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Diagn Microbiol Infect Dis 2004,50(4):237–245.PubMedCrossRef SCH772984 concentration 19. Maukonen J, Simoes C, Saarela M: The

currently used commercial DNA-extraction methods give different results of clostridial and actinobacterial populations derived from human fecal samples. FEMS Microbiol Ecol 2012,79(3):697–708.PubMedCrossRef 20. Bahl MI, Bergstrom A, Licht TR: Freezing fecal samples prior to DNA extraction affects the Firmicutes to Bacteroidetes ratio determined by downstream quantitative PCR analysis. FEMS Microbiol Lett 2012,329(2):193–197.PubMedCrossRef 21. RNAlater®: Preserving RNA Before Isolation TechNotes. 11(4): Life Technologies. Accessed 14 November 2013, http://​www.​lifetechnologies​.​com/​us/​en/​home/​references/​ambion-tech-support/​rna-isolation/​tech-notes/​rnalater-faqs.​html 22. Boesenberg-Smith KA, Pessarakli MM, Wolk DM: Assessment of DNA yield and purity: an overlooked detail of PCR troubleshooting. Clin Microbiol Newsl 2012,34(1):1–6.CrossRef PD-1 antibody inhibitor 23. U.S. Preventive Services Task Force: Guide to Clinical Preventive Services, 2008: recommendations of the U.S.

Services Task Force. Rockville, MD: Agency for Healthcare Research and Quality; 2008. [AHRQ Publication No. 08–05122] 24. Allison JE: Review article: faecal occult blood testing for colorectal cancer. Aliment Pharmacol Ther 1998,12(1):1–10.PubMedCrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions CD performed the statistical analysis and drafted the manuscript. JW carried out the sequencing assays and drafted the manuscript. RBH participated in the design of the study and helped to draft the manuscript. JA conceived the study, participated in its design and coordination, and helped to draft manuscript. All authors read and approved the final manuscript.”
“Background Bio-aerosols are airborne particles Arachidonate 15-lipoxygenase that originate from living microorganisms such as bacteria, fungi, and viruses generally found as part of the patient’s endogenous flora. Their components have negative effects

especially on the health of immuno-compromised people [1]. The infectious aerosols are small and may remain suspended and viable in the air stream over long periods of time. Attributable to the above-mentioned facts, the risk of airborne infections especially in hospitals and other health-care settings can be high as there can be confined spaces in which aerosols may build up to infectious levels [1]. The buildup of infectious aerosols exacerbates healthcare challenges in developing countries as the role of bio-aerosols in hospital-acquired infections (HAIs) has been recognized; studies have uncovered increasing evidence regarding the spread of disease via the aerial route [2]. Consequently, the presence of bio-aerosols in health-care settings needs to be monitored and controlled to limit their dispersal.

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