Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection
Michelle Nelson1, Neil Burton2, Alejandro Nunez3
1CBR Division, Defence Science and Technology Laboratory (Dstl), Porton Down, Salisbury, Wiltshire, United Kingdom.
Abstract:
Burkholderia pseudomallei is the causative agent of melioidosis and presents with diverse clinical manifestations. Naturally occurring infection occurs following contamination of cuts or skin abrasions, or ingestion of contaminated water, and occasionally through inhalational of infected soil or water particles. The influence of the route of disease acquisition on the efficacy of medical countermeasures has not been explored in humans or in appropriate animal models. The efficacy of co-trimoxazole against melioidosis acquired by different routes of exposure was assessed in postexposure prophylaxis (PEP) and treatment studies in marmoset models of melioidosis. Following challenge with B. pseudomallei by the inhalational, subcutaneous, or ingestion routes of administration, animals were given co-trimoxazole at 12 hourly intervals for 14 days, starting either 6 h postchallenge or at the onset of fever. Animals were then observed for 28 days. All animals that received antibiotic 6 h postchallenge survived the duration of dosing. All animals that received antibiotics at the onset of fever completed the treatment, but 10%, 57%, and 60% of those with ingestion, subcutaneous, and inhalation challenge relapsed, respectively. Bacteriological and histological differences were observed between placebo-control animals and those that relapsed. Immunological profiles indicate difference between animals given placebo and those that relapsed or survived the duration of the study. A broad T-cell activation was observed in animals that survived. Overall, these data suggest the efficacy of co-trimoxazole, as measured in the incidence of relapse, differs depending on the disease-acquisition route. Therefore, there are implications in treating this disease in regions of endemicity.
Insights
The antibiotic co-trimoxazole
Area of Science:
- Infectious Diseases
- Microbiology
- Pharmacology
Background:
- Melioidosis, caused by Burkholderia pseudomallei, exhibits varied clinical presentations.
- Infection routes include skin/abrasion contamination, water ingestion, and inhalation.
- The impact of acquisition route on medical countermeasure efficacy remains understudied.
Purpose of the Study:
- To evaluate co-trimoxazole efficacy against melioidosis based on the route of B. pseudomallei infection.
- To assess postexposure prophylaxis (PEP) and treatment effectiveness in a marmoset model.
Main Methods:
- Marmosets were challenged with B. pseudomallei via inhalation, subcutaneous, or ingestion routes.
- Co-trimoxazole was administered 6 hours post-challenge or at fever onset for 14 days.
- Animals were monitored for 28 days, with relapse, bacteriological, histological, and immunological assessments.
Main Results:
- All animals receiving early co-trimoxazole (6h post-challenge) survived.
- Relapse rates after treatment at fever onset varied: 10% (ingestion), 57% (subcutaneous), and 60% (inhalation).
- Distinct immunological profiles, including T-cell activation, were observed in survivors versus relapsed animals.
Conclusions:
- Co-trimoxazole's efficacy in preventing melioidosis relapse is significantly influenced by the route of disease acquisition.
- Treatment strategies for melioidosis may need to be tailored based on infection route, especially in endemic areas.


