Airborne bacteria are components of the atmospheric aerosol particles and can be responsible of allergic disease, regardless of their viability. In this paper, we report a method for the determination of total (viable and nonviable) bacterial content in airborne particles, using muramic and dipicolinic acids as biomarkers of bacteria and bacterial spores, respectively. The analytical procedure was optimized with bacteria and spores of Bacillus subtilis. After extraction and purification, the two biomarkers were analyzed by HPLC-ESI-MS/MS and their percentage was evaluated to be used as conversion factor. The present method for the determination of the total bacterial content was then applied to environmental samples, after a proper collection in an urban site. Thanks to the use of a low pressure impactor, capable of fractionating particles into the range of 0.03–10 μm, it was also possible to study the bacterial content in ultrafine, fine, and coarse particulate matter. The results from this study showed that muramic and dipicolinic acids can be determined together in one chromatographic run in reversed phase ion pair chromatography. Bacteria were more abundant than bacterial spores in the urban atmosphere, both showing a higher concentration in the coarse fraction of particles, although bacteria and bacterial spore amounts per unit mass of ultrafine particles were higher than in fine and coarse particles. © 2016, Springer-Verlag Berlin Heidelberg.

Muramic and dipicolinic acids in atmospheric particulate matter as biomarkers of bacteria and bacterial spores / Di Filippo, Patrizia; Pomata, Donatella; Riccardi, Carmela; Buiarelli, Francesca; Uccelletti, Daniela; Zanni, Elena. - In: ANALYTICAL AND BIOANALYTICAL CHEMISTRY. - ISSN 1618-2650. - STAMPA. - 409:6(2017), pp. 1657-1666. [10.1007/s00216-016-0111-y]

Muramic and dipicolinic acids in atmospheric particulate matter as biomarkers of bacteria and bacterial spores

Di Filippo, Patrizia
;
Pomata, Donatella;Buiarelli, Francesca
Conceptualization
;
Uccelletti, Daniela;Zanni, Elena
2017

Abstract

Airborne bacteria are components of the atmospheric aerosol particles and can be responsible of allergic disease, regardless of their viability. In this paper, we report a method for the determination of total (viable and nonviable) bacterial content in airborne particles, using muramic and dipicolinic acids as biomarkers of bacteria and bacterial spores, respectively. The analytical procedure was optimized with bacteria and spores of Bacillus subtilis. After extraction and purification, the two biomarkers were analyzed by HPLC-ESI-MS/MS and their percentage was evaluated to be used as conversion factor. The present method for the determination of the total bacterial content was then applied to environmental samples, after a proper collection in an urban site. Thanks to the use of a low pressure impactor, capable of fractionating particles into the range of 0.03–10 μm, it was also possible to study the bacterial content in ultrafine, fine, and coarse particulate matter. The results from this study showed that muramic and dipicolinic acids can be determined together in one chromatographic run in reversed phase ion pair chromatography. Bacteria were more abundant than bacterial spores in the urban atmosphere, both showing a higher concentration in the coarse fraction of particles, although bacteria and bacterial spore amounts per unit mass of ultrafine particles were higher than in fine and coarse particles. © 2016, Springer-Verlag Berlin Heidelberg.
2017
bacteria; bacterial spores; bioaerosol; conversion factors; dipicolinic acid; muramic acid
01 Pubblicazione su rivista::01a Articolo in rivista
Muramic and dipicolinic acids in atmospheric particulate matter as biomarkers of bacteria and bacterial spores / Di Filippo, Patrizia; Pomata, Donatella; Riccardi, Carmela; Buiarelli, Francesca; Uccelletti, Daniela; Zanni, Elena. - In: ANALYTICAL AND BIOANALYTICAL CHEMISTRY. - ISSN 1618-2650. - STAMPA. - 409:6(2017), pp. 1657-1666. [10.1007/s00216-016-0111-y]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/946246
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