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Salicylanilides - New Weapon for Clostridium Difficile Infections

by Madhumathi Palaniappan on September 16, 2016 at 5:20 PM
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Highlights:

A research team from the Scripps Research Institute (SRI) have discovered that several class of existing anthelmintic drugs (deworming drugs) called salicylanilides to be effective against Clostridium difficile bacteria. Clostridium difficile infections are found to be a major cause for most of the intestinal infections in United States.


The study found that several strains including epidemic and hypervirulent strains of Clostridium difficile bacterium which recurs after treatment were also killed using salicylanilides.

‘Salicylanilide drugs are now found to combat Clostridium difficile infections.’

The research study focusing on C.difficile infections was published online in the Scientific Reports.

Research Study on Salicylanilides

Salicylanilides are chemical amide compounds of salicylic acid and anilines. Drugs like niclosamide, oxyclozanide, rafoxanide are some of the salicylanilides which are effective anthelminitics.

Kim D. Janda, the Ely R. Callaway, Jr. Professor of Chemistry, Director of the Worm Institute for Research & Medicine (WIRM) , Member of The Skaggs Institute for Chemical Biology at TSRI and senior author of the study said that "These salicylanilide compounds have all the right features, and they've long been used in animals, so I think they can be quickly repurposed against C. difficile infections in people"

Closantel a veterinary drug for deworming cattle, sheep and goat was used as a control for the discovery of new compounds for C.difficle infections. After noting its effectiveness , Gooyit and Janda tested niclosamide, oxyclozanide and rafoxanide for treating C.difficle infections.

Oxyclozanide and rafoxanide are approved veterinary drugs for deworming animals. Niclosamide is used for the treatment of tapeworm infections in humans.

Gooyit said "We found that these salicylanilides inhibited the growth of a broad selection of strains, including the BI/NAP1/027 strain, with similar and sometimes greater in vitro activity than metronidazole's and vancomycin's"

The findings of the study reported that closantel and rafoxanide were effective in killing the stationary phase cells of C. difficile infections. These cells are important toxins which damage gut wall and stimulates inflammation in C.difficile infections. Stationary phase cells are hard seed-like spores which tend to stay on the surface for long time and is responsible for high transmission rates of infections in the hospitals.

Favorable Properties of Salicylanilides

Mechanism Behind Salicylanilide Effectiveness

Previous studies suggest that salicylanilides are found to act by altering the electrical properties of the cell membrane which disrupts the existence of C.difficile bacterium.

New salicylanilide compounds were designed by improving membrane targeting effects for killing C.difficile infections.

Clostridium difficile Infections

Clostridium difficile infections are bacterial infections which lead to diarrhea and colitis infections (inflammation of colon). According to an analysis in 2011 from the Center for Disease Control and Prevention(CDC), it was estimated that 450,000 cases and 30,000 deaths were due to C.difficile infections in United States.

These infections mostly occur after treatment with antibiotics (mainly broad spectrum antibiotics which act against several types of bacteria), people with weak immune system, staying in a hospital for long time or any other conditions like inflammatory disease.

Symptoms of Clostridium difficile infections may include:

Source: Medindia

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