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Authors
Info
R.A. Santos1, N.J. Sau1,
M.T. Certucha2, F.J. Almend?riz2,
A.O. Monge2, I.J. Zepeda3
and L.J. Hern?ndez1*
1Centro de
Investigaciones Biol?gicas del Noroeste SC, Hermosillo CP 83106, M?xico
2Divisi?n de
Ingenier?a, Departamento de Ingenier?a Qu?mica y Metalurgia, Universidad de
Sonora,? Hermosillo CP 83000, M?xico
3Coordinaci?n
General de Infraestructura, Desarrollo Urbano y Ecolog?a, Instituto Municipal
de Ecolog?a, Hermosillo CP 83270, M?xico
*Corresponding
Author Email :
jhlopez04@cibnor.mx
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Abstract
Aim: The microorganisms
present in the air have great biological and economic importance because they
can seriously affect living organisms. The aim of this work was to implement
a real-time PCR technique as a rapid method for detecting Enterococcus
faecalis in filters containing airborne particles, seeking to avoid the
loss of time in bacterial culture on agar plates.
Methodology: Air filter
samples were collected from four monitoring stations. Filter samples with PM10
and TSP particles were subjected to nucleic acid extraction and PCR for
identification of E. faecalis.
Results: The PCR technique
developed in this work showed high sensitivity and good specificity for
detecting the presence of E. faecalis in airborne particles. The
results of the microbiological analysis using traditional identification
techniques confirmed the presence of E. faecalis in all sampling
sites. Winter was the period with the highest percentage of positive samples.
Interpretation: The results
suggest that PCR technique can be used for rapid detection of E. faecalis
in filters containing PM10 and TSP particles.
Key words: Air borne particles, Atmospheric, Enterococcus
faecalis, Real-Time PCR
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