Abstract

Acrylamide (AA) has been extensively examined for its potential toxicological effects on humans and animals, but its impacts on gut microbiota and effects on hosts’ susceptibility to enteric infection remain elusive. The present study was designed to evaluate the effect of AA on gut microbiota of mice and susceptibility of mice to S. Typhimurium infection. After four weeks’ intervention, mice fed with AA exhibited significantly decreased body weight. Meanwhile, 16S rRNA gene sequencing showed reduced relative abundance of Firmicutes and increased abundance of Bacteroidetes in AA-treated mice prior to infection. In addition, we observed high relative abundance of Burkholderiales and Erysipelotrichales, more specifically the genus Sutterella and Allobaculum, respectively, in AA-treated mice before infection. Subsequently, the mice were orally infected with S. Typhimurium. The histological changes, systemic dissemination of S. Typhimurium, and inflammatory responses were examined. Compared to mice fed with normal diet, mice fed AA exhibited higher level of bacterial counts in liver, spleen, and ileum, which was consistent with exacerbated tissue damage determined by histological analyses. In addition, higher expression of pro-inflammaroty cytokines, p-IκBα, and p-P65 and lower mRNA expressions of mucin2, occludin, zo-1, claudin-1, and E-cadherin were detected in AA-treated mice. These findings provide novel insights into the potential health impact of AA consumption and the detailed mechanism for its effect on S. Typhimurium infection merit further exploration.

Highlights

  • The mature, complex gut microbiota inhabiting the mammalian intestinal tract has an important role on the host immune system and defense functions during infection [1]

  • The Effect of AA on the Diversity and Composition of Gut Microbiota 3.2.TThheecEomffepctosoiftiAoAn aonndthaebDunivdearnsicteyoafngduCtommipcroosibtiioontaooffGmuitcMe wicarsobainotaalyzed and compared by 16S TrRhNe AcoammppolisciotinonseaqnudenacbinugnadnaanlyceseosfinguNtCmaincdroAbiAotgarouf pms.icAe twotaasl oanf 9a6ly2zoepderaantdioncoalmtaxpoanreodmbicyu1n6itSsrwReNreAidaemnptilficeodninse1q3ufecnaclinsagmapnlaelsy(sFeisguinreN2CA)a.nSdeqAueAncgirnoguapnsa. lAystisotoaflfoecfa9l62 saomppelreastifornomal tAaxAongoromuipc umniictes pwreordeuicdeedntainfieadveinra1g3e foefca2l55sa.3m33p±les11(F.8i8g5uroebs2eArv).eSdesqpueecniceisng coamnpalayrseids otof fNecCalgsraomuple(3s7f5r.o5m00A±A6g.9r8o5u)p(Tmaibclee pSr2o)d. uTcheed caonmamveurnagitey orfic2h5n5e.3ss33(C±h1a1o.8185 observed species compared to normal control (NC) group (375.500 ± 6.985) (Table S2)

  • The β-diversity analysis based on the principal coordinate analysis (PCoA) of the weighted UniFrac distance showed significant difference between NC and AA group (Figure 2F)

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Summary

Introduction

The mature, complex gut microbiota inhabiting the mammalian intestinal tract has an important role on the host immune system and defense functions during infection [1]. These gut microbiota has a large impact on the prevention of pathogen infection by direct and indirect mechanisms [2]. Typhimurium can cause systemic infection in mice and foodborne gastroenteritis in humans [7] It has been widely used in a laboratory model to understand the biological mechanisms involved in multiple intracellular behaviors including invasion, proliferation, dissemination, and transmission to host cell and resultant host immune responses [8]. The pathogenic potential of the pathogen, such as invasion and colonization, are likely to be influenced by many environmental factors including endogenous and exogenous physic-chemical signals in gastrointestinal phase

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