Screening of indigenous strains of lactic acid bacteria for development of a probiotic for poultry.
ABSTRACT : In an attempt to develop a probiotic pro·bi·ot·ic
A dietary supplement containing live bacteria or yeast that supplements normal gastrointestinal flora, given especially after depletion of flora caused by infection or ingestion of an antibiotic drug. formulation for poultry feed, a number of lactic acid bacteria The Lactic Acid Bacteria (LAB) comprise a clade of Gram positive, low-GC, acid tolerant, non-sporulating, non-respiring rod or cocci that are associated by their common metabolic and physiological characteristics. (LAB) were isolated from chicken intestinal specimens and a series of in vitro experiments were performed to evaluate their efficacy as a potential probiotic candidate. A total of 650 LAB strains were isolated and screened for their antagonistic potential against each other. Among all the isolates only three isolates (TMU TMU Taipei Medical University
TMU Tokyo Metropolitan University
TMU Traffic Management Unit (BCOPD)
TMU Texture Mapping Unit (3D video rendering hardware)
TMU Time Measurement Unit 121, 094 and 457) demonstrated a wide spectrum of inhibition and were thus selected for detailed investigations. All three selected isolates were able to inhibit the growth of E. coli and Salmonella species, although to variable extent. The nature of the inhibitory substance produced by the isolates TMU121 and 094 appeared to be associated with bacteriocin bacteriocin /bac·te·rio·cin/ (bac-ter´e-o?-sin) any of a group of substances, e.g., colicin, released by certain bacteria that kill other strains of bacteria by inducing metabolic block. , as their activity was completely lost after treatment with proteolytic enzymes, while pH neutralization neutralization, chemical reaction, according to the Arrhenius theory of acids and bases, in which a water solution of acid is mixed with a water solution of base to form a salt and water; this reaction is complete only if the resulting solution has neither acidic nor and catalase catalase /cat·a·lase/ (kat´ah-las) a hemoprotein enzyme that catalyzes the decomposition of hydrogen peroxide to water and oxygen, protecting cells. enzyme had no effect on the residual activity. In contrast, isolate TMU457 was able to resist the effect of proteolytic enzymes while pH neutralization completely destroyed its activity. Attempts were made to study the acid, bile tolerance and cell surface hydrophobicity of these isolates. TMU121 showed high bile salt tolerance (0.3%) and high cell surface hydrophobicity compared to the other two strains studied, while TMU094 appeared the most pH resistant strain. Based on these results, the three selected LAB isolates were considered as potential ingredients for a chicken probiotic feed formulation and were identified to species level based on their carbohydrate fermentation pattern by using API 50CH test kits. The three strains were identified as Lactobacillus lactobacillus
Any of the rod-shaped, gram-positive (see gram stain) bacteria that make up the genus Lactobacillus. They are widely distributed in animal feeds, manure, and milk and milk products. fermentum TMU121, Lactobacillus rhamnosus TMU094, and Pediococcus pentosaceous TMU457. (Key Words : Lactic Acid Bacteria, Probiotics, In vitro, Broiler broiler
a young (about 8 weeks old) male or female chicken weighing 3 to 3.5 lb. )
The gram positive lactic acid bacteria (LAB) have been well known for thousands of years for their important role in the food industry due to their fermentative fer·men·ta·tive
1. Causing or having the ability to cause fermentation.
2. Relating to or of the nature of fermentation. capacities (McKay and Boldvin, 1990). In recent years, the role of these bacteria in health and functionality of human and animal intestine has been well emphasized, mainly because of their ability to lower the pH and to produce antimicrobial agents (Delves-Broughton, 1990; Ten Brink et al., 1994; Collins et al., 1998). Controlled introduction of bacterial cultures to chicks was originated by Nurmi and Rantala (1973) for salmonella control and, subsequently, for improvement of performance by numerous authors (Tortuero, 1973; Mulder et al., 1997; Jin et al., 1998a, b). Those bacterial cultures demonstrating antibacterial actions and possessing desirable properties were later termed probiotics. Probiotics are live, nonpathogenic bacteria that contribute to the health and balance of the intestinal tract (Fuller, 1989). They are given orally to poultry to help the birds fight illness and disease. Addition of probiotics to feed is one of the alternatives to be used as a replacement for antibiotics which have created great public concerns due to emergence of antibiotic resistance (Reid and Friendship, 2002; Patterson and Burkholder, 2003).
Most common routes of administering probiotics are feed and drinking water supplementation and, much less frequently, in ovo injection, spray and oral dosing (Ghadban, 2002). In all of the above-mentioned applications of probiotics, the microorganisms must pass through the gastrointestinal tract to their targets, such as the lower part of the intestines and ceca. Essentially, these microorganisms must survive low pH and high concentrations of bile salts available in upper parts of the gastrointestinal tract to reach the hind gut in an active and functional form and to exert their beneficial properties (Kim et al., 2006). In our research, we aimed to evaluate the probiotic potential of the LAB strains isolated from chicken intestinal specimens under in vitro conditions.
MATERIALS AND METHODS
Isolation and Identification of LAB Samples from the digestive tracts of healthy broilers at market age (42-50 days of age) were cultured in MRS MRS - Modifiable Representation System.
An integration of logic programming into Lisp.
["A Modifiable Representation System", M. Genesereth et al, HPP 80-22, CS Dept Stanford U 1980]. broth (Merck, Germany) and subcultured in MRS agar under micro-aerophilic conditions at 37[degrees], until pure isolates were obtained. A total of 659 isolates were identified as belonging to lactic acid bacteria based on their gram reaction, morphology and catalase test.
The selected LAB strains were further identified to species level by subjecting them to biochemical reactions and identifying them according to the key in Bergey's manual of determinative bacteriology bacteriology
Study of bacteria. Modern understanding of bacterial forms dates from Ferdinand Cohn's classifications. Other researchers, such as Louis Pasteur, established the connection between bacteria and fermentation and disease. (Buchanan and Gibbons, 1994). Finally, these species were confirmed by using API 50CH test kits (Bio Merieux, France) according to the manufacturer's instruction.
All cultures were maintained as stocks in MRS broth at -20[degrees]C, with 15% glycerol glycerol, glycerin, glycerine, or 1,2,3-propanetriol (prō`pāntrī'ŏl), CH2OHCHOHCH2OH, colorless, odorless, sweet-tasting, syrupy liquid. .
Antagonistic activity of the isolated LAB strains (659) against a number of pathogenic bacteria was determined by the agar well diffusion method (Schillinger and Lucke, 1989; Jin et al., 1996; Juven et al., 1991, 1992). Only those strains demonstrating a wide spectrum of activity were selected for further studies. The antibacterial activity of these strains against poultry pathogens, including Salmonella (serotypes Enteritidis, Pullorum and Typhimurium) and E. coli (serotypes O1:K1, O2:K1 and O78:K80), was also determined by the above-mentioned method. To determine the nature of the inhibitory substance produced by the LAB isolates demonstrating antibacterial activity, the cell free supernatant of these strains was subjected to 0.5 mg/ml of enzymes including pepsin pepsin, enzyme produced in the mucosal lining of the stomach that acts to degrade protein. Pepsin is one of three principal protein-degrading, or proteolytic, enzymes in the digestive system, the other two being chymotrypsin and trypsin. , trypsin trypsin, enzyme that acts to degrade protein; it is often referred to as a proteolytic enzyme, or proteinase. Trypsin is one of the three principal digestive proteinases, the other two being pepsin and chymotrypsin. , lysozyme lysozyme: see immunity.
An enyme that was first identified and named by Alexander Fleming, who recognized its bacteriolytic properties. and catalase (Lewus et al., 1991). The remaining activity was determined after 2 h of incubation at 37[degrees]C by the agar well diffusion method. Furthermore, to rule out the possibility of organic acids accounting for the inhibitory action, the cell free supernatants of the LAB isolates were neutralized with 1 M NaOH and the remaining activity determined.
The freshly grown lactic acid bacteria in MRS broth were centrifuged at 5,000 g for 10-15 min at 4[degrees]C and the pellet collected in a sterile tube. The pellet was washed twice with PBS PBS
in full Public Broadcasting Service
Private, nonprofit U.S. corporation of public television stations. PBS provides its member stations, which are supported by public funds and private contributions rather than by commercials, with educational, cultural, , pH 7.0 before inoculation in MRS broth adjusted to pH 2.0 (by addition of 1 M HCl). The mixture was enumerated for the presence of viable cells after 2 h by measuring the OD (650 nm) and survival count. The strains exhibiting pH tolerance of 2.0 exceeding 1 h of incubation were considered as selection criteria (Gilliland et al., 1984; Toit et al., 1998).
Bile salt tolerance was assayed by the method of Gilliland and Walker (1990). The growth of the LAB strains was monitored in MRS broth supplemented with 0.3 and 1.0% W/V of bile salts (Quelab, Canada). At hourly intervals, the bacterial growth was monitored by measuring absorbance absorbance /ab·sor·bance/ (-sor´bans)
1. in analytical chemistry, a measure of the light that a solution does not transmit compared to a pure solution. Symbol .
2. at 650 nm for a period of 12 h. The bile tolerance of each strain was based on the time in minutes required for the absorbance value to increase by 0.3 units (Erkkila and Petaja, 2000).
Cell surface hydrophobicity
The bacterial adhesion to hydrocarbons (BATH) test was adopted to screen the isolated lactic acid bacteria for their cell surface hydrophobicity, using hydrocarbon (hexadecane) by the method of Gusils et al. (1999).
Antibiotic susceptibility of the three selected isolates was determined using commercial antibiotic discs (Padtan Teb, Iran). The diameters of clear zone appearing around the discs were measured and recorded using a digital caliper (Treagan and Pulliam, 1982). All the tests were run in triplicate and the results compared to determine the susceptibility of the strains to given antibiotics.
All quantitative data were subjected to analysis of variance using SAS (1) (SAS Institute Inc., Cary, NC, www.sas.com) A software company that specializes in data warehousing and decision support software based on the SAS System. Founded in 1976, SAS is one of the world's largest privately held software companies. See SAS System. (SAS, 1990). A test of least significant differences was used to separate means; differences between means were considered statistically significant at p<0.05 (Steel and Torrie, 1980).
RESULTS AND DISCUSSION
A total of 659 isolates appearing as gram positive cocci cocci /coc·ci/ (kok´si) plural of coccus.
[L.] plural of coccus. or rods, catalase negative and non-spore forming were identified as lactic acid bacteria (LAB) and were further screened for their probiotic properties in vitro. If a probiotic preparation is used mainly for excluding potential pathogenic microorganisms, antagonistic properties are of utmost importance (Huis in't Veld veld or veldt (both: vĕlt, Du. fĕlt) [Du.,=field], term applied to the grassy undulating plateaus of the Republic of South Africa and of Zimbabwe. and Shortt, 1996). In our studies, only three isolates demonstrated a wide spectrum of inhibitory action when tested against each other and were thus selected for detailed investigations (Table 2). These isolates were further identified according to their morphological and cultural properties and an API 50 CHL CHL crown-heel length. kit analyzed by API LAB Plus software version 4.0 database (Bio Merieux, France). A brief list of important morphological and biochemical results used in identification procedures is illustrated (Table 1). The selected LAB isolates were able to inhibit the growth of some poultry pathogens against which they were tested, although to a variable extent. All three strains appeared more effective in inhibiting the growth of Salmonella than E. coli serotypes. S. Pullorum was found to be the most susceptible of all the Salmonella serotypes tested in this study. Similar results have been observed previously by Jin et al. (1996).
As reported earlier, the antagonistic activity of LAB towards pathogens can be attributed to the production of bactericidal bactericidal /bac·te·ri·ci·dal/ (bak-ter?i-si´d'l) destructive to bacteria.
An agent that destroys bacteria (e.g. substances like bacteriocins, organic acids and hydrogen peroxide (Upreti and Hinsdill, 1975; Joerger and Klaenhammer, 1986). During our investigations we evaluated the nature of the inhibitory substance produced by the three selected LAB strains (Table 3). The inhibitory effects of the culture supernatants of LAB isolates were retained after treatment with catalase and lysozyme, which eliminates the involvement of hydrogen peroxide and carbohydrate moiety moiety: see clan. in inhibitory actions. In contrast to P. pentosaceus TMU457, treatment of the culture supernatant fluids of L. fermentum TMU121 and L. rhamnosus TMU094 with proteolytic enzymes completely destroyed the inhibitory effects in these two strains, indicating the protein nature of the antagonistic substances. Consequently, the antagonistic action in these two species may be attributed to the presence of bacteriocin or bacteriocin-like substance. However, the culture supernatant fluid of P. pentosaceus TMU457 lost its inhibitory action after pH neutralization, showing the possibility of organic acids in antagonistic effects in this isolate. Similarly to our results, Gusils et al. (2002) reported that the inhibitory action of 100 LAB strains isolated from the gastrointestinal tract of pigs was not affected by catalase treatment, while pH neutralization resulted in complete loss of activity.
One of the most important properties for a probiotic to provide health benefits is that it must be able to overcome physical and chemical barriers such as acid and bile in the gastrointestinal tract (Gibson et al., 2000). Stresses to organisms begin in the stomach, with pH between 1.5 and 3.0, and in the upper intestine which contains bile (Lankaputhra and Shah, 1995; Corzo and Gilliland, 1999). Although stomach pH can be as low as 1.0, in most in vitro assays pH 3.0 has been preferred (Garriga et al., 1998; Suskovic et al., 2001). Thus, survival at pH 3.0 for 2 h and at a bile concentration of 1,000 mg/L is considered an optimal acid and bile tolerance for probiotic strains (Usman, 1999). The acid and bile tolerance of the three selected LAB isolates is presented in Table 4. In this study, one of the strains designated TMU094, identified as L. rhamnosus, was able to resist low pH values of 2.0 and showed maximum growth at this pH within an hour of incubation. However, L. fermentum TMU121 showed moderate resistance to this pH value and lost about half of its viable counts within an hour of incubation, while P. pentosaceus TMU457 showed a sharp decline in its growth rate immediately after exposure to this pH (2.0). This phenomenon has previously been observed in a number of probiotic bacteria where a substantial decrease in the viability of strains was often observed at pH 2.0 or below (Hood and Zottola, 1988; Gupta et al., 1996). However, as reported by Prasad Prasāda (Sanskrit: प्रसाद), prasād/prashad (Hindi), Prasāda in (Kannada), prasādam (Tamil), or prasadam and his co-workers (1999), the probiotic strains are likely to be buffered by food or other carrier matrix molecules following consumption and are thus not likely to be exposed to the extremes of pH in the stomach.
Another important characteristic for a probiotic that enables it to survive and then grow and exert its action in the small intestine is its bile tolerance. Selection of bile tolerant strains at bile concentrations between 0.1 and 4.0% w/v in growth media is typical (Gilliland and Speck, 1977; Mayara-Makinen et al., 1983). Gilliland et al. (1984) reported that bile tolerant lactobacilli Lactobacilli,
n a type of bacteria that may play an important role in tooth decay. It is usually found in small amounts in dental plaque. Its concentration increases with high sugar intake. occur in high numbers in the upper section of the intestine. Although the bile concentrations in the gastro-intestinal tract vary, the mean intestinal bile concentration is believed to be 0.3% w/v (Sjovall, 1959; Gilliland et al., 1985). In our studies, the most bile resistant strain was L. fermentum TMU121 which was able to survive in the presence of high bile salt concentrations (0.3%), while P. pentosaceus TMU457 showed minimum growth in the presence of this salt. Owing to the high tolerance of bile salt by L. fermentum TMU121, we expect the strain to be effective in bile salt deconjugation and consequently effective in lowering serum cholesterol in broilers. This phenomenon was also observed by Begley and his colleagues (2005), who reported that hydrolysis hydrolysis (hīdrŏl`ĭsĭs), chemical reaction of a compound with water, usually resulting in the formation of one or more new compounds. of bile salts by bile tolerant bacteria results in increased usage of cholesterol to synthesize new bile salts and this resulted in lowering of serum cholesterol levels. However, it is worth mentioning that too high bile salt hydrolase hydrolase /hy·dro·lase/ (hi´dro-las) one of the six main classes of enzymes, comprising those that catalyze the hydrolytic cleavage of a compound.
n. activity in the intestinal lumen can result in low availability of conjugated bile salts needed for lipid digestion (Kim and Lee, 2005).
The beneficial effect of probiotic bacteria has been attributed to their ability to colonize col·o·nize
v. col·o·nized, col·o·niz·ing, col·o·niz·es
1. To form or establish a colony or colonies in.
2. To migrate to and settle in; occupy as a colony.
3. human and animal gastrointestinal tracts (Dharmawan et al., 2006). Several factors are involved in the adhesion of probiotics; one is the hydrophobicity of the bacterial cell surface. It has been reported by Wadstrom and his co-workers (1987) that, compared to hydrophilic hydrophilic /hy·dro·phil·ic/ (-fil´ik) readily absorbing moisture; hygroscopic; having strongly polar groups that readily interact with water.
adj. strains, hydrophobic lactobacilli adhered better to intestinal epithelial cells. As bacterial cells alter their membrane fluidity under various environmental conditions, growth conditions may have a profound effect on the fatty acid composition of their lipids and subsequently on the hydrophobicity and adhesion ability of bacterial strains. As Table 4 depicts, L. rhamnosus TMU094 had the highest cell surface hydrophobicity compared to L. fermentum TMU121 and P. pentosaceus TMU457. As suggested by others, the high cell surface hydrophobicity of the mentioned strain could indicate its potential to attach to the epithelial cell lining of the intestine and resist the movement of digesta (Yu et al., 2007).
Antibiotic susceptibility profiles of selected LAB are shown in Table 5. All three LAB had some degree of antibiotic resistance against some of the tested antibiotics. In a previous report, Nemcova et al. (1997) investigated the antimicrobial susceptibility of 13 lactobacilli strains isolated from suckling piglets and found they were susceptible to many common feed additive antibiotics. Although it is clear that simultaneous application of susceptible probiotics with oral antibiotics is generally unreasonable, in the case of microbial microbial
pertaining to or emanating from a microbe.
the breakdown of organic material, especially feedstuffs, by microbial organisms. infection it might be possible to use these resistant probiotics in combination with appropriate antibiotics (Marounec and Rada, 1995).
To conclude, we might suggest the three selected LAB strains, namely Lactobacillus rhamnosus TMU094, Lactobacillus fermentum TMU121 and Pediococcus pentosaceus TMU457, to be potential candidates in developing a probiotic formulation for poultry feed. Although all three strains varied in some of their properties, when used in combination they could provide beneficial and desirable properties as a probiotic.
Received January 16, 2008; Accepted May 6, 2008
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M. A. Karimi Torshizi, Sh. Rahimi *, N. Mojgani (1), S. Esmaeilkhanian (2), and J. L. Grimes (3)
Department of Poultry Science, College of Agriculture, Tarbiat Modares University Colleges
Tarbiat Modares University (TMU) is a fully Accredited Graduate University and a prestigious center for higher education in Iran. TMU has 7 colleges: Arts, Engineering, Agriculture, Basic Sciences, Humanities, Natural Resources, Marine Sciences and Medical Sciences. Tehran, P.O. Box 14115-336, Iran
(1) Department of Biotechnology The Centre for Biotechnology at Acharya Nagarjuna University was established in year 1994 inaugurated by the then Secretary, Department of Biotechnology, Government of India, Dr.C.R.Bhatia. The centre was offering two academic programs, M.Sc. (Biotechnology) and M.Tech. , Razi Vaccine and Serum Research Institute, Karaj, Iran.
(2) Department of Biotechnology, Animal Science Research Center, Esfehan, Iran.
(3) Department of Poultry Science, North Carolina State University History
* Corresponding Author: Sh. Rahimi. Tel: +98-21-44196522, Fax: +98-21-44196524, E-mail: firstname.lastname@example.org
Table 1. Some important morphological and biochemical data used in isolate identification P. L. L. pentosaceus fermentum rhamnosus TMU457 TMU121 TMU094 Morphology Cocci * Rod Rod L-arabinose + - - D-xylose + - - L-sorbose - - + L-rhamnose + - + Inositol - - + D-mannitol - - + D-sorbitol - - + Methyl-a D- - - + Glucopyranoside N-acetyl glucosamine + - + Amygdalin + - + Arbutin + - + D-maltose - + + D-sucrose - + - D-trehalose + - + D-melezitose - - + Gentibiose + - + D-turanose - - + D-xylose - - + D-tagatose + - + Potassium 2-Keto + - - gluconate * Diplococcus. + : Able to ferment the substrate. - : Not able to ferment the substrate. Table 2. Antagonistic activity demonstrated by the three selected LAB strains assayed by measuring the zone diameter around the wells (Mean [+ or -] SD) LAB Escherichia coli O78:K80 O2 :K1 P. pentosaceus TMU457 16.4 (a,**) [+ or -] 0.9 14.1 (a,*) [+ or -] 1.0 L. fermentum TMU121 11.7b [+ or -] 2.1 10.2b [+ or -] 1.3 L. rhamnosus TMU094 10.5b [+ or -] 1.3 10.4b [+ or -] 2.0 LAB Escherichia coli Salmonella O1:K1 Enteritidis P. pentosaceus TMU457 16.7 (a,*) [+ or -] 1.4 17.3 (a,*) [+ or -] 0.6 L. fermentum TMU121 11.9 (b) [+ or -] 2.1 13.7 (b) [+ or -] 1.5 L. rhamnosus TMU094 12.4 (b) [+ or -] 2.0 14.7 (b) [+ or -] 1.5 LAB Salmonella Pullorum Typhimurium P. pentosaceus TMU457 20.3 (a,**) [+ or -] 1.5 17.7 (a,**) [+ or -] 1.5 L. fermentum TMU121 16.0 (b) [+ or -] 1.0 13.0 (b) [+ or -] 1.0 L. rhamnosus TMU094 17.0 (b) [+ or -] 1.0 14.0 (b) [+ or -] 1.5 (a, b) Means with different superscripts in columns are significantly different (* p<0.05, ** p<0.01). Table 3. Nature of antagonistic properties exerted by culture supernatant of three selected LAB Supernatant P. Pentosaceus L. fermentum L. rhamnosus treatment TMU457 TMU121 TMU094 Control + + + pH neutralization - + + Catalase + + + Pepsin - - - Trypsin + - - Lysozyme + + + + Inhibitory effect observed/- Inhibitory effect not observed. Table 4. Acid and bile tolerance and degree of hydrophobicity of three selected LAB strains (Mean [+ or -] SD) Selected LAB % Survivability at pH 2.0 after 2 h P. pentosaceus TMU457 55.89 (b) [+ or -] 1.86 L. fermentum TMU121 51.58 (b) [+ or -] 1.48 L. rhamnosus TMU094 67.76 (a) [+ or -] 2.66 Selected LAB OD (650 nm) in the presence of 0.3% bile salt after 12 h P. pentosaceus TMU457 35.00 (b) [+ or -] 4.58 L. fermentum TMU121 296.67 (a) [+ or -] 15.28 L. rhamnosus TMU094 43.67 (b) [+ or -] 3.51 Selected LAB Hydrophobicity (%) P. pentosaceus TMU457 3.64 (b) [+ or -] 0.19 L. fermentum TMU121 79.94 (a) [+ or -] 9.70 L. rhamnosus TMU094 93.53 (a) [+ or -] 3.10 (a, b) Means with different superscripts in columns are significantly different (p<0.01). Table 5. Antibiotic susceptibility profile of three selected LAB Antibiotics P. pentosaceus L. fermentum L. rhamnosus TMU457 TMU121 TMU094 Amikasin S I R Enrofloxacin R R R Cephalexin R R R Gentamicin S S S Kanamycin S S I Chloramphenicol S S I Tetracycline R S R Trimethoprim R I R +Sulfamethoxazole Lincospectin R S S Flumequin I S I Novobiocin R R R Nalidixic acid R S R Synotrime S S S Penicilin R R R Vancomicin R R R Bacitracin I S I Neomycin R R R R = Resistant; I = Intermediate; S = Susceptible.