Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Treponema denticola is frequently isolated together with Porphyromonas gingivalis from the lesions seen in cases of chronic periodontitis and is considered a major pathogen of this disease. It has several virulence factors, including a major surface protein (Msp) and a major surface protease, dentilisin. The effect of these virulence factors on the host immune response remains to be elucidated, however. Toll-like receptors (TLRs) in the host can recognize pathogen-associated molecular patterns. Bacteria stimulate TLRs and activate the pro-inflammatory nuclear factor-kappa B pathway. Therefore, the aim of this study was to investigate the effect of T. denticola on TLR pathways. Toll-like receptor 4 and TLR2 reporter cell lines, which secrete alkaline phosphatase in response to TLR signals, were infected with the T. denticola wild type, an Msp-deficient mutant, a dentilisin-deficient mutant, or their extracts obtained via sonication. Signals from TLR2 or TLR4 cells were evaluated by alkaline phosphatase activity. Toll-like receptor 2 signals were detected in all T. denticola strains and sonication extracts, while no TLR4 signal was detected. Infection with the dentilisin-deficient mutant induced the strongest TLR2 signal among the strains. Sonication extracts of the wild type and Msp-deficient mutant showed the same level of TLR2 signaling. The TLR2 signal in the sonication extracts from the wild type was inhibited by Sparstolonin B, an antagonist of TLR2, in a dose-dependent manner. These results indicate that T. denticola is recognized by epithelial cells mainly via TLR2. The outer sheath structure may conceal potential ligands for TLR2.
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http://dx.doi.org/10.2209/tdcpublication.2024-0023 | DOI Listing |