Advances in Antiwolbachial Drug Discovery for Treatment of Parasitic Filarial Worm Infections

The intracellular bacteria now known as <i>Wolbachia</i> were first described in filarial worms in the 1970s, but the idea of <i>Wolbachia</i> being used as a macrofilaricidal target did not gain wide attention until the early 2000s, with research in filariae suggesting the r...

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Main Authors: Malina A. Bakowski, Case W. McNamara
Format: Article
Language:English
Published: MDPI AG 2019-07-01
Series:Tropical Medicine and Infectious Disease
Subjects:
Online Access:https://www.mdpi.com/2414-6366/4/3/108
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spelling doaj-80458e72c7044c079265749970d675fa2020-11-25T01:07:49ZengMDPI AGTropical Medicine and Infectious Disease2414-63662019-07-014310810.3390/tropicalmed4030108tropicalmed4030108Advances in Antiwolbachial Drug Discovery for Treatment of Parasitic Filarial Worm InfectionsMalina A. Bakowski0Case W. McNamara1Calibr at Scripps Research, La Jolla, CA 92037, USACalibr at Scripps Research, La Jolla, CA 92037, USAThe intracellular bacteria now known as <i>Wolbachia</i> were first described in filarial worms in the 1970s, but the idea of <i>Wolbachia</i> being used as a macrofilaricidal target did not gain wide attention until the early 2000s, with research in filariae suggesting the requirement of worms for the endosymbiont. This new-found interest prompted the eventual organization of the Anti-<i>Wolbachia</i> Consortium (A-WOL) at the Liverpool School of Tropical Medicine, who, among others have been active in the field of antiwolbachial drug discovery to treat filarial infections. Clinical proof of concept studies using doxycycline demonstrated the utility of the antiwolbachial therapy, but efficacious treatments were of long duration and not safe for all infected. With the advance of robotics, automation, and high-speed computing, the search for superior antiwolbachials shifted away from smaller studies with a select number of antibiotics to high-throughput screening approaches, centered largely around cell-based phenotypic screens due to the rather limited knowledge about, and tools available to manipulate, this bacterium. A concomitant effort was put towards developing validation approaches and in vivo models supporting drug discovery efforts. In this review, we summarize the strategies behind and outcomes of recent large phenotypic screens published within the last 5 years, hit compound validation approaches and promising candidates with profiles superior to doxycycline, including ones positioned to advance into clinical trials for treatment of filarial worm infections.https://www.mdpi.com/2414-6366/4/3/108<i>Wolbachia</i>filariaparasitic worms<i>Onchocerca</i><i>Brugia</i>drug discoveryantiwolbachialendosymbiontneglected tropical diseasehigh-throughput screening
collection DOAJ
language English
format Article
sources DOAJ
author Malina A. Bakowski
Case W. McNamara
spellingShingle Malina A. Bakowski
Case W. McNamara
Advances in Antiwolbachial Drug Discovery for Treatment of Parasitic Filarial Worm Infections
Tropical Medicine and Infectious Disease
<i>Wolbachia</i>
filaria
parasitic worms
<i>Onchocerca</i>
<i>Brugia</i>
drug discovery
antiwolbachial
endosymbiont
neglected tropical disease
high-throughput screening
author_facet Malina A. Bakowski
Case W. McNamara
author_sort Malina A. Bakowski
title Advances in Antiwolbachial Drug Discovery for Treatment of Parasitic Filarial Worm Infections
title_short Advances in Antiwolbachial Drug Discovery for Treatment of Parasitic Filarial Worm Infections
title_full Advances in Antiwolbachial Drug Discovery for Treatment of Parasitic Filarial Worm Infections
title_fullStr Advances in Antiwolbachial Drug Discovery for Treatment of Parasitic Filarial Worm Infections
title_full_unstemmed Advances in Antiwolbachial Drug Discovery for Treatment of Parasitic Filarial Worm Infections
title_sort advances in antiwolbachial drug discovery for treatment of parasitic filarial worm infections
publisher MDPI AG
series Tropical Medicine and Infectious Disease
issn 2414-6366
publishDate 2019-07-01
description The intracellular bacteria now known as <i>Wolbachia</i> were first described in filarial worms in the 1970s, but the idea of <i>Wolbachia</i> being used as a macrofilaricidal target did not gain wide attention until the early 2000s, with research in filariae suggesting the requirement of worms for the endosymbiont. This new-found interest prompted the eventual organization of the Anti-<i>Wolbachia</i> Consortium (A-WOL) at the Liverpool School of Tropical Medicine, who, among others have been active in the field of antiwolbachial drug discovery to treat filarial infections. Clinical proof of concept studies using doxycycline demonstrated the utility of the antiwolbachial therapy, but efficacious treatments were of long duration and not safe for all infected. With the advance of robotics, automation, and high-speed computing, the search for superior antiwolbachials shifted away from smaller studies with a select number of antibiotics to high-throughput screening approaches, centered largely around cell-based phenotypic screens due to the rather limited knowledge about, and tools available to manipulate, this bacterium. A concomitant effort was put towards developing validation approaches and in vivo models supporting drug discovery efforts. In this review, we summarize the strategies behind and outcomes of recent large phenotypic screens published within the last 5 years, hit compound validation approaches and promising candidates with profiles superior to doxycycline, including ones positioned to advance into clinical trials for treatment of filarial worm infections.
topic <i>Wolbachia</i>
filaria
parasitic worms
<i>Onchocerca</i>
<i>Brugia</i>
drug discovery
antiwolbachial
endosymbiont
neglected tropical disease
high-throughput screening
url https://www.mdpi.com/2414-6366/4/3/108
work_keys_str_mv AT malinaabakowski advancesinantiwolbachialdrugdiscoveryfortreatmentofparasiticfilarialworminfections
AT casewmcnamara advancesinantiwolbachialdrugdiscoveryfortreatmentofparasiticfilarialworminfections
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