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Biology subjects

Yousif, M.

Publications and source records attributed to Yousif, M..

2 recordsLinked to original sources

Time restricted feeding ameliorates colitis through clock-dependent and nutrition-dependent processes

Inflammatory Bowel Disease (IBD) is rising worldwide and requires the development of preventative strategies to lower its incidence. Circadian rhythms, daily cycles of physiology, have been shown to be implicated in IBD in both clinical and laboratory studies. We tested if a 12-hour Time-Restricted Feeding (TRF) dietary regimen, that improves circadian rhythms, could ameliorate colitis using a mouse model of disease. We find that TRF indeed protects mice from the damaging effects of colitis, and boosts the rhythmic expression of transcripts related to the clock, cell proliferation, and barrier function. Under TRF, mice exhibit lower disease symptoms, changes in microbiota, and reduced inflammatory tissue damage. These outcomes are not clock-dependent: colitis in Bmal1 mutants without circadian rhythms is also rescued by TRF. However, in this context alterations to the transcriptome are distinct from that found in clock-wildtype controls. Together our data support the translation of a 12-hour TRF in IBD, and highlight clock-dependent and nutrition-dependent changes accompanying colitis rescue.

physiology↗

Salmonella-vectored vaccine delivering three Clostridium perfringens antigens protects poultry against necrotic enteritis.

Necrotic enteritis is an economically important poultry disease caused by the bacterium Clostridium perfringens. There are currently no necrotic enteritis vaccines available for use in broiler birds, the most important target population. Salmonella-vectored vaccines represent a convenient and effective option for controlling this disease. We used a single attenuated Salmonella vaccine strain, engineered to lyse within the host, to deliver up to three C. perfringens antigens. Two of the antigens were toxoids, based on C. perfringens -toxin and NetB toxin. The third antigen was fructose-1,6-bisphosphate aldolase (Fba), an metabolic enzyme with an unknown role in virulence. Oral immunization with a single Salmonella vaccine strain producing either Fba, -toxoid and NetB toxoid, or all three antigens, was immunogenic, inducing serum, cellular and mucosal responses against Salmonella and the vectored C. perfringens antigens. All three vaccine strains were protective against virulent C. perfringens challenge. The strains delivering Fba only or all three antigens provided the best protection. We also demonstrate that both toxins and Fba are present on the C. perfringens cell surface. The presence of Fba on the cell surface suggests that Fba may function as an adhesin.

microbiology↗