“
“Crucell – Johnson and Johnson, Leiden, The Netherlands Nontypeable Haemophilus influenzae (NTHi) is a Gram-negative microbe that frequently colonizes the human host without obvious signs of inflammation, but is also a frequent cause of otitis media in children and exacerbations in chronic obstructive pulmonary disease patients. Accumulating data suggest that NTHi can reside in biofilms during both colonization and infection. Recent literature proposes

roles for phosphorylcholine, sialic acid, bacterial DNA, but also eukaryotic DNA in the development of NTHi biofilms. However, many questions remain. Until now, there are insufficient data GSK458 concentration to explain how NTHi forms biofilms. Here, we review the recent advances IDO inhibitor in NTHi biofilm formation with particular focus on the role that neutrophils may play in this process. We propose that recruitment of neutrophils facilitates NTHi biofilm formation on mucosal sites by the initiation

of neutrophil extracellular traps. “
“Avian pathogenic Escherichia coli (APEC) are bacteria associated with extraintestinal diseases in poultry. A method to generate markerless deletions of APEC genome is described. Lambda Red recombination is used to introduce a LoxP cassette (loxP-rpsL-neo-loxP) containing the rpsL gene for streptomycin sensitivity and the neo gene for kanamycin/neomycin resistance into the APEC genome, with attendant deletion of a desired chromosomal gene. The loxP sites are incorporated into primers used to amplify the rpsL-neo marker during the construction of the LoxP cassette, making the method rapid and efficient. The cassette is specifically integrated into the fiu gene or intergenic region 2051-52, and the Cre/lox system is used to remove the marker, hence deletion of the drug-resistance genes. The results demonstrate Beta adrenergic receptor kinase that the Cre/lox system

can successfully be used to generate markerless deletions in APEC, and rpsL counter-selection can be used to select the deletions so that one does not have to pick and test to find the desired product. Avian pathogenic Escherichia coli (APEC) are extraintestinal E. coli that cause systemic disease in poultry, collectively known as avian colibacillosis and associated with major economic losses in the poultry industry worldwide (Dho-Moulin & Fairbrother, 1999; Dziva & Stevens, 2008). Availability of experimental infection models in target hosts and the recently available complete genome sequence of APEC O1:K1:H7 (Johnson et al., 2007) provides the basis for comprehensive understanding of the organism’s pathogenesis (Dziva & Stevens, 2008). Together with several gene manipulations such as site-directed mutagenesis, construction of strains with mutations in chromosomal genes remains the ‘gold standard’ for many functional genomic analyses (Gerlach et al., 2009). Deletions in the E. coli genome using the Cre/lox system have been reported (Yoon et al., 1998; Fukiya et al., 2004).