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Relevant bibliographies by topics / Cutibacterium spp

Academic literature on the topic 'Cutibacterium spp'

Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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Journal articles

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Journal articles on the topic "Cutibacterium spp"

1

Goldenberger, Daniel, Kirstine K. Søgaard, Aline Cuénod, Helena Seth-Smith, Daniel de Menezes, Peter Vandamme, and Adrian Egli. "Cutibacterium modestum and “Propionibacterium humerusii” represent the same species that is commonly misidentified as Cutibacterium acnes." Antonie van Leeuwenhoek 114, no. 8 (May 7, 2021): 1315–20. http://dx.doi.org/10.1007/s10482-021-01589-5.

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AbstractCutibacterium spp. play an increasing role in soft tissue and implant-associated infections. We isolated a novel Cutibacterium spp. from an implant and investigated this isolate using multiple identification approaches. Correct identification was hampered by inconsistent reference data. The isolate was characterised using conventional methods such as Gram stain, MALDI-TOF MS, and antimicrobial susceptibility testing against multiple antimicrobials. Partial 16S rRNA gene sequencing and whole genome sequencing were also performed. In addition, we summarised the available published sequence data and compared prior data to our strain. Conventional phenotypic identification of our isolate resulted in Cutibacterium spp. After analysis of 16S rRNA gene and genome sequences, our isolate was identified as C. modestum, a very recently described species. The 16S rRNA gene analysis was hampered by three incorrect nucleotides within the 16S rRNA gene reference sequence of C. modestum M12T (accession no. LC466959). We also clearly demonstrate that this novel species is identical to tentatively named “Propionibacterium humerusii”. Retrospective data analysis indicates that C. modestum is a clinically important Cutibacterium species often misidentified as C. acnes. The isolation and identification of Cutibacterium spp. is still a challenge. The correct description of very recently named C. modestum and the availability of a correct 16S rRNA sequence of the type strain may help to clarify the taxonomical uncertainty concerning “P. humerusii”. The novel C. modestum is an additional, clinically important species within the genus Cutibacterium and may represent a new member of the human skin microbiome.

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2

Gisler, Valentin, Lorin Benneker, and Parham Sendi. "Late Spinal Implant Infection caused by Cutibacterium acnes." Journal of Bone and Joint Infection 4, no. 4 (July 25, 2019): 163–66. http://dx.doi.org/10.7150/jbji.36802.

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Abstract. Cutibacterium spp. have been frequently associated with foreign-body material infections. The vast majority of these infections occur via the exogenous route. Rarely, haematogenous infections occur, possibly seeding from pilosebaceous glands. A late spinal implant-associated infection is presented in this case report, and the possible sources of haematogenous seeding are discussed.

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3

Bronnec, Vicky, and Oleg A. Alexeyev. "In vivo model of Propionibacterium (Cutibacterium) spp. biofilm in Drosophila melanogaster." Anaerobe 72 (December 2021): 102450. http://dx.doi.org/10.1016/j.anaerobe.2021.102450.

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4

Lima, Rayssa Durães, Gabrielle Antunes dos Reis, Juliana da Silva Reviello, Thaís Glatthardt, Larissa da Silva Coimbra, Carla Ormundo Gonçalves Ximenes Lima, Luis Caetano Martha Antunes, and Rosana Barreto Rocha Ferreira. "Antibiofilm activity of Cutibacterium acnes cell-free conditioned media against Staphylococcus spp." Brazilian Journal of Microbiology 52, no. 4 (October 2, 2021): 2373–83. http://dx.doi.org/10.1007/s42770-021-00617-w.

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5

Renz, Nora, Stasa Mudrovcic, Carsten Perka, and Andrej Trampuz. "Orthopedic implant-associated infections caused by Cutibacterium spp. – A remaining diagnostic challenge." PLOS ONE 13, no. 8 (August 20, 2018): e0202639. http://dx.doi.org/10.1371/journal.pone.0202639.

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6

Salar-Vidal, Llanos, Marta Martin-Garcia, Alvaro Auñón, and Jaime Esteban. "Cutibacterium spp. isolated from orthopaedic implant-associated infection: A not-so-slowly growing organism." Enfermedades infecciosas y microbiologia clinica (English ed.) 39, no. 6 (June 2021): 287–90. http://dx.doi.org/10.1016/j.eimce.2020.05.017.

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7

Olejniczak-Staruch, Irmina, Magdalena Ciążyńska, Dorota Sobolewska-Sztychny, Joanna Narbutt, Małgorzata Skibińska, and Aleksandra Lesiak. "Alterations of the Skin and Gut Microbiome in Psoriasis and Psoriatic Arthritis." International Journal of Molecular Sciences 22, no. 8 (April 13, 2021): 3998. http://dx.doi.org/10.3390/ijms22083998.

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Numerous scientific studies in recent years have shown significant skin and gut dysbiosis among patients with psoriasis. A significant decrease in microbiome alpha-diversity (abundance of different bacterial taxa measured in one sample) as well as beta-diversity (microbial diversity in different samples) was noted in psoriasis skin. It has been proven that the representation of Cutibacterium, Burkholderia spp., and Lactobacilli is decreased and Corynebacterium kroppenstedii, Corynebacterium simulans, Neisseria spp., and Finegoldia spp. increased in the psoriasis skin in comparison to healthy skin. Alterations in the gut microbiome in psoriasis are similar to those observed in patients with inflammatory bowel disease. In those two diseases, the F. prausnitzii, Bifidobacterium spp., Lactobacillus spp., Parabacteroides and Coprobacillus were underrepresented, while the abundance of Salmonella sp., Campylobacter sp., Helicobacter sp., Escherichia coli, Alcaligenes sp., and Mycobacterium sp. was increased. Several research studies provided evidence for the significant influence of psoriasis treatments on the skin and gut microbiome and a positive influence of orally administered probiotics on the course of this dermatosis. Further research is needed to determine the influence of the microbiome on the development of inflammatory skin diseases. The changes in microbiome under psoriasis treatment can serve as a potential biomarker of positive response to the administered therapy.

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8

Sancak, B., H. Cenk Mirza, B. Altun, and F. Tunçkanat. "Identification and distribution of anaerobic bacteria isolated from clinical specimens in a University Hospital: 4 years’ experience." Microbiology Independent Research Journal (MIR Journal) 9, no. 1 (July 29, 2022): 75–81. http://dx.doi.org/10.18527/2500-2236-2022-9-1-75-81.

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Anaerobes, which are components of microbiota, can cause life-threatening infections. Because of their fastidious nature, they are difficult to isolate and are often overlooked. The goal of this study was to identify the anaerobic bacteria isolated from clinical specimens at the Central Laboratory of Hacettepe University Hospital in 2015-2018 and to evaluate the distribution of the isolated bacterial species among the different specimen types. The anaerobic bacteria isolated from the specimens were identified by the conventional methods and MALDI-TOF MS.Overall, 15,300 anaerobic cultures were studied. Of these, 14,434 (94.3%) were blood samples and 866 (5.7%) were other clinical specimens. A total of 138 anaerobic bacteria were isolated: 62 (44.9%) were isolated from blood samples and 76 (55.1%) from other specimens. The most isolated anaerobes from blood cultures were Bacteroides spp. (41.9%), followed by Cutibacterium acnes (25.8%) and Clostridium spp. (9.7%). The most isolated anaerobes from the other specimens were Gram-negative bacilli, including Bacteroides spp. (15.8%), Fusobacterium spp. (14.5%), Prevotella spp. (14.5%), and Porphyromonas spp. (2.6%). Anaerobic Finegoldia magna represented the major species among the isolated Gram-positive bacteria (10.5%). Anaerobic growth was observed in 0.4% of all the blood cultures and in 5.8% of the positive blood cultures. The results of our study showed that the incidence of anaerobic bacteremia was stable during the 2015-2018 period.

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9

Hermawan, Melyawati, Enty Tjoa, Inneke Hidajat, Maria Teressa, Eka Layadi, and Alegra Wolter. "Prevalence of Cutibacterium acnes and Staph spp. in the lesions of acne vulgaris in Jakarta." Journal of General - Procedural Dermatology & Venereology Indonesia 5, no. 2 (June 30, 2021): 86–91. http://dx.doi.org/10.19100/jdvi.v5i2.218.

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10

Benito, Natividad, Isabel Mur, Alba Ribera, Alex Soriano, Dolors Rodríguez-Pardo, Luisa Sorlí, Javier Cobo, et al. "The Different Microbial Etiology of Prosthetic Joint Infections according to Route of Acquisition and Time after Prosthesis Implantation, Including the Role of Multidrug-Resistant Organisms." Journal of Clinical Medicine 8, no. 5 (May 13, 2019): 673. http://dx.doi.org/10.3390/jcm8050673.

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The aim of our study was to characterize the etiology of prosthetic joint infections (PJIs)—including multidrug-resistant organisms (MDRO)—by category of infection. A multicenter study of 2544 patients with PJIs was performed. We analyzed the causative microorganisms according to the Tsukayama’s scheme (early postoperative, late chronic, and acute hematogenous infections (EPI, LCI, AHI) and “positive intraoperative cultures” (PIC)). Non-hematogenous PJIs were also evaluated according to time since surgery: <1 month, 2–3 months, 4–12 months, >12 months. AHIs were mostly caused by Staphylococcus aureus (39.2%) and streptococci (30.2%). EPIs were characterized by a preponderance of virulent microorganisms (S. aureus, Gram-negative bacilli (GNB), enterococci), MDROs (24%) and polymicrobial infections (27.4%). Conversely, coagulase-negative staphylococci (CoNS) and Cutibacterium species were predominant in LCIs (54.5% and 6.1%, respectively) and PICs (57.1% and 15.1%). The percentage of MDROs isolated in EPIs was more than three times the percentage isolated in LCIs (7.8%) and more than twice the proportion found in AHI (10.9%). There was a significant decreasing linear trend over the four time intervals post-surgery for virulent microorganisms, MDROs, and polymicrobial infections, and a rising trend for CoNS, streptococci and Cutibacterium spp. The observed differences have important implications for the empirical antimicrobial treatment of PJIs.

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