Viruses mechanisms

Starr CE, Pavan-Langston D. Varicella-zoster virus mechanisms of pathogenicity and corneal disease. Ophthalmol CUn North Am 2002 15 7-15. 

Fujinami RS, Oldstone MB (1985) Amino acid homology between the encephalitogenic site of myelin basic protein and virus Mechanism for autoimmunity. Science 230 1043-1045. 

PLASMIDS DERIVED FROM EPSTEIM-BARR VIRUS MECHANISMS OF PLASMID MAINTENANCE AND APPLICATIONS IN MOLECULAR BIOLOGY... 

The immune system in vertebrates provides a defense mechanism against foreign parasites such as viruses and bacteria. Three main properties are essential to its successful operation specific recognition of foreign molecules, the ability to destroy the foreign parasite, and a memory mechanism that allows a more rapid response to a second infection by the same microorganism. 

Figure 16.1 Viruses vary in size and shape from the simplest satellite viruses (a) that need another virus for their replication to the T-even bacteriophages (d) that have developed sophisticated mechanisms for injecting DNA into bacteria. Four different virus particles are shown to scale.

Viruses are the 2nd most problematic pathogen, behind protozoa. As with protozoa, most waterborne viral diseases don t present a lethal hazard to a healthy adult. Waterborne pathogenic viruses range in size from 0.020-0.030 jtim, and are too small to be filtered out by a mechanical filter. All waterborne enteric viruses affecting humans occur solely in humans, thus animal waste doesn t present much of a viral threat. At the present viruses don t present a major hazard to people drinking surface water in the U.S., but this could change in a survival situation as the level of human sanitation is reduced. Viruses do tend to show up even in remote areas, so a case can be made for eliminating them now. 

Unrestricted use of reclaimed wastewater for drinking water, however, requires careful examination. While practically a complete barrier to viruses, bacteria, and other toxic entities that must be kept out of a potable supply, RO membranes could pose serious problems should any defect develop in their separation mechanism. Given the purity and clarity of RO-treated wastewaters, however, it might be advantageous to use RO and then subject the product to well-established disinfection procedures. 

Since the preparation of the PEO and PVP silicas was carried out under the circumstances corresponding to the plateau part of isotherms, it obviously led to tailed structures of the stationary phases. Their inherent repellency ensured the size-exclusion mechanism for chromatography of viruses and large proteins. 

Extracts from 152 plant species, representing 46 different families, were screened for effects on tobacco mosaic virus (TMV) replication in cucumber cotyledons. Twenty species have shown enough activity to warrant further study. Several members of the Caprifoliaceae family increased virus replication. An extract of Lonicera involucrata enlarged the virus lesions in local lesion hosts and produced a thirty fold increase in virus titer, but had no effect on virus replication in systemic hosts. The active material appears to affect the virus defense mechanism of local lesion hosts. An extract of common geranium is an active virus inhibitor. It inactivates TMV and TMV-RNA (ribonucleic acid) in vitro by forming non-infectious complexes. In vivo, it also inhibited starch lesion formation in cucumber cotyledons incited by TMV infection. 

Therefore, in the cucumber-TMV system, tannic acid treatment had no effect on the establishment of infection it merely suppressed the expression of starch lesions and at the same time interfered with the defense mechanism of the host, permitting systemic spread of the virus. 

In both cases, a seeming virus stimulator (twinberry extract) and a virus inhibitor (tannic acid) operated in a more or less similar way in the cucumber-TMV system. They both affect the host defense mechanism against virus infection. The active component in twin-berry extract exhibits a mild and temporary interference, thus permitting virus to make further rounds of gain (ringlike patterns) while tannic acid produces a strong and permanent interference. 

Humoral immunity depends on soluble, noncellular effector mechanisms of the immune system. These include defensins and complement components (proteins of the innate immune system) and antibodies (products of the adaptive immune system). They are capable of reacting with foreign substances (e.g., bacteria and viruses) to produce detoxification and elimination. 

Bacterial and viral myositis is well recognized as a clinical entity by muscle pathologists. The viruses most commonly involved appear to be the Coxsackie viruses, the arboviruses, influenza virus, and HIV, but the mechanism whereby the viral infection gives rise to the myositic syndrome is not known. A detailed discussion of such problems is presented later on pages 333-334. 

Phillips, B., Abravaya, K., Morimoto, R.l. (1991), Analysis of the specificity and mechanism of the transcriptional activation of the human hsp70 gene during infection by DNA viruses. J. Virol. 11, 5680-5692. 

Although the details of the replication mechanism differ significantly between viruses, all viruses undergo the general replication steps outlined in Fig. 2. First, the... 

Substances that do not target the active site but display inhibition by allosteric mechanisms are associated with a lower risk of unwanted interference with related cellular enzymes. Allosteric inhibition of the viral polymerase is employed in the case of HIV-1 nonnucleosidic RT inhibitors (NNRTl, see chapter by Zimmermann et al., this volume) bind outside the RT active site and act by blocking a conformational change of the enzyme essential for catalysis. A potential disadvantage of targeting regions distant from the active site is that these may be subject to a lower selective pressure for sequence conservation than the active site itself, which can lower the threshold for escape of the virus by mutation. 

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