• Je něco špatně v tomto záznamu ?

Changes in Caenorhabditis elegans life span and selective innate immune genes during Staphylococcus aureus infection

G. JebaMercy, SK. Pandian, K. Balamurugan,

. 2011 ; 56 (5) : 373-80.

Jazyk angličtina Země Česko

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc12035209

Caenorhabditis elegans has been increasingly used to study the innate immunity and for the screening of microbe/host-specific pathogenic factors. Staphylococcus aureus-mediated infections with live C. elegans were performed on solid (full-lawn) and liquid assays. S. aureus required 90 ± 10 h for the complete killing of C. elegans, but the infection was started only after 32 h of exposure with 20% inoculum of S. aureus. The short time exposure studies revealed that, in 20% of inoculum, continuous exposure to the pathogen was required for the killing of nematode. In 100% of inoculum, only 8 h of exposure was sufficient to kill the C. elegans. To evaluate kinetically at the innate immune level, the regulation of representative candidate antimicrobial genes was investigated. Both semi-quantitative reverse transcriptase polymerase chain reaction (PCR) and real-time PCR analyses indicated the regulation of candidate immune regulatory genes of lysozyme (lys-7), cysteine protease (cpr-2), and C-type lectin (clec-60 and clec-87) family members during the course of S. aureus infections, indicating the possible contribution of the above players during the host immune response against S. aureus exposures.

000      
00000naa a2200000 a 4500
001      
bmc12035209
003      
CZ-PrNML
005      
20121213145217.0
007      
ta
008      
121023s2011 xxu f 000 0|eng||
009      
AR
035    __
$a (PubMed)21853381
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xr
100    1_
$a JebaMercy, Gnanasekaran $u Department of Biotechnology, Alagappa University, Karaikudi, 630 003, India. jebmercy@gmail.com
245    10
$a Changes in Caenorhabditis elegans life span and selective innate immune genes during Staphylococcus aureus infection / $c G. JebaMercy, SK. Pandian, K. Balamurugan,
520    9_
$a Caenorhabditis elegans has been increasingly used to study the innate immunity and for the screening of microbe/host-specific pathogenic factors. Staphylococcus aureus-mediated infections with live C. elegans were performed on solid (full-lawn) and liquid assays. S. aureus required 90 ± 10 h for the complete killing of C. elegans, but the infection was started only after 32 h of exposure with 20% inoculum of S. aureus. The short time exposure studies revealed that, in 20% of inoculum, continuous exposure to the pathogen was required for the killing of nematode. In 100% of inoculum, only 8 h of exposure was sufficient to kill the C. elegans. To evaluate kinetically at the innate immune level, the regulation of representative candidate antimicrobial genes was investigated. Both semi-quantitative reverse transcriptase polymerase chain reaction (PCR) and real-time PCR analyses indicated the regulation of candidate immune regulatory genes of lysozyme (lys-7), cysteine protease (cpr-2), and C-type lectin (clec-60 and clec-87) family members during the course of S. aureus infections, indicating the possible contribution of the above players during the host immune response against S. aureus exposures.
650    _2
$a zvířata $7 D000818
650    _2
$a Caenorhabditis elegans $x genetika $x imunologie $x metabolismus $7 D017173
650    _2
$a proteiny Caenorhabditis elegans $x genetika $x imunologie $x metabolismus $7 D029742
650    _2
$a počet mikrobiálních kolonií $7 D015169
650    _2
$a cysteinové proteasy $x genetika $x imunologie $x metabolismus $7 D057056
650    _2
$a bakteriální léková rezistence $7 D024881
650    _2
$a exprese genu $7 D015870
650    _2
$a interakce hostitele a patogenu $7 D054884
650    _2
$a přirozená imunita $7 D007113
650    _2
$a lektiny typu C $x genetika $x imunologie $x metabolismus $7 D037181
650    _2
$a muramidasa $x genetika $x imunologie $x metabolismus $7 D009113
650    _2
$a kvantitativní polymerázová řetězová reakce $7 D060888
650    _2
$a polymerázová řetězová reakce s reverzní transkripcí $7 D020133
650    _2
$a stafylokokové infekce $x genetika $x imunologie $x mikrobiologie $7 D013203
650    _2
$a Staphylococcus aureus $x fyziologie $7 D013211
650    _2
$a virulence $7 D014774
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Pandian, Shunmugiah Karutha $u -
700    1_
$a Balamurugan, Krishnaswamy $u -
773    0_
$w MED00011005 $t Folia microbiologica $x 1874-9356 $g Roč. 56, č. 5 (2011), s. 373-80
856    41
$u https://pubmed.ncbi.nlm.nih.gov/21853381 $y Pubmed
910    __
$a ABA008 $b $c $y a
990    __
$a 20121023 $b ABA008
991    __
$a 20121102114656 $b ABA008
999    __
$a ok $b bmc $g 961634 $s 792709
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2011 $b 56 $c 5 $d 373-80 $i 1874-9356 $m Folia microbiologica $n Folia microbiol. (Prague) $x MED00011005
LZP    __
$a Pubmed-20121023-FolMibiolPha11Zahr

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...