, 1994). We cannot exclude that in contrast to pri2 in S. commune,

priB does play a role in mushroom formation in L. edodes. The monokaryotic Δjmj3 strain was also indistinguishable from the wild-type strain. However, the dikaryotic Δjmj3Δjmj3 strain grew somewhat slower than the wild type and formed a less dense mycelium. Yet, the mutant did form sporulating fruiting bodies (data not shown). Taken together, we have shown that the relative incidence of gene inactivation by homologous integration is drastically increased in a Δku80 strain when compared with the wild type. This strain will therefore be highly www.selleckchem.com/products/AZD2281(Olaparib).html instrumental in the functional analysis of genes in S. commune and, in this way, contribute towards our understanding of the biology of mushroom-forming basidiomycetes. This research was supported by the Dutch Technology Foundation STW, the Applied Science division of NWO and the Technology Program of the Ministry of Economic Affairs. “
“It is expected that Mannheimia hemolyticaA1 expresses a particular collection of genes during infection in the host. The bacterial gene products are produced in the in vivo environment to facilitate growth and survival. Here, we examined gene expression

by M. hemolyticaA1 in the bovine host after 6 days of infection. Total RNA from M. hemolyticaA1 recovered from pneumonic lungs of two animals was used to produce Quizartinib in vitro cDNA to screen a custom M. hemolyticaA1 microarray. The expression profile was compared to a RNA sample from an in vitro grown culture. The data showed that 44 genes were differentially expressed by more than eightfold when compared with the in vitro sample. Seventeen genes were found Erastin research buy to have higher expression in vivo and 27 genes had lower expression. Several virulence-associated genes including those encoding leukotoxin, a capsule biosynthetic enzyme and the serotype-specific antigen, Ssa, had reduced expression, suggesting that their products may not be important during the later stages of infection. Most of the genes up-regulated in vivo encoded hypothetical or conserved hypothetical

proteins. Three Mu-like bacteriophage-related genes were up-regulated in the in vivo sample, suggesting that the prophage may be transcriptionally active. The results provide a glimpse of gene expression by the bacterium in the host after pulmonary infection has been established. Bovine pneumonic pasteurellosis is the major cause of morbidity and mortality in beef cattle in North America and results in significant economic loss to the cattle industry (Griffin, 1997). The primary causative agent of pneumonic pasteurellosis is Mannheimia hemolytica A1, a Gram-negative, non-motile bacterium that is a part of the normal flora of the upper respiratory mucosa of cattle (Frank, 1988). To-date, there is no information pertaining to the global gene expression of M. hemolytica A1 within the bovine host during an infection. Roehrig et al. (2007) examined the transcriptome profile of M.