Wikipedia

Lactobacillus acidophilus

(Redirected from Acidophilus milk)

Lactobacillus acidophilus (Neo-Latin 'acid-loving milk-bacillus') is a rod-shaped, Gram-positive, homofermentative, anaerobic microbe first isolated from infant feces in the year 1900.[1] The species is commonly found in humans, specifically the gastrointestinal tract and oral cavity as well as some speciality fermented foods such as fermented milk or yogurt, though it is not the most common species for this. The species most readily grows at low pH levels (below 5.0), and has an optimum growth temperature of 37 °C. Certain strains of L. acidophilus show strong probiotic effects, and are commercially used in dairy production. The genome of L. acidophilus has been sequenced.

Lactobacillus acidophilus
"Lactobacillus acidophilus", Numbered ticks are 11 μm (micrometers)
Lactobacillus acidophilus, Numbered ticks are 11 μm
Scientific classification Edit this classification
Domain: Bacteria
Phylum: Bacillota
Class: Bacilli
Order: Lactobacillales
Family: Lactobacillaceae
Genus: Lactobacillus
Species:
L. acidophilus
Binomial name
Lactobacillus acidophilus
(Moro 1900) Hansen & Mocquot 1970

L. acidophilus has antagonistic effects on the growth of Staphylococcus aureus, Escherichia coli, Salmonella typhimurium, and Clostridium perfringens.[2] Out of the four organisms, Staphylococcus aureus is the most affected. Along with S. aureus, the other Gram-positive bacteria, C. perfringens, was affected more by L. acidophilus, than the two other bacteria that are Gram-negative. L. acidophilus is found to also reduce oral plaque formation by Streptococcus mutans.[3]

History

edit

Lactobacillus acidophilus was first isolated from the human gastrointestinal tract in 1900 by Ernst Moro with the original name Bacillus acidophilus. Over time, there have been many changes to the methods for characterizing taxonomy of organisms, leading to the genus distinction of Lactobacillus in 1929. Complication around finding the original strain arose when multiple strains of a single isolate were given a variety of names. Most studies on L. acidophilus was focused on one particular strain, Lactobacillus acidophilus NCFM. With the large amount of information discovered about L. acidophilus NCFM, the US Food and Drug Administration has adjudged the microbe to be an approved ingredient in beverages, dairy products, and other probiotic foods.[4]

Biological and biochemical features

edit

Morphology

edit
 
Lactobacillus acidophilus image taken with a scanning electron microscope (SEM).
 
A Lactobacillus acidophilus culture

Lactobacillus acidophilus is an immobile rod-shaped (bacillus), gram-positive organism that ranges in size from 2-10 μm in size. L. acidophilus has one phospholipid bilayer membrane with a large cell wall consisting of peptidoglycan exterior to the membrane. The cell wall of L. acidophilus is interwoven with teichoic acids and surface proteins, with anionic and neutral polysaccharides as well as an S-layer lining the exterior of the cell.[5] The S-layer proteins of L. acidophilus have been shown to adhere to epithelial cells as well as mucus and other extracellular proteins.[6] The S-layer is made of two structural domains. The C-terminal domain is responsible for cell wall anchoring, while the N-terminal domain is responsible for interacting with the cell environment, as well as S-layer self assembly.[6] In the L. acidophilus species, the N-terminal region shows high amino acid variability along with low sequence homology (31-72%). However, the C-terminus shows low amino acid variability and high amino acid sequence homology (77-99%).[6]L. acidophilus does not have any extracellular means of motion like a flagellum or pilli, and therefore is an immobile microbe.

 
Lactobacillus acidophilus under microscope with dark light background.

Metabolism

edit
 
Pathway by which glucose is converted to lactic acid as a means of energy production

L. acidophilus is a homofermentative anaerobic microorganism, meaning it only produces lactic acid as an end product of fermentation; and that it can only ferment hexoses (not pentoses) by way of the EMP pathway (glycolysis).[5] L. acidophilus has a slower growth time in milk than when in a host due to limited available nutrients. Because of its use as a probiotic in milk, a study done by the American Journal of Dairy Science examined the nutrient requirements of L. acidophilus in an effort to increase its low growth rate. The study found that glucose and the amino acids cysteine, glutamic acid, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tyrosine, valine, and arginine are essential nutrients to the growth of L. acidophilus, with glycine, calcium-pantothenate, and Mn2+ acting as stimulatory nutrients.[7] The study helps to explain the low growth rate of L. acidophilus in milk, as some of the amino acids necessary to L. acidophilus growth are lacking in milk. Adding amino acids with high rates of consumption to fermented milk is a possible solution to the problem.[7]

Genomics

edit

The specialization of prokaryotic genomes is distinguishable when recognizing how the prokaryote replicates its DNA during replication. In L. acidophilus, replication begins at an origin called oriC and moves bi-directionally in the form of replication forks.[5] The DNA is synthesized continuously on the leading strand and in discontinuous Okazaki fragments on the lagging strand with help from the DNA polymerase III enzyme.[8] An RNA primer is needed to initiate the DNA synthesis on the leading and lagging strands. DNA polymerase III follows the RNA primer with the synthesis of DNA in the 5' to 3' direction.[8] L. acidophilus consists of a small genome with a low guanine-cytosine content, approximately 30%.[5] A study comparing 46 genomes of varying strains of L. acidophilus found the genome size ranged from 1.95 Mb to 2.09 Mb, with an average size of 1.98 Mb.[1] The average number of coding sequences in the genome was 1780, with the strains isolated from fermented foods and commercial probiotics having more coding sequences on average than those isolated from humans.[1] L. acidophilus has an open state pan-genome (all of the genes within a species), meaning that the pan-genome size increased as the number of genomes sequenced increased. The core-genome (the genes shared by all individuals of a species) consist of around 1117 genes in the case of L. acidophilus. [1] Genetic analysis also revealed that all L. acidophilus strains contained at least 15 families of glycosyl hydrolases, which are the key enzymes in carbohydrate metabolism. Each of the 15 GH families were involved in metabolizing common carbohydrates, such as glucose, galactose, fructose, sucrose, starch, and maltose. Genes encoding antibiotic resistance by means of antibiotic efflux, antibiotic target alteration, and antibiotic target protection were present in all L. acidophilus strains, providing protection against 18 different classes of antibiotic across all strains. Fluoroquinolone, glycopeptide, lincosamide, macrolide and tetracycline were the five classes of antibiotic to which L. acidophilus displayed the highest level of tolerance, with more than 300 genes relevant to these classes.[1]

Environment

edit
 
Columnar epithelial cells from a mammal's intestinal tract. L. acidophilus easily adheres to and commonly grows on this cell type

L. acidophilus grows naturally in the oral, intestinal, and vaginal cavities of mammals.[9] Nearly all Lactobacillus species have special mechanisms for heat resistance which involves enhancing the activity of chaperones. Chaperones are highly conserved stress proteins that allow for enhanced resistance to elevated temperatures, ribosome stability, temperature sensing, and control of ribosomal function at high temperatures.[10] This ability to function at high temperatures is extremely important to cell yield during the fermentation process, and genetic testing on L. acidophilus in order to increase its temperature tolerance is currently being done.[1] When being considered as a probiotic, it is important for L. acidophilus to have traits suitable for life in the gastrointestinal tract. Tolerance of low pH and high toxicity levels are often required. These traits vary and are strain specific. Mechanisms by which these tolerances are expressed include differences in cell wall structure, along with other changes is protein expression.[9] Changes in salt concentration have been shown to affect L. acidophilus viability, but only after exposure to higher salt concentrations. In another experiment highlighted by the American Dairy Science Association, viable cell counts only showed a significant reduction after exposure to NaCl concentrations of 7.5% or higher.[11] Cells were also observed to distinctly elongate when grown in conditions of 10% NaCl concentration or higher.[11] L. acidophilus is also very well suited for living in a dairy medium, as fermented milk is the ideal method of delivery for introducing L. acidophilus into a gut microbiome.[7] The viability of L. acidophilus cells encapsulated by spray drying technology stored at refrigerated condition (4 °C) is higher than the viability of cells stored at room temperature (25 °C).[12]

Quorum sensing

edit

Quorum sensing among cells is the process among which cell signaling can lead to coordinated activities which can ultimately help bacteria control gene expression in a consecutive sequence. This is accomplished via detection of small autoinducers which are secreted in response to increasing cell-population density.[13] In Lactobacillus acidophilus, which can be found in the gastrointestinal tract, quorum sensing is important for bacterial interaction when considering biofilm formation and toxin secretion.[14] In L. acidophilus, along with many other bacteria, the luxS-mediated quorum sensing is involved in the regulation of behavior. In monoculture, the production of luxS increased during the exponential growth phase and started to plateau as it progressed to the stationary phase. Up-regulation of luxS can occur when L. acidophilus is placed in co-cultivation with another Lactobacillus species.[13]

Vaginal microbiota

edit

Lactobacillus acidophilus is relatively rare in the vaginal microbiome;[15][16][17] it is more common in the gut.[16] Other species in the genus are more common, including Lactobacillus crispatus, Lactobacillus gasseri, Lactobacillus jensenii, and Lactobacillus iners.[18][19][20][21] In experiments, L. acidophilus seemed to decrease Candida albicans’ ability to adhere to vaginal epithelial cells; however, L. acidophilus’ use in preventing yeast infections is unclear because this species of Lactobacilli has also been found not to have a very strong ability to adhere to (and thereby colonize) the vaginal cells.[22]

Therapeutic uses

edit
 
A capsule containing L. acidophilus used for vaginal health

Research has shown that the presence of L. acidophilus can produce a variety of probiotic effects in humans, such as acting as a barrier against pathogens, assisting in lactose digestion, enhancing immune response, and reducing cholesterol level. L. acidophilus must exist in concentrations of 10^5 - 10^6 c.f.u (colony-forming units) per mL in order for these effects to be seen.[8] A study conducted at the Wake Forest School of Medicine examined the effects of L. acidophilus on the structure and composition of the gut microbiome of mice with respect to the age of the mice. The research established the importance of the interactions between microbes within a gut microbial environment on the overall health of the organism, and the data showed that mice supplemented with L. acidophilus had reduced proteobacteria levels, and increased levels of other probiotic bacteria when compared to other mice of similar age.[23] Another study conducted at Maranatha Christian University studied the impact of L. acidophilus cell free supernatants (a liquid medium containing the metabolites produced by microbial growth)[24] on the growth pattern of Salmonella typhi, the microbe associated with Typhoid fever. The study showed that the presence of L. acidophilus metabolites significantly inhibited the growth curves displayed by S. typhi,[25] supporting the idea that L. acidophilus presence has a positive impact on the species makeup of a gut microbial community, providing the organism with intestinal health benefits. The innate immune system of L. acidophilus also produces antimicrobial peptides.[26] The group of short peptides found there have shown antimicrobial properties such as their strength against viruses and other cell types, including cancer cells.[27] There is also some evidence supporting the use of a symbiotic gel (containing L. acidophilus) in treating gastrointestinal symptoms in patients who had received a hemodialysis treatment. This gel also reduced the occurrence of vomit, heartburn, and stomachaches. Further study concerning this subject is needed to draw firm conclusions.[28]

Dairy industry usage

edit
 
An example of fermented milk, a dairy product L. acidophilus is commonly added to for probiotic effects

As stated in a journal from the American Dairy Science Association, "Lactobacillus acidophilus is a commercial strain and probiotic that is widely used in the dairy industry to obtain high-quality fermentation products."[7] Increased levels of beneficial bacteria, and decreased levels of pathogenic bacteria within the intestine due to the consumption of fermented milk containing strains of L. acidophilus has a range of probiotic effects. Reduced serum cholesterol levels, stimulated immune response, and improved lactic acid digestion are all probiotic effects associated with intestinal L. acidophilus presence. L. acidophilus was also effective in reducing Streptococcus mutans levels in saliva, as well as decreasing risk factors associated with the development of nonalcoholic fatty liver disease.[7] The strain of L. acidophilus that has been most widely researched, and is most widely used as a probiotic and is referred to as NCFM.[1]

The most common species of Lactobacillus for use in the production of yoghurt is Lactobacillus delbrueckii subsp. bulgaricus.

Side effects

edit

Although probiotics are generally safe, when they are used by oral administration there is a small risk of passage of viable bacteria from the gastrointestinal tract to the blood stream (bacteremia), which can cause adverse health consequences.[29] Some people, such as those with a compromised immune system, short bowel syndrome, central venous catheters, cardiac valve disease and premature infants, may be at higher risk for adverse events.

See also

edit

References

edit
  1. ^ a b c d e f g Huang Z, Zhou X, Stanton C, Ross RP, Zhao J, Zhang H, et al. (September 2021). "Comparative Genomics and Specific Functional Characteristics Analysis of Lactobacillus acidophilus". Microorganisms. 9 (9): 1992. doi:10.3390/microorganisms9091992. PMC 8464880. PMID 34576887.
  2. ^ Gilliland SE, Speck ML (December 1977). "Antagonistic Action of Lactobacillus acidophilus Toward Intestinal and Foodborne Pathogens in Associative Cultures 1". Journal of Food Protection. 40 (12): 820–823. doi:10.4315/0362-028x-40.12.820. PMID 30736216.
  3. ^ Tahmourespour A, Kermanshahi RK (February 2011). "The effect of a probiotic strain (Lactobacillus acidophilus) on the plaque formation of oral Streptococci". Bosnian Journal of Basic Medical Sciences. 11 (1): 37–40. doi:10.17305/bjbms.2011.2621. PMC 4362563. PMID 21342140.
  4. ^ Bull M, Plummer S, Marchesi J, Mahenthiralingam E (December 2013). "The life history of Lactobacillus acidophilus as a probiotic: a tale of revisionary taxonomy, misidentification and commercial success". FEMS Microbiology Letters. 349 (2): 77–87. doi:10.1111/1574-6968.12293. PMID 24152174.
  5. ^ a b c d Crawley AB, Barrangou R (2018-08-01). "Conserved Genome Organization and Core Transcriptome of the Lactobacillus acidophilus Complex". Frontiers in Microbiology. 9: 1834. doi:10.3389/fmicb.2018.01834. PMC 6099100. PMID 30150974.
  6. ^ a b c Kong W, Gan J, Su M, Xiong B, Jiang X, Zhang T, et al. (October 2022). "Identification and Characterization of Domains Responsible for Cell Wall Binding, Self-Assembly, and Adhesion of S-layer Protein from Lactobacillus acidophilus CICC 6074". Journal of Agricultural and Food Chemistry. 70 (40): 12982–12989. doi:10.1021/acs.jafc.2c03907. PMID 36190122. S2CID 252681628.
  7. ^ a b c d e Meng L, Li S, Liu G, Fan X, Qiao Y, Zhang A, et al. (January 2021). "The nutrient requirements of Lactobacillus acidophilus LA-5 and their application to fermented milk". Journal of Dairy Science. 104 (1): 138–150. doi:10.3168/jds.2020-18953. PMID 33131816. S2CID 226234977.
  8. ^ a b c Alberts BM (1987). "Prokaryotic DNA Replication Mechanisms". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 317 (1187): 395–420. Bibcode:1987RSPTB.317..395A. doi:10.1098/rstb.1987.0068. ISSN 0080-4622. JSTOR 2396708. PMID 2894677. S2CID 39640563.
  9. ^ a b Horackova S, Vesela K, Klojdova I, Bercikova M, Plockova M (August 2020). "Bile salt hydrolase activity, growth characteristics and surface properties in Lactobacillus acidophilus". European Food Research & Technology. 246 (8): 1627–1636. doi:10.1007/s00217-020-03518-8. S2CID 218877607. Retrieved November 17, 2022.
  10. ^ Adikari AM, Priyashantha H, Disanayaka JN, Jayatileka DV, Kodithuwakku SP, Jayatilake JA, et al. (October 2021). "Isolation, identification and characterization of L actobacillus species diversity from Meekiri: traditional fermented buffalo milk gels in Sri Lanka". Heliyon. 7 (10): e08136. Bibcode:2021Heliy...708136A. doi:10.1016/j.heliyon.2021.e08136. PMC 8503854. PMID 34660933.
  11. ^ a b Gandhi A, Shah NP (April 2016). "Effect of salt stress on morphology and membrane composition of Lactobacillus acidophilus, Lactobacillus casei, and Bifidobacterium bifidum, and their adhesion to human intestinal epithelial-like Caco-2 cells". Journal of Dairy Science. 99 (4): 2594–2605. doi:10.3168/jds.2015-10718. hdl:10722/238772. PMID 26874411.
  12. ^ Arepally D, Reddy RS, Goswami TK (2020). "Encapsulation of Lactobacillus acidophilus NCDC 016 cells by spray drying: characterization, survival after in vitro digestion, and storage stability". Food & Function. 11 (10): 8694–8706. doi:10.1039/D0FO01394C.
  13. ^ a b Moslehi-Jenabian S, Vogensen FK, Jespersen L (October 2011). "The quorum sensing luxS gene is induced in Lactobacillus acidophilus NCFM in response to Listeria monocytogenes". International Journal of Food Microbiology. 149 (3): 269–273. doi:10.1016/j.ijfoodmicro.2011.06.011. PMID 21784546.
  14. ^ Uhlig F, Hyland NP (May 2022). "Making Sense of Quorum Sensing at the Intestinal Mucosal Interface". Cells. 11 (11): 1734. doi:10.3390/cells11111734. PMC 9179481. PMID 35681429.
  15. ^ Eschenbach DA, Davick PR, Williams BL, Klebanoff SJ, Young-Smith K, Critchlow CM, et al. (February 1989). "Prevalence of hydrogen peroxide-producing Lactobacillus species in normal women and women with bacterial vaginosis". Journal of Clinical Microbiology. 27 (2): 251–256. doi:10.1128/jcm.27.2.251-256.1989. PMC 267286. PMID 2915019.
  16. ^ a b Bilodeau K (2019-12-27). "Should you use probiotics for your vagina?". Harvard Health. Retrieved 2024-04-21.
  17. ^ Antonio MA, Hawes SE, Hillier SL (December 1999). "The identification of vaginal Lactobacillus species and the demographic and microbiologic characteristics of women colonized by these species". The Journal of Infectious Diseases. 180 (6): 1950–1956. doi:10.1086/315109. PMID 10558952.
  18. ^ Fijan S (May 2014). "Microorganisms with claimed probiotic properties: an overview of recent literature". International Journal of Environmental Research and Public Health. 11 (5): 4745–4767. doi:10.3390/ijerph110504745. PMC 4053917. PMID 24859749.
  19. ^ Aagaard K, Riehle K, Ma J, Segata N, Mistretta TA, Coarfa C, et al. (2012). "A metagenomic approach to characterization of the vaginal microbiome signature in pregnancy". PLOS ONE. 7 (6): e36466. Bibcode:2012PLoSO...736466A. doi:10.1371/journal.pone.0036466. PMC 3374618. PMID 22719832.
  20. ^ Senok AC, Verstraelen H, Temmerman M, Botta GA (October 2009). "Probiotics for the treatment of bacterial vaginosis". The Cochrane Database of Systematic Reviews (4): CD006289. doi:10.1002/14651858.CD006289.pub2. PMID 19821358.
  21. ^ Nardis C, Mosca L, Mastromarino P (September–October 2013). "Vaginal microbiota and viral sexually transmitted diseases". Annali di Igiene. 25 (5): 443–456. doi:10.7416/ai.2013.1946. PMID 24048183.
  22. ^ Can Yogurt Prevent Yeast Infections? Archived 2012-03-09 at the Wayback Machine. Planned Parenthood Advocates of Arizona. 28 February 2012. Retrieved 28 February 2012.
  23. ^ Vemuri R, Martoni CJ, Kavanagh K, Eri R (February 2022). "Lactobacillus acidophilus DDS-1 Modulates the Gut Microbial Co-Occurrence Networks in Aging Mice". Nutrients. 14 (5): 977. doi:10.3390/nu14050977. PMC 8912519. PMID 35267950.
  24. ^ Mani-López E, Arrioja-Bretón D, López-Malo A (January 2022). "The impacts of antimicrobial and antifungal activity of cell-free supernatants from lactic acid bacteria in vitro and foods". Comprehensive Reviews in Food Science and Food Safety. 21 (1): 604–641. doi:10.1111/1541-4337.12872. PMID 34907656. S2CID 245228355.
  25. ^ Rahardja F, Shahib MN, Tjahjani S, Prasetyo D (December 2019). "The Inhibition of Salmonella Typhi Growth by the Cell Free Supernatans of Lactobacillus Acidophilus Cultures". Carpathian Journal of Food Science & Technology. 11 (5): 6–10. doi:10.34302/crpjfst/2019.11.5.1. S2CID 243406198.
  26. ^ da Silva BS, Díaz-Roa A, Yamane ES, Hayashi MA, da Silva Junior PI (2022-10-29). "Doderlin: Isolation and Characterization of a Broad-Spectrum Antimicrobial Peptide from Lactobacillus acidophilus". Research in Microbiology. 174 (3): 103995. doi:10.1016/j.resmic.2022.103995. ISSN 0923-2508.
  27. ^ Salem M, Keshavarzi Arshadi A, Yuan JS (September 2022). "AMPDeep: hemolytic activity prediction of antimicrobial peptides using transfer learning". BMC Bioinformatics. 23 (1): 389. doi:10.1186/s12859-022-04952-z. PMC 9511757. PMID 36163001.
  28. ^ Viramontes-Hörner D, Márquez-Sandoval F, Martín-del-Campo F, Vizmanos-Lamotte B, Sandoval-Rodríguez A, Armendáriz-Borunda J, et al. (May 2015). "Effect of a symbiotic gel (Lactobacillus acidophilus + Bifidobacterium lactis + inulin) on presence and severity of gastrointestinal symptoms in hemodialysis patients". Journal of Renal Nutrition. 25 (3): 284–291. doi:10.1053/j.jrn.2014.09.008. PMID 25455039.
  29. ^ Durchschein F, Petritsch W, Hammer HF (February 2016). "Diet therapy for inflammatory bowel diseases: The established and the new". World Journal of Gastroenterology (Review). 22 (7): 2179–2194. doi:10.3748/wjg.v22.i7.2179. PMC 4734995. PMID 26900283.
edit
 
Wikimedia Commons has media related to Lactobacillus acidophilus.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Lactobacillus_acidophilus&oldid=1251134695"