Literature DB >> 32999236

Additional Bacteriological Examinations Might be Required for the Correct Identification of Staphylococcus warneri.

Takahiko Fukuchi1, Hitoshi Sugawara1.   

Abstract

Entities:  

Keywords:  16S rRNA gene sequencing; Staphylococcus pasteuri; Staphylococcus warneri; matrix-assisted laser desorption ionisation time-of-flight mass spectrometry; rRNA restriction fragment length polymorphism analysis

Year:  2020        PMID: 32999236      PMCID: PMC7990647          DOI: 10.2169/internalmedicine.5675-20

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


× No keyword cloud information.
To the Editor We read with great interest the article, “Native valve endocarditis due to Staphylococcus warneri developing in a patient with type 1 diabetes,” by Yamamoto et al. (1). This article described the patient's clinical course in detail, as well as the clinical decision making that was involved, the deductive interpretation of underlying heart disease, the pathogenicity of coagulase-negative Staphylococci, including Staphylococcus warneri, and diabetes as an accelerating factor. We appreciate the authors' contribution to furthering our understanding of infective endocarditis caused by the extremely rare pathogen S. warneri. However, an Australian case report described an elderly man suffering from native valve endocarditis caused by S. pasteuri, which has been frequently misidentified as S. warneri because of the strong phenotypic similarity (2). This pathogen was detected by both a biochemical procedure (VITEKⓇ) and matrix-assisted laser desorption ionisation time-of-flight mass spectrometry (MALDI-TOF MS). In addition, an article published by a European microbiological laboratory group revealed that four of the nine S. warneri strains were correctly identified based on their phenotype and molecular methods (3). An rRNA restriction fragment length polymorphism analysis (ribotyping) correctly identified all nine S. warneri strains. Furthermore, partial 16S rRNA gene sequencing correctly identified coagulase-negative Staphylococci, which included S. warneri and S. pasteuri (4). Therefore, we wonder if an additional analysis, such as MALDI-TOF MS, ribotyping or 16S rRNA gene sequencing, was performed for the identification of this rarely isolated microorganism. Although, to our knowledge, no article has yet determined the difference in the clinical course between S. warneri and S. pasteuri, the correct identification of the pathogen is ultimately the most important point when treating infectious diseases. The authors state that they have no Conflict of Interest (COI).
  4 in total

1.  Identification of coagulase-negative staphylococci other than Staphylococcus epidermidis by automated ribotyping.

Authors:  E Carretto; D Barbarini; I Couto; D De Vitis; P Marone; J Verhoef; H De Lencastre; S Brisse
Journal:  Clin Microbiol Infect       Date:  2005-03       Impact factor: 8.067

2.  Comparison of growth on mannitol salt agar, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, VITEK® 2 with partial sequencing of 16S rRNA gene for identification of coagulase-negative staphylococci.

Authors:  Funmilola A Ayeni; Camilla Andersen; Niels Nørskov-Lauritsen
Journal:  Microb Pathog       Date:  2017-02-28       Impact factor: 3.738

3.  Staphylococcus pasteuri infective endocarditis: A case report.

Authors:  Jaineel Ramnarain; Jang Yoon; Naomi Runnegar
Journal:  IDCases       Date:  2019-10-14

4.  Native Valve Endocarditis due to Staphylococcus warneri Developing in a Patient with Type 1 Diabetes.

Authors:  Junpei Yamamoto; Akira Endo; Hiroto Sugawara; Tomohito Izumi; Kenji Takahashi; Saori Yamamoto; Masatoshi Akiyama; Osamu Adachi; Keizo Kaneko; Shojiro Sawada; Junta Imai; Yoshikatsu Saiki; Hiroaki Shimokawa; Hideki Katagiri
Journal:  Intern Med       Date:  2020-06-15       Impact factor: 1.271

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.