Abstract

Disseminated disease from non-typhoidal Salmonella enterica strains results in >20% mortality globally. Barriers to effective treatment include emerging multidrug resistance, antibiotic treatment failure, and risk factors such as malnutrition and related micronutrient deficiencies. Individuals in sub-Saharan Africa are disproportionately affected by non-typhoidal S. enterica bloodstream infections. To inform a clinical trial in people, we investigated vitamin A as a treatment in the context of antibiotic treatment failure in a mouse model of vitamin A deficiency. Vitamin A-deficient (VAD) mice exhibited higher systemic bacterial levels with a multidrug-resistant clinical isolate in comparison to mice on a control diet. Sex-specific differences in vitamin A deficiency and disseminated infection with S. enterica serotype Typhimurium (S. Typhimurium) were observed. VAD male mice had decreased weight gain compared to control male mice. Further, infected VAD male mice had significant weight loss and decreased survival during the course of infection. These differences were not apparent in female mice. In a model of disseminated S. Typhimurium infection and antibiotic treatment failure, we assessed the potential of two consecutive doses of vitamin A in alleviating infection in male and female mice on a VAD or control diet. We found that subtherapeutic antibiotic treatment synergized with vitamin A treatment in infected VAD male mice, significantly decreasing systemic bacterial levels, mitigating weight loss and improving survival. These results suggest that assessing vitamin A as a therapy during bacteremia in malnourished patients may lead to improved health outcomes in a subset of patients, especially in the context of antibiotic treatment failure.

Highlights

  • In susceptible populations globally, there is a vicious cycle of infection and malnutrition [1]

  • Vitamin A and antibiotics synergize against antibiotic resistant Salmonella

  • Typhimurium in liver, spleen and blood were significantly higher in Vitamin A-deficient (VAD) mice compared to control (Fig 1B), and there was no sex difference observed in bacterial colonization (S1A Fig)

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Summary

Introduction

There is a vicious cycle of infection and malnutrition [1]. Severe or recurrent infections can lead to vitamin A deficiency due to impaired nutrient absorption and decreased food intake, as well as direct nutrient loss through urine [3, 4]. Non-typhoidal serotypes of S. enterica cause significant morbidity and mortality worldwide, resulting in 93.8 million cases of gastroenteritis and 155,000 associated deaths annually [6]. Invasive non-typhoidal Salmonella (iNTS) infection, a severe febrile illness with bacteremia, disproportionately affects infants, older adults and immunosuppressed individuals. An estimated 3.4 million cases of invasive disease occur globally per year, resulting in 680,000 deaths [7]. Malnutrition and concurrent malaria are key risk factors for systemic disease, and populations in sub-Saharan Africa are disproportionately affected [8]. The mortality rate due to iNTS in children reaches 20–25% [10], indicating that more effective treatment is vital

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