- Home
- A-Z Publications
- Current Drug Targets - Infectious Disorders
- Previous Issues
- Volume 5, Issue 3, 2005
Current Drug Targets - Infectious Disorders - Volume 5, Issue 3, 2005

Volume 5, Issue 3, 2005
-
-
Combination Antifungal Therapy for Invasive Aspergillosis: Utilizing New Targeting Strategies
More LessThe optimal therapy for invasive aspergillosis (IA) is unknown, and there is little agreement on the exact antifungal management of IA. The previously stagnant landscape of antifungal choices for IA is rapidly changing with newer antifungals and newer targets. While amphotericin B has historically been the preferred therapy, recent studies support voriconazole as primary therapy or caspofungin as salvage therapy. How Read More
-
-
-
Paracoccidioides brasiliensis, Paracoccidioidomycosis, and Antifungal Antibiotics
Authors: G. Visbal, G. San-Blas, J. Murgich and H. FrancoParacoccidioides brasiliensis is the causative agent of paracoccidioidomycosis (PCM), a human systemic, chronic and progressive mycosis. Preferred antifungals are sulfamethoxazol-trimethoprim, itraconazole, amphotericin B. Treatment is lengthy, the drugs may have undesirable side effects, and some are costly. Occasional resistant strains have been reported. Therefore, the search for more selective and efficient anti Read More
-
-
-
Quinolone-Based Drugs Against Toxoplasma gondii and Plasmodium spp
Authors: Guillaume Anquetin, Jacques Greiner and Pierre VierlingOwing to the rapid emergence of multi-resistant strains of Plasmodium spp. (the causative agents of malaria) and the limitations of drugs used against Toxoplasma gondii (an important opportunistic pathogen associated with AIDS and congenital birth defects), the discovery of new therapeutical targets and the development of new drugs are needed. The presence of the prokaryotic-like organelle in apicomplexan pa Read More
-
-
-
Dendrimers and Antivirals: A Review
Authors: A. Rosa Borges and C.- L. SchengrundIn response to the need for antiviral agents, dendrimers, hyper-branched, well-defined, and chemically versatile molecules, have been found to have a number of potential uses. How they are used is based on knowledge of 1) how a virus interacts with its target cells, 2) how it replicates, and 3) which viral components are recognized by the immune response of the host. Many viral-host cell interactions are initiated by viral pro Read More
-
-
-
Insulin Resistance in the HIV-Infected Population: The Potential Role of Mitochondrial Dysfunction
Authors: C. M. Shikuma, L. J. Day and M. GerschensonInsulin resistance is accepted as the underlying fundamental defect that predates and ultimately leads to the development of type 2 (adult onset) diabetes mellitus in the general non-human immunodeficiency virus (HIV)-infected population. Insulin resistance is also a major component of the metabolic syndrome that, in association with other factors such as hypertension, hypercholesterolemia, and central obesity, defines a pr Read More
-
-
-
Mechanisms of Drug Resistance in Mycoplasma pneumoniae
Authors: C. M. Bebear and S. PereyreMycoplasma pneumoniae is a pathogenic mycoplasma responsible for respiratory tract infections in humans, occurring worldwide in children and adults. This review briefly focuses on its antibiotic susceptibility profile and on the development of acquired resistance for this microorganism. The lack of a cell wall in mycoplasmas makes them intrinsically resistant to β-lactams and to all antimicrobials which target the cell wall. Intri Read More
-
-
-
The Molecular Basis for the Mode of Action of Bicyclomycin
Authors: Harold Kohn and William WidgerBicyclomycin (1) is a clinically useful antibiotic exhibiting activity against a broad spectrum of Gram-negative bacteria and against the Gram-positive bacterium, Micrococcus luteus. Bicyclomycin has been used to treat diarrhea in humans and bacterial diarrhea in calves and pigs and is marketed by Fujisawa (Osaka, Japan) under the trade name Bicozamycin. The structure of 1 is unique among antibiotics, and our studies documen Read More
-
-
-
Identification of Inhibitors of Bacterial Enoyl-Acyl Carrier Protein Reductase
More LessThe FabI-related enoyl-ACP reductase enzymes of bacteria meet many of the criteria for antibacterial targets. These enzymes are essential for the growth of several pathogenic species, have no significant mammalian homologs, catalyze a rate-limiting step in a vital macromolecular biosynthetic pathway, and are already the targets of antibacterials used in the clinic (isoniazid) and in consumer products (triclosan). The suitability o Read More
-
Most Read This Month
Article
content/journals/cdtid
Journal
10
5
false
en
