Chlamydophila psittaci DNA detection in the faeces of cage birds


SAREYYÜPOĞLU B., Cantekin Z., Bas B.

ZOONOSES AND PUBLIC HEALTH, cilt.54, sa.6-7, ss.237-242, 2007 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 54 Sayı: 6-7
  • Basım Tarihi: 2007
  • Doi Numarası: 10.1111/j.1863-2378.2007.01060.x
  • Dergi Adı: ZOONOSES AND PUBLIC HEALTH
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.237-242
  • Anahtar Kelimeler: cage birds, Chlamydophila psittaci, faeces, polymerase chain reaction, POLYMERASE-CHAIN-REACTION, CHLAMYDIA-PSITTACI, FECAL SAMPLES, PCR, QUANTIFICATION, PURIFICATION
  • Ankara Üniversitesi Adresli: Evet

Özet

In this study, we investigated the shedding of Chlamydophila psittaci in faecal samples from cage birds using PCR testing. A total of 47 faeces samples were collected from four different aviaries. Main symptoms determined after clinical investigation and owner histories of the birds showed that the birds had respiratory system problems changing from mild to severe. They also showed conjunctivitis, diarrhoea or no symptoms at all. DNA extractions from faeces were performed with the QIAamp DNA Stool Mini Kit. Following PCR with Cp. psittaci specific primers, 43 (91.5%) samples were determined to harbour-specific DNA. Only one bird from each aviary was found to be negative by PCR. As all the samples from birds showing clinical signs were PCR positive, these signs could be correlated to psittacosis in these birds. Cp. psittaci shedding in faeces was detected in all the aviaries. After restriction analysis of PCR amplicons with AluI enzyme, all the isolates showed the same RFLP (Restriction Fragment Length Polymorphism) patterns with the control Cp. psittaci DNA. PCR following QIAamp DNA stool mini kit extraction of faecal samples was found to be a rapid, specific, sensitive, reproducible test, which did not need additional nested PCR of samples.