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Kihlberg, Pernilla
Publications (2 of 2) Show all publications
Kihlberg, P., Bech Johannesen, T., Stegger, M., Cajander, S. & Söderquist, B. (2025). Reliability of disc diffusion testing and molecular epidemiology of penicillin-susceptible Staphylococcus aureus bacteraemia. Journal of Antimicrobial Chemotherapy, 80(8), 2187-2193
Open this publication in new window or tab >>Reliability of disc diffusion testing and molecular epidemiology of penicillin-susceptible Staphylococcus aureus bacteraemia
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2025 (English)In: Journal of Antimicrobial Chemotherapy, ISSN 0305-7453, E-ISSN 1460-2091, Vol. 80, no 8, p. 2187-2193Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Recent studies have reported an increasing prevalence of penicillin-susceptible Staphylococcus aureus (PSSA) worldwide. The reliability of disc diffusion testing for detecting penicillin-resistance has been questioned, and the molecular epidemiology of PSSA has not been studied to the same extent as that of MRSA strains.

OBJECTIVES: To investigate the reliability of the disc diffusion method for detecting penicillin-resistance in S. aureus, and to examine the prevalence and molecular epidemiology of PSSA in bloodstream infections.

METHODS: A total of 258 bacteraemic isolates obtained from one geographic region in Sweden during 2018-2019 were analysed using the disc diffusion test to detect penicillin-resistance, and genome sequenced to examine the prevalence of the blaZ gene and the molecular epidemiology of PSSA.

RESULTS: Phenotypic susceptibility to penicillin correlated strongly with the absence of the blaZ gene, with nearly 98% concordance. The prevalence of PSSA among patients with bacteraemia was 35.1%, highlighting the need for penicillin-susceptibility testing. Additionally, population structure analyses revealed substantial genetic diversity, underscoring the complexity of the PSSA epidemiology. The PSSA belonged to diverse clonal lineages, with CC5 and CC45 dominating our cohort, similar to findings in Spain, Australia, and other parts of Sweden. However, our study revealed a higher prevalence of CC12 compared with other regions, underscoring the importance of local epidemiological surveillance.

CONCLUSIONS: These findings validate the reliability of EUCAST's disc diffusion method, showing a high prevalence of PSSA, and provide insight into the genetic underpinnings of penicillin-susceptibility in S. aureus.

Place, publisher, year, edition, pages
Oxford University Press, 2025
National Category
Infectious Medicine
Identifiers
urn:nbn:se:oru:diva-121571 (URN)10.1093/jac/dkaf187 (DOI)001504912200001 ()40492523 (PubMedID)2-s2.0-105012413161 (Scopus ID)
Funder
Region Örebro County, OLL-985410Region Örebro County, OLL-999643Region Örebro County, OLL-982875Region Örebro County, OLL-936003Region Örebro County, OLL-933344
Note

Funding Agencies:

This study was supported by ALF funding from Region Örebro Län (grant numbers OLL-985410 and OLL-999643); the Research Committee of Region Örebro Län (grant numbers OLL-982875, OLL-936003, and OLL-933344); and Regionala Forskningsrådet Uppsala/Örebro (grant number RFR-931422).

Available from: 2025-06-11 Created: 2025-06-11 Last updated: 2026-01-23Bibliographically approved
Nestor, D., Andersson, H., Kihlberg, P., Olson, S., Ziegler, I., Rasmussen, G., . . . Sundqvist, M. (2021). Early prediction of blood stream infection in a prospectively collected cohort. BMC Infectious Diseases, 21(1), Article ID 316.
Open this publication in new window or tab >>Early prediction of blood stream infection in a prospectively collected cohort
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2021 (English)In: BMC Infectious Diseases, E-ISSN 1471-2334, Vol. 21, no 1, article id 316Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Blood stream infection (BSI) and sepsis are serious clinical conditions and identification of the disease-causing pathogen is important for patient management. The RISE (Rapid Identification of SEpsis) study was carried out to collect a cohort allowing high-quality studies on different aspects of BSI and sepsis. The aim of this study was to identify patients at high risk for BSI who might benefit most from new, faster, etiological testing using neutrophil to lymphocyte count ratio (NLCR) and Shapiro score.

METHODS: Adult patients (≥ 18 years) presenting at the emergency department (ED) with suspected BSI were prospectively included between 2014 and 2016 at Örebro University Hospital. Besides extra blood sampling, all study patients were treated according to ED routines. Electronic patient charts were retrospectively reviewed. A modified Shapiro score (MSS) and NLCR were extracted and compiled. Continuous score variables were analysed with area under receiver operator characteristics curves (AUC) to evaluate the ability of BSI prediction.

RESULTS: The final cohort consisted of 484 patients where 84 (17%) had positive blood culture judged clinically significant. At optimal cut-offs, MSS (≥3 points) and NLCR (> 12) showed equal ability to predict BSI in the whole cohort (AUC 0.71/0.74; sensitivity 69%/67%; specificity 64%/68% respectively) and in a subgroup of 155 patients fulfilling Sepsis-3 criteria (AUC 0.71/0.66; sensitivity 81%/65%; specificity 46%/57% respectively). In BSI cases only predicted by NLCR> 12 the abundance of Gram-negative to Gram-positive pathogens (n = 13 to n = 4) differed significantly from those only predicted by MSS ≥3 p (n = 7 to n = 12 respectively) (p < 0.05).

CONCLUSIONS: MSS and NLCR predicted BSI in the RISE cohort with similar cut-offs as shown in previous studies. Combining the MSS and NLCR did not increase the predictive performance. Differences in BSI prediction between MSS and NLCR regarding etiology need further evaluation.

Place, publisher, year, edition, pages
BioMed Central (BMC), 2021
Keywords
Bacteremia, Clinical decision rules, Sepsis
National Category
Infectious Medicine
Identifiers
urn:nbn:se:oru:diva-90961 (URN)10.1186/s12879-021-05990-3 (DOI)000636178800001 ()33810788 (PubMedID)2-s2.0-85103852609 (Scopus ID)
Note

Funding Agencies:

Research Committee of Örebro County Council  

Örebro University 

Available from: 2021-04-13 Created: 2021-04-13 Last updated: 2026-04-13Bibliographically approved
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