scholarly journals 696: A RARE CASE OF STREPTOCOCCUS INTERMEDIUS BRAIN ABSCESS WITH VENTRICULITIS IN A PREGNANT PATIENT

2021 ◽  
Vol 50 (1) ◽  
pp. 342-342
Author(s):  
Clinton Ezekiel ◽  
Nikhil Organti
2019 ◽  
Vol 14 (2) ◽  
pp. 168-170
Author(s):  
Ali Fuat Tekin ◽  
Hakan Yilmaz ◽  
Turgay Kara ◽  
Erdi Seçkin ◽  
Muhsin Nuh Aybay ◽  
...  

2017 ◽  
Vol 18 (4) ◽  
pp. 254-257
Author(s):  
Vladimír Mihál ◽  
Marta Neklanová ◽  
Eva Klásková ◽  
David Krahulík ◽  
Kamila Michálková

2021 ◽  
Vol 3 (3) ◽  
pp. 164-176
Author(s):  
Buket Erturk Sengel ◽  
Elif Tukenmez Tigen ◽  
Fatmanur Yıldız ◽  
Yusuf Olur ◽  
Nurver Ulger ◽  
...  
Keyword(s):  

Pathogens ◽  
2019 ◽  
Vol 8 (1) ◽  
pp. 22 ◽  
Author(s):  
Elio Issa ◽  
Tamara Salloum ◽  
Balig Panossian ◽  
David Ayoub ◽  
Edmond Abboud ◽  
...  

Streptococcus intermedius (SI) is associated with prolonged hospitalization and low survival rates. The genetic mechanisms involved in brain abscess development and genome evolution in comparison to other members of the Streptococcus anginosus group are understudied. We performed a whole-genome comparative analysis of an SI isolate, LAU_SINT, associated with brain abscess following sinusitis with all SI genomes in addition to S. constellatus and S. anginosus. Selective pressure on virulence factors, phages, pan-genome evolution and single-nucleotide polymorphism analysis were assessed. The structural details of the type seven secretion system (T7SS) was elucidated and compared with different organisms. ily and nanA were both abundant and conserved. Nisin resistance determinants were found in 47% of the isolates. Pan-genome and SNPs-based analysis didn’t reveal significant geo-patterns. Our results showed that two SC isolates were misidentified as SI. We propose the presence of four T7SS modules (I–IV) located on various genomic islands. We detected a variety of factors linked to metal ions binding on the GIs carrying T7SS. This is the first detailed report characterizing the T7SS and its link to nisin resistance and metal ions binding in SI. These and yet uncharacterized T7SS transmembrane proteins merit further studies and could represent potential therapeutic targets.


Author(s):  
Sevliya Öcal Demir ◽  
Eda Kepenekli Kadayifci ◽  
Gülşen Akkoç ◽  
Nurhayat Yakut ◽  
Adnan Dağçınar ◽  
...  

1999 ◽  
Vol 158 (10) ◽  
pp. 872-873 ◽  
Author(s):  
T. Nagatomo ◽  
S. Ohga ◽  
M. Saito ◽  
H. Takada ◽  
Y. Sasaki ◽  
...  

CHEST Journal ◽  
2016 ◽  
Vol 150 (4) ◽  
pp. 448A ◽  
Author(s):  
Shyam Shankar ◽  
Sushilkumar Gupta ◽  
Ishan Malhotra ◽  
Mangalore Amith Shenoy ◽  
Hatem Desoky ◽  
...  

2021 ◽  
pp. 491-493
Author(s):  
Nalini Sharma ◽  
Vinayak Jante ◽  
Rituparna Das ◽  
Subrat Panda ◽  
Mandeep Sagar

Hydranencephaly (HE) is a rare condition occurring in <1/10,000 births worldwide. It is one of the recognized forms of brain malformations that are usually associated with intrauterine fetal demise rarely seen in postnatal life. HE can often be misdiagnosed due to certain common features with other neurological abnormalities such as hydrocephalus, holoprosencephaly, and porencephaly. Here, we report the case of a 26-year-old pregnant patient at 34 weeks who was referred with ultrasonography finding of HE which was confirmed by fetal MRI. The decision to deliver the baby was taken expecting an extremely poor outcome after discussing with the family.


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