Effects of morphine on replication of herpes simplex virus type 1 and 2

Several drugs are being used in treatment of HSV (Herpesviridae) infection in human but still introducing an effective safe drug is desirable. We investigated the inhibitory effect of morphine on replication of HSV in vitro. The results indicated that a concentration of up to 200 ìg/ml morphine had a limited effect on Vero cell viability. At this concentration, the growth of HSV was inhibited considerably and after the third passage in presence of morphine it was completely eliminated. The presence of viral antigens in infected cells in presence of morphine by immunoflourescent staining showed that after the first passage a small number of infected cells contained viral proteins and at the third passage no cells with viral antigen was observed. This was confirmed by page and immunobloting techniques. Electronmicroscopy observation in cellular section indicated that there was no virus present in treated cells as compared with control untreated infected cells

Primary Human mDC1, mDC2, and pDC Dendritic Cells Are Differentially Infected and Activated by Respiratory Syncytial Virus

Respiratory syncytial virus (RSV) causes recurrent infections throughout life. Vaccine development may depend upon understanding the molecular basis for induction of ineffective immunity. Because dendritic cells (DCs) are critically involved in early responses to infection, their interaction with RSV may determine the immunological outcome of RSV infection. Therefore, we investigated the ability of RSV to infect and activate primary mDCs and pDCs using recombinant RSV expressing green fluorescent protein (GFP). At a multiplicity of infection of 5, initial studies demonstrated ∼6.8% of mDC1 and ∼0.9% pDCs were infected. We extended these studies to include CD1c−CD141+ mDC2, finding mDC2 infected at similar frequencies as mDC1. Both infected and uninfected cells upregulated phenotypic markers of maturation. Divalent cations were required for infection and maturation, but maturation did not require viral replication. There is evidence that attachment and entry/replication processes exert distinct effects on DC activation. Cell-specific patterns of RSV-induced maturation and cytokine production were detected in mDC1, mDC2, and pDC. We also demonstrate for the first time that RSV induces significant TIMP-2 production in all DC subsets. Defining the influence of RSV on the function of selected DC subsets may improve the likelihood of achieving protective vaccine-induced immunity

Incp2 Group Of Pseudomonas, A Class Of Uniquely Large Plasmids

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/62848/1/274715a0.pd