Comparison of bloodstream infections due to Corynebacterium striatum, MRSA, and MRSE.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
17 Sep 2024
Historique:
received: 11 04 2024
accepted: 05 09 2024
medline: 18 9 2024
pubmed: 18 9 2024
entrez: 17 9 2024
Statut: epublish

Résumé

Corynebacterium striatum (C. striatum), a common skin and mucosal colonizer, is increasingly considered as an opportunistic pathogen causing bloodstream infections (BSIs). This study aims to investigate the clinical features and outcomes of C. striatum-BSI. We included hospitalized cases with C. striatum-positive blood cultures from January 2014 to June 2022 and classified them into C. striatum-BSI group and contamination group; Clinical characteristics, treatments, and outcomes were compared between the C. striatum-BSI group and contamination group, Methicillin-resistant Staphylococcus aureus (MRSA)-BSI and Methicillin-resistant Staphylococcus epidermidis (MRSE)-BSI. Fifty-three patients with positive C. striatum blood cultures were identified. Among them, 25 patients were classified as C. striatum-BSI, with 21 as contamination cases. And 62 cases of MRSA-BSI and 44 cases of MRSE-BSI were identified. Compared to the contaminated group, the C. striatum-BSI group had a shorter time to positivity of blood cultures (27.0 h vs. 42.5 h, P = 0.011). C. striatum-BSI group had a longer time to positivity (27 h) when compared to both the MRSA (20 h) and MRSE groups (19 h) (p < 0.05). Appropriate therapy within 24 h of BSI onset was significantly lower in the C. striatum group (28%) compared to the MRSA (64.5%) and MRSE (65.9%) groups (p < 0.005). The 28-day mortality was higher in the C. striatum group (52.0%) compared to the MRSA (25.8%) and MRSE (18.2%) groups.  CONCLUSIONS: Given the distinct characteristics of C. striatum-BSI, including a longer time to positivity than other Gram-positive bacteria and higher mortality rates, we suggest prescribing early appropriate antibiotics if C. striatum-BSI is suspected.

Sections du résumé

BACKGROUND BACKGROUND
Corynebacterium striatum (C. striatum), a common skin and mucosal colonizer, is increasingly considered as an opportunistic pathogen causing bloodstream infections (BSIs). This study aims to investigate the clinical features and outcomes of C. striatum-BSI.
METHODS METHODS
We included hospitalized cases with C. striatum-positive blood cultures from January 2014 to June 2022 and classified them into C. striatum-BSI group and contamination group; Clinical characteristics, treatments, and outcomes were compared between the C. striatum-BSI group and contamination group, Methicillin-resistant Staphylococcus aureus (MRSA)-BSI and Methicillin-resistant Staphylococcus epidermidis (MRSE)-BSI.
RESULTS RESULTS
Fifty-three patients with positive C. striatum blood cultures were identified. Among them, 25 patients were classified as C. striatum-BSI, with 21 as contamination cases. And 62 cases of MRSA-BSI and 44 cases of MRSE-BSI were identified. Compared to the contaminated group, the C. striatum-BSI group had a shorter time to positivity of blood cultures (27.0 h vs. 42.5 h, P = 0.011). C. striatum-BSI group had a longer time to positivity (27 h) when compared to both the MRSA (20 h) and MRSE groups (19 h) (p < 0.05). Appropriate therapy within 24 h of BSI onset was significantly lower in the C. striatum group (28%) compared to the MRSA (64.5%) and MRSE (65.9%) groups (p < 0.005). The 28-day mortality was higher in the C. striatum group (52.0%) compared to the MRSA (25.8%) and MRSE (18.2%) groups.  CONCLUSIONS: Given the distinct characteristics of C. striatum-BSI, including a longer time to positivity than other Gram-positive bacteria and higher mortality rates, we suggest prescribing early appropriate antibiotics if C. striatum-BSI is suspected.

Identifiants

pubmed: 39289626
doi: 10.1186/s12879-024-09883-z
pii: 10.1186/s12879-024-09883-z
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article Comparative Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

988

Informations de copyright

© 2024. The Author(s).

Références

Funke G, von Graevenitz A, Clarridge JE, Bernard KA. Clinical microbiology of coryneform bacteria. Clin Microbiol Rev. 1997;10(1):125–59. https://doi.org/10.1128/CMR.10.1.125 .
pubmed: 8993861 pmcid: 172946
Silva-Santana G, Silva CMF, Olivella JGB, et al. Worldwide survey of Corynebacterium striatum increasingly associated with human invasive infections, nosocomial outbreak, and antimicrobial multidrug-resistance, 1976–2020. Arch Microbiol. 2021;203(5):1863–80. https://doi.org/10.1007/s00203-021-02246-1 .
pubmed: 33625540 pmcid: 7903872
Human Microbiome Project Consortium. Structure, function and diversity of the healthy human microbiome. Nature. 2012;486(7402):207–14. https://doi.org/10.1038/nature11234 .
Rasmussen M, Mohlin AW, Nilson B. From contamination to infective endocarditis—a population-based retrospective study of Corynebacterium isolated from blood cultures. Eur J Clin Microbiol Infect Dis. 2020;39(1):113–9. https://doi.org/10.1007/s10096-019-03698-6 .
pubmed: 31485919
Abe M, Kimura M, Maruyama H, et al. Clinical characteristics and drug susceptibility patterns of Corynebacterium species in bacteremic patients with hematological disorders. Eur J Clin Microbiol Infect Dis. 2021;40(10):2095–104. https://doi.org/10.1007/s10096-021-04257-8 .
pubmed: 33895886
Kimura S, Gomyo A, Hayakawa J, et al. Clinical characteristics and predictive factors for mortality in coryneform bacteria bloodstream infection in hematological patients. J Infect Chemother. 2017;23(3):148–53. https://doi.org/10.1016/j.jiac.2016.11.007 .
pubmed: 28011352
Garcia CM, McKenna J, Fan L, Shah A. Corynebacterium Striatum Bacteremia in End-Stage Renal Disease: A Case Series and Review of Literature. R I Med J (2013). 2020;103(8):46–9.
pubmed: 33003679
Tang J, Kornblum D, Godefroy N, et al. Corynebacterium striatum thrombophlebitis: a nosocomial multidrug-resistant disease? Access Microbiol. 2021;3(12): 000307. https://doi.org/10.1099/acmi.0.000307 .
pubmed: 35024563 pmcid: 8749143
Yamamuro R, Hosokawa N, Otsuka Y, Osawa R. Clinical Characteristics of Corynebacterium Bacteremia Caused by Different Species, Japan, 2014–2020. Emerg Infect Dis. 2021;27(12):2981–7. https://doi.org/10.3201/eid2712.210473 .
pubmed: 34812137 pmcid: 8632174
Yanai M, Ogasawasa M, Hayashi Y, Suzuki K, Takahashi H, Satomura A. Retrospective evaluation of the clinical characteristics associated with Corynebacterium species bacteremia. Braz J Infect Dis. 2018;22(1):24–9. https://doi.org/10.1016/j.bjid.2017.12.002 .
pubmed: 29360429 pmcid: 9425686
Oliva A, Belvisi V, Iannetta M, et al. Pacemaker lead endocarditis due to multidrug-resistant Corynebacterium striatum detected with sonication of the device. J Clin Microbiol. 2010;48(12):4669–71. https://doi.org/10.1128/JCM.01532-10 .
pubmed: 20943861 pmcid: 3008477
Kalt F, Schulthess B, Sidler F, et al. Corynebacterium Species Rarely Cause Orthopedic Infections. J Clin Microbiol. 2018;56(12):e01200-e1218. https://doi.org/10.1128/JCM.01200-18 .
pubmed: 30305384 pmcid: 6258853
Sturm PDJ, Scholle D. Arthritis caused by Corynebacterium striatum: spontaneous infection? J Clin Microbiol. 2007;45(6):2097. https://doi.org/10.1128/JCM.00298-07 . author reply 2097.
pubmed: 17548460 pmcid: 1933092
Ge Y, Lu J, Feng S, Ji W, Tong H. A case of catheter related bloodstream infection by Corynebacterium striatum. IDCases. 2020;22: e00987. https://doi.org/10.1016/j.idcr.2020.e00987 .
pubmed: 33194547 pmcid: 7644921
Ishiwada N, Watanabe M, Murata S, Takeuchi N, Taniguchi T, Igari H. Clinical and bacteriological analyses of bacteremia due to Corynebacterium striatum. J Infect Chemother. 2016;22(12):790–3. https://doi.org/10.1016/j.jiac.2016.08.009 .
pubmed: 27654073
Milosavljevic MN, Milosavljevic JZ, Kocovic AG, et al. Antimicrobial treatment of Corynebacterium striatum invasive infections: a systematic review. Rev Inst Med Trop Sao Paulo. 2021;63: e49. https://doi.org/10.1590/S1678-9946202163049 .
pubmed: 34161555 pmcid: 8216692
Chow JW, Yu VL. Combination antibiotic therapy versus monotherapy for gram-negative bacteraemia: a commentary. Int J Antimicrob Agents. 1999;11(1):7–12. https://doi.org/10.1016/S0924-8579(98)00060-0 .
pubmed: 10075272
Horan TC, Andrus M, Dudeck MA. CDC/NHSN surveillance definition of health care–associated infection and criteria for specific types of infections in the acute care setting. Am J Infect Control. 2008;36(5):309–32. https://doi.org/10.1016/j.ajic.2008.03.002 .
pubmed: 18538699
Osaki S, Kikuchi K, Moritoki Y, et al. Distinguishing coagulase-negative Staphylococcus bacteremia from contamination using blood-culture positive bottle detection pattern and time to positivity. J Infect Chemother. 2020;26(7):672–5. https://doi.org/10.1016/j.jiac.2020.02.004 .
pubmed: 32131983
Sathaporn N, Khwannimit B. Risk Factor for Superimposed Nosocomial Bloodstream Infections in Hospitalized Patients with COVID-19. Infect Drug Resist. 2023;16:3751–9. https://doi.org/10.2147/IDR.S411830 .
pubmed: 37333683 pmcid: 10276631
Watanabe N, Otsuka Y, Watari T, Hosokawa N, Yamagata K, Fujioka M. Time to positivity of Corynebacterium in blood culture: Characteristics and diagnostic performance. PLoS ONE. 2022;17(12): e0278595. https://doi.org/10.1371/journal.pone.0278595 .
pubmed: 36512568 pmcid: 9747040
Lakhundi S, Zhang K. Methicillin-Resistant Staphylococcus aureus: Molecular Characterization, Evolution, and Epidemiology. Clin Microbiol Rev. 2018;31(4):e00020-e118. https://doi.org/10.1128/CMR.00020-18 .
pubmed: 30209034 pmcid: 6148192
Kleinschmidt S, Huygens F, Faoagali J, Rathnayake IU, Hafner LM. Staphylococcus epidermidis as a cause of bacteremia. Future Microbiol. 2015;10(11):1859–79. https://doi.org/10.2217/fmb.15.98 .
pubmed: 26517189
Ruiz-Giardín JM, Martin-Díaz RM, Jaqueti-Aroca J, Garcia-Arata I, San Martín-López JV, Sáiz-Sánchez BM. Diagnosis of bacteraemia and growth times. Int J Infect Dis. 2015;41:6–10. https://doi.org/10.1016/j.ijid.2015.10.008 .
pubmed: 26482387
Verroken A, Bauraing C, Deplano A, et al. Epidemiological investigation of a nosocomial outbreak of multidrug-resistant Corynebacterium striatum at one Belgian university hospital. Clin Microbiol Infect. 2014;20(1):44–50. https://doi.org/10.1111/1469-0691.12197 .
pubmed: 23586637
Leonard RB, Nowowiejski DJ, Warren JJ, Finn DJ, Coyle MB. Molecular evidence of person-to-person transmission of a pigmented strain of Corynebacterium striatum in intensive care units. J Clin Microbiol. 1994;32(1):164–9. https://doi.org/10.1128/jcm.32.1.164-169.1994 .
pubmed: 7907342 pmcid: 262989
Renom F, Garau M, Rubí M, Ramis F, Galmés A, Soriano JB. Nosocomial outbreak of Corynebacterium striatum infection in patients with chronic obstructive pulmonary disease. J Clin Microbiol. 2007;45(6):2064–7. https://doi.org/10.1128/JCM.00152-07 .
pubmed: 17409213 pmcid: 1933039
Elting LS, Rubenstein EB, Rolston KV, Bodey GP. Outcomes of bacteremia in patients with cancer and neutropenia: observations from two decades of epidemiological and clinical trials. Clin Infect Dis. 1997;25(2):247–59. https://doi.org/10.1086/514550 .
pubmed: 9332520
Nørgaard M, Larsson H, Pedersen G, Schønheyder HC, Sørensen HT. Risk of bacteraemia and mortality in patients with haematological malignancies. Clin Microbiol Infect. 2006;12(3):217–23. https://doi.org/10.1111/j.1469-0691.2005.01298.x .
pubmed: 16451407
Gupta S, Sakhuja A, Kumar G, McGrath E, Nanchal RS, Kashani KB. Culture-Negative Severe Sepsis: Nationwide Trends and Outcomes. Chest. 2016;150(6):1251–9. https://doi.org/10.1016/j.chest.2016.08.1460 .
pubmed: 27615024
Kang Y, Chen S, Zheng B, et al. Epidemiological Investigation of Hospital Transmission of Corynebacterium striatum Infection by Core Genome Multilocus Sequence Typing Approach. Van Tyne D, ed. Microbiol Spectr. 2023;11(1):eo1490-22. https://doi.org/10.1128/spectrum.01490-22 .
Ramos JN, Souza C, Faria YV, et al. Bloodstream and catheter-related infections due to different clones of multidrug-resistant and biofilm producer Corynebacterium striatum. BMC Infect Dis. 2019;19(1):672. https://doi.org/10.1186/s12879-019-4294-7 .
pubmed: 31357945 pmcid: 6664767
Cc D, Be L, Il C, et al. Antimicrobial Susceptibility Testing for Corynebacterium Species Isolated from Clinical Samples in Romania. Antibiotics (Basel, Switzerland). 2020;9(1). https://doi.org/10.3390/antibiotics9010031 .

Auteurs

Shu-Hua He (SH)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.

Yan Chen (Y)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.

Hong-Li Sun (HL)

Department of Clinical Laboratory, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.

Shan Li (S)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.

Shi-Tong Diao (ST)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.

Yi-Fan Wang (YF)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.

Zhuo-Xin He (ZX)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.

Li Weng (L)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.

Jin-Min Peng (JM)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China. pjm731@hotmail.com.

Bin Du (B)

Medical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China. dubin98@gmail.com.

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