<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-07-21T17:17:16Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/16047" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/16047</identifier><datestamp>2025-05-08T13:08:55Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19609</setSpec><setSpec>col_20.500.12105_25179</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">dc</subfield>
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      <subfield code="a">Amblar, Monica</subfield>
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      <subfield code="a">Zaballos, Ángel</subfield>
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      <subfield code="a">de la Campa, Adela G</subfield>
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      <subfield code="c">2022-12-17</subfield>
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      <subfield code="a">PatAB is an ABC bacterial transporter that facilitates the export of antibiotics and dyes. The overexpression of patAB genes conferring efflux-mediated fluoroquinolone resistance has been observed in several laboratory strains and clinical isolates of Streptococcus pneumoniae. Using transformation and whole-genome sequencing, we characterized the fluoroquinolone-resistance mechanism of one S. pneumoniae clinical isolate without mutations in the DNA topoisomerase genes. We identified the PatAB fluoroquinolone efflux-pump as the mechanism conferring a low-level resistance to ciprofloxacin (8 µg/mL) and levofloxacin (4 µg/mL). Genetic transformation experiments with different amplimers revealed that the entire patA plus the 5'-terminus of patB are required for levofloxacin-efflux. By contrast, only the upstream region of the patAB operon, plus the region coding the N-terminus of PatA containing the G39D, T43A, V48A and D100N amino acid changes, are sufficient to confer a ciprofloxacin-efflux phenotype, thus suggesting differences between fluoroquinolones in their binding and/or translocation pathways. In addition, we identified a novel single mutation responsible for the constitutive and ciprofloxacin-inducible upregulation of patAB. This mutation is predicted to destabilize the putative rho-independent transcriptional terminator located upstream of patA, increasing transcription of downstream genes. This is the first report demonstrating the role of the PatAB transporter in levofloxacin-efflux in a pneumoccocal clinical isolate.</subfield>
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      <subfield code="a">Antibiotics (Basel). 2022 Dec 17;11(12):1837.</subfield>
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      <subfield code="a">10.3390/antibiotics11121837</subfield>
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      <subfield code="a">2079-6382</subfield>
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      <subfield code="a">Antibiotics (Basel, Switzerland)</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/16047</subfield>
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      <subfield code="a">PatAB</subfield>
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      <subfield code="a">Streptococcus pneumoniae</subfield>
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      <subfield code="a">Efflux-pump</subfield>
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      <subfield code="a">Fluoroquinolone-resistance</subfield>
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      <subfield code="a">Levofloxacin-efflux</subfield>
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      <subfield code="a">Role of PatAB Transporter in Efflux of Levofloxacin in Streptococcus pneumoniae</subfield>
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