key: cord-0018841-n1hg0oze
authors: Wang, Baikui; Ye, Xiaolin; Zhou, Yuanhao; Zhao, Pengwei; Mao, Yulong
title: Glycyrrhizin Attenuates Salmonella Typhimurium-Induced Tissue Injury, Inflammatory Response, and Intestinal Dysbiosis in C57BL/6 Mice
date: 2021-06-22
journal: Front Vet Sci
DOI: 10.3389/fvets.2021.648698
sha: a2feb88fe1fdbc90cda16ed6dd129f5fe9162934
doc_id: 18841
cord_uid: n1hg0oze

Salmonellae are one of the most important foodborne pathogens, which threaten the health of humans and animals severely. Glycyrrhizin (GL) has been proven to exhibit anti-inflammatory and tissue-protective properties. Here, we investigated the effects of GL on tissue injury, inflammatory response, and intestinal dysbiosis in Salmonella Typhimurium-infected mice. Results showed that GL or gentamicin (GM) significantly (P < 0.05) alleviated ST-induced splenomegaly indicated by the decreased spleen index, injury of liver and jejunum indicated by the decreased hepatocytic apoptosis, and the increased jejunal villous height. GL significantly (P < 0.05) increased secretion of inflammatory cytokines (IFN-γ, IL-12p70, IL-6, and IL-10) in spleen and IL-12p40 mRNA expression in liver. Meanwhile, GL or GM pre-infection treatments significantly (P < 0.05) decreased ST-induced pro-inflammatory cytokine (IFN-γ, TNF-α, and IL-6) expression in both spleen and liver and increased (P < 0.05) anti-inflammatory cytokine IL-10 secretion in spleen. Furthermore, GL or GM pre-infection treatment also regulates the diversities and compositions of intestinal microbiota and decreased the negative connection among the intestinal microbes in ST-infected mice. The above findings indicate that GL alleviates ST-induced splenomegaly, hepatocytic apoptosis, injury of jejunum and liver, inflammatory response of liver and spleen, and intestinal dysbacteriosis in mice.

Salmonellae are facultative intracellular bacterial pathogens, which can invade and survive inside many cell types, such as epithelial cells, macrophages, microfold (M) cells, and dendritic cells (1, 2) . As one of the most common foodborne pathogens, Salmonellae had strong pathogenicity, which colonizes, adheres to, and damages the intestinal epithelium by producing enterotoxins and then invade organs (such as liver, spleen, and kidney) by secreting invasive protein to induce organic swellings and inflammation (3, 4) . Salmonellae-induced Salmonellosis poses a great threat to the health of food animals and humans. It is reported that Salmonellae-contaminated food-induced Salmonellosis is one of the major causes of diarrhea of humans globally (5) , and the total economic loss caused by Salmonellosis is estimated to be over $3.5 billion per year in the US (6) . Salmonellae infection not only causes enteric diseases that compromise growth performance and overall health of animals and thereby lead to serious economic loss for food animal industry but also leads to serious Salmonellae-contaminated raw food animal products (meat and eggs) (6, 7) . Salmonellae-contaminated poultry products (raw meat and eggs) are considered as the leading food sources for human Salmonellosis (8) . Traditionally, in-feed antibiotics is the main strategy to prevent or control Salmonellae-induced enteric diseases in animal production (9) . As growth promoters, antibiotics have been widely used in livestock production since the 1940's to improve growth performance and overall health of animals (10) . However, with the increasing concerns about antimicrobial resistance (AMR) and foodborne antibiotic residues, many countries, including China, have banned the use of antibiotics in animal husbandry production (11) (12) (13) . With the strict ban of the in-feed antibiotic growth promoters (AGPs), gastrointestinal infectious diseases of food animals and zoonotic pathogen contamination in animal products severely threaten the health of animals and humans (11, 14) . Therefore, it is a priority to explore the proper alternatives to AGP under the post-AGP era (13) . In recent years, many studies have been reported that some natural agents, such as natural plant extracts, probiotics, and prebiotics, are beneficial for improving growth performance and reducing morbidity and mortality of food animals, and are considered "Generally Recognized as Safe (GRAS)" alternatives to AGP (13, (15) (16) (17) .

Glycyrrhizin (GL), a triterpene glycoside that is extracted from licorice root, consists of one molecule 18-β-glycyrrhetinic acid and two molecules of glucuronic acid and is the most important active ingredient of licorice root (18, 19) . GL has been proven to exert a variety of pharmacological activities, such as anti-microbial, anti-inflammatory, anti-viral, anti-oxidative, anti-tumor, and hepatoprotective activities (18, (20) (21) (22) . GL can activate specific and non-specific immune responses by enhancing phagocytosis and bactericidal activities of macrophage (18) , inducing maturation of dendritic cells (DCs) and proliferation of T lymphocytes (23) , augmenting natural killer (NK) cell activity (24) , and inducing cytokine secretion (18) . GL exhibits anti-inflammatory and tissueprotective properties by binding to high-mobility group box (HMGB1) to inhibit cytokine secretion activities (25) . Many studies showed that as an alternative to antibiotics, GL had a beneficial effect in preventing or controlling multi-drugresistant pathogen infection (26, 27) . As a potential substitute for AGP, licorice extract showed beneficial effects on the growth performance of broiler (28, 29) . Our previous studies also found that GL exerts anti-Salmonella activities by inducing M1 polarization of murine bone marrow-derived macrophages (BMDMs) and maturation of murine bone marrow-derived dendritic cells (BMDCs) (18, 30) . The present study was aimed to further investigate whether GL as a potential AGP substitute has protective effects against ST-induced tissue injury, inflammatory response, and intestinal dysbiosis in C57BL/6 mice.

GL was purchased from Sigma-Aldrich (purity ≥95.0%, St. Louis, MO, USA). Gentamicin (GM) was purchased from Sigma-Aldrich (St. Louis, MO, USA). ELISA kits for IFN-γ, IL-12p70, TNF-α, IL-6, and IL-10 were obtained from eBioscience (San Diego, CA, USA). Caspase-1 activity assay kit was purchased from Beyotime Institute of Biotechnology (Shanghai, China).

ST CMCC 50115 was generously provided by Dr. Weihuan Fang (Institute of Preventive Veterinary Medicine, Zhejiang University). ST was cultured at 37 • C in Luria-Bertani broth overnight under aerobic conditions. The ST pellet was harvested by centrifugation at 4000 ×g for 15 min at 16 • C and then washed three times with sterile phosphate-buffered saline (pH 7.2). Finally, the optical density method (SpectraMax M5, MD, USA) and spreading plate method were conducted to adjust the final ST.

Male C57BL/6 mice (6 weeks old, Slac Animal Inc., Shanghai, China) were raised in the Experimental Animal Center of Zhejiang University under light-controlled (12-h light/dark cycle) and temperature-controlled (22 ± 1 • C) conditions and had free access to water and food. Fifty male C57BL/6 mice were randomly divided into five groups (n = 10/group): Control group, glycyrrhizin-treated group (GL), ST-infected group (ST), glycyrrhizin protective group (GL + ST), and gentamicin protective group (GM + ST, as a positive protective group). Mice in the Control and ST groups were drinking sterile water. The mice in the GL, GL + ST, and GM + ST groups were drinking sterile water containing 0.4 mg/ml GL (80 mg/kg weight) or 0.4 mg/ml GM (80 mg/kg weight) every day, respectively (30) . All mice were fed a basal diet and weighted every 3 days. After 3 weeks, mice were orally infected with 200 µl of Salmonella Typhimurium (2 × 10 9 CFU/ml) (31) . Mice were euthanized at day 3 post-infection. Spleen was weighted, and liver, jejunum, and cecum were collected for further analysis. Spleen index (n = 10/group) was calculated according to the formula: Spleen index = spleen weight (mg)/body weight (g).

For photonic microscope observations, the liver and jejunal samples (n = 5/group) of mice were fixed in 4% paraformaldehyde, embedded in paraffin, sliced, dehydrated with gradient concentrations of alcohol, and then stained with hematoxylin and eosin (H&E). Images were captured, and the villus height was measured by an Olympus microsystem (Tokyo, Japan). The TUNEL assay was determined by using TUNEL Assay Kit (Abcam, Cambridge, United States) according to the manufacturer's instructions. Briefly, the paraffin-embedded liver sections were deparaffinized with xylene, hydrated with gradient concentrations of alcohol, and covered with proteinase K. Slides were incubated with terminal deoxynucleotidyl transferase 

The spleen and liver samples (n = 5/group) were homogenized with ice-cold sterile saline solution (1:9, w/v) and centrifuged at 4000 ×g for 20 min at 4 • C. Then, the collected supernatant was used for ELISA and caspase-1 activity analyses. Levels of interferon-γ (IFN-γ), interleukin-12 subunit p70 (IL-12p70), tumor necrosis factor-α (TNF-α), IL-6, and IL-10 in the spleen homogenates were colorimetrically determined by enzyme-linked immunosorbent assay (ELISA) kits (eBioscience, San Diego, CA) according to the manufacturer's instructions. Caspase-1 activity in liver homogenates were determined by caspase-1 activity assay kit according to the manufacturer's instructions.

Total RNA (n = 5/group) was extracted from spleen tissue using RNAiso Plus kit (TAKARA, Dalian, China). Reverse transcription was performed using the PrimeScript II 1st Strand cDNA Synthesis Kit (TAKARA) according to the manufacturer's recommendation. RT-qPCR was conducted using SYBR PremixEx TaqII (TAKARA) by the StepOne real-time PCR system (Applied Biosystems). All primer sequences for target genes (including TNF-α, IL-12p40, IL-6, IFN-γ, and IL-10) are listed in Table 1 . Fold changes were calculated after normalizing to the housekeeping gene β-actin using the 2 − Ct method.

The cecal bacterial genomic DNA (n = 4/group) was extracted using the TIANamp Stool DNA Kit (Tiangen, Beijing, China) according to the manufacturer's instructions, and the quality of extracted DNA was checked by agarose gel electrophoresis and spectrophotometric analysis. The V3-V4 region of the 16S rRNA gene was amplified using the primer pair 341F/805R, and sequencing was performed on MiSeq platform (Illumina Inc., San Diego, CA, USA). Sequences were filtered and clustered into operational taxonomic unit (OTU) at 97% similarity by QIIME software (version 1.9.1). Bacterial OTU representative sequences were assigned to a taxonomic lineage by Ribosomal Database Project (RDP) classifier based on the SILVA database (SILVA 132 release). Alpha diversity (observed OTUs and PD_whole_tree) and beta diversity were analyzed based on a subsample of a minimum number of sequences (12,722) by QIIME software. Beta diversity was displayed by principal coordinates analysis (PCoA) using R software (https://www.r-project.org/). Analysis of similarities (ANOSIM), permutational multivariate analysis of variance (PERMANOVA), and multi response permutation procedure (MRPP) were calculated using "vegan" package of R software to determine significant differences in bacterial beta diversity among the five groups (based on the Bray-Curtis distance matrices) (32).

Pearson correlation between phenotypic variables and the relative abundance of microbial communities (phylum level) were analyzed and visualized by the package "corrplot" of R software. The co-occurrence networks of microbial communities in different treatments were built based on significant correlations (Spearman's R > 0.6 and FDR-adjusted P < 0.05) (33) and were visualized by Gephi TM software (https:// gephi.org/). The topological properties of the co-occurrence network were also calculated to describe the complex patterns of the interrelationships by Gephi software. Comparison of the intestinal bacteria among different treatments was analyzed and visualized by statistical analysis of taxonomic and functional profiles (STAMP) with a 95% confidence interval. The rest of the data were evaluated by ANOVA, and the contrast of means was performed by Tukey's multiple range test, using SPSS TM software (SPSS Inc., Chicago, IL, USA), and the graphs were generated using Origin 8.5 TM (OriginLab, Berkeley, CA, USA). The statistical significance was set at P < 0.05.

H&E staining showed that compared with the Control group, GL treatment had little effect on villous height (P > 0.05) and jejunal structure, which exhibited integrated structure, ordered jejunal villi, and completed gland (Figure 1) . However, compared with the Control group, ST infection significantly (P < 0.05) decreased the villous height of jejunum. Compared with the ST group, GL or GM significantly (P < 0.05) prevented jejunum injury indicated by the higher villous height (Figure 1) . 

As shown in Figure 2 , compared with the Control group, the spleen index of mice was significantly (P < 0.05) increased in the ST-infected group by 50.18%. GL or GM pretreatments significantly (P <0.05) attenuated ST-induced splenomegaly by 15.16 or 26.35%, while there was no significant difference between the two pretreated groups (P > 0.05).

Compared with the Control group, GL treatment did not cause hepatocytic apoptosis exhibiting completed structure, hepatic lobule, and intact cell and unincreased apoptosis index (P > 0.05) (Figures 3A,B) . However, ST infection caused hepatocytes with fragmented and pyknotic nuclei ( Figure 3A , H&E, black arrows indicted) and hepatocytic apoptosis ( Figure 3A , TUNEL, cells labeled as brown) and significantly (P < 0.05) increased apoptosis index (Figure 3B) , which could be significantly (P < 0.05) alleviated by GL or GM pretreatments (Figures 3A,B) . Compared with the Control group, GL treatment had no effect on caspase-1 activity (P > 0.05), while ST infection significantly (P < 0.05) increased the activity of caspase-1, which could be significantly (P < 0.05) reversed by GL or GM pretreatments ( Figure 3C) . 

As shown in Figure 4 , compared with the Control group, GL treatment significantly (P < 0.05) increased the secretions of IFN-γ, IL-12p70, IL-6, and IL-10 in spleen, whereas, it had no (P > 0.05) effect on the protein level of TNF-α. ST infection significantly (P < 0.05) increased the secretion of proinflammatory cytokines (IFN-γ, IL-12p70, TNF-α, and IL-6) and anti-inflammatory cytokine (IL-10) in spleen. As expected, GL or GM pretreatments effectively (P < 0.05) decreased the increased pro-inflammatory cytokines (IFN-γ, TNF-α, and IL-6) induced by ST infection, whereas, they increased anti-inflammatory cytokine IL-10 secretion (P < 0.05).

Furthermore, the mRNA expression of cytokines in liver showed that compared with the Control group, GL treatment significantly (P < 0.05) upregulated the IL-12p40 mRNA expression, whereas, it had no significant (P > 0.05) effect on the expression of IFN-γ, TNF-α, IL-6, and IL-10 ( Figure 5) . ST infection significantly (P < 0.05) increased the mRNA expression of pro-inflammatory cytokines (IFN-γ, IL-12p40, TNF-α, and IL-6) and anti-inflammatory cytokine (IL-10). Similarly, GL or GM pretreatments also significantly (P < 0.05) decreased the mRNA expression of IFN-γ, TNF-α, and IL-6 ( Figure 5 ).

Alpha diversity analysis showed that compared with the Control group, GL treatment significantly (P < 0.05) increased the alpha diversities (including observed OTUs, PD_whole_tree index, Chao1, and Ace) of the intestinal microbiota, while ST infection had no (P > 0.05) effect on the alpha diversities (Figure 6) . Additionally, the alpha diversity indices of the microbial communities in the GL + ST and GM + ST treatment were significantly (P < 0.05) lower than those of the ST group. PCoA of microbial communities based on Bray-Curtis distance suggested variation of the bacterial community structure with treatments (Figure 7 ). Significant differences in beta diversity among treatments were further confirmed by ANOSIM, PERMANOVA, and MRPP analysis ( Table 2) , except for that between the Control and GL treatments.

The differences of the intestinal bacterial compositions among groups were also analyzed (Figure 8) . The results showed that GL treatment significantly (P < 0.05) increased the relative abundance of Oscillibacter, Millionella, and Bilophila, whereas, it decreased (P < 0.05) the relative abundance of Verrucomicrobiales, Family XIII AD3011 group, Ruminiclostridium 9, and Lachnospiraceae UCG-001. ST infection significantly (P < 0.05) increased the relative abundance of Alphaproteobacteria, Verrucomicrobiales, To determine the co-occurrence patterns of microbes in the different groups, five networks were constructed based on the genus and species levels (Figure 9 and Table 3 ). Network analysis showed that the values of average degree and graph density in the ST group were higher than those of the other groups Pearson's correlation coefficient was calculated to reveal correlations between the phenotypic variables and the relative abundance of microbial communities (phylum level) (Figure 10) . Correlation analysis showed that the relative abundances of Verrucomicrobia, Cyanobacteria, Tenericutes, and Actinobacteria were negatively correlated with the final body weight (P < 0.05 or P < 0.01). The relative abundances of Verrucomicrobia and Cyanobacteria were positively correlated with the spleen index, caspase-1 activity, and apoptosis index (P < 0.05 or P < 0.01), while the relative abundance of Tenericutes was positively correlated with caspase-1 activity (P < 0.01) and apoptosis index (P < 0.05).

Salmonellosis, caused by food-borne Salmonella, is largely associated with tissue injury and intestinal dysbiosis, which accounts for approximately 109.9 million cases and 264,300 deaths globally per year (34) . With the strict prohibition of AGP, there is an increasing interest in exploring dietary natural extract products to reduce or prevent against zoonotic enteric pathogen infection and food-borne contamination in industrial livestock production. Previous studies found that FIGURE 10 | Pearson's correlation analysis between phenotypic variables and the relative abundance of microbial communities (phylum level, n = 4/group). The color and dot size represent the correlation coefficient within rows. *P < 0.05; **P < 0.01.

GL, an extract from licorice root, could ameliorate HFDmediated intestinal dysbiosis (20) and Streptococcus aureusinduced acute lung injury (25) in murine models. Our previous study found that GL could effectively ameliorate the body weight loss of mice infected with S. Typhimurium infection (30) , which may be related to the beneficial effects of GL in reducing the inflammation and tissue damage associated with S. Typhimurium infection. Salmonella Typhimurium may migrate to the liver and spleen via the blood circulatory system due to the damage of the intestinal barrier to cause the hepatosplenomegaly, which is characterized by cell apoptosis and inflammatory infiltration (35, 36) . In the present study, we found that GL pretreatment significantly prevented S. Typhimuriuminduced jejunal injury indicated by the higher villous height and splenomegaly indicated by the decreased the spleen index of mice. Additionally, liver injury induced by S. Typhimurium infection was also relieved by GL or GM pretreatments as evidenced by the decreased hepatocytic apoptosis and the reduced caspase-1 enzyme activity. GL pretreatment significantly inhibited S. Typhimurium colonization in ileum and colon and translocation to spleen and liver (30) . In addition, GL enhanced the phagocytosis and bactericidal capacity of BMDM by inducing the JNK/NF-??B signaling pathway-mediated polarization of M1 macrophages that participate in polarized Th1 responses and act as the primary line of defense against intracellular pathogens (18, 37) . These results indicate that the attenuated injury of tissues in the GL + ST group may be related to the inhibition of colonization and invasion of S. Typhimurium (30), polarization of M1 macrophages (18) , improved inflammation response, and intestinal dysbacteriosis.

Inflammatory responses induced by pathogenic infection is one of the most common symptoms of splenomegaly and hepatomegaly (38) . The expression of pro-inflammatory cytokines (such as IFN-γ, IL-6, IL-12, and TNF-α) is necessary for the initiation of the innate immune response for pathogen clearance (39) . However, excessive pro-inflammatory responses could be extremely harmful to the host (40) . Thus, excessive pro-inflammatory responses are tightly balanced by antiinflammatory cytokines (such as IL-10 and TGF-β) and associated negative feedback loops (41) . The ameliorated tissue injury of S. Typhimurium-infected mice in GL-or GMpretreated group mentioned above may be due to the attenuated inflammatory response. Indeed, compared with the uninfected group, S. Typhimurium infection significantly induced inflammatory responses as evidenced by the upregulation of pro-inflammatory cytokines (IFN-γ, IL-6, IL-12, and TNF-α) and anti-inflammatory cytokine IL-10 in spleen and liver of mice. Interestingly, GL pretreatment effectively decreased the upregulation of pro-inflammatory cytokines (IFN-γ, TNF-α, and IL-6) induced by ST infection in spleen and liver, and increased secretion of anti-inflammatory cytokine IL-10 in spleen. The results indicate that GL effectively alleviates S. Typhimurium-induced inflammatory response by exerting an anti-inflammatory activity.

Intestinal microbes play an important role in maintaining gastrointestinal homeostasis. The intestinal beneficial and commensal microbiota protect host against Salmonella colonization via competition of adhesion site and nutrition and secretion of metabolite (SCFAs, indole, and bacteriocin) (42, 43) . It is reported that S. Typhimurium infection is tightly accompanied by intestinal dysbiosis (44, 45) . Salmonella outcompetes the resident microbes by inducing the host intestinal immune system to secrete reactive oxygen species (ROS) and antimicrobial peptides that are non-specific harmful to the beneficial and commensal microbes (43) . In this study, we observed that Salmonella infection led to dysbiosis by altering microbial beta diversity and composition. Salmonella Typhimurium infection significantly increased the abundances of Alphaproteobacteria, Verrucomicrobiales, DTU014, Prevotellaceae NK3B31 group, and Ruminococcaceae UCG-013, whereas, it decreased the abundances of Desulfovibrionaceae, Rikenellaceae, ASF356, Rikenella, Ruminococcaceae UCG-009, Lachnospiraceae UCG-010, Alistipes, Odoribacter, and Muribaculum. Knowledge about the altered bacteria caused by S. Typhimurium infection remains unclear and needs further investigation. Oral administration of GL significantly increased microbial alpha diversity and altered microbial composition. GL significantly increased the relative abundances of Oscillibacter, Millionella, and Bilophila, whereas, it decreased the relative abundances of Verrucomicrobiales, Family XIII AD3011 group, Ruminiclostridium 9, and Lachnospiraceae UCG-001.

Oscillibacter was proposed to exert an anti-inflammatory effect (46) . Administration of probiotics increased cecal Millionella abundance of mice (47) . Bilophila, a sulfate-reducing bacterium, is associated with animal-based and fat-enriched diets (48) . The intestinal dysbiosis caused by Salmonella infection can be reshaped by dietary or antibiotic interventions (31, 49) . In the present study, GL or GM pretreatments significantly reshaped the intestinal microbes by reducing microbial alpha diversity, modulating beta diversity, and microbial compositions.

The results indicate that the altered microbial diversities and compositions induced by GL pretreatment may be related to the attenuated injury of tissues and pro-inflammatory responses induced by S. Typhimurium infection, although, more direct evidences are needed.

Co-occurrence pattern analysis was performed to investigate the microbial interactions, and we found that the values of average degree and graph density of microbial network in the S. Typhimurium infected group were higher than those of the other groups (Control, GL, GL + ST, and GM + ST), suggesting that S. Typhimurium infection increased the connection among the microbes. All the modularity values of the co-occurrence networks were higher than 0.4, suggesting that these networks had a modular structure (50) . The microbial network in the S. Typhimurium-infected group was not easier to form a "small world" as evidenced by lower modularity value than those of the other groups (33) . Additionally, negative correlation of the microbial networks in the other groups was less than that of the S. Typhimurium-infected group, which could be interpreted as a reduction in competitive relationships within intestinal microbes (51) . Finally, the correlations between phenotypic variables and microbial communities (alpha diversity and phylum level) were further investigated. The final body weight was obtained from our previous study (30) and reanalyzed with the relative abundance of bacterial phyla. Pearson's correlation analysis showed that the final body weight of mice was negatively correlated with cecal Verrucomicrobia, Cyanobacteria, Tenericutes, and Actinobacteria. Verrucomicrobia and Cyanobacteria were positively correlated with the spleen index, caspase-1 activity, and apoptosis index. Tenericutes was positively correlated with caspase-1 activity and apoptosis index. The above results indicate that the relieved negative effect caused by S. Typhimurium infection may be related to the altered microbial diversities and compositions induced by GL pretreatment.

Collectively, the present study demonstrates that GL exerts the anti-inflammatory and tissue-protective properties to attenuate ST infection, as indicated by alleviating ST-induced splenomegaly, hepatocytic apoptosis, injury of jejunum and liver, and inflammatory response of liver and spleen in mice. Moreover, we found that GL modulates ST-induced intestinal dysbacteriosis. These findings might give a new perspective into the function of GL in regulating the host immune and intestinal microbiota to defense against pathogen infection. However, further studies about the role of the intestinal microbiota in the progress of GL-mediated anti-Salmonella infection are needed.

According to the manufacturer's instructions (eBioscience, San Diego, CA), the detailed information about the used ELISA kits is IFN-γ (Assay range: 15.6-1,000 pg/ml; Analytical sensitivity: 1.7 pg/ml; Intra-and Inter-assay CV: <6.8 and <7.4%), IL-12p70 (Assay range: 15.6-1,000 pg/ml; Analytical sensitivity: 10.0 pg/ml; Intra-and Inter-assay CV: 8.3 and 11.0%), TNF-α (Assay range: 31.3-2000 pg/ml; Analytical sensitivity: 3.7 pg/ml; Intra-and Inter-assay CV: 6.5 and 5.7%), IL-6 (Assay range: 31.3-2,000 pg/ml; Analytical sensitivity: 6.5 pg/ml; Intra-and Inter-assay CV: 5 and 8.9%), and IL-10 (Assay range: 39.1-2,500 pg/ml; Analytical sensitivity: 5.28 pg/ml; Intra-and Inter-assay CV: 6.7 and 10.1%).

Raw sequences have been deposited in the Genome Sequence Archive (GSA) of the BIG Data Center (https://bigd.big.ac.cn/gsa/) under accession number PRJCA004208/CRA003756.

All animal experiments were conducted according to the guidelines and approval of the Institutional Animal Care and Use Committee of Zhejiang University (Permission number: ZJU20160416).

YM: conceptualization, supervision, and project administration. BW, XY, and PZ: writing-original draft preparation and writing-review and editing. BW, YZ, and PZ: investigation, methodology, and visualization. All authors have read and agreed to the published version of the manuscript. 

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The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.Copyright © 2021 Wang, Ye, Zhou, Zhao and Mao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.