Septic Polyarthritis by Staphylococcus aureus of “Unknown Origin”

2020 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Soraia Azevedo ◽  
Joana Sousa-Neves ◽  
Daniela Santos-Faria ◽  
Joana Leite Silva ◽  
Joana Ramos Rodrigues ◽  
...  
2017 ◽  
Vol 44 (4) ◽  
pp. 488-489 ◽  
Author(s):  
Jacopo Colombo ◽  
Luigia Elzi ◽  
Giorgio Treglia ◽  
Andreas Perren

2019 ◽  
Vol 46 (6) ◽  
pp. 1351-1358 ◽  
Author(s):  
Mette Bordinggaard Brøndserud ◽  
Court Pedersen ◽  
Flemming S. Rosenvinge ◽  
Poul F. Høilund-Carlsen ◽  
Søren Hess

2020 ◽  
Author(s):  
Darius Gawlik ◽  
Antje Ruppelt-Lorz ◽  
Elke Müller ◽  
Annett Reißig ◽  
Helmut Hotzel ◽  
...  

AbstractAn Eritrean patient was admitted with suspected tuberculous cervical lymphadenitis. While no mycobacteria were detected in pus from this process, culture yielded PVL-positive, methicillin-susceptible Staphylococcus aureus. Microarray hybridisation assigned the isolate to clonal complex (CC) 80 but revealed unusual features, including the presence of the ORF-CM14 enterotoxin homologue and of an ACME-III element as well as the absence of etD and edinB. The isolate was subjected to both, Illumina and Nanopore sequencing allowing characterisation of deviating regions within the strain’s genome. Atypical features of this strain were attributable to the presence of two genomic regions that originated from other S. aureus lineages and that comprised, respectively, 3% and 1.4% of the genome. One deviating region extended from walJ to sirB. It comprised ORF-CM14 and the ACME-III element. A homologous, but larger fragment was also found in an atypical S. aureus CC1/ST567 strain whose lineage might have served as donor of this genomic region. This region itself is a chimera comprising fragments from CC1 as well as fragments of unknown origin. The other region of another 3% of the genome comprised the region from htsB to ecfA2. It was very similar to CC1 sequences. This suggests either an incorporation of CC1 DNA into the study strain, or it might alternatively suggest a recombination event affecting “canonical” CC80. As the study strain bears witness of several recombination events, such complex and large-scale events cannot be rare and exceptional, despite a mainly clonal nature of S. aureus. Although the exact mechanism is not yet clear, chimerism seems to be an additional pathway in the evolution of S. aureus, possibly being responsible for the transmission also of virulence and resistance factors. An organism that can shuffle, swap or exchange major parts of its genome by a yet unknown mechanism would have an evolutionary advantage compared to a strictly clonal organism.


2021 ◽  
Vol 10 (37) ◽  
Author(s):  
Brianna L. McCall ◽  
J. A. C. Vriezen

Many Staphylococcus and Pseudomonas species, such as Staphylococcus aureus and Pseudomonas aeruginosa , are opportunistic human pathogens. However, Pseudomonas species are also known to produce bioactive compounds. Here, we report on the genome sequences of a Pseudomonas isolate and a Staphylococcus species of unknown origin that it inhibits.


2009 ◽  
Vol 58 (4) ◽  
pp. 313-314 ◽  
Author(s):  
Ramachandran Vignesh ◽  
Esaki Muthu Shankar ◽  
Nagalingeswaran Kumarasamy ◽  
Paulas Irene ◽  
Kailapuri G. Murugavel ◽  
...  

2013 ◽  
Vol 21 (4) ◽  
pp. 217-221
Author(s):  
Jose F. Camargo ◽  
George Sakoulas ◽  
Jonathan D. Dodd ◽  
Sigridh Muñoz-Gomez ◽  
Khatuna Kadeishvili ◽  
...  

2015 ◽  
Vol 53 (6) ◽  
pp. 1836-1841 ◽  
Author(s):  
W. S. N. Lekkerkerk ◽  
W. J. B. van Wamel ◽  
S. V. Snijders ◽  
R. J. Willems ◽  
E. van Duijkeren ◽  
...  

Fifteen percent of all methicillin-resistantStaphylococcus aureus(MRSA) clonal complex 398 (CC398) human carriers detected in The Netherlands had not been in direct contact with pigs or veal calves. To ensure low MRSA prevalence, it is important to investigate the likely origin of this MRSA of unknown origin (MUO). Recently, it was shown that CC398 strains originating from humans and animals differ in the presence of specific mobile genetic elements (MGEs). We hypothesized that determining these specific MGEs in MUO isolates and comparing them with a set of CC398 isolates of various known origin might provide clues to their origin. MUO CC398 isolates were compared to MRSA CC398 isolates obtained from humans with known risk factors, a MRSA CC398 outbreak isolate, livestock associated (LA) MRSA CC398 isolates from pigs, horses, chickens, and veal calves, and five methicillin-susceptibleStaphylococcus aureus(MSSA) CC398 isolates of known human origin. All strains werespatyped, and the presence or absence of,scn,chp, φ3int, φ6int, φ7int,rep7,rep27, andcadDXwas determined by PCRs. The MRSA CC398 in humans, MUO, or MRSA of known origin (MKO) resembled MRSA CC398 as found in pigs and not MSSA CC398 as found in humans. The distinct human MSSA CC398spatype, t571, was not present among our MRSA CC398 strains; MRSA CC398 was tetracycline resistant and carried no φ3 bacteriophage withscnandchp. We showed by simple PCR means that human MUO CC398 carriers carried MRSA from livestock origin, suggestive of indirect transmission. Although the exact transmission route remains unknown, direct human-to-human transmission remains a possibility as well.


2019 ◽  
Vol 101 (5) ◽  
pp. e125-e127
Author(s):  
S Capella ◽  
T Mahesan ◽  
J Taylor ◽  
A Chetwood

Cavernosal abscess is a rare diagnosis. Disparity exists in the literature but the most common colonising agents appear to be Neisseira gonorrhoea and Staphylococcus aureus. We describe a 75-year-old man who presented with sepsis and was found to have Escherichia coli positive blood and urinary cultures. Following initial treatment for sepsis of unknown origin, computed tomography demonstrated a bilateral cavernosal abscess. The patient was successfully treated with incision and drainage, multiple re-looks and a delayed closure, alongside a course of appropriate antibiotics. A defect in the bulbar urethra was identified and repaired with bladder drainage via both suprapubic and urethral catheters. Following discharge, a urethrogram showed no urethral leak or stricture and the patient is now catheter free.


Author(s):  
Masaatsu Koike ◽  
Koichi Nakashima ◽  
Kyoko Iida

Penicillin exerts the activity to inhibit the peptide cross linkage between each polysaccharide backbone at the final stage of wall-peptidoglycan biosynthesis of bacteria. Morphologically, alterations of the septal wall and mesosome in gram-positive bacteria, which were occurred in early time after treatment with penicillin, have been observed. In this experiment, these alterations were cytochemically investigated by means of silver-methenamine staining after periodate oxidation, which is applied for detection of localization of wall mucopolysaccharide.Staphylococcus aureus strain 209P treated with 100 u/ml of penicillin G was divided into two aliquotes. One was fixed by Kellenberger-Ryter's OSO4 fixative at 30, 60 and 120 min after addition of the antibiotic, dehydrated through alcohol series, and embedded in Epon 812 (Specimen A). The other was fixed by 21 glutaraldehyde, dehydrated through glycolmethacrylate series and embedded in glycolmethacrylate mixture, according to Bernhard's method (Specimen B).


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