Comparative Assessment of the Bioremedial Potentials of Potato Resistant Starch-Based Microencapsulated and Non-encapsulated Lactobacillus plantarum to Alleviate the Effects of Chronic Lead Toxicity

Lead (Pb) is a well-recognized and potent heavy metal with non-biodegradable nature and can induce the oxidative stress, degenerative damages in tissues, and neural disorders. Certain lactic acid bacterial strains retain the potential to mitigate the lethal effects of Pb. The present work was carried out to assess the Pb bio-sorption and tolerance capabilities of Lactobacillus plantarum spp. Furthermore, potato resistant starch (PRS)-based microencapsulated and non-encapsulated L. plantarum KLDS 1.0344 was utilized for bioremediation against induced chronic Pb toxicity in mice. The experimental mice were divided into two main groups (Pb exposed and non-Pb exposed) and, each group was subsequently divided into three sub groups. The Pb exposed group was exposed to 100 mg/L Pb(NO3)2 via drinking water, and non-Pb exposed group was supplied with plain drinking water during 7 weeks prolonged in vivo study. The accumulation of Pb in blood, feces, renal, and hepatic tissues and its pathological damages were analyzed. The effect of Pb toxicity on the antioxidant enzyme capabilities in blood, serum, as well as, on levels of essential elements in tissues was also calculated. Moreover, KLDS 1.0344 displayed remarkable Pb binding capacity 72.34% and Pb tolerance (680 mg/L). Oral administration of both non- and PRS- encapsulated KLDS 1.0344 significantly provided protection against induced chronic Pb toxicity by increasing fecal Pb levels (445.65 ± 22.28 μg/g) and decreasing Pb in the blood up to 137.63 ± 2.43 μg/L, respectively. KLDS 1.0344 microencapsulated with PRS also relieved the renal and hepatic pathological damages and improved the antioxidant index by inhibiting changes in concentrations of glutathione peroxidase, glutathione, superoxide dismutase, malondialdehyde, and activated oxygen species, which were affected by the Pb exposure. Overall, our results suggested that L. plantarum KLDS 1.0344 either in free or encapsulated forms hold the potentiality to deliver a dietetic stratagem against Pb lethality.


INTRODUCTION
A prompt industrial expansion, farm mechanization, and indiscreet utilization of agricultural manures, invigilancy to dispose-off solid wastes, and inappropriate mining operations are imperiling the human health and ecosystems because of the constant discharge of lethal heavy metals (Huang et al., 2015;Lai et al., 2016;Sidhu et al., 2016;Liang et al., 2017a). Lead (Pb) has been documented as a critical, heavy metal contaminant, and it possesses grievous eco-toxicological indications with the elongated persistency in the environment due to its non-biodegradable behavior (Flora et al., 2012;Liang et al., 2017b). Even at very low concentrations, Pb is incredibly pestilent, and it is generally accumulated in the kidneys, liver, bones (Patra et al., 2001), and muscles instigating numerous dreadful ailments, like oxidative stress (Patra et al., 2001;Khordad et al., 2013), carcinogenesis (Valverde et al., 2002), disturbance of calcium homeostasis, degenerative variations (Sansar et al., 2011(Sansar et al., , 2012, and tissue illnesses, mostly in the kids (Ahyayauch et al., 2013).
Numerous researches suggest that oxidative stress is among the mechanisms significantly involved in the baneful effects of Pb (Hosseini et al., 2015). Chelation therapy is the most typical treatment for heavy metal lethality by utilizing the chelating agents such as Meso-2,3-dimercaptosuccinic acid (DMSA) and calcium disodium versenate (CaNa 2 EDTA). However, adversative effects, including skin reactions, malaise, renal injury, vomiting, and nausea occur (Bayer, 2015). These chelating agents can also cause subsequent deficiencies of zinc, copper, and other crucially important trace nutrients, which are a vital part of the body's antioxidant defense system (Yadav et al., 2014). According to several studies, kidney is the main organ in the body where the development of chronic Pb toxicity can occur (Bidlack, 2002;Brzóska et al., 2003). Howsoever, most part of the absorbed Pb all through chronic exposure is originally deposited in the liver before its transportation to the kidney by the bloodstream (Zhai et al., 2014;Javed et al., 2016;Morcillo et al., 2016;Zhang S. et al., 2016;Ashraf and Tang, 2017).
As sorption matrices, there are several biodegradable natural polymers that have increased attention because of their metal chelating competence, simplicity of processing, non-toxicity, and worldwide afford-ability (Li and Buschle-Diller, 2017). Recently, some plant polymer extracts have been found to have the capacity to decrease tissue Pb levels and Pb-induced oxidative stress (Yadav et al., 2014;Liu et al., 2018). Owing to low cost, biodegradability and renewability starch is considered among the agricultural biopolymers that are expansively utilized in the food and food-related industry (Soto et al., 2015(Soto et al., , 2016Peng et al., 2016). The potato resistant starch (PRS) is consisted of compact structured granules of native potato starch, having resistance to enzymatic hydrolysis and higher contents of amylopectin (Dragan et al., 2014;Cieśla et al., 2015). Potato starch possesses unique features to form Werner-type complexes (Ciesielski and Tomasik, 2004a,b), and these complexes contain the ability to ligate a metal atom to the lone electron pairs of hydroxyl groups from phosphate groups and D-glucose units in the starch (Bhat et al., 2015;Soto et al., 2016). The potentially possible sites for metal ions interaction with polysaccharide chains are the hydroxyl groups of D-glucose units of starch granules and in this regard, the PRS has greater ability to bind cations (Blennow et al., 2000(Blennow et al., , 2006Ciesielski and Tomasik, 2004a). Bhat et al. (2015) conducted a study to assess the efficiency of PRS against heavy metals and stated that it could be effective adsorbent with 78.1% efficiency against Pb adsorption.
According to some studies, anti-oxidative defense system in lactic acid bacteria (LAB) either enzymatic or non-enzymatic might critically perform its role in detoxifying the damages produced by the oxidative stress (Halttunen et al., 2008;Huang et al., 2017;Yi et al., 2017). Furthermore, LAB are recognized to possess anti-oxidative characteristics in human, which might be additional imperative property to provide protection against Pb-induced noxiousness (Monachese et al., 2012). Bhakta et al. (2012), Tian et al. (2012), and Zhai et al. (2013Zhai et al. ( , 2015, conducted studies on the healing effects of oral administration of the LABs' and their shielding effect against Pb noxiousness by reducing Pb levels in the tissues and blood and, impeding Pb-induced oxidative strain. The study conducted by  has also provided the information that some Lactobacillus strains possess a positive impact to alleviate the acute Pb toxicity. In our previously published work , we successfully incorporated PRS for the microencapsulation of Lactobacillus Plantarum KLDS 1.0344. Presently, there is no specific natural remedy has been developed to deal with the chronic Pb poisoning. Therefore, introducing some new strategies tackling chronic Pb toxicity is the dire need of the day. To the best available information, the healing effects of L. plantarum 1.0344 microencapsulated with polysaccharides, like PRS, have not been studied so far to remedify the chronic Pb toxicities. Based on the findings of our previous  studies, the present work has been designed to appraise the alleviation and adsorption of Pb by PRS-microencapsulated and non-encapsulated L. plantarum KLDS 1.0344 and, their effects on anti-oxidative responses (enzymatic and non-enzymatic), oxidative stress, as well as, the Pb tolerance and anti-oxidative mechanisms, decrease in intestinal Pb absorption, reduction of Pb accretion in tissues, and alleviation of hepatic and renal oxidative stress have been assessed. Overall, the aims of the current study were set to evaluate and to compare the role of L. plantarum 1.0344 in nonencapsulated and microencapsulated forms for the alleviation of the induced chronic Pb toxicity by using the adult female BALB/c mice as a model animal.

Bacterial Strain and Culture
Lactobacillus plantarum KLDS strains were isolated from the traditional fermented cheese in Inner Mongolia and were stored in KLDS (Key Laboratory of Dairy Science) under the patronage of Chinese Ministry of Education. Frozen stock culture of L. plantarum strains were reactivated twice in MRS (de Man, Rogosa and Sharpe) broth, and incubation was done at 37 • C up to the stationary phase. Then, culture was centrifuged at 4 • C for 10 min at 10,000 g to collect the cell pellets. Thermo Sorvall Legend Micro, 21 microcentrifuge was used for the centrifugation purpose. The pellets were again washed three times and suspended in distilled and sterilized water.

Microencapsulation, Survivability During Storage, and in Vitro Digestion
The probiotics (L. plantarum KLDS 1.0344) were microencapsulated by using PRS. Buchi B-290, Flawil, Switzerland (laboratory-scale spray dryer) was used to execute the microencapsulation process. Survivability during storage and in vitro digestion was carried out as formerly reported in our previously published article . As the formulations with PRS gave us the best results during microencapsulation process, storage, and in vitro digestibility in the previous study, we selected these microencapsulated strains for the animal experiments. Lyophilization of the microencapsulated cells was done by mixing the skim milk with the encapsulated cells, and cells were then stored at −20 • C. Skim milk was utilized as a cryoprotectant agent. Before doing the animal experiments, viability of the lyophilized cells was done by the colony counting method. In short, the freeze-dried cells were reactivated with the ultrapure water. After the colony counting, viability of the cells was documented as around 2.7 × 10 9 CFU/mL. Thereof, the mice were orally gavage 0.5 mL of the reactivated lyophilized cells in skimmed milk, and it is conformed to 1.3 × 10 9 CFU of the bacterial cells.

Appraisal of the Binding and Tolerance of Pb
The ability of seven KLDS strains to bind the Pb was investigated as formerly described by , with little amendments. Incubation of all strains was carried out for 16 h, and the centrifugation of the cultivated biomass was done at 10,000 g for 10 min at 4 • C. The cell pellets were obtained after two times washing of the centrifuged mass with ultrapure water. Concentration of the bacteria was set to 1 g/L (wet weight) with ultrapure water having 100 mg/L lead nitrate, and incubation of the samples was done for 24 h at 37 • C. Afterwards, centrifugation of the samples was carried out for 20 min at 10,000 g, and the concentrations of the residual Pb in the supernatants were determined by (Spectra AA 220; Varian, Palo Alto, CA, United States) flame atomic absorption spectrophotometer. Following equation was used to determine the metal removal efficiency on the basis of mass balance in Equation (1) where C e and C i are the respective residual Pb concentrations and initial Pb concentrations after removal. The MIC (Minimum inhibitory concentration) approach was followed to determine the Pb tolerance of each strain according to the methods as described by Abou-Shanab et al. (2007) and Gupta et al. (2012). Preparation of the MRS agar medium having (100 to 1000 mg/L) lead nitrate solution was carried out. Each cultured LAB strain (10 µL) was spread on the MRS agar medium and the inoculum level was taken as 1 × 10 9 CFU/mL. Then incubation was done at 37 • C for 48 h, and subsequently the LAB growth was determined.
In the present study, the least concentration of Pb that entirely repressed the LAB growth was taken as MIC.
Comparison of Protective Potentials of Non-encapsulated and Microencapsulated L. plantarum KLDS 1.0344 Against Chronic Pb Toxicity in Vivo Study

Experimental Design of the Animal Trial
The mice used in all of the animal experiments were adult female BALB/c mice, and these were procured from the Beijing Vital River Lab. Animal Technology Co., Ltd. (China). Stainless steel cages and a well-equipped room to retain a 12 h lightdark cycle, controlled humidity, and temperature were used to keep the mice. Mice were given the standard commercial mouse food, and Pb-containing and Pb-free water were also supplied ad libitum in therapy groups. The entire protocols for the present study were approved by the Ethics Committee of Huazhong Agricultural University and Hubei provincial Animal Care Committee, Wuhan, China. The procedures and techniques of this study were strictly followed according to the European Community guidelines for the use and care of experimental animals (directive 2010/63/EU). Such as presented in Table 1, the mice were distributed into six subgroups, control (no Pb or KLDS 1.0344), Pb only, nonencapsulated L. plantarum KLDS 1.0344 only, encapsulated L. plantarum KLDS 1.0344 only, Pb plus non-encapsulated L. plantarum KLDS 1.0344, and Pb plus encapsulated L. plantarum KLDS 1.0344 with 10 mice in every respective group. The mice were given orally a dosage of 1.3 × 10 9 CFU of L. plantarum KLDS 1.0344 mixed in 0.5 mL of skim milk through gavage once in a day. Pb exposure of the mice was done by (Pb containing) drinking water, 100 mg/liter (0.05 mg/kg-day) −1 oral dose of Pb from lead nitrate in drinking water was taken for modeling of environment related concentration of Pb exposure)  were done during the treatment period of 7 weeks. The fecal samples were collected at the end of every week while, each mouse was relocated into an empty and clean cage for 1 h. Mice were individually moved to metabolic cages and kept there for 24 h at the end of the 7th week. Latterly, under light ether anesthesia, all the mice were sacrificed, and the blood was taken in heparinized tubes in order to obtain plasma. After scarifying the animals, the kidneys and livers were removed, and saline solution (prepared with sodium chloride and sterilized distilled water) was utilized to wash the samples. Prior to histopathological studies, the samples were removed and preserved in formalin saline (10%) for 48 h. The remaining kidney and liver samples were wrapped in aluminum foils, put into the Eppendorf tubes and stored at −80 • C to assess the chemical elements and biochemical assays (Zhai et al., 2014.

Quantifying Chemical Elements in Tissues
The tissue samples were moved to digestion vessels. The vessels were metal free, manufactured by Omni; CEM, United Kingdom. Then, samples were digested in concentrated nitric acid by using the Microwave Digestion System manufactured by MARS; CEM, United Kingdom. Concentrations of calcium (Ca), zinc (Zn), magnesium (Mg), and iron (Fe) in the kidneys and liver were measured with the use of graphite furnace or flame atomic absorption spectrophotometer (Zhai et al., 2014).

Measurement of Pb in the Blood, Feces, and Tissues
BH 2100 kit (Beijing Bohui Innovation Technology Co., Ltd.) was used to determine the levels of Pb from the whole blood samples. The samples of feces and tissues were digested in a microwave digestion system using concentrated HNO 3 . The concentration of Pb in the feces, kidneys, and livers was measured by an atomic absorption spectrophotometer, i.e., graphite furnace or flame spectrophotometer (Specter. AA; Varian or AAS). The quantity of Pb was given in mg/g of feces (wet weight) and µg/g of tissue (Dobrakowski et al., 2016).

Biochemical Assays
The MDH, GSH level, activities of GSH-Px, SOD, CAT in the mice tissues while, AST and ALT in the serum were determined with the respective kits obtained from the Jiancheng Bioengineering Institute. All assays were done in triplicate in accordant to the manufacturer's guidelines (Dobrakowski et al., 2016).

Histopathological Analyses
The kidney and liver tissues were split into 5 µm thickness with rotary microtome and fixed in paraffin. These sliced tissues were stained with hematoxylin-eosin and then observed by light microscopy .

Statistical Analyses
Entire analyses were completed in triplicate, and the data were compiled. Tukey method was utilized by using the statistical program Statistics 8.1 (Analytical Software, United States) for analysis of variance (ANOVA) and comparison of means. Statistically, the difference was considered as significant when the P < 0.05. Standard errors and mean values were deliberated and demonstrated in charts as coordinate pairs with error bars.

Lead Biosorption and Tolerance of the LAB Strains
Abilities of seven Lactobacillus KLDS strains to bind and tolerate the Pb have been presented in Table 2. The tested strains showed a range of 20.23 ± 0.51% to 72.34 ± 2.55% to remove the Pb (Table 2), while initially the concentration of Pb was 100 mg/L. Among all the seven tested strains L. plantarum, KLDS 1.0344 exhibited the greatest binding ability. On the basis of the binding ability L. plantarum, KLDS 1.0344 was taken as the best suitable candidate to be investigated for further in vivo assays. Additionally, PRS-encapsulated L. plantarum KLDS 1.0344 also showed more Pb binding ability followed by the non-encapsulated bacteria (Figure 1).

Body Weight of Mice
On the basis of Pb biosorption and tolerance of the LAB strains, we selected L. plantarum KLDS 1.0344 to evaluate its effect on the Pb toxicity in the forms of microencapsulated and nonencapsulated bacteria. Increment of weight was observed in every mouse through 7 week experimentation, and there was no significant (P > 0.05) difference was found among all the groups. Maximum body weight witnessed in control 27.11 ± 0.6 g succeeding by 26.96 ± 0.83 g in PRS microencapsulated KLDS 1.0344+Pb group, contrary to the Pb group only (25.72 ± 1.11 g) at 7th week given in Figure 2.  Pb Contents in the Excreta, Liver, Kidneys, and Blood The Pb concentrations in excreta of mice (groups) given Pb orally, were suggestively greater than all of the other (deprived of Pb in drinking water) groups (P < 0.01). The variations in the Pb concentrations in excreta are demonstrated in the Pb oral ( Figure 3B) and Pb free oral (Figure 3A) groups. In Pb free oral groups, the lower most Pb intensity in excreta was perceived in control 0.18 ± 0.00 µg/g (wet) feces during first week ( Figure 3A). While, in Pb oral groups, the orally given PRS encapsulated KLDS 1.0344+Pb were substantially (P < 0.05) incremented fecal Pb quantities, compared to the Pb-only group, after each week of the experimentation. The highest Pb fecal concentrations (445.6 ± 12.2 µg/g wet feces) were displayed by the PRS encapsulated KLDS 1.0344+Pb only oral groups followed by the KLDS 1.0344+Pb in 7th week ( Figure 3B). During the 7 week study, the elimination quantities of Pb in the Pb group and therapy groups (including the KLDS 1.0344 in skim milk given through gavage) were smaller in all successive weeks, indicating that PRS encapsulated and non-encapsulated KLDS 1.0344 were potentially effective against the chronic Pb toxicity. The concentrations of Pb in the kidneys, liver, and blood in the non-orally exposed Pb groups were significantly smaller than the orally exposed Pb groups (P < 0.05) of entire cliques and are publicized in Figure 3C. In the kidneys and blood, the declining levels of Pb in all Pb dose groups were suggestively different from the results noticed for the Pb group only (P < 0.05). Likened with the Pb-only groups, non-encapsulated and PRS encapsulated L. plantarum KLDS 1.0344 treatments expressively decreased the Pb contents in the blood and tissues. The tissue Pb contents in the control, nonencapsulated, and PRS encapsulated KLDS 1.0344-only groups were very low in the liver and 0.30 µg/g ± 0.04, 0.05 ± 0.008 µg/g, 0.03 ± 0.001 µg/g, respectively, in the kidney in Figure 3C. Comparing with the orally exposed Pb only (20.22 ± 0.98 µg/g in liver 24.8 ± 0.6 µg/g in kidney), non-encapsulated KLDS 1.0344+Pb (9.11 ± 0.06 µg/g in liver 16.78 ± 0.5 µg/g in kidney), and PRS encapsulated KLDS 1.0344+Pb (8.56 ± 0.09 µg/g in liver 15.32 ± 0.7 µg/g in kidney) significantly (P < 0.05) decreased the concentrations of Pb in the hepatic and renal tissues of the mice. The Pb contents in blood (µg/L) of mice are presented in Figure 3C. As compared to the Pb-only group (185.46 ± 2.57 µg/L), PRS encapsulated L. plantarum KLDS 1.0344+Pb (137.63 ± 2.44 µg/L) considerably reduced the Pb concentration in blood and tissues and provided protection to counter Pb burden in the blood and tissues.

Ca, Zn, Fe, and Mg Quantities in the Kidneys and Liver
Exposure of the Pb brought about variations of the Zn, Ca, Mg, and Fe metal quantities in both the liver and the kidneys (Tables 3A,B, respectively). Maximum of these changes were suggestively inverted in the non-encapsulated and encapsulated KLDS 1.0344+Pb groups (P < 0.05) in kidneys except for zinc. However, in liver, significant results were witnessed for increased metal levels in all others groups as compared to the Pb group only.

MDA, GSH, SOD, GPx, and CAT in Liver and Kidneys
The antioxidant capacity levels in the kidney and liver of mice are presented in Figure 4. In both orally and non-orally exposed Pb groups, chronic Pb exposure initiated noticeable reduction in levels of CAT (Figure 4A), GSH (Figure 4C), and SOD ( Figure 4B), accompanied by increased concentrations of MDA ( Figure 4E) and GSH-Px ( Figure 4D). Utilization of the PRS encapsulated L. plantarum 1.0344 treatment was efficacious in maximizing CAT (181.21 ± 2.16 U/mgprot as compared to the Pb only group 112.62 ± 2.03 U/mgprot in liver), GSH and SOD degrees and decreasing MDA and GSH-Px (52.64 ± 0.54 U/mgprot as compared to the Pb only group 66.48 ± 1.09 U/mgprot in liver) levels (P < 0.05). KLDS 1.0344 either in non-encapsulated or PRS-based encapsulated form had substantial protecting properties on the antioxidant capacity (P < 0.05). Co-treatment with non-encapsulated and PRS encapsulated KLDS 1.0344+Pb significantly protected against the variations of these parameters in the oral introduction. In kidneys prolonged Pb acquaintance produced an apparent increase in MDA and GSH-Px, whereas, there was improvement in CAT, GSH, and SOD activity. The activity of the marker enzymes ALT and AST in the serum of mice are given in Figure 4F.

Histopathological Appraisal
Prolonged Pb contact instigated a notable damage to the mice tissues. Demonstrated photomicrographs of liver and kidney tissue specimen from all groups are presented in Figures 5A,B.
Treatments with Pb plus non-encapsulated and PRS encapsulated KLDS 1.0344 considerably relieved such hepatic damages. In the kidneys, cloudy swelling and necrosis of tubules and enlargement of glomeruli were apparent in Pb only treated animals, contrary to the control group. It was witnessed likewise that, the renal and hepatic morphology of the non-encapsulated and PRS encapsulated KLDS 1.0344 groups was not varying from that of the control group.

DISCUSSIONS
In the emerging nations like China, India, and Thailand, Pb noxiousness has been the utmost premeditated communal health evils, particularly for specific hazardous professions including painting and mining (Ibrahim et al., 2006;Halttunen et al., 2007) The use of biomass such as bacteria, fungi, and algae as biosorbents have great potentials for cleaning up the environmental contaminants due to the availability of a broad range of sorption sites which can, not only, retain metallic ions and metals but also several other organic materials (Jiménez-Pranteda et al., 2012;Kinoshita et al., 2013). The chelation treatment has been found deficient of safety and effectiveness, leading us to strive for certain novel approaches against Pb lethality. Lactobacilli are found to have capabilities to bind and eliminate numerous heavy metals like Pb, cadmium, and copper in vitro (Ibrahim et al., 2006;Halttunen et al., 2007;Schut et al., 2011). A variety of approaches are employed in bioremediation and among these approaches, encapsulation of bacterial cells is considered to be the most promising due to their potential in removing specific contaminants within a carrier matrix (Bruschi et al., 2003). Encapsulation has variety of auspicious implications in multiple fields, from bioreactors to numerous medicines. Protection from severe external environments, easiness of separation, and a decreased vulnerability to adulteration by external organisms are the potential benefits of encapsulated cells. Coacervation and/or emulsifying-crosslinking and spray-drying are among the most common encapsulation approaches (San Keskin et al., 2018). There are several encapsulating compounds that have been utilized for these objectives. A frequent use of polysaccharides for microencapsulation is due to the reason as they have constituents or matrices which could be degraded by intestinal microorganisms and, consequently, allow and support the probiotics to be delivered at targeted sites in the human intestine (de Vos et al., 2010;Mahmoud et al., 2015). Lead is a widespread pollutant present into the environment with a negative impact on biological activities. It causes adverse damage to the host by inducing oxidative stress. According to several researchers LAB have been reported to possess the ability to give relief from oxidative stress by sequestering the Pb and repairing the damage caused by Pb induced oxidative stress (Fewtrell et al., 2004;Okoro et al., 2015). Numerous properties should be taken into considerations while screening out the LAB against Pb noxiousness. First of all, the LAB should possess the higher capability to bind the Pb, facilitating them to attach the Pb before the Pb could be absorbed into the intestine of the host. The ability to resist the Pb to avoid Pb poisonous is the second pre-requisite of the LAB strains. Furthermore, it is obligatory for the screened strains to retain viability into the highly acidic concentrations and harsh environments of bile and stomach to accomplish Pb elimination in the gastrointestinal tract. In our present investigation, among the seven tested strains the L. plantarum KLDS 1.0344 strain displayed the highest Pb binding capability ( Table 2) and showed a significant forbearance against the Pb. Additionally, PRS based microencapsulated L. plantarum KLDS 1.0344 presented a remarkable survival in the simulated gastrointestinal conditions (data not shown). Due to the structural differences in bacterial species different metal biosorption mechanisms have been proposed, including micro precipitation and chelation, ion exchange, complexation, and adsorption (Monachese et al., 2012). The Gram-positive bacteria contain polysaccharides, proteins, peptidoglycans, and teichoic acids in their cell walls (Schär-Zammaretti and Ubbink, 2003;Passot et al., 2015). The negatively charged functional groups are present in these contents. These functional groups act as primary sites on a bacterial surface of metal ion sorption (Mishra et al., 2013;Yadav et al., 2014). On cell surface of bacteria the carboxyl and phosphate groups (present in teichoic acids and peptidoglycans) are the key sites to bind metal ions (Kazy et al., 2009).
To imitate prolonged contact, we supplied Pb orally by means of drinking water at the concentration of 100 mg/L, the quantity of which was chosen conferring to the normal human and animal Pb ingestion, animal body weight and concentrations in the contaminated zones, for demonstration of the relevant ecological Pb exposure (Fan et al., 2008). Hereby, we have testified that encapsulated L. plantarum 1.0344, not only, demonstrated a better Pb chelating capability and might propose substantial protection to counter Pb noxiousness in vivo assisted by chelating action of PRS and lessening the Pb intensities in the blood and tissues (Figure 3C), as well as, KLDS 1.0344 prevented the variations in the levels of GSH, GSH-Px, MDA, SOD. We noticed that non-encapsulated and encapsulated L. plantarum 1.0344 have supremely significant effect on mechanism of Pb noxiousness. High MDA level accelerates the oxidative stress and the lipid peroxidation process. Ultimately affects the antioxidant defense system, by disturbing the enzyme activity of SOD, GSH-Px, and GSH  discovered the properties of L. plantarum CCFM8661 on reducing Pb concentrations in tissues and blood, improving the enzymatic action of antioxidant protection mechanism and easing the oxidative trauma  revealed that L. bulgaricus, not only, decreased the oxidative stress induced by Pb, but also, played a protective role by facilitating the reduction in the concentrations of of lipid peroxide and MDA and escalating the levels of other antioxidants, like, GSH, T-SOD, and GSH-Px in the kidneys and liver. The impairment of energy metabolism and mitochondrial dysfunction is due to the depletion of GSH (Pereira and Oliveira, 2000). It was stated that lactobacilli could sequester Pb quickly, and the bio-sorption was steady in vitro, and hence was not smooth for desorption (Halttunen et al., 2008;Schut et al., 2011).
Moreover, KLDS 1.0344 by itself did not cause the loss of crucially essential metals, like Mg, Ca, Zn, and Fe from the mice tissues (Tables 3A,B). Certain vital components even escalated in concentration, like Fe in the kidneys and Ca in the liver. Our study showed that the PRS-basedˆmicencapsulated KLDS 1.0344 therapy group contains the higher capability to excrete greater quantity of Pb through feces than non-encapsulated KLDS 1.0344 groups. Analogous results were witnessed for the other lactobacilli, which could restrain absorption of heavy metals in intestine in mice by excreting heavy metals through feces (Jomova and Valko, 2011;Zhai et al., 2013Zhai et al., , 2014. Huang et al. (2011) and Liu et al. (2018) stated that the modified starches retain the capability of sequestering Pb (Pb 2+ ) and mercury (Hg 2+ ) ions. Normally, the eminent adsorption capabilities of (modified) starches for Hg 2+ and Pb 2+ ions are 131.2 and 123.2 mg/g, correspondingly.
Moreover, San Keskin et al. (2018) observed that cyclodextrin fiber encapsulated Lysinibacillus sp. has high efficiency to remove the heavy metals(70 ± 0.2%, 58 ± 1.4%, and 82 ± 0.8% for 30 mg L −1 concentrated solutions of the Ni(II), Cr(VI), respectively). Concentrations of 30 mgL −1 are already above the acceptable limits of environmental concerns. The obtained results suggested that the cyclodextrin CD-F encapsulated Lysinibacillus sp. bio-composite system was appropriately suitable for the potential application in Ni (II), Cr (VI), and reactive dye bioremoval.
Numerous research works have described a probable relation between disruption of metal ion homeostasis and the oxidative stress (Valko et al., 2005;Jomova and Valko, 2011;Odewabi and Ekor, 2017). AST/ALT is an imperative biochemical indicator and alterations in the AST and ALT levels are frequently utilized for liver pathological studies (Vijayavel and Balasubramanian, 2006;Agrahari and Gopal, 2009). Liver cell plasma is the main place where ALT exists. Levels of ALT are elevated in the blood by changing the permeability of liver-cell-membrane when the damage of the liver cell is lower. While in contrast, the increasing levels of AST in the blood are due to the severe damage to the liver cells data presented in Figure 4F. On the basis of this discussion, it could be concluded that elevated AST/ALT ratios indicate a severe damage to the liver cells. , Liu et al. (2018), andSan Keskin et al. (2018) also described that the treatment of LAB like, L. bulgaricus could possibly improve the levels of ALT and AST, and encapsulation of LAB with modified starches could increase the capability of these bacteria to adsorb the heavy metals by proving them better choice to be adopted as natural bio-sorbents.

CONCLUSION
Lead is a lethal heavy metal and contrasting to other noxious compounds this is barely degradable. Consequently, chronic exposure even to very minute quantity could be resulted in developing adversative health effects. Taking into consideration the other effects, such as oxidative stress, body weight gain, histopathological changes and renal, hepatic damage biomarkers, we are certain of that PRS-based microencapsulated KLDS 1.0344 treatment is safe. Additionally, the intestinal pH is about 7-8 slightly alkaline, which increased the capability of PRS and KLDS 1.0344 for detoxication of Pb ++ in vivo study. Both PRS and KLDS 1.0344 contributed to alleviate the Pb levels in mice body by fecal elimination, minimal absorption of Pb to the blood, maintaining the antioxidant defense system, eventually safeguarded the major body organs from Pb toxicity. The restoration of these natural parameters in the mice with the oral administration of the PRS-based microencapsulated KLDS 1.0344 further approves the protecting properties of this probiotic against prolonged and chronic Pb toxicity.

AUTHOR CONTRIBUTIONS
ZM has designed and carried out the present research work, conducted experiments, and has written the present manuscript. This is the major part of the thesis research work of ZM. RR helped in analyzing the statistical data, elaborating, and drawing the figures. SZ and HH provided help during the experimentation. AH, AB, YD, and LW also helped with technical issues, provided help in proofreading and presenting the work in its present form. SP provided place, lab facilities, and funding for the present work.