioned study, we extended our susceptibility analyses to an even larger collection of specimens (507 isolates collected in 6 years), this time grouping the isolates according to their 16S genotypes, i.e., we differentiated between EM-90-like and LF-89-like strains. Remarkably, this approach revealed only wild-type antibiotic susceptible, host-specific isolates in the EM-90-like group.</p>
<p>After applying a lineage segmentation on the dataset we published in 2016, the overlapped bimodal distribution of florfenicol susceptibility became clearly unimodal for the EM-90-like isolates. According to tests on normal distribution, the latter likely included only wild-type microorganisms, but this was not the case for their LF-89-like counterparts (Figure <xref ref-type="fig" rid="F1">1</xref>). A similar &#x0201C;strain effect&#x0201D; becomes evident when re-analyzing MIC values of quinolones and oxytetracycline. Therefore, regardless of the methodology used for ECOFF calculations, it seems that the overlapped bimodal distribution of MICs can at least partially be explained by the fact that data obtained from two kinds of bacteria were exploited in our studies and that of Contreras-Lynch et al. (<xref ref-type="bibr" rid="B2">2017</xref>). Contreras-Lynch and colleagues argued on the taxonomic heterogeneity as a source of imprecision, assuming a high level of homogeneity in their own dataset. But both Figure <xref ref-type="fig" rid="F1">1</xref> of this commentary as well as the results presented by Contreras-Lynch et al. (<xref ref-type="bibr" rid="B2">2017</xref>) show that MIC data are derived from a mixed <italic>P. salmonis</italic> population in either case. Consequently, ECOFF calculations will yield different results when the subspecies criterion is considered.</p>
<fig id="F1" position="float">
<label>Figure 1</label>
<caption><p>Florfenicol susceptibility profiles deduced from the dataset published in Saavedra et al. (<xref ref-type="bibr" rid="B5">2016</xref>). The <bold>upper</bold> plot shows the MIC distribution as displayed by the whole collection, which contains EM-90-like and LF-89-like <italic>P. salmonis</italic> isolates. The <bold>lower</bold> panels show strain-specific MIC distributions.</p></caption>
<graphic xlink:href="fmicb-09-00483-g0001.tif"/>
</fig>
<p>We think that the setting of ECOFF values is a starting point to establish rules for the interpretation of susceptibility to antimicrobials, yet it remains only a step on the way to clinical breakpoints. In this regard, a clinically relevant conclusion of our work is that the identification of the <italic>P. salmonis</italic> strain or genotype allows for a forecast of the efficacy of antimicrobial therapies, especially when a highly disseminated and fully susceptible strain is responsible for the majority of outbreaks in the current situation of piscirickettsiosis. We highlight the significance of this finding since the efforts for reducing the use of antibiotics made by the Chilean industry in recent years could benefit not only from antibiotic susceptibility surveillance, but also from genotyping of isolates. Altogether, due to the importance of <italic>P. salmonis</italic> genotypes as discussed above, we miss a more in-depth genetic characterization of the bacteria analyzed by Contreras-Lynch and colleagues.</p>
<sec id="s1">
<title>Author contributions</title>
<p>The author confirms being the sole contributor of this work and approved it for publication.</p>
<sec>
<title>Conflict of interest statement</title>
<p>The author declares 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>
</body>
<back>
<ack><p>We gratefully acknowledge the comments and suggestions on the manuscript made by Dr. Melanie Kaiser.</p>
</ack>
<ref-list>
<title>References</title>
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<fn-group>
<fn fn-type="financial-disclosure"><p><bold>Funding.</bold> This work was funded by Grant &#x00023; 14IDL2-30005 from Corporaci&#x000F3;n de Fomento de la Producci&#x000F3;n, CORFO.</p>
</fn>
</fn-group>
</back>
</article> 