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Evaluation of the Probiotic Profile of the Lactobacillus Acidophilus Used in Pharmaceutical and Food Applications/Avaliacao do perfil probiotico de Lactobacillus acidophilus utilizado em aplicacoes farmaceuticas e alimentares.


Probiotics are considered as GRAS ingredients (generally recognized as safe) (Mattia & Merker, 2008), and their consumption reduces the viable number of pathogens while strengthening the body's natural defenses (Bertazzoni-Minelli & Benini, 2008; Madureira et al., 2008; Larsen, Michaelsen, Paerregaard, Vogensen, & Jakobsen, 2009; Savard et al., 2011). Hence, they help boost the immune system and thus lower the risk of gastrointestinal diseases, cancer, diabetes, and elevated serum cholesterol levels while improving digestion itself (De Vrese & Schrezenmeir, 2008; Kumar et al., 2012).

The ingestion of probiotic microorganisms may be in the form of pharmaceutical preparations such as powdered compounds, tablets, or capsules, or as yogurts and other fermented foods. These products may contain only one or several distinct species of microorganisms (Nagpal et al., 2012).

The use of Lactobacillus acidophilus as a probiotic provides benefits such as reduction in abdominal pain or discomfort in patients with irritable bowel syndrome (Sinn DH, Song JH, Kim HJ, et al., 2008), reduction in total cholesterol levels, LDL-c, and triacyclglycerols in animals (Park et al., 2007; Park et al., 2008) and a reduction in insulin resistance (Andreasen et al., 2010).

The ability of probiotic microorganisms to survive and develop in the host strongly influences their probiotic effects. The microorganism that is metabolically stable in the product and survives the passage through the digestive tract with high viability may have beneficial effects when present in the host intestine (Anal & Singh, 2007).

Viability and activity are not the only key factors in the action of a probiotic. The microorganism level must be sufficiently high (Stefe, Alves, & Ribeiro, 2008). In Brazil, to market products containing probiotics, the National Agency of Sanitary Surveillance (ANVISA) requests the submission of an analysis report that proves the minimum viable quantity of the microorganism needed to exercise functional property at the end of the product's shelf life and in the use, storage, and distribution conditions (National Agency of Sanitary Surveillance [ANVISA], 2016).

The lack of information regarding the activity of probiotic microorganisms administered by means of pharmaceutical forms, such as capsules, often called nutraceuticals, and food products of different origins justifies this study, which aims to evaluate the differences in the probiotic profile.

The objective of this article is to compare the probiotic profile of Lactobacillus acidophilus of different origins. For this, their growth was evaluated in the presence of commercial use antibiotics, as well as their resistance in conditions that simulate in vitro the gastrointestinal environment. We aimed to investigate the in vitro adhesion abilities of these probiotic cultures, as well as evaluate the production capacity of bile salt hydrolase enzymes and the production of inhibitory compounds with bactericidal characteristics.

Material and methods

a. Microorganisms

Lactobacillus acidophilus from three different origins were used:

--Origin 1 (LA1): Lactobacillus acidophilus from a manipulated supplement, marketed in the form of capsules or sachets to regulate the intestinal microbiota in case of diarrhea or constipation. According to the Ache supplier's specification, each gram of lyophilized product contained [10.sup.9] CFU.

--Origin 2 (LA2): Lactobacillus acidophilus, used in food formulations as fermented products, kindly provided by SACCO[R] Brazil. According to the supplier's specification, each gram of lyophilized product contained [10.sup.11] CFU.

--Origin 3 (LA3): Lactobacillus acidophilus of allopathic origin, marketed in dispensing pharmacies, also with the purpose of regulating the intestinal microbiota. According to the supplier's specification, each capsule contained the equivalent of [10.sup.9] CFU [g.sup.-1].

b. Microorganism activation

The microorganisms were placed in 10% (v/v) TSB medium (Tryptic Soy Broth--Acumidia-Maryland) and incubated for 24 hours in an anaerobic jar at 37 [+ or -] 1[degrees]C. After this incubation period, centrifugation was performed for 5 minutes and they were washed three times with a pH 7.0 phosphate-buffered saline solution.

c. Cellular viability evaluation

Cell viability was determined by the depth seeding technique (Zayed & Winter, 1995) using the MRS agar medium (Man Rogosa and Sharp). The incubation was carried out for a period of 48h, in an anaerobic jar, at 37 [+ or -] 1[degrees]C. The analyses were performed in duplicate, with two repetitions.

For counting, plaques that presented between 30 and 300 colonies were used, and the individual result was multiplied by the respective dilution. The mean dilution results were expressed in CFU [g.sup.-1] of product.

d. Inoculum preparation

To ensure that in all tests performed the number of microbial cells added would be exactly the same, the bacterial inoculum was standardized and the absorbance was equivalent to a standard solution equal to 0.5 on the Mac Farland scale to a wavelength of 625nm, where the desired optical density was between 0.08 to 0.10, which equated to 1,5 x 108 CFU (National Committee For Clinical Laboratory Standards [NCCLS], 2015).

e. Evaluation of resistance to different commercial use antibiotics

The antimicrobial resistance profile in Lactobacillus acidophilus was determined from the antibiogram, which was performed in duplicate, with three repetitions, according to the adapted antimicrobial susceptibility technique by diffusion of the drug in disks (Charteris et al., 1998). The following antimicrobials were tested: Ampicillin (10 [micro]g), Clindamycin (2 [micro]g), Chloramphenicol (30 [micro]g), Doxycycline (30 [micro]g), Erythromycin (15 [micro]g), Gentamicin (10 [micro]g), and Tetracycline (30 [micro]g) (Laborclin, Brazil).

f. Resistance in acidic conditions

The Lactobacillus acidophilus resistance to hydrochloric acid was tested according to the procedure described by Charteris et al.

g. Determination of gastrointestinal transit tolerance

Simulating the conditions of the stomach and small intestine, the viability of the microorganisms was determined against pepsin at pH 2.0 and pancreatin at pH 8.0, respectively, according to the methodology described by Charteris et al. (1998).

h. Adherence to cell surface solvents for Lactobacilli test

The hydrophobicity of the bacterial cell surface was evaluated by measuring the microbial adhesion to solvents (MATS), as described by Rosenberg, Gutnick, and Rosenberg (1980) and Pelletier et al. (1997). (2003). The percentage of bacterial adherence to the solvent was calculated as

MATS = ((1 - A1/A0) x 100

A0 = Absorbance reading of the cell suspension in KN[O.sub.3].

A1 = Absorbance reading of the aqueous phase, after 30 minutes of exposure to organic solvents.

The isolated were classified as high (66.67 to 100%), medium (33.37 to 66.66%), and low hydrophobicity (0 to 33.33%) as proposed by Nader-Macias, Otero, Espeche, and Maldonado (2008). The results obtained were based on the average of three experiments.

i. Antagonistic substances production

To verify the production of antibacterial substances, the multilayer inhibition technique described by Diep, Havarstein, and Nes (1995) was used.

j. Bile salt hydrolase activity (BSH)

In the present study, we used the methodology by Tanaka, Hashiba, Kok, and Mierau (2000) based on the deconjugation of TDCA (sodium tauro deoxycholate hydrate--Sigma Aldrich) and GDCA (Glyco deoxy cholic acid monohydrate Sigma Aldrich) bile salts per Lactobacillus acidophilus strains.

k. Statistical analyses

For tests of resistance to different commercial use antibiotics, resistance to acid conditions, tolerance to the gastrointestinal tract and hydrophobicity, we applied the variance analysis and the averages of the treatments were compared among themselves by the Tukey test with 5% probability, using the Statistica[R]7.0 and Minitab 14[R] programs.

Results and discussion

Cellular viability evaluation

To ensure that the amount of microorganism reported on the product packaging was consistent, the microbial cell count viability test was performed. Table 1 shows the concentrations of the microorganisms under study.

The results obtained are in accordance with the information presented by the manufacturers /suppliers.

Barreto et al. (2003) evaluated the viability of Lactobacillus acidophilus, bifidobacteria, and total bacteria in 177 samples from 15 brands of probiotic products marketed in Brazil from January to August 2001. In their study, they found that most products had a total count of viable microorganisms above [10.sup.7] CFU [g.sup.-1].

Evaluation of resistance to different commercial use antibiotics

The results presented in Table 2 demonstrate that the cultures with inhibition halos greater than the reference values were considered as sensitive to antibiotics. Cultures that presented inhibition zones smaller than the reference values were considered moderately sensitive and resistant. Lactobacillus species are generally sensitive to inhibitors of protein synthesis, such as chloramphenicol, erythromycin, clindamycin, and tetracycline, and more resistant to aminoglycosides (neomycin, kanamycin, streptomycin, and gentamicin) (Darsanaki, Aliabadi, & Chakoosari, 2013). This is partially presented in our results, where all lactobacilli were inhibited by chloramphenicol, doxycycline, and tetracycline. And also by the cell wall synthesis inhibitor (ampicillin). However, when analyzing the inhibition halo of the antibiotic erythromycin, we observed that LA1 and LA2 are in the moderately sensitive range, while LA3 is resistant. Similarly, Thumu, and Halami (2012) found that Lactobacillus plantarum isolated from dairy products was resistant to erythromycin.

When analyzing the antibiotic clindamycin, LA2 was in the range between moderately sensitive and sensitive. This fact can be explained by the use of strains of different origins. Antimicrobial susceptibility evaluation studies in bacteria of the genus Lactobacillus, conducted by Danielsen and Wind (2003), indicated that the level of susceptibility is dependent on the origin of the strains.

Resistance was observed for the antibiotic gentamicin (aminoglycoside) in the three microorganisms tested. This fact occurs due to the inhibition of antibiotic transport in the bacterial cell since the entry of this drug into prokaryotic cells is O2-dependent. This explains the natural resistance of strictly anaerobic bacteria to this antibiotic (Gueimonde, Sanchez, Los Reyes-Gavilan, & Margolles, 2013).

It is also known that aminoglycosides are more widely used against Gram-negative and non-Gram-positive enteric bacteria such as the genus Lactobacillus (Gueimonde et al., 2013).

Many resistance mechanisms in probiotic cultures are attributed to complex intrinsic characteristics such as cell wall structure or metabolic properties, and impermeability is the most frequently observed intrinsic resistance mechanism (Charteris et al., 1998).

At the same time, although many strains of lactic bacteria, particularly Lactobacillus spp., are resistant to certain antibiotics, this resistance is not normally mediated by plasmids and is not transmissible (Stefe et al., 2008). This feature is beneficial as it enables the use of Lactobacillus in therapy associated with antibiotics.

Resistance to acidic conditions

In order to reach the intestine and ensure its functionality, probiotic bacteria must have resistance to gastric juice as one of its characteristics, as shown in Table 3.

The medium at pH 2.0 over the incubation time caused a gradual reduction in the number of viable cells, but at the end of 3 hours, viable cells remained.

At pH 3.0, there was no significant difference (p > 0.05) in the viable cell count for the LAs evaluated.

The ability to survive at pH 3.0 over an approximate period of three hours is a fundamental characteristic for a microorganism to have a probiotic profile, since that it is the stomach's pH after food ingestion and the average permanence time of the food under these conditions (Collado, Isolauri, Salminen, & Sanz, 2009).

It was observed that the microorganisms tested had the same growth characteristic at pH 4.0 and pH 6.5 (control pH) during the incubation period, i.e., there was no significant difference during the incubation time (p > 0.05). Although pH 4.0 was considered acid, an increase in cell viability was observed at the end of the exposure time of these microorganisms. This occurred because this pH range (from 4 to 6.5) is considered ideal for the growth of Lactobacillus species (Park & Floch, 2007).

The nature of the food affects the transit time through the stomach, but normally the food remains for 2 to 4 hours (Collado et al., 2009), as well as the pH of the gastric contents. These factors affect the action of probiotic bacteria and indicate that the recommendation of ingestion of this microorganism type, whether in the form of capsules or fermented foods. should not be made while fasting, but soon after meals so that their effects are maintained or potentiated.

Determination of tolerance to the gastrointestinal tract

In vitro methodologies represent an important way to characterize GT tolerance, since, in addition to guaranteeing reliable results, they are performed more easily than in vivo studies (Charteris et al., 1998).

As proposed by Charteris, Kelly, Morelli, and Collins. (1998), we considered tolerant microorganisms for the gastric simulation survival test those that decreased their cellular concentration to a maximum of 30%.

According to the results presented in table 4, the three strains of LA presented a considerable decrease in viability, superior to the recommended 30% for the simulation of gastric conditions, however, it is still possible to observe viable cells after 180 minutes.

We found that, of the three strains, the one that presented the highest number of viable cells at the end of the experiment was LA2--Lactobacillus acidophilus for food applications.

Vizoso Pinto, Franz, Schillinger, and Holzapfel (2006) presented a study where isolated Lactobacillus strains from African fermented dairy products as well as human intestinal isolates were identified and investigated in vitro for their functional and technological characteristics as the potential for new probiotic strains. For the test that simulates gastrointestinal conditions, in the passage through the stomach model, five strains identified as L. plantarum and two identified as L. johnsonii showed good survival.

With respect to intestinal resistance, it is recommended that the microorganism have a reduction of at most 1.5 log of its initial count. As shown in Table 5, all strains remained within this range, and LA2 was the strain that showed the greatest resistance against pancreatin.

A similar result was found by Pithva, Shekh, Dave, and Vyas (2014). When testing Lactobacillus-based commercial fermented products they found that the greatest reduction in strain viability after the simulation of intestinal transit occurred with a mean reduction of 1.3 log.

The incubation time for the gastric treatment (120 min) and intestinal fluid (180 min) test simulates food intake and the passage time from the stomach to the intestine during digestive processes (Cordonnier et al., 2015).

Adherence to surface solvents

The hydrophobicity index can be used to predict the adhesion potential of the strains by facilitating their contact with the hydrophobic surface of the eukaryotic epithelial cells or with the hydrophilic nature of the mucus covering the surface of the epithelium in some specific areas (Nader- Macias, Otero, Espeche, & Maldonado, 2008).

Bacterial adhesion depends in part on reversible or irreversible interactions. The initial and reversible stage is mediated by a complex of physicochemical interactions, including hydrophobicity and loads, which are not considered specific but important properties (Pelletier et al., 1997).

Through the microbial adhesion to solvents test (MATS), it is possible to qualitatively evaluate how polar or apolar the bacterial surface is since it would indicate the potential of adhesion of the probiotic to the apolar surfaces of the intestinal and vaginal epithelium. However, we propose that the test be only the primary indicator for microorganism adhesion (Mangoni et al., 2011).

Cell surface hydrophobicity and hydrophilicity were evaluated by separating cells between the aqueous and organic phases.

According to the classification proposed by Nader-Macias et al. (2008), where the high hydrofibicity is between 66.67 to 100%, average between 33.37 to 66.66%, and low hydrophobicity is 0 to 33.33%, we see that the adhesion of LA1 cells to xylol is in the range of medium adhesion, whereas for the ethyl acetate and chloroform solvent the adhesion may be considered high. The same profile was observed for LA2 and LA3 strains. Among the three strains evaluated, the one with the highest adhesion values was LA2.

In contrast to the results found in this work, when evaluating the cell surface hydrophobicity of isolates from six distinct species of lactobacilli from industrial products, Pelletelier et al. (1997) performed the MATS test for xylol, an organic non-polar solvent, and verified that the microorganisms studied were relatively hydrophilic, with solvent adhesion percentages varying between 2.7 and 26.5%.

The highest adhesion value for L. plantarum FAbM2 microorganisms was obtained from chloroform with a maximum of 72% (Sathyabama, Vijayabharathi, Brinda Priyadarisini, Ranjithkumar, & Bruntha, 2012).

A study with L. plantarum showed an affinity above 40% for an apolar solvent, generally present with high hydrophobic characteristics (Giarous, Chapot-Chartier, & Briandet, 2009).

According to Giarous et al. (2009), probiotic strains must have a hydrophobic surface because they have a high adhesion capacity to intestinal cells and solid materials.

The ability to adhere to mucosal surfaces of the intestine and subsequent long-term or short-term colonization has been one of the most commonly encountered criteria for the selection of probiotic strains (Lebeer, Vanderleyden, & De Keersmaecker, 2008; Collado et al., 2009).

Antagonist activity against pathogens

The mechanisms of antibacterial activity in Lactobacillus probiotic strains appear to be multifactorial (Castillo, de Moreno de LeBlanc, Galdeano, & Perdigon, 2013) and are due to the presence of bacteriocins and/or organic acids produced by them.

The bacteria tested in the present work presented antagonistic activity for Gram-positive and Gram-negative pathogens.

The three strains of L. acidophilus presented inhibitory halos for all the pathogenic microorganisms tested, as follows: Salmonella spp., Escherichia coli, Staphylococcus sp., and Listeria monocytogenes. In some plates, a greater number of halos is verified when compared to others, however, the methodology used does not allow the quantification of the activity, only determines presence or absence of inhibition.

The inhibitory effect may be due to the production of [H.sub.2][O.sub.2], lactic acid, bacteriocins (substances that act as antibiotics), or the combination of several of these compounds (Gillor, Etzion, & Riley, 2008), which are characteristic substances of these microorganisms' metabolism, demonstrating the importance and interest in the use of these bacteria in food or pharmaceutical compounds for the purpose of becoming part of the human and animal microbiota.

Using the same methodology, Pereira and Gomez (2007) reported inhibition of E. coli and S. aureus by L. acidophilus obtained from a commercial lyophilized probiotic culture.

Similar results were described by Costa, Suguimoto, Miglioranza, and Gomez (2012), who achieved inhibition of E. coli by culturing a strain of L. acidophilus through the multilayer methodology.

Bile salt hydrolase activity (BSH)

BSH is an enzyme produced by several microorganisms, including probiotics. Many studies involving the kinetics of this enzyme have reported its efficiency in hydrolyzing tauroconjugated bile salts and, because of this action, it has been demonstrated that this mechanism assists in the reduction of total blood cholesterol concentrations (Tanaka et al., 2000), which is why the production of this enzyme by probiotic bacteria has been widely studied.

For the medium containing GDCA there was no growth of LA strains.

The three strains of Lactobacillus acidophilus decongest bile salts present in a TDCA-containing medium. This effect was observed by the formation of white precipitation around the colonies in an MRS medium containing bile salts.

Evidence suggests that probiotics exert various biological health properties, one of which is the activity of anticholesterolemic bile salts through hydrolysis and cholesterol uptake (Nagpal et al., 2012). The selection of specific strains and the evidence of their efficacy results in a control of lipemic values that can be exploited to formulate new probiotic foods or supplements that, in turn, may play a role in the prevention of cardiovascular diseases.

The properties of lactobacilli, which influence cholesterol decrease, have been evaluated in vivo in several studies in humans and animal models, mostly consisting of the consumption of supplements and fermented foods containing selected Lactobacillus strains (Kumar, Batish, & Grover, 2011; Jones, Tomaro-Duchesneau, Martoni, & Prakash, 2013). Schillinger, Guigas, and Holzapfel (2005), in a study which isolated different Lactobacillus from commercial yogurts, found that all L. acidophilus strains produced precipitation zones in the BSH plaque trial.


The results obtained show that LA2 used in fermented foods was distinguished in relation to the other origins, since it presented a higher growth rate, advantage in intestinal colonization, and an antibiotic resistance profile against clindamycin, gentamicin, and erythromycin, helping to restore intestinal flora during antibiotic therapy. It registered greater resistance to digestive and intestinal enzymes and adherence to the MATS test.

Thus, it is possible to have equal or better probiotic effect using products fermented with Lactobacillus acidophilus as compared to products purchased in compounding or dispensing pharmacies.

Doi: 10.4025/actascihealthsci.v40i1.36664


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Received on April, 11, 2017.

Accepted on July 27, 2017.

License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Jucelaine Deon Schmitt (1), Luciana Oliveira de Farina (1), Marcia Simoes (1) and Luciana Bill Mikito Kottwitz (2) *

(1) Programa de Pos-Graduacao em Ciencias Farmaceuticas, Universidade Estadual do Oeste do Parana, Cascavel, Parana, Brazil. (2) Colegiado de Farmacia, Universidade Estadual do Oeste do Parana, Rua Universitaria, 2069, 85819-110, Cascavel, Parana, Brazil. * Author for correspondence. E-mail:
Table 1. Lactobacillus acidophilus viability according to origin.

Origin   [CFU.sup.-1] log   Declared reliability *

LA1            9.20                  9
LA2           11.16                  11
LA3            9.06                  9

* Viability declared in the report and/or package insert provided by
the manufacturer.

Table 2. Lactobacillus acidophilus' sensitivity to antimicrobials
according to the origin demonstrated by the mean diameter of the
inhibition halos, followed by the standard deviation.

                           Inhibition Halo mean diameter (mm)

Antibiotic                  LA1                        LA2

Ampicillin        34.00 [+ or -] 0.82 (a)    21.25 [+ or -] 2.06 (c)
Clindamycin       16.75 [+ or -] 2.88 (a)    12.00 [+ or -] 1.15 (a)
Chloramphenicol   29.50 [+ or -] 0.57 (ac)   27.25 [+ or -] 0.95 (c)
Doxycycline       23.50 [+ or -] 2.51 (c)    32.50 [+ or -] 2.08 (ad)
Erythromycin      15.70 [+ or -] 2.21 (a)    16.75 [+ or -] 0.95 (a)
Gentamicin        08.25 [+ or -] 0.5 (a)     09.25 [+ or -] 0.5 (a)
Tetracycline      20.75 [+ or -] 1.5 (b)     31.50 [+ or -] 1.9 (a)

                  Inhibition Halo mean        Sensitivity Profile *
                      diameter (mm)

Antibiotic                  LA3                          *R

Ampicillin        29.20 [+ or -] 1.89 (b)    [less than or equal to] 12
Clindamycin       16.75 [+ or -] 1.15 (a)    [less than or equal to] 8
Chloramphenicol   31.25 [+ or -] 2.75 (ab)   [less than or equal to] 13
Doxycycline       31.75 [+ or -] 0.5 (bd)    [less than or equal to] 14
Erythromycin      13.50 [+ or -] 2.38 (a)    [less than or equal to] 13
Gentamicin        09.50 [+ or -] 0.57 (a)    [less than or equal to] 12
Tetracycline      31.00 [+ or -] 1.82 (a)    [less than or equal to] 14

                       Sensitivity Profile *

Antibiotic         *MS                 *S

Ampicillin        13-15   [greater than or equal to] 16
Clindamycin       9-11    [less than or equal to] 12
Chloramphenicol   14-17   [greater than or equal to] 18
Doxycycline       15-18   [greater than or equal to] 19
Erythromycin      14-17   [greater than or equal to] 18
Gentamicin         --     [greater than or equal to] 13
Tetracycline      15-18   [greater than or equal to] 19

* Averages followed by the same letter in the line do not differ
statistically from each other by the Tukey test (p > 0.05). The
results are expressed as R (resistant), S (susceptible) or MS
(moderately susceptible) (Charteris et al., 1998a).

Table 3. Average growth (CFU [g.sup.-1] log) followed by the standard
deviation of microorganisms exposed to hydrochloric acid (HCl P.A.)
for up to 3 hours.

ORIGIN   Exposure     Exposure to different pH (CFU [g.sup.-1] log)
         (hours)             pH 2                      pH 3

LA1         0       5.46 [+ or -] 0.15 (aA)   5.85 [+ or -] 0.06 (aA)
            1       1.90 [+ or -] 0.21 (bA)   5.67 [+ or -] 0.32 (aA)
            3       1.52 [+ or -] 0.11 (cA)   5.78 [+ or -] 0.46 (aA)

LA2         0       6.08 [+ or -] 0.14 (aA)   5.87 [+ or -] 0.10 (aA)
            1       2.07 [+ or -] 0.38 (bA)   5.54 [+ or -] 0.09 (aA)
            3       1.99 [+ or -] 0.01 (bA)   4.25 [+ or -] 0.07 (bB)

LA3         0       5.78 [+ or -] 0.46 (aA)   5.57 [+ or -] 0.39 (aA)
            1       2.11 [+ or -] 0.44 (bA)   4.83 [+ or -] 0.24 (aA)
            3       1.90 [+ or -] 0.14 (bA)   4.66 [+ or -] 0.15 (aB)

ORIGIN     Exposure to different pH (CFU [g.sup.-1] log)

                  pH 4                 control pH (6.5)

LA1      5.54 [+ or -] 0.34 (aA)   5.62 [+ or -] 0.32 (bA)
         5.97 [+ or -] 0.17 (aA)   6.21 [+ or -] 0.15 (bA)
         6.01 [+ or -] 0.44 (aA)   7.18 [+ or -] 0.11 (aA)

LA2      6.06 [+ or -] 0.09 (aA)   6.12 [+ or -] 0.03 (aA)
         6.16 [+ or -] 0.02 (aA)   6.30 [+ or -] 0.19 (aA)
         6.05 [+ or -] 0.22 (aA)   6.80 [+ or -] 0.31 (aA)

LA3      5.52 [+ or -] 0.06 (aA)   5.83 [+ or -] 0.12 (Ca)
         5.89 [+ or -] 0.30 (aA)   6.27 [+ or -] 0.16 (acA)
         6.27 [+ or -] 0.37 (aA)   6.87 [+ or -] 0.18 (aA)

* Equal lowercase letters in the same column and uppercase letters on
the same line correspond to the same averages by the Tukey test (p >

Table 4. Total viable cells resistant to the gastric tolerance
simulation test at different exposure times.

Origin         Exposure to pepsin (CFU [mL.sup.-1] log)

                  1 min..                    90 min..

LA1      7.93 (aA) ([+ or -] 0.02)   5.74 (bB) ([+ or -] 0.08)
LA2      7.94 (aA) ([+ or -] 0.03)   6.04 (bA) ([+ or -] 0.11)
LA3      7.93 (aA) ([+ or -] 0.05)   5.75 (bB) ([+ or -] 0.05)

Origin    Exposure to pepsin (CFU
             [mL.sup.-1] log)

                 180 min..

LA1      3.60 (cC) ([+ or -] 0.05)
LA2      4.66 (cA) ([+ or -] 0.04)
LA3      3.79 (cB) ([+ or -] 0.03)

* Equal lowercase letters in the same row do not differ from each
other for the Tukey Test with p > 0.05. Equal uppercase letters in the
same column do not differ from each other for Tukey's test with p >

Table 5. Total viable cells resistant to the gastric transit tolerance
simulation test at different exposure times.

Origin       Exposure to pancreatin (CFU [mL.sup.-1] log)

                  1 min.                     240 min.

LA1      7.87 (aA) ([+ or -] 0.03)   6.57 (bC) ([+ or -] 0.07)
LA2      7.89 (aA) ([+ or -] 0.03)   7.38 (bA) ([+ or -] 0.04)
LA3      7.89 (aA) ([+ or -] 0.04)   6.79 (bB) ([+ or -] 0.02)

* Equal lowercase letters in the same row do not differ from each
other for the Tukey Test with p > 0.05. Equal uppercase letters in
the same column do not differ from each
other for Tukey's test with p > 0.05.

Table 6. Hydrophobicity of the Lactobacillus acidophilus strains' cell
surface by bacterial adhesion to hydrocarbons.

Origins            Adhesion                        %

                    Xylol                     Ethyl acet.

LA1       45.00 (cA) ([+ or -] 1.88)   72.52 (bB) ([+ or -] 3.01)
LA2       55.75 (cA) ([+ or -] 1,25)   84.16 (bA) ([+ or -] 1.60)
LA3       48.96 (bA) ([+ or -] 1.37)   77.34 (aB) ([+ or -] 1.89)

Origins           Chloroform

LA1       84.03 (aB) ([+ or -] 1.60)
LA2       98.41 (aA) ([+ or -] 0.90)
LA3       76.90 (aC) ([+ or -] 1.04)

* Values are represented by mean [+ or -] standard deviation of three
independent experiments. Equal lowercase letters in the same row do
not differ from each other for the Tukey Test with p > 0.05. Equal
uppercase letters in the same column do not differ from each other for
Tukey's test with p > 0.05.
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