Overweight and obesity result from abnormal adipose deposition and function and are considered as major pathophysiological symptoms of metabolic syndrome (Olufadi & Byrne, 2008). Originating from insulin resistance, metabolic syndrome may be reflected by several clinical manifestations such as atherosclerosis, hyperglycemia, dyslipidemia, hypertension, reduced high density lipoprotein (HDL) cholesterol and type 2 diabetes mellitus (Furukawa et al., 2017). Based on typical pathological symptoms, broadly defined as excessive fat mass in the body (specifically the abdomen), the prevalence of obesity has rapidly increased during the last two decades (Kobyliak et al., 2017). Also referred to as “obesity pathogenesis,” obesity is considered as a disorder of the energy homeostasis system rather than the result of passive weight accumulation (Schwartz et al., 2017). In spite of the recent intensive research input, a deeper understanding of pathogenesis and the underlying mechanisms of obesity are still lacking, while, in fact, the causality of obesity has been explained from different viewpoints and disciplines of science such as genetics, endocrinology and psychology (Schwartz et al., 2017).
Following up on classical approaches, recent studies show that the microbiota can play a key role in host obesity and metabolic syndrome (Gérard, 2016). Thereby, new clinical diagnostic perspectives were opened on the influence of the gut microbiota on the status of metabolic disorders. This potential has been highlighted in a review by Boulange et al. (2016), at the same time underlining the complex etiology of these disorders. The current understanding of the mechanisms linking the gut microbiota with metabolic syndrome still appears to be “vague” (Chattophadyay & Mathili, 2018). Indeed, numerous studies have reported on qualitative and quantitative discrepancies in the microbiota of the gastrointestinal tract (GIT) when comparing healthy subjects with people suffering from metabolic diseases (Turnbaugh et al., 2006, 2008; Ley et al., 2005; Cani & Delzenne, 2009; Armougom et al., 2009).
The International Scientific Association for Probiotics and Prebiotics, after a grammatic correction, has condoned the FAO/WHO consensus definition of probiotics as “live microorganisms that, when administered in adequate amounts, confer a health benefit on the host” (Hill et al., 2014). There is general agreement that probiotics support the balance of the host gut microbiota, and scientific evidence is steadily accumulating regarding the positive impact of probiotics on human health such as improvement of immune disorders, inflammatory bowel disease, type 2 diabetes and atherosclerosis (Amar et al., 2011; Kim et al., 2016; Ritze et al., 2014; Schroeder et al., 2018; Vemuri, Gundamaraju & Eri, 2017). In spite of increasing evidences of beneficial effects, information is still sparse on the way in which gut microbiota communicates with distant sites in the host, and also on the mechanisms underlying their influence on host physiology with regard to (e.g.,) the respiratory system, the skin, brain, heart and host metabolism (Reid et al., 2017). The best recognized mechanisms among the studied probiotics appear to be related to colonization resistance, acid and short-chain fatty acid production, regulation of intestinal transit, normalization of perturbed microbiota, increasing turnover of enterocytes, and competitive exclusion of pathogens (Hill et al., 2014). Using a high-calorie induced obesity BALB/c mouse model a single strain of Lactobacillus casei IMV B-7280, and a combination of Bifidobacterium animalis VKL, B. animalis VKB and L. casei IMV B-7280 were shown to be effective in reducing weight gain and cholesterol levels, in the restoration of liver morphology and in modulating the gut microbiome in a beneficial manner (Bubnov et al., 2017). However, key issues such as strain-specificity and characterization of dose-dependent effects still remain to be solved. For this purpose, the further development of both in vitro and in vivo models appears to be strongly justified. Evidence-based recommendations for probiotics presently suggest a dose of 109 CFU/day or higher (WGO, 2017). A former study involving volunteers demonstrated a dose of 1011 CFU/day (of probiotic strains B. animalis subsp. lactis BB-12 and L. paracasei subsp. paracasei CRL-341) to be effective (Larsen et al., 2006). For the clinical success of anti-obesity treatment, selection of an optimal dose and an optimal administration time frame of probiotics are considered to be essential for inducing beneficial changes, both in gut microbiome diversity and in the metabolism of obese humans (Bubnov et al., 2017).
Various modes of probiotic action were elucidated by using in vitro studies (including development of dedicated in vitro models) while efficacy was investigated by both in vivo (preclinical) studies (Park et al., 2016; Wang et al., 2015) and clinical trials (Kadooka et al., 2010; Woodard et al., 2009). These therapeutic benefits were all related to anti-obesity effects of probiotics (Kadooka et al., 2010; Park et al., 2016; Wang et al., 2015; Woodard et al., 2009). Yet, the anti-obesity efficacy of probiotics has not been fully elucidated in spite of various clinical trials, and scientific evidence for a “minimal dose effect level” remains relatively sparse (Tanentsapf, Heitmann & Adegboye, 2011; Raoult, 2009; Mekkes et al., 2013). The concept of a minimal effective dose is complicated due to the large (and diverse) number of microbial and host-related factors (Salminen et al., 1998), and will also depend on the kind of key criteria and the “end-points” selected. The dose of intolerance is generally considered to be high; thus, allowing a relatively broad “therapeutic window” (Collins, Thornton & Sullivan, 1998), it may be difficult to find a suitably low effective dose above the minimal level. Yet, precisely defining an effective dose has remained an arbitrary issue, and thus the pragmatic suggestion by an FAO/WHO Working Group (FAO/WHO, 2002) that “the suggested serving size must deliver the effective dose of probiotics related to the health claim.” Convincingly delivering this kind of evidence has remained difficult until this day, in particular for commercial distribution of (food or pharmaceutical) strains claimed to be probiotics. In an early report Perdigón, Alvarez & De Ruiz Holgado (1991) suggested a dose related impact of L. casei on the secretory immune response and protective capacity in intestinal infections. A placebo-controlled study designed to evaluate the therapeutic value of four different non-antibiotic preparations (including Saccharomyces boulardii, and heat-killed microbial strains) indicated a non-significant dose dependency for either prophylaxis or treatment of traveller’s diarrhoea (Kollaritsch et al., 1989, 1993). Yet, substantial evidence supports the principle of dose-dependency of probiotics to modulate systemic and mucosal immune function, improve intestinal barrier function, alter gut microbiota, and exert metabolic effects on the host, also in a strain-dependent manner (Alemka et al., 2010; Madsen, 2012; Larsen et al., 2013). Everard et al. (2011) reported a dose-dependent immunomodulation of human dendritic cells by the probiotic L. rhamnosus Lcr35, leading, at high doses, to the semi-maturation of the cells and to a strong pro-inflammatory effect. Against this background, the present study was designed with the challenge of involving a hitherto rarely reported species (L. sakei) and its potential for alleviation of obesity (in a diet-induced obese (DIO) mouse model). In addition, there was the prospect of gaining additional insights in intra-species (strain-specific) functional diversity by using established biomarkers.
In this study we administered three different 10-fold dose levels of three different L. sakei strains separately to a DIO C57BL/6 murine model and monitored body weight during the full experimental period. Organ weights and serum biomarkers were monitored to elucidate the dose-dependent anti-obesity effect of three different L. sakei strains.
Materials and Methods
The animal study was approved by the Ethical Committee of KPC Ltd. in Korea (P150067), in full compliance with ethical standards as specified by Korean law. A total of 5 week-old, specific pathogen free male C57BL/6 mice were supplied from Orient Bio, Korea. Either a high-fat diet (HFD) (Research Diets D12492) (60% kcal fat), or low-fat diet (LFD) (Purina Laboratory Rodent Diet 38057) (12% kcal fat) (negative control) and autoclaved tap water were provided ad libitum, while the animals were housed at 23 °C, 55 ± 10% humidity, in a 12 h light/dark cycle. At the age of 5 weeks mice were fed with either a low-fat control diet containing 12% kcal of total energy from fat (12.41% kcal fat, 24.52% protein, 63.07% kcal carbohydrate (Purina Laboratory Rodent Diet 38057; Purina Korea Inc., Seoul, Korea)) or a HFD with 60% kcal fat ((90% of the fat from lard, 10% from soybean oil), 20% kcal protein, 20% kcal carbohydrate (D12492; Research Diets Inc., New Brunswick, NU, USA)) for 6 weeks. For this study, a HFD of 60% kcal fat was chosen, as this is one of the most commonly used diets to induce obesity and ectopic lipid storage in in vivo studies. Detailed analytical information on the diet composition is given in Table S1 (see also Table 1). The NIH guidelines were followed by providing sufficient cage surface area based on the weight of the mice. In total 120 mice were separated into 12 different groups (five animals per cage and two cages per group) with each group receiving a different treatment. Study design is given in Table 2 and information on the diets in Table 1.
|Protein (%)||Fat (%)||Fiber (%)||Minerals (%)||Vitamins (%)|
|Fat||12.41%||Arginine (1.26) Glycine (0.87) Isoleucine (0.82) Leucine (1.47) Lysine (1.01) Phenylalanine (0.98) Valine (0.91) Others||Linoleic Acid (1.10) Linolenic Acid (0.12) ArachidonicAcid (0.02) Omega-3 Fatty Acids (1.11)||Crude fiber||Ash (7.25) Calcium (1.20) Phosphorus (0.62) Potassium (0.82) Others||Vitamins A, D3, E, K, Riboflavin, Niacin Others|
|Calories (kcal%)||Ingredients (g)|
|Fat||60.00%||Casein, 80 Mesh (200) L-Cystine (3) Maltodextrin 10 (125) Sucrose (68.8) Cellulose, BW 200 (50) Soybean Oil (25) Lard (245) Mineral Mix, S10026 (10) DiCalcium Phosphate (13) Calcium Carbonate (5.5) Potassium Citrate.1H2O (16.5) Vitamin Mix, V10001 (10) Choline Bitartrate (2) FD&Blue Dye #1 (0.05)|
(A) Low-fat diet (Purina Laboratory Rodent Diet 38057); (B) high-fat diet (Research Diets D12492).
|LFD||LFD||300 μL PBS (non-obese control)|
|HFD||HFD||300 μL PBS (obese control)|
|Orlistat||HFD||40 mg/kg suspended in 300 μl PBS|
|CJB38 L||HFD||1 × 108 CFU/day of L. sakei L338 suspended in 300 μL PBS|
|CJB38 M||HFD||1 × 109 CFU/day of L. sakei L338 suspended in 300 μL PBS|
|CJB38 H||HFD||1 × 1010 CFU/day of L. sakei L338 suspended in 300 μL PBS|
|CJB46 L||HFD||1 × 108 CFU/day of L. sakei L446 suspended in 300 μL PBS|
|CJB46 M||HFD||1 × 109 CFU/day of L. sakei L446 suspended in 300 μL PBS|
|CJB46 H||HFD||1 × 1010 CFU/day of L. sakei L446 suspended in 300 μL PBS|
|CJLS03 L||HFD||1 × 108 CFU/day of L. sakei LS03 suspended in 300 μL PBS|
|CJLS03 M||HFD||1 × 109 CFU/day of L. sakei LS03 suspended in 300 μL PBS|
|CJLS03 H||HFD||1 × 1010 CFU/day of L. sakei LS03 suspended in 300 μL PBS|
LFD, low-fat diet (negative control); HFD, high-fat diet; CJB38, CJB46 and CJLS03 denote the three Lactobacillus sakei strains; the three dose levels of each strain administered together with the HFD were 1 × 1010 CFU/ml (high-dose, H), 1 × 109 (medium-dose, M) and 1 × 108 CFU/mL (low-dose, L).
The experiment comprised 1 week of adaptation followed by 6 weeks of obesity induction using a HFD while the LFD group was maintained on LFD feeding. A total number of 110 mice received the test substances, with exception of those with the upper and lower body weights after the 6-week period of obesity induction. All treatments were by oral gavage and were performed twice a day, at the same daytime (10.00 and 17.00), for 7 weeks. Each group was treated with either the microbial culture suspended in phosphate buffered saline (PBS), orlistat suspended in PBS, as chemical control, or only PBS as negative control. Orlistat was provided as Xenical (with 120 mg/g of orlistat as active pharmaceutical ingredient, and microcrystalline cellulose, sodium starch glycolate, sodium lauryl sulfate, povidone and talc as inactive ingredients). The contents of the Xenical capsules were added to PBS, as explained in Table 1. As orlistat is insoluble in water, it was suspended by vortexing and sonication and then orally administered to the animals. For oral administration each microbial strain was washed twice with PBS and the supernatant discarded after centrifugation. The microbial pellet was resuspended in PBS to suit the dose for administration. On the last day of the experiment, the mice were sacrificed by dislocation of the cervical vertebrata. The organs (liver, femoral muscle, brown adipose tissue, epididymal adipose tissue, subcutaneous adipose tissue and mesenteric adipose tissue) were collected, weighed, and stored at −80 °C. Each perfused liver was embedded in paraffin and sectioned (four μm) on a microtome. Hematoxylin and eosin (H&E) staining was performed on each high dose L. sakei group and assessed by light microscopy (Olympus MVX10 microscope, equipped with a DC71 camera; Center Valley, PA, USA; Olympus, Tokyo, Japan).
Serum triglycerides (TG), glucose (GLU), total cholesterol (TC), HDL, low-density lipoprotein (LDL) and aspartate transaminase (AST; a marker of liver toxic injuries of hepatocytes (Aulbach & Amuzie, 2017)), were measured using an automated biochemical analyzer BS-200 (Mindray, China) in Pohang Technopark, Pohang (South Korea).
Lactobacillus sakei strain CJLS03 was isolated from kimchi, while L. sakei strains CJB38 and CJB46 originated from human fecal samples. These strains were selected among nine different strains (comprising four L. brevis, three L. sakei, one L. plantarum and one Bifidobacterium longum) on the basis of the lowest weight gain in a preliminary study using a DIO mouse model (data shown in Fig. S1).
The three L. sakei strains were grown daily in MRS broth (Difco Laboratories INC., Franklin Lakes, NJ, USA) for feeding during the 7-week period of intervention. Strains were grown for 8 h to reach their late log phase and were collected by centrifugation (3,546g, 5 min, 5 °C) (Hanil Science Inc., Gangneung, South Korea) and washed two times with PBS. Each strain was prepared in an approximate number of 1 × 1010 CFU/ml using a mathematical equation derived from a pre-optimised standard curve (Fig. S2) using optical density by SPECTROstar Nano (BMG Labtech, Durham, NC, USA). A stock suspension of 1 × 1010 CFU/mL (high-dose, H) was prepared of each strain, then diluted 10-fold to 1 × 109 (medium-dose, M) and 1 × 108 CFU/mL (low-dose, L), respectively, and finally suspended in 300 μl of PBS to be administered to each mouse by oral gavage.
Experimental determinants were statistically calculated using ANOVA and Dunnett’s multiple comparison test to distinguish the level of significance based on probability of 0.05 (*), 0.01 (**) and 0.001 (***).
High-fat diet feeding resulted in a strong increase in body mass as compared to those animals receiving LFD administration (Fig. 1A) over the 48-day feeding period. Moreover, elevated levels of serum biomarkers such as TG, TC, GLU, LDL and AST were detected in the HFD group (Fig. 2), concomitantly with quantitative increases in epididymal, mesenteric and subcutaneous adipose tissues (Fig. 3). Orlistat therapy did not cause any mentionable side-effects in the treated animals. No animals in any of the groups died during the study period.
Three different doses (108–1010) of the three L. sakei strains (CJB38, CJB46 and CJLS03) were orally administered to high fat DIO C57BL/6 mice for 7 weeks, and body weight and food consumption were measured daily. During the test period, three strains were found to exhibit reduced weight gain compared to the HFD group (Figs. 1B–1D), with strain CJLS03 showing, dose-dependently, the strongest effect of the three strains. LFD, Orlistat, the full CJB46 group, and medium and high dose of the CJLS03 groups showed significantly lower weight increase compared to the HFD group (Fig. 1E; Fig. S3). The weight loss of CJB38 or CJB46 was not dependent of the dose while only strain CJLS03 showed a dose-dependent weight reduction effect, and with the highest efficacy of all groups for CJLS03 H (Fig. 1E). The onset time of weight loss showed significance compared to the HFD at days 4, 21, 21 and 7 for the Orlistat, CJB38, CJB46 and CJLS03 groups, respectively (Table S2). The daily dietary intake was significantly higher in the LFD, Orlistat and CJLS03 M groups compared to the HFD group (Fig. 1F).
Serum biochemical analysis showed an overall increase in the lipid profile (TC, TG, HDL, LDL), liver (AST) and the GLU level of the HFD group compared to the LFD group, demonstrating that a HFD intake may impact various biomarkers associated with pathophysiological symptoms of obesity (Fig. 2). Compared to the HFD group, the serum TG level decreased in all test groups (Fig. 2A) while the LDL level was significantly reduced in all test groups except CJB46 H (Fig. 2E). Significant reduction of TC was only detected in LFD, Orlistat and in the groups treated with higher doses (M and H) of L. sakei CJB38 H, CJB46 M, CJB46 H, CJLS03 M and CJLS03 H (Fig. 2C). In particular, the CJLS03 group, shown to be superior regarding weight gain inhibition, appears to be effective in a dose-dependent manner (Figs. 2A–2C). HDL levels were not significantly different from the HFD group in all the test groups, however, all L. sakei treated groups except CJB46 L, CJLS03 M and CJLS03 H showed significant increase when the ratio of HDL to TC level was calculated; this is reflected in Fig. 2D. Serum AST values (indicating liver function) were found to be approximately 1.7 times higher for the HFD compared to the LFD group (Fig. 2F), while the Orlistat group showed no significant change in AST level compared to the HFD group. All nine groups receiving the L. sakei strains showed a trend toward reduced AST levels but with only the high dose of CJLS03 (CJLS03 H) differing significantly when compared to the HFD group (Fig. 2F). CJLS03 showed the highest overall effectivity and a dose-dependent anti-obesity function; at the same time, it induced a dose-dependent improvement of serum obesity-associated biomarkers and liver function. Liver H&E staining optically demonstrated normal histology in LFD mice with minor lipid accumulation. Comparing the visual differences, the HFD-fed mice showed extensive fat accumulation and moderate vacuolations around the portal triad. In the groups treated with the higher dose of L. sakei CJB38 H, CJB46 H and CJLS03 H inhibition of lipid accumulation was visually evident and was comparable to that of the LFD group (Fig. S4).
Compared to HFD the LFD group showed significantly lower weights of epididymal, mesenteric, subcutaneous and brown adipose tissues while insignificant organ weight differences were measured in liver and femoral muscles (Fig. 3). Every dose of all three strains of L. sakei and the orlistat treatment resulted in significantly lower subcutaneous adipose tissue weight while only CJLS03 H showed significant reduction of visceral adipose tissue including epididymal and mesenteric adipose tissue, when compared to the HFD group (Figs. 3A–3C). CJLS03 M treatment significantly reduced epididymal adipose tissue weight when compared to the HFD group (Fig. 3A). These results suggest that the three different L. sakei strains inhibited the accumulation of subcutaneous adipose tissue but that the CJLS03 group responded by dose-dependent reduction of visceral adipose tissues including the epididymal and mesenteric adipose tissues (Figs. 3A and 3B). Orlistat and L. sakei treatment did not result in significant weight differences regarding brown adipose tissue, liver and femoral muscle (Figs. 3D–3F).
The impact of a HFD on various biomarkers associated with pathophysiological symptoms of obesity is well established and supported in current literature (Chandler et al., 2017; Lee, 2013; Ludwig et al., 2018; Siri-Tarino et al., 2010). The body mass increase resulting from HFD feeding (as compared to a LFD) in this study (Fig. 1) was also accompanied by significant increases in serum biomarkers such as TG, TC, GLU, LDL and AST (Fig. 2) and also increases in epididymal, mesenteric and subcutaneous adipose tissues (Fig. 3). Definition of an ideal HFD and its exact composition is generally considered difficult (Buettner, Schölmerich & Bollheimer, 2007). However, the standardization of the specific laboratory and feeding conditions for the purpose of metabolic studies is essential. In our studies, we have used exactly defined and commercially available HFD and LFD. The selected murine model (male C57BL/6 mice) is widely preferred as in vivo model for obesity and metabolic studies (Khan et al., 2014) and related investigations (Neuhofer et al., 2014).
The anti-obesity influence of administered probiotics is a heavily debated issue, yet, an indisputable fact is that the host gut microbiota is exercising a leverage over energy efficiency and adipose tissue accumulation (Kobyliak et al., 2017; Greiner & Bäckhed, 2011; Delzenne et al., 2011). At the same time, probiotics have been reported to impact the host microbiota in a positive way (Hemarajata & Versalovic, 2013) and to beneficially influence gut homeostasis and reduce the symptoms of gastrointestinal diseases (Bron et al., 2017). The beneficial effect of probiotics on the levels of alanine aminotransferase, AST, TC, HDL, tumor necrosis factor-α and also on insulin resistance (assessed in a homeostasis model (HOMA-IR)) have been reported earlier (Ma et al., 2013). In a study using C57BL/6J mice L. rhamnosus GG (LGG) showed a protective effect against nonalcoholic fatty liver disease (NAFLD) induced by a high-fructose diet (Ritze et al., 2014). This potential is supported by meta-analysis of data from randomized controlled trials in patients with NAFLD, showing probiotic therapy to result in a significant decrease of NAFLD (Ma et al., 2013; Al-muzafar & Amin, 2017). Moreover, probiotic therapy has been shown to be typically associated with a reduction in liver aminotransferase levels (Aller et al., 2011; Buss et al., 2014; Shavakhi et al., 2013). The significant reduction of liver AST levels by L. sakei CJLS03 H in our study suggests its possible therapeutic potential for alleviation of NAFLD. The potential advantages of probiotics as complementary treatment for metabolic disorders and as therapy for NAFLD are increasingly recognized (Le Barz et al., 2015; Ma, Zhou & Li, 2017). Moreover, the modulatory effect of probiotics on the gut microbiota suggests their potential as a “promising and innovative add-on therapeutic tool” for the treatment of NAFLD (Paolella et al., 2014). In our study, inhibition of hepatic lipid accumulation in HFD animals was revealed by Liver H&E staining and was particularly obvious for the groups treated with orlistat and CJLS03 H which also compared well with the normal histological features of the LFD group (Fig. S4).
The function of orlistat in assisting weight loss is well established and has been supported by Cochrane meta-analysis of various randomized controlled trials (Drew, Diuxon & Dixon, 2007). Obesity control may be by several mechanisms, one of which being that orlistat prevents fat hydrolysis by acting as a gastric and pancreatic lipase inhibitor (Heck, Yanovski & Calis, 2012; Yanovski & Yanovski, 2014). It has been successfully used as anti-obesity control in animal experiments involving high fat DIO rats (Karimi et al., 2015) and DIO C57BL/6 mice (Chung et al., 2016). The latter studies also included clinical trials, and the authors (Chung et al., 2016) claimed orlistat to be the most popular anti-obesity pharmaceutical drug, both in animal (DIO C57BL/6 mice) experiments and clinical trials. The DIO C57BL/6 mouse is now widely accepted as an in vivo model of choice. It has been reported to closely reflect human metabolic disorders such as obesity, hyperinsulinemia, hyperglycemia and hypertension (Collins et al., 2004). In particular, the metabolic abnormalities of DIO C57BL/6 after HFD feeding are considered reported to closely resemble those of human obesity development patterns (Speakman et al., 2007), and also regarding properties such as adipocyte hyperplasia, fat deposition in the mesentery and increased fat mass (Inui, 2003).
Probiotic administration increasingly enjoys consideration as a promising approach for beneficially modulating the host microbiota (Jia et al., 2008; Steer et al., 2000). Numerous reports confirmed the beneficial effects of specific probiotic strains against diarrhoea and inflammatory bowel diseases (Ahmadi, Alizadeh-Navaei & Rezai, 2015; Gionchetti et al., 2000; Ouwehand, Salminen & Isolauri, 2002). Recently, anti-obesity effects of probiotics were also reported and confirmed in clinical trials (Kadooka et al., 2010; Woodard et al., 2009; Minami et al., 2015, 2018; Borgeraas et al., 2017) and animal models (Kim et al., 2016; Alard et al., 2016; Wang et al., 2015; Ji et al., 2012). Kadooka et al. (2010) investigated the anti-obesity effect of the probiotic L. gasseri SBT2055 by conducting a double-blind, randomized, placebo-controlled intervention trial with 87 overweight and obese subjects for 12 weeks. The data confirmed that the abdominal visceral and subcutaneous fat area, weight, BMI, as well as waist and hip measures were significantly reduced in the group consuming the probiotic. In another study (Woodard et al., 2009) 44 morbid obese patients were operated for weight loss by surgery (gastric bypass surgery) and were randomly divided in a probiotic administered group and a control group. A significantly higher weight loss was recorded in the group receiving the probiotic (described as “Puritan’s Pride®,” containing a mixture of 2.4 billion live cells of Lactobacillus spp.). Park et al. (2013) reported a significant weight reduction of a C57BL/6 mice model after L. curvatus HY7601 and L. plantarum KY1032 consumption, however, faecal microbiota modulation of major groups such as Firmicutes and Bacteroidetes was not monitored.
One of the major hurdles for an accurate clinical trial is to understand the effective dose of a probiotic at a strain-specific level. Selecting the correct dose of a probiotic for a specific purpose such as the alleviation of diarrhoea was suggested in various studies; yet, there is a general lack of scientific proof of a concept to define the functional dose of a probiotic (Kollaritsch et al., 1989, 1993; Islam, 2016). Chen et al. (2015) used a range of five different 10-fold doses of L. acidophilus in a colitis-induced animal model and reported 106 CFU/10 g of the animal weight as the most effective application level for modulating the bacterial profile in the distal colon. In our study we have monitored dose-related effects of three different strains of L. sakei and found only one strain, CJLS03, to show a dose-dependent anti-obesity effect while the anti-obesity impact of the other two strains was lower and dose-independent (Fig. S3). At dose levels from 1 × 108 to 1 × 1010 CFU/mL administration of strain CJLS03 resulted in a dose-related (progressive) reduction in the levels of TC, TG, AST, mesenteric adipose tissue and epididymal adipose tissue (Fig. S3). Adipose tissues were reduced relative to weight gain, and TG and TC showed the most significant reduction in the L. sakei treated groups compared to the HFD control group. Another L. sakei strain (OK67) isolated from kimchi was reported to ameliorate HFD-induced blood GLU intolerance and obesity in mice; mechanisms for this effect have been suggested to be by inhibition of gut microbial lipopolysaccharide production and the inducing of colon tight junction protein expression (Lim et al., 2016).
Our study has confirmed the relevance of a strain-specific approach when selecting functional strains suitable for (costly and time-consuming) clinical studies. The importance of this issue has been emphasized in recent papers with regard to pre-clinical physiological studies on putative probiotic strains of lactic acid bacteria and Bifidobacterium. These studies involved features such as adhesion potential, antibiotic resistance and survival under simulated conditions of the upper GIT, in addition to the modulation of the gut microbiome (Bubnov et al., 2018).
This in vivo investigation showed that beneficial effects of putative probiotics are both strain-specific and dose-related. For only one (CJLS03) out of three L. sakei strains an anti-obesity effect could be detected, which, at the same time, was found to be dose-dependent. The highest of three doses (1 × 1010 CFU/day) of CJLS03 gave the most favorable (significant) biomarker-related effects with regard to cholesterol and triglyceride reduction, when compared to the HFD control.
Raw data on animal experiments.
Raw data obtained during the animal experiments in four subsections, comprising information on weight, feed consumption, organ weight and blood chemistry.
Detailed analytical composition of the low-fat (LFD) and high-fat (HFD) diets used in this study.
Detailed analytical composition of the low-fat (LFD) and high-fat (HFD) diets used in this study. (A) Low fat diet (38057; Purina Laboratory Rodent Diet); (B) High fat diet (D12492; Research Diets Inc., New Brunswick, NU, USA).
Effect of the test materials/strains on body weight in HFD-induced obese mice.
Effect of the test materials/strains on body weight in HFD-induced obese mice. LFD, low-fat diet; HFD, high-fat diet; CJB38, CJB46 and CJLS03 denote the three Lactobacillus sakei strains; the three dose levels of each strain administered together with the HFD were 1 X 1010 CFU/mL (high-dose, H), 1 X 109 (medium-dose, M) and 1 X 108 CFU/mL (low-dose, L). Data expressed as mean ± SD (n=10). *, **: significantly different from ND group at p<0.05, p<0.01; #, ##:: significantly different from HFD group at p<0.05, p<0.01.
Reduced weight gain effect of different microorganisms administered in a diet induced obesity mouse model after 8 weeks study period.
Reduced weight gain effect of different microorganisms administered in a diet induced obesity mouse model after 8 weeks study period. After 1 week of acclimatization, 120 of 6 weeks old male C57/BL6 mice were divided into 12 different groups receiving a low-fat diet with 300 μL PBS as carrier (LFD), high-fat diet with 300 μL PBS (HFD), high-fat diet with 80 mpk of orlistat. The other 9 groups received a high-fat diet with 1x109 CFU of either Lactobacillus plantarum 301 (LP 301), L. sakei CJLS03 (LS 03), L. sakei LS 338, L. sakei LS 446, L. brevis LB 29, L. brevis LB 33, L. brevis LB 54, L. brevis LB 55 or B. longum BL 83. Feed and sterilized water supply were provided ad libitum and weight gains were measured by subtracting the average weight of week 0 from that of week 8. Asterisks denote the level of significance (Dunnett’s multiple comparison test) compared to HFD as *: p<0.05, **: p<0.01 and ***: p<0.001.
Equation, growth curves and plate counting.
Equation, growth curves and plate counting results for L. sakei LS03, L. sakei L338 and L. sakei L446.
Dose dependent anti-obesity effects of CJLS03 with regard to weight gain, serum biomarkers and adipose tissue weight.
Dose dependent anti-obesity effects of CJLS03 with regard to weight gain, serum biomarkers and adipose tissue weight. All data were measured at the end of the experimental period (at 48 days) and RE expressed as mean value (n=10). LFD, normal diet (low-fat diet); HFD, high-fat diet; OLS, Orlistat 40 mg/kg. L (high-dose), 1 X 1010 CFU/mL; M (medium-dose), 1 X 109 CFU/mL; L (low-dose), 1 X 108 CFU/mL. TG, serum triglycerides; TC, total cholesterol; AST, aspartate transaminase.
Histological analyses of hepatic lipid accumulation.
Histological analyses of hepatic lipid accumulation. Representative HE-stained liver sections are shown (magnification, 200X). Mice fed a high-fat diet showed considerable hepatic lipid accumulation compared with normal pellet diet. Moderate vacuolations around the portal triad are shown in the HFD-fed mouse. LFD, normal diet (low-fat diet); HFD, high-fat diet; OLS, Orlistat 40 mg/kg; CJB38H, CJB46H, and CJLS03H received 1 X 1010 CFUs respectively of the L. sakei strains CJB38, CJB46, and CJLS03.