Weschka Dennis, Mousavi Soraya, Biesemeier Nina, Bereswill Stefan, Heimesaat Markus M
Gastrointestinal Microbiology Research Group, Institute of Microbiology, Infectious Diseases and Immunology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 12203 Berlin, Germany.
Microorganisms. 2021 May 23;9(6):1127. doi: 10.3390/microorganisms9061127.
The prevalence of infections with the zoonotic enteritis pathogen is increasing. Probiotic formulations constitute promising antibiotic-independent approaches to reduce intestinal pathogen loads and modulate pathogen-induced immune responses in the infected human host, resulting in acute campylobacteriosis and post-infectious sequelae. Here, we address potential antipathogenic and immuno-modulatory effects of the commercial product Aviguard during experimental campylobacteriosis. Secondary abiotic IL-10 mice were infected with a patient isolate on days 0 and 1, followed by oral Aviguard treatment on days 2, 3 and 4. Until day 6 post-infection, Aviguard treatment could lower the pathogen burdens within the proximal but not the distal intestinal tract. In contrast, the probiotic bacteria had sufficiently established in the intestines with lower fecal loads of obligate anaerobic species in -infected as compared to uninfected mice following Aviguard treatment. Aviguard application did not result in alleviated clinical signs, histopathological or apoptotic changes in the colon of infected IL-10 mice, whereas, however, Aviguard treatment could dampen pathogen-induced innate and adaptive immune responses in the colon, accompanied by less distinct intestinal proinflammatory cytokine secretion. In conclusion, Aviguard constitutes a promising probiotic compound to alleviate enteropathogen-induced proinflammatory immune responses during human campylobacteriosis.
人畜共患肠炎病原体感染的发生率正在上升。益生菌制剂是一种有前景的不依赖抗生素的方法,可降低肠道病原体载量并调节受感染人类宿主中病原体诱导的免疫反应,从而导致急性弯曲菌病和感染后后遗症。在此,我们探讨了商业产品Aviguard在实验性弯曲菌病期间的潜在抗病原体和免疫调节作用。在第0天和第1天,将二级无生物活性的IL-10小鼠用一株患者分离株感染,随后在第2、3和4天进行口服Aviguard治疗。直到感染后第6天,Aviguard治疗可降低近端肠道而非远端肠道内的病原体负担。相比之下,与未感染的小鼠相比,在Aviguard治疗后,益生菌在肠道中已充分定植,感染小鼠中 obligate anaerobic species的粪便载量较低。Aviguard的应用并未减轻感染的IL-10小鼠结肠的临床症状、组织病理学或凋亡变化,然而,Aviguard治疗可抑制结肠中病原体诱导的先天性和适应性免疫反应,同时肠道促炎细胞因子分泌不那么明显。总之,Aviguard是一种有前景的益生菌化合物,可减轻人类弯曲菌病期间肠道病原体诱导的促炎免疫反应。