Dietary Bacillus licheniformis improves the effect of Astragalus membranaceus extract on blood glucose by regulating antioxidation activity and intestinal microbiota in InR[E19]/TM2 Drosophila melanog

14 Sep.,2022

 

yeast hydrolysate

The obtained results showed that dietary supplementation with BL and AE, under the synergistic effect of BL and AE, not only prolonged the lifespan of InR [E19] /TM2 D. melanogaster, increased body weight, and improved the body’s antiaging enzyme activity but also effectively improved the types and quantities of beneficial bacteria in the intestinal flora of InR [E19] /TM2 D. melanogaster to improve the characteristics of diabetes symptoms. This study provides scientific evidence for a safe and effective dietary therapeutic method for diabetes mellitus.

In this study, Bacillus licheniformis (BL) and Astragalus membranaceus extract (AE) were given with food to InR [E19] /TM2 Drosophila melanogaster, and the blood glucose, antioxidation activity and intestinal microbiota were investigated. The obtained results showed that BA (BL and AE combination) supplementation markedly decreased the blood glucose concentration compared with the standard diet control group, accompanied by significantly increased enzymatic activities of catalase (CAT), decreased MDA levels and prolonged lifespan of InR [E19] /TM2 D. melanogaster. The treatments with BL, AE and BA also ameliorated intestinal microbiota equilibrium by increasing the population of Lactobacillus and significantly decreasing the abundance of Wolbachia. In addition, clearly different evolutionary clusters were found among the control, BL, AE and BA-supplemented diets, and the beneficial microbiota, Lactobacillaceae and Acetobacter, were found to be significantly increased in male flies that were fed BA. These results indicated that dietary supplementation with AE combined with BL not only decreased blood glucose but also extended the lifespan, with CAT increasing, MDA decreasing, and intestinal microbiota improving in InR [E19] /TM2 D. melanogaster.

This study aims to clarify the influence of B. licheniformis and the extracts of A. membranaceus or a combination of both on the lifespan, antioxidants, blood glucose and gut microbial community structure of InR [E19] /TM2 D. melanogaster, which may help us to evaluate the interaction between the probiotics and the extracts of A. membranaceus in insulin deficiency. This work will provide the possible antidiabetic mechanisms of B. licheniformis and the extract of A. membranaceus in InR [E19] /TM2 D. melanogaster.

Drosophila and mammals have a high degree of similarity in terms of molecular and biological characteristics [ 19 , 20 ]. In the last two decades, Drosophila melanogaster has been extensively used to elucidate the mechanisms of beneficial host-gut microbiota interactions. As a burgeoning material, D. melanogaster is frequently used for intestinal microbiota and metabolism research [ 19 – 21 ]. As a model, D. melanogaster is much easier to maintain in large quantities due to its body size and lifespan [ 22 – 24 ]. Therefore, D. melanogaster is often used to investigate immune regulation, diet, and probiotic characteristics that are related to ageing [ 22 , 23 ]. Furthermore, flies can achieve homeostasis via the insulin signalling pathway, Drosophila with InR defects (insulin receptor mutant) showed significantly lower insulin tolerance [ 21 , 22 ], and they can serve as a screening model for potential probiotic foods for diabetes management [ 25 , 26 ].

Bacillus licheniformis is a probiotic that is widely used in enteritis, diarrhoea and intestinal endotoxaemia therapy with no evident adverse reactions [ 15 ]. Previous studies have demonstrated that B. licheniformis supplementation could improve the growth parameters of animals [ 15 , 16 ]. Since 2007, the European Food Safety Authority (EFSA) has designated 12 Bacillus species, including B. licheniformis, as coming under the qualified presumption of safety status [ 17 ]. Recent studies have shown that B. licheniformis decreases postprandial hyperglycaemia, counteracting the activity of α-glucosidase and preventing the onset of diabetes [ 18 ]. However, there is no report about the effects of B. licheniformis as a supplement in anti-diabetic treatment. Can supplementation with B. licheniformis improve the extracts of A. membranaceus for diabetes treatment? If there is a complementary advantage, the obtained results may provide guidance for improving diabetes symptoms.

Astragalus membranaceus, prepared from the roots of Astragali Radix known as “Huangqi”, is used in traditional Chinese food and medicine for its beneficial immune-regulatory functions [ 3 , 4 ]. It has been reported that flavonoids and polysaccharides of Astragalus are the primary active components. In particular, the extracts of A. membranaceus are effective in alleviating clinical symptoms and related complications of diabetes [ 3 – 5 ] and should also work with other traditional Chinese medicines or chemical drugs to achieve complementary advantages, reduce toxicity and increase efficiency [ 6 ]. Yang et al. (2021) showed that A. membranaceus prolongs lifespan by regulating antioxidant ability and insulin/IGF-1 signalling and may be explored as a novel agent for slowing the ageing process [ 7 ].

The prevalence of diabetes mellitus (DM) is rapidly increasing in most parts of the world and has become a vital health problem [ 1 , 2 ]. Type 2 diabetes mellitus (T2DM) is caused by insulin resistance and the insulin production and secretion decline of β-cells. The current therapies for T2DM only control blood glucose levels; thus, patients always develop tolerance requiring higher medicine doses with more side effects [ 1 , 2 ]. Therefore, a safe and effective dietary therapeutic method for the prevention and control of T2DM is urgently needed.

Flies from days 10, 20 and 30 were rinsed in 50% bleach, followed by 70% ethanol, and then washed with sterile PBS before dissection. Samples were dissected from 20 flies in phosphate buffered saline. The intestines were collected after removing the Malpighian tubules and trachea under a stereomicroscope. Genomic DNA was extracted using a QIAGEN DNeasy® Blood and Tissue Kit (Qiagen, 69504). The genomic DNA was sent to Novogene (Beijing, China) for sequencing by Illumina MiSeq and sequence library construction. The 16S rRNA amplicon sequencing was conducted using the Illumina MiSeq (300-bp paired-end reads) platform. The extracted DNA (20–30 ng μL -1 ) was used as the template to amplify the V3-V4 region of the 16S rRNA gene in triplicate using the primer set 515F (5′-GTGCCAGCMGCCGCGGTAA-3′) and 806R (5’-GGACTACHVGGGTWTCTAAT-3′). The polymerase chain reaction (PCR) was performed in a 30-μL reaction system that contained 15 μL of 2 × PCR buffer, 1 μL of 0.2 μmol L -1 of each primer, 0.5 μL of Taq DNA enzyme, 1 μL of template DNA within, and 2 μL of ddH 2 O. The thermal cycle conditions consisted of initial denaturation at 98°C for 1 min, followed by 30 cycles of 10 s at 98°C, 30 s at 50°C, and 30 s at 72°C, then finally ending with a final extension of 5 min at 72°C. PCR amplification was performed using an ABI GeneAmp® 9700 PCR instrument. The 16S rRNA reference database and sequence clustering were aligned by VSEARCH (1.9.6) and Silva 132. Operational taxonomic unit (OTU) clustering was performed for unique sequences with 97% similarity. During the clustering process, chimeric sequences were removed to obtain the representative sequences of OTUs. Random sampling was used to calculate the Shannon and Chao1 α diversity index according to the OTU analysis. Weighted UniFrac analysis was applied to compare differences in microbial communities. Beta diversity was visualized by principal coordinate analysis (PCoA) and nonmetric multidimensional scaling (NMDS). In addition, redundancy analysis (RDA) was performed by the Hellinger method. PICRUSt (phylogenetic investigation of communities by reconstruction of unobserved states) and Kyoto Encyclopedia of Genes and Genomes (KEGG) orthologues were used to evaluate the bacterial functional genes. All data have been uploaded to the NCBI database (PRJNA838651).

The preserved Drosophila melanogaster were washed with 70% ethanol and sterile phosphate buffered saline 3 times, and then 9 times normal saline was added according to the ratio of weight (g): volume (mL) = 1:9. The tissue was ground, the homogenate was prepared in an ice water bath and centrifuged at 3000 rpm for 10 minutes, and the supernatant was collected to obtain 10% homogenate supernatant. Antioxidant activity changes in homogenate supernatant were evaluated by catalase (CAT) with a CAT assay kit (B518131, Nanjing Jiancheng Bioengineering Institute, China). Because the absorbance of hydrogen peroxide reached the maximum value at 240 nm, the CAT activity was expressed as the decomposition of H 2 O 2 as measured by the decrease in absorbance at 240 nm for 3 min. CAT activity was expressed on a protein basis, and the protein content of the enzyme extract was determined using bovine serum albumin (BSA) as a standard according to the method described by Bradford (1976) [ 27 ]. The malondialdehyde (MDA) level of the homogenate supernatant was quantified using the thiobarbituric acid (TBA) method (B518191, Nanjing Jiancheng Bioengineering Institute, China). Briefly, homogenate supernatant was reacted with a solution mixed with 5% trichloroacetic acid (TCA) and 0.5% TBA in 0.2 mol L -1 HCl. The sample was incubated in a 95°C water bath for 40 min and then cooled to room temperature. After centrifugation at 3500 rpm for 10 min, the supernatant absorbance was determined at 532 nm, and 1,1,3,3-tetramethoxypropane was used as a standard. Blood glucose levels of InR [E19] /TM2 D. melanogaster were measured according to the method described by Tennessen et al. (2014) [ 28 ].

The body weight of Drosophila melanogaster was recorded on the 10 th , 20 th and 30 th day. Each group of fruit flies was anaesthetized with CO 2 gas, and then the weight of each group of samples was measured with an ultrasensitive electronic analytical balance (Mettler Toledo AL204). The average weight of fruit flies in each group was calculated. Then, those flies were stored at -80°C for later enzyme and intestinal microbiota assays.

A total of 480 male virgin flies that emerged and did not mate within 8 h were selected and divided into 4 groups under CO 2 anaesthesia, with 6 bottles in each group and 20 in each bottle. They were put into the corresponding test tube, and the test tube mouth was sealed with a cotton plug made of sterilized absorbent cotton. At the same time, all fruit flies were cultured in a light dark cycle for 12 h under constant temperature (25°C) and relative humidity (60%). The culture medium was changed once every 5 days, and the survival number of Drosophila was observed and recorded at 8:30 every day until the last Drosophila died. Drosophila melanogaster that died accidentally due to excessive anaesthesia or other human factors was not included. According to the counting results, the lifespan of fruit flies in each group was analysed.

The final concentration of A. membranaceus extract was 2%. A. membranaceus extract: 100 g of A. membranaceus was added to 500 mL of distilled water and soaked in warm water for 3 h with constant stirring to ensure adequate soaking. Then, 500 mL of water was added, boiled at 100°C for 1 h, and filtered with double gauze for retention. Then, 1 L of water was added to the remaining residue, boiled for 1 h, filtered with double gauze for retention, combined twice to retain the liquid, and concentrated to a 10% concentration of A. membranaceus decoction (1 L).

The B. licheniformis strain was isolated with LB medium from the probiotic product Zhengchangsheng (Northeast Pharmaceutical Group Shenyang No.1 Pharmaceutical Co., Ltd, Shenyang, China), which is an innovative probiotic drug containing B. licheniformis bacteria for acute and chronic enteritis and diarrhoea therapy. It is a microbial pharmaceutics approved by the China Food and Drug Administration (Permission Number: S10950019). The bacteria were cultured at 37°C and 180 rpm for 18 h. The bacteria were added to the diets (40°C) at 1×10 8 CFU mL -1 .

InR [E19] /TM2 D. melanogaster (#9646) was purchased from Bloomington Drosophila Stock Center (Indiana University, Bloomington, IN, USA). InR [E19] /TM2 is an inducible mutation model induced by ethyl methanesulfonate exposure. In this study, male flies were selected after anaesthetization with CO 2 and emerged within 8 h without mating. The yeast-sucrose-cornmeal diet included 9 g of soybean meal, 66.825 g of corn flour, 30 g of sucrose, 0.5 g of sodium benzoate, 25 g of yeast, 6.5 g of agar, and 6.8 mL of propionic acid per litre. D. melanogaster was grown at 25°C and 65% humidity with a 12 h:12 h light-dark cycle.

The NMDS and PCoA analyses revealed that the microbial communities of the control, BL, AE and BA groups were clustered separately from each other (ANOSIM R = 0.98, p = 0.001) at day 30 ( Fig 6 ). LEfSe analysis was used to identify overrepresented OTUs and compare their relative abundances in different groups. As shown in Fig 7 , evolutionary clusters were clearly different from those in the control, BL, AE and BA-supplemented diets. Among the beneficial microbiota, Lactobacillaceae and Acetobacter were found to remarkably increase in male flies that were fed BA, and Enterobacteriaceae was enriched in the BL group; Alphaproteobacteria was relatively higher in the control diet group.

In total, 4,473,148 sequences were obtained, and 2,236,574 clean sequences were detected for subsequent analysis. The alpha diversities of gut microbiota in InR [E19] /TM2 D. melanogaster in the control, BL, AE and BA groups are shown in Fig 4 . Compared to the control, the species evenness and richness of the gut microbiota in flies were not significantly enhanced in the BL, AE and BA groups, according to Shannon, Chao1, ACE and Simpson effective counts. At day 30, BL, AE and BA markedly increased the abundance of Lactobacillus (p = 0.006; p = 0.003; p = 0.004) ( Fig 5 ). Furthermore, Wolbachia was found to be significantly reduced in the AE and BA groups at day 30 (p = 0.009; p = 0.003) ( Fig 5 ).

From the 10 th to 30 th day, the CAT enzyme activity of InR [E19] /TM2 D. melanogaster in the BA and BL groups was significantly higher than that in the control ( Fig 3A ). On day 30, the MDA content of InR [E19] /TM2 D. melanogaster in the BA group was significantly decreased compared to that in the control group ( Fig 3B ). From the 20 th to 30 th day, the blood glucose concentration of InR [E19] /TM2 D. melanogaster in the BA group was significantly decreased compared to that in the control, and that in the AE group was significantly decreased compared to that in the control at day 30 of growth in InR [E19] /TM2 D. melanogaster ( Fig 3C ).

On the 10 th and 20 th days, the body weight of InR [E19] /TM2 D. melanogaster in the AE, BL and BA groups was significantly higher than that in the control group (all p < 0.05), but on the 30 th day, the body weight of InR [E19] /TM2 D. melanogaster was significantly increased in the BA group compared to that in the control group (p < 0.05, Fig 2 ).

The lifespan of male Drosophila (InR [E19] /TM2) that were fed BL, AE, and BA showed significant differences compared to that of the control ( Fig 1 ). The Kaplan–Meier test of survival curves demonstrated increased longevity for BL (p < 0.0001), AE (p < 0.0001) and BA (p < 0.0001, S1 Table ). Compared to the control group, InR [E19] /TM2 D. melanogaster in the AE, BL and BA groups increased their mean lifespan by 32.55%, 45.31% and 34.29%, median lifespan by 56.81%, 69.10% and 44.43% and maximum lifespan by 51.19%, 74.25% and 32.86%, respectively ( S1 Table ). The longevity-promoting activities of BA and BL were higher than those of AE ( Fig 1 ).

Discussion

The study investigated the effects of BL supplied with AE as diet supplements on blood glucose in InR [E19]/TM2 D. melanogaster. The obtained results revealed that the blood glucose concentration significantly decreased in the BA groups, accompanied by an increase in the lifespan of InR[E19]/TM2 D. melanogaster on day 30. The mechanism of AE- and BL-mediated blood glucose levels and lifespan extension of InR[E19]/TM2 D. melanogaster were explored by measuring changes in antioxidant capacity and the gut microbiota.

A. membranaceus has been reported to have a variety of functions, such as enhancing immunity, resisting ageing, lowering blood glucose and preventing lipid peroxidation [29–31]. AEs have been proven to be a safe healthy food in China, and we can use AEs to prevent diabetic symptoms [3–5, 17]. Our results showed that the BA group significantly improved blood glucose parameters; the results were even better than those in the control positive group in the InR[E19]/TM2 D. melanogaster model. At day 30, the blood glucose concentration of InR[E19]/TM2 D. melanogaster in the AE group was also decreased compared with that in the control. When AE was supplied with BL, the blood glucose concentration of InR[E19]/TM2 D. melanogaster in the BA group was significantly decreased compared with that in the control group from day 20. This result shows that the positive effect of AE combined with BL improved diabetic symptoms better than BL and AE, while further investigation is needed to explore the mechanisms of AE coordinated with BL.

The effect of A. membranaceus crude extract on lifespan was assessed. As shown in Fig 1, AE can significantly prolong the lifespan of fruit flies, which is consistent with previously reported results [4, 29]. Intriguingly, the effects of the BL and BA targets were stronger than those of the AE and control targets. This result suggests that the AE in fruit flies is correlated with the prolonging lifespan capacity, and BL can also improve the capacity, which provides another evidence to explain the beneficial effects of B. licheniformis on A. membranaceus towards InR[E19]/TM2 D. melanogaster.

The underlying mechanism by which AE and BL prolong lifespan may be related to free radical scavenging. Generally, organism deterioration is caused by free radical species, while antioxidants can overcome this issue [32, 33]. The radical scavenging activity of BL and AE is always related to antioxidant enzymes: CAT detoxifies hydrogen peroxide and converts lipid hydroperoxides to nontoxic substances. The antioxidant enzyme activities were assayed to determine the antioxidant properties of BL and AE. BL treatment significantly enhanced CAT activity and decreased the MDA level, which is a product of lipid peroxidation caused by free radicals in vivo. In this study, we found a significant increase in CAT activity in BL and BA fed InR[E19]/TM2 D. melanogaster, suggesting that consuming BL or BA has the potential to clean up free radical molecules in InR[E19]/TM2 D. melanogaster [34]. MDA, the product of lipid peroxidation, causes structural and functional alterations associated with ageing organs [35]. BL treatment significantly increased the antioxidant enzyme CAT activity and decreased the MDA level. When AE was combined with BL, it improved CAT activity and further decreased MDA (Fig 3). We suggest that this may be an important reason contributing to the BL- and AE-mediated blood glucose decrease and prolongation of lifespan in Drosophila. Further studies will be conducted to evaluate potential molecular markers of lifespan-increasing properties in other animal models.

The comparison of lifespan has been accepted as an important protocol for examining the physiological effects of substances on animal models [19–21]. In this study, dietary supplementation with BL or AE was proven to prolong the lifespan of InR[E19]/TM2 D. melanogaster (S1 Table, Fig 1). As beneficial living microorganisms, probiotics always survive in the gastrointestinal tract and play important roles in balancing the intestinal flora, involving barrier defence and mucosal immunity [8, 9]. B. licheniformis has been widely used as a supplement for animal feed, human food and medical treatment [15, 36, 37]. For example, dietary supplementation with B. licheniformis improved animal performance and eased necrotic enteritis induced by Clostridium perfringens [15, 16]. Recently, B. licheniformis Dahb1 was reported to increase the growth and antioxidant activity of catfish Pangasius hypophthalmus [38]. Midhun et al. reported that the B. licheniformis strain HGA8B possessed in vitro probiotic activity [39, 40]. In addition, the B. licheniformis preparation could relieve radiation therapy-related gastrointestinal symptoms and inflammatory reactions in central nervous system tumour (CNST) patients during radiotherapy [41].

Metagenome analyses demonstrated that the intestinal microbiota was modified in type 2 diabetes (T2D), and significant differences were observed between the patient and control groups. Impaired glucose metabolism is related to changes in the bacterial community, and several attempts have been made to target the gut microbiota [10–13]. Many experiments have proven that gut microbiota diversity can be modulated [42, 43]. In this study, the results of 16S amplicon analysis implied that BL, AE and BA might affect the diversity of commensal microbes (Fig 4). Compared to the control, the species evenness and richness of the gut microbiota in flies were not significantly enhanced in the BL, AE and BA groups, according to Shannon, Chao1, ACE and Simpson effective counts. However, the distinct clusters of microbial communities among BL, AE, BA and the control demonstrated an alteration in the beta diversity of intestinal flora, and this may be the factor that affects the lifespan of InR[E19]/TM2 D. melanogaster.

The bacterial genus Lactobacillus is a vital bacterium in the intestinal flora of Drosophila that promotes the growth and development of Drosophila [44, 45]. Lactobacillus has been reported to regulate the insulin/insulin-like growth factor-like signalling pathway and act as a Drosophila nutrient sensing system to modulate host homeostasis, growth rate and individual size [44, 45]. In this study, we found that all treatments markedly increased the abundance of Lactobacillus at day 30 (Fig 5). It has been reported that Lactobacillus reuteri strains can regulate T2D-related factors and improve insulin resistance in a rat model [46]. Balakumar et al. (2018) demonstrated that the Lactobacillus strain combination could improve insulin sensitivity in mice [47]. The results of this study revealed that the abundance of the Lactobacillus genus was higher in the gut content of the B. licheniformis-treated group, and the abundance of the Lactobacillus genus was positively correlated with that of B. licheniformis, which implied that probiotic supplementation promotes the beneficial bacterial population and, thus, maintains a healthier intestinal system, thereby improving the growth lifespan and body weight parameters. Additionally, Lactobacillaceae and Acetobacter were found to be significantly increased in flies fed BA. As the dominant microbial genus in Drosophila melanogaster, Acetobacter species are commonly acetic acid-producing bacteria, which may help regulate host glucose levels, accelerate host development, and increase body size and growth rate in D. melanogaster [44, 48, 49]. It has been described that Acetobacter spp. also influenced the nutrient-sensing insulin/insulin-like growth factor signalling pathways through acetic acid [44]. In the BA group, the increasing abundance of the Acetobacter genus suggested the influence of the dietary supplementation of BL and AE combination on improving lifespan of InR[E19]/TM2 D. melanogaster.

The results presented in this work indicated that Wolbachia was significantly reduced in the AE and BA groups at day 30 (p = 0.009; p = 0.003) (Fig 5). Wolbachia bacteria are intracellular bacteria present in the insect and parasitic nematode microbiota. Wolbachia bacteria have been shown to influence the reproduction, development and lifespan of insect biology [50, 51]. Although Wolbachia has been reported to affect the longevity of hosts, some inconsistency remains [52, 53]. For example, Wolbachia was reported to substantially increase the lifespan and competitiveness of infected females under laboratory conditions [52]; nevertheless, some Wolbachia strains, such as MelPop, have been shown to shorten the lifespan of Drosophila [53]. Interestingly, our results showed that BL, AE and BA significantly reduced the proportion of Wolbachia in intestinal flora, and more research is needed to confirm the relationship between decreased Wolbachia and lifespan extension of male InR[E19]/TM2 D. melanogaster.