Effect of human immunodeficiency virus on blood-brain barrier integrity and function: an update

The blood-brain barrier (BBB) is a diffusion barrier that has an important role in maintaining a precisely regulated microenvironment protecting the neural tissue from infectious agents and toxins in the circulating system. Compromised BBB integrity plays a major role in the pathogenesis of retroviral associated neurological diseases. Human Immunodeficiency Virus (HIV) infection in the Central Nervous System (CNS) is an early event even before the serodiagnosis for HIV positivity or the initiation of antiretroviral therapy (ART), resulting in neurological complications in many of the infected patients. Macrophages, microglia and astrocytes (in low levels) are the most productively/latently infected cell types within the CNS. In this brief review, we have discussed about the effect of HIV infection and viral proteins on the integrity and function of BBB, which may contribute to the progression of HIV associated neurocognitive disorders

Feline immunodeficiency virus decreases cell-cell communication and mitochondrial membrane potential.

The in vitro effects of viral replication on mitochondrial membrane potential (MMP) and gap junctional intercellular communication (GJIC) were evaluated as two parameters of potential cellular injury. Two distinct cell types were infected with the Petaluma strain of feline immunodeficiency virus (FIV). Primary astroglia supported acute FIV infection, resulting in syncytia within 3 days of infection, whereas immortalized Crandell feline kidney (CRFK) cells of epithelial origin supported persistent FIV infection in the absence of an obvious cytopathic effect. An examination of cells under conditions that included an infection rate of more than 90% for either population revealed that the astroglia produced about four times more virus than the CRFK cells. The mitochondrial uptake of the cationic fluorescent dye rhodamine 123 in infected astroglia was less than 45% of that of normal control cells, whereas the MMP of the CRFK cells, which produced about one-fourth as much virus, was 80.8% of that of the normal cells. Cell-cell communication between adjacent cells was determined by the recovery of fluorescence following photobleaching of a single cell. In spite of the lower level of innate cell-cell communication among cultured CRFK cells than among astroglia, viral replication resulted in a 30% decrease in the GJIC of both astroglia and CRFK cells. These studies indicate that cell injury, as defined by an inhibition of MMP and GJIC, can occur as a result of persistent and acute infection with the Petaluma strain of FIV

The characteristics of altered cellular functions of the Crandell cell line (CFRK) and feline fetal astroglia infected with the Petaluma strain of the feline immunodeficiency virus

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HIV PREVALENCE AND RISK FACTORS IN A SUBURBAN REGION

OBJECTIVES: Human immunodeficiency virus (HIV) infection and acquired immunodeficiency syndrome have created havoc due to high morbidity and mortality. Apart from anti - retroviral therapy (ART) there is no effective line of management available for this infection. Pr eventive strategies remain the mainstay to curb this epidemic. We undertook this study for estimating the prevalence and risk factors of HIV infection in our local population. This would help us to plan appropriate interventions for minimizing and preventi ng HIV infections. MATERIALS AND METHODS: The study was conducted from January – December 2004, in Integrated Counselling and Testing Center (ICTC) affiliated to our institute. After pre - test counselling, blood samples were collected from 1694 patients. Th ey were subjected to Enzyme Linked Immunosorbent Assay (ELISA) and rapid tests - Comb AIDS, Tri Dot & ACON under strict quality control. RESULTS: Out of 1694 patients, seropositive males and females were 297 (17.53%) and 166 (9.79%) respectively. Heterosexual behaviour (35.20%) and parent to child transmission (10.36%) were the major routes of transmission of HIV infection. Amongst infected patients labourers, farmers and housewives were high in numbers. CONCLUSIONS: Behavioural interventions and risk factor modifications are important targets in controlling the HIV epidemi

Feline immunodeficiency virus decreases cell-cell communication and mitochondrial membrane potential

The in vitro effects of viral replication on mitochondrial membrane potential (MMP) and gap junctional intercellular communication (GJIC) were evaluated as two parameters of potential cellular injury. Two distinct cell types were infected with the Petaluma strain of feline immunodeficiency virus (FIV). Primary astroglia supported acute FIV infection, resulting in syncytia within 3 days of infection, whereas immortalized Crandell feline kidney (CRFK) cells of epithelial origin supported persistent FIV infection in the absence of an obvious cytopathic effect. An examination of cells under conditions that included an infection rate of more than 90% for either population revealed that the astroglia produced about four times more virus than the CRFK cells. The mitochondrial uptake of the cationic fluorescent dye rhodamine 123 in infected astroglia was less than 45% of that of normal control cells, whereas the MMP of the CRFK cells, which produced about one-fourth as much virus, was 80.8% of that of the normal cells. Cell-cell communication between adjacent cells was determined by the recovery of fluorescence following photobleaching of a single cell. In spite of the lower level of innate cell-cell communication among cultured CRFK cells than among astroglia, viral replication resulted in a 30% decrease in the GJIC of both astroglia and CRFK cells. These studies indicate that cell injury, as defined by an inhibition of MMP and GJIC, can occur as a result of persistent and acute infection with the Petaluma strain of FIV.</jats:p