2011
DOI: 10.1292/jvms.10-0222
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Detection of Chlamydophila psittaci by Using SYBR Green Real-Time PCR

Abstract: ABSTRACT. Chlamydophila psittaci is the causative agent of human psittacosis and avian chlamydiosis. This zoonotic pathogen is frequently transmitted from infected birds to humans. Therefore proper and rapid detection of C. psittaci in birds is important to control this disease. We developed a method for detecting C. psittaci by using SYBR Green Real-time PCR based on targeting the cysteinerich protein gene (envB) of C. psittaci. This one step procedure was highly sensitive and rapid for detection and quantifi… Show more

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Cited by 9 publications
(5 citation statements)
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“…The PCR and real-time PCR tests, although highly sensitive and used to detect Chlamydia in different animals in other countries ( 92–96 ) have seldom been used on a large scale due to high cost. The omp1 gene, which is very conservative, was used as a target gene to detect Chlamydia in different animals when IHA results were ambiguous ( 16, 97 ).…”
Section: Diagnostic Methodsmentioning
confidence: 99%
“…The PCR and real-time PCR tests, although highly sensitive and used to detect Chlamydia in different animals in other countries ( 92–96 ) have seldom been used on a large scale due to high cost. The omp1 gene, which is very conservative, was used as a target gene to detect Chlamydia in different animals when IHA results were ambiguous ( 16, 97 ).…”
Section: Diagnostic Methodsmentioning
confidence: 99%
“…DNAs from the specimens were extracted using a PureLink Genomic DNA kit (Thermo Fisher Scientific, Waltham, MA, USA) following the manufacturer's instructions. pecorum with a high sensitivity and a detection limit of 10 inclusion-forming units (IFUs) [19].…”
Section: Specimensmentioning
confidence: 99%
“…The reaction was performed with the Premix Ex-Taq (TaKaRa Bio, Kusatsu, Japan) on a Thermal Cycler Dice TP800 (TaKaRa Bio) in accordance with the manufacturer's instructions. The SYBR Green real-time PCR targeted envB as described previously[19] using the following primers: Env-F (). The reaction was performed with the SYBR Premix Ex-Taq (TaKaRa Bio) on a Thermal Cycler TP800 (TaKaRa Bio) inaccordance with the manufacturer's instructions.…”
mentioning
confidence: 99%
“…A curva de dissociação do fragmento de DNA de C. psittaci, amplificado a partir das amostras fecais, apresentou temperatura de dissociação de 83,2 a 83,4ºC (Fig. 1) A positividade para infecção por C. psittaci é variável em função de situações que predispõem as aves à infecção, presença de enfermidade clínica e ao teste diagnóstico utilizado (Stewardson e Grayson, 2010;Okuda et al, 2011). Há relatos desde positividade de 6,3% (2/32) em papagaios-verdadeiros (A. aestiva) e de 26,7% (12/45) em araras-azuis (Anodorhynchus hyacinthinus), procedentes de aves jovens do Pantanal do Mato Grosso do Sul, Brasil (Raso et al, 2006), 52,6% (61/116) em pombos na Espanha (Vázquez et al, 2010) e 90% (43/47) em várias espécies de aves de gaiola na Turquia (Sareyyupoglu et al, 2007).…”
Section: Resultsunclassified