{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,5]],"date-time":"2026-03-05T02:51:02Z","timestamp":1772679062604,"version":"3.50.1"},"reference-count":43,"publisher":"Microbiology Society","issue":"2","license":[{"start":{"date-parts":[[2024,2,1]],"date-time":"2024-02-01T00:00:00Z","timestamp":1706745600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,2,1]]},"abstract":"<jats:p>\n                    <jats:bold>Introduction.<\/jats:bold>\n                    <jats:italic>\n                      <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3419\" xlink:type=\"simple\">Haemophilus influenzae<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    (\n                    <jats:italic>Hi<\/jats:italic>\n                    ) was long known as an easy-to-treat bacterium, but increasing resistance against beta-lactams and other critically important antibiotics is now a growing concern. We describe here the whole-genome sequencing (WGS) analysis of three non-typeable\n                    <jats:italic>Hi<\/jats:italic>\n                    isolates received in 2018\u20132019 by the Belgian National Reference Centre (NRC) for\n                    <jats:italic>\n                      <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3419\" xlink:type=\"simple\">Haemophilus influenzae<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    , as they presented an unusual multi-resistant profile.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>Methods.<\/jats:bold>\n                    All three isolates were sequenced by WGS and mapped to the reference isolate\n                    <jats:italic>Hi<\/jats:italic>\n                    Rd KW20. Shorten uptake signal sequences (USSs) known to be associated with homologous recombination were sought in\n                    <jats:italic>ftsI, murE<\/jats:italic>\n                    and\n                    <jats:italic>murF<\/jats:italic>\n                    genes, and inner partial sequences were compared against the\n                    <jats:sc>blast<\/jats:sc>\n                    nucleotide database to look for similarity with other\n                    <jats:italic>\n                      <jats:named-content content-type=\"genus\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3418\" xlink:type=\"simple\">Haemophilus<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    species. Their antimicrobial resistance (AMR) genotype was studied. Core-genome multilocus sequence typing (MLST) was performed on the NTHi database pubMLST to place our isolates in the actual worldwide epidemiology.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>Results.<\/jats:bold>\n                    The isolates also harboured interspecies recombination patterns in the\n                    <jats:italic>murF-murE-ftsI<\/jats:italic>\n                    region involved in cell wall synthesis. The three isolates were multidrug resistant and two of them were also resistant to amoxicillin\u2013clavulanic acid and showed a reduced susceptibility to meropenem. All three isolates belonged to the MLST clonal complex (CC) 422, and WGS revealed that the three were very similar. They harboured mobile genetic elements (carrying\n                    <jats:italic>blaTEM-1B<\/jats:italic>\n                    ,\n                    <jats:italic>mefA<\/jats:italic>\n                    and\n                    <jats:italic>msrD<\/jats:italic>\n                    genes associated with resistance), mutations in\n                    <jats:italic>gyrA<\/jats:italic>\n                    and\n                    <jats:italic>parC<\/jats:italic>\n                    linked to fluoroquinolone resistance as well as remodelling events in\n                    <jats:italic>ompP2<\/jats:italic>\n                    that might be related to lower carbapenem susceptibility.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>Conclusion.<\/jats:bold>\n                    The\n                    <jats:italic>Hi<\/jats:italic>\n                    evolution towards antimicrobial multiresistance (AMR) is a complex and poorly understood phenomenon, although probably linked to a large degree to the presence of USSs and exchange within the family\n                    <jats:italic>\n                      <jats:named-content content-type=\"family\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3370\" xlink:type=\"simple\">Pasteurellaceae<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    . To better understand the respective roles of clonal expansion, horizontal gene transfers, spontaneous mutations and interspecies genetic rearrangements in shaping\n                    <jats:italic>Hi<\/jats:italic>\n                    AMR, both analysis of\n                    <jats:italic>Hi<\/jats:italic>\n                    communities over time within individuals and worldwide monitoring of non-typeable\n                    <jats:italic>Hi<\/jats:italic>\n                    causing infections should be conducted.\n                  <\/jats:p>","DOI":"10.1099\/acmi.0.000649.v3","type":"journal-article","created":{"date-parts":[[2024,2,12]],"date-time":"2024-02-12T09:17:33Z","timestamp":1707729453000},"source":"Crossref","is-referenced-by-count":7,"title":["Multiple interspecies recombination events documented by whole-genome sequencing in multidrug-resistant Haemophilus influenzae clinical isolates"],"prefix":"10.1099","volume":"6","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0250-2664","authenticated-orcid":false,"given":"Charlotte","family":"Michel","sequence":"first","affiliation":[{"name":"Department of Microbiology, Laboratoire Hospitalier Universitaire de Bruxelles (LHUB-ULB), Rue Haute 322, 1000 Brussels, Belgium"},{"name":"Belgian National Reference Centre for Haemophilus influenzae, Laboratoire Hospitalier Universitaire de Bruxelles (LHUB-ULB), Rue Haute 322, 1000 Brussels, Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria De Los Angeles","family":"Argud\u00edn","sequence":"additional","affiliation":[{"name":"Department of Molecular Biology, Cliniques Universitaires Saint Luc (CUSL), Avenue Hippocrate 10, 1200, Brussels, Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Magali","family":"Wautier","sequence":"additional","affiliation":[{"name":"Belgian National Reference Centre for Haemophilus influenzae, 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