2011
DOI: 10.1016/j.vetmic.2010.07.006
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Deletion of sua gene reduces the ability of Streptococcus uberis to adhere to and internalize into bovine mammary epithelial cells

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Cited by 18 publications
(13 citation statements)
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“…The same group demonstrated that bovine serum and milk containing anti-SUAM or anti-pepSUAM antibodies significantly inhibited adherence to and internalization of S. uberis into BMEC . This observation was further confirmed by a study using a sua-gene deletion mutant strain of S. uberis UT888 (Chen et al, 2011). Using 3 different prediction methods, the N-terminal pepSUAM (also designated as SUAM peptide I), 3 other regions in the middle portion of SUAM [peptide II (AA 342-356), peptide III (AA 357-371), and peptide IV (AA 439-453], and a region at the C-terminus of SUAM [peptide V (AA 705-719)] were predicted to be surfaced exposed B-cell epitopes Luther et al, 2010).…”
mentioning
confidence: 55%
“…The same group demonstrated that bovine serum and milk containing anti-SUAM or anti-pepSUAM antibodies significantly inhibited adherence to and internalization of S. uberis into BMEC . This observation was further confirmed by a study using a sua-gene deletion mutant strain of S. uberis UT888 (Chen et al, 2011). Using 3 different prediction methods, the N-terminal pepSUAM (also designated as SUAM peptide I), 3 other regions in the middle portion of SUAM [peptide II (AA 342-356), peptide III (AA 357-371), and peptide IV (AA 439-453], and a region at the C-terminus of SUAM [peptide V (AA 705-719)] were predicted to be surfaced exposed B-cell epitopes Luther et al, 2010).…”
mentioning
confidence: 55%
“…Invasion, persistence, and internalization are up regulated by binding of SUAM to lactoferrin, which is primarily synthesized in those cells (ALMEIDA et al, 2006;CHEN et al, 2011;LUTHER et al, 2008). This gene is reported to be highly conserved (LUTHER et al, 2008;PERRIG et al, 2015), supporting its potential utility for the development of vaccines.…”
Section: Resultsmentioning
confidence: 97%
“…Streptococcus uberis UT888, originally isolated from a clinical case of mastitis, and ∆sua S. uberis UT888 were used (Chen et al, 2011). For challenge, S. uberis strains were plated onto trypticase soy blood agar plates (BAP, Becton Dickinson and Company, Franklin Lakes, NJ, USA), and incubated overnight at 37°C in 5% CO 2.…”
Section: Bacteria and Culture Conditionsmentioning
confidence: 99%
“…In following studies, we created a sua-gene deletion mutant clone of S. uberis UT888 unable to express SUAM showing reduced adherence to and internalization of the SUAM mutant into BMEC (Chen et al, 2011). However, although all these data suggested the virulence attributes of SUAM the confirmation of the pathogenic role of SUAM under in vivo conditions was still missing.…”
Section: Intramammary Infectionsmentioning
confidence: 99%
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