Evaluating the performance of Fourier transform infrared spectroscopy for typing and outbreak investigation of methicillin-resistant and -susceptible <i>Staphylococcus aureus</i>

dc.contributor.authorSilvola, Jaakko
dc.contributor.authorHarju, Inka
dc.contributor.authorKallonen, Teemu
dc.contributor.authorGröndahl-Yli-Hannuksela, Kirsi
dc.contributor.authorKanerva, Mari
dc.contributor.authorVuopio, Jaana
dc.contributor.authorRantakokko-Jalava, Kaisu
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.converis.publication-id523056901
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/523056901
dc.date.accessioned2026-04-30T15:26:43Z
dc.description.abstract<p>Infections caused by methicillin-susceptible <em>Staphylococcus aureus</em> (MSSA) and methicillin-resistant <em>Staphylococcus aureus</em> (MRSA) can be life-threatening and complicated to manage. Especially in the healthcare environment, MRSA is a notorious cause of outbreaks inflicting a significant disease burden. Assessing the relatedness of isolates is a key challenge for outbreak management. We aimed to assess the utility and performance of Fourier transform infrared (FTIR) spectroscopy (IR Biotyper; Bruker Daltonics GmbH & Co. KG, Bremen, Germany) by comparing it with <em>spa</em> typing and whole-genome sequencing (WGS). <em>S. aureus</em> was cultured under standard conditions on Müller-Hinton agar, and the second subculture was used for spectral acquisition. Eighty-eight MRSA isolates and 89 MSSA isolates were included from both screening and clinical MRSA specimens, and blood culture MSSA specimens were identified at the clinical microbiology laboratory of Turku University Hospital, Southwest Finland. Among non-outbreak strains, two or three possible subtypes were detected with FTIR within 16 different <em>spa</em> types. Two suspected healthcare-associated outbreaks comprising nine and four isolates, respectively, were detected. WGS confirmed the outbreak with four isolates. Within the other outbreak, WGS revealed five closely related and four unrelated isolates. FTIR analysis correctly differentiated two of the unrelated isolates, while two unrelated isolates were erroneously clustered in a principal component analysis. Although the discriminatory power of FTIR was lower than WGS, false-negative clustering was not observed. FTIR showed a lower analysis cost per specimen and was superior in processing speed to both WGS and <em>spa</em> typing. Our findings suggest the potential use of FTIR in preliminary screening, supporting almost real-time outbreak analysis and hence outbreak management.<br></p>
dc.identifier.eissn2165-0497
dc.identifier.urihttps://www.utupub.fi/handle/11111/60198
dc.identifier.urlhttps://doi.org/10.1128/spectrum.03245-25
dc.identifier.urnURN:NBN:fi-fe2026043036731
dc.language.isoen
dc.okm.affiliatedauthorSilvola, Jaakko
dc.okm.affiliatedauthorKallonen, Teemu
dc.okm.affiliatedauthorGröndahl-Yli-Hannuksela, Kirsi
dc.okm.affiliatedauthorKanerva, Mari
dc.okm.affiliatedauthorVuopio, Jaana
dc.okm.affiliatedauthorRantakokko-Jalava, Kaisu
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline1183 Plant biology, microbiology, virologyen_GB
dc.okm.discipline1183 Kasvibiologia, mikrobiologia, virologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherAmerican Society for Microbiology
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.articlenumbere03245-25
dc.relation.doi10.1128/spectrum.03245-25
dc.relation.ispartofjournalMicrobiology spectrum
dc.titleEvaluating the performance of Fourier transform infrared spectroscopy for typing and outbreak investigation of methicillin-resistant and -susceptible <i>Staphylococcus aureus</i>
dc.year.issued2026

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