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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Diagnostic approaches based on PCR methods are increasingly used in the field of parasitology, particularly to detect . Consequently, many different PCR methods are available, both "in-house" and commercial methods. The aim of this study was to compare the performance of eight PCR methods, four "in-house" and four commercial methods, to detect species. On the same DNA extracts, performance was evaluated regarding the limit of detection for both and specificity and the ability to detect rare species implicated in human infection. Results showed variations in terms of performance. The best performance was observed with the FTD Stool parasites method, which detected and with a limit of detection of 1 and 10 oocysts/gram of stool respectively; all rare species tested were detected (, and ), and no cross-reaction was observed. In addition, no cross-reactivity was observed with other enteric pathogens. However, commercial methods were unable to differentiate species, and generally, we recommend testing each DNA extract in at least triplicate to optimize the limit of detection.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224656 | PMC |
http://dx.doi.org/10.3390/pathogens10060647 | DOI Listing |