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Ampicillin Resistance Mechanisms in Clinical Haemophilus influenzae: What is Happening in Portugal?

dc.contributor.authorBajanca-Lavado, Maria Paula
dc.date.accessioned2017-02-13T16:00:54Z
dc.date.available2017-02-13T16:00:54Z
dc.date.issued2016-11-29
dc.descriptionComunicação por convitept_PT
dc.description.abstractHaemophilus influenzae (Hi) remains a key etiological agent of upper and lower respiratory tract infections. Two major mechanisms are involved in ampicillin (AMP) resistance: β-lactam hydrolysis due to β-lactamase production (TEM-1 or ROB-1) and decreased affinity of penicillin-binding protein 3 (PBP3) for β-lactam antibiotics as a result of ftsI gene mutations encoding PBP3. Isolates exhibiting this latter resistant mechanism are termed β-lactamase-non-producing ampicillin-resistant (BLNAR), while isolates with both resistant mechanisms are defined as β-lactamase-positive amoxicillin-clavulanic acid-resistant (BLPACR). A variety of amino acid (AA) substitutions within the transpeptidase domain of PBP3 are mainly responsible for resistance. According to specific substitutions, these isolates have been classified in one of three mutational groups: I-III. Group II was further divided into subgroups IIa-IId. More recently, a new group was described, “III-like”, with additionally AA substitutions to the ones described in group III. Decreased ampicillin susceptibility have been associated to group I and II, while group III is normally associated with high resistance levels to ampicillin. Isolates with the non enzymatic resistance mechanisms have been described and emerging worldwide. In this context, we aimed to characterize ampicillin resistance mechanisms in clinical Hi strains isolated in Portugal. Amplification and sequencing of ftsI gene was performed in 568 clinical Hi isolates. Analysis of mutations characterized 61% of isolates as gBLNAR or gBLPACR. Most of the strains were included in group II (85%), with predominance of IIb (61%). Rare isolates were of group I and no isolate was classified in group III, although few strains were of group III-like. Our results are indicative of wide dissemination of a non-enzymatic resistance mechanism to β-lactams among H. influenzae isolates circulating in our country, probably due to inappropriate use of oral antibiotics, which is a matter of concern. A better understanding of this issue may help to establish adequate therapeutic and preventive measures to avoid selection or dissemination of such strains.pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/4154
dc.language.isoengpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.subjectHaemophilus Influenzaept_PT
dc.subjectPBP3pt_PT
dc.subjectAmpicillin Non-enzymatic Resistancept_PT
dc.subjectAntibiotic Resistancept_PT
dc.subjectInfecções Respiratóriaspt_PT
dc.subjectPortugalpt_PT
dc.titleAmpicillin Resistance Mechanisms in Clinical Haemophilus influenzae: What is Happening in Portugal?pt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceValência, Espanhapt_PT
oaire.citation.title4th World Congress on Infection Prevention and Control, 28–29 November 2016pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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