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Medically Reviewed by Dr. Atmika Paudel, PhD
Bacillus Laterosporus BOD was supposedly discovered by Boyd J.
O'Donnell in the late 1980's while he was visiting Iceland. He was
intrigued by the health of the plants they grew without the aid of
fertilizers. Soil samples were taken and further studies revealed the
soil's growing power to be a species of bacteria that was later named
Bacillus Laterosporus BOD. O'Donnell patented this bacteria as a candida
yeast and Aspergillus killer in 1994 and all sub-strains thereof. (1)
Brevibacillus Laterosporus is a spore bearing bacteria so it survives the
stomach acids intact. Spore bearing means it is basically encapsulated
within itself. It does not have to be refrigerated so it will not spoil
and grow molds. Once introduced to the intestine the spores
begin to germinate and multiply every 32 minutes. However, this is a
soil based bacteria and like all soil based bacteria, it will
not set up large long-term colonies of bacteria in the intestine. The
effects are transitory and the colonies will begin to die within 3 days
Testing has shown it to be completely safe.
There are numerous studies published in the American Society of Microbiology journals that have been performed on over 30 substrains of B. laterosporus as an insecticide for mosquito's.
A published study in the Brazilian Journal of Microbiology in 2012, has shown that the compounds B. laterosporus produces does have antimicrobial activity against Streptococcus mutans, Staphylococcus aureaus, Clostridium and Gram- negative Bacteria such as Escherichia coli and Pseudomonas putrefaciens. It also had antifungal activities against the yeast Candida albicans.(Source)
Another published medical study in February of 2013 in Applied Microbiology and Biotechnology, reveals that B. laterosporus produces chitinase enzymes that exhibited antifungal activity against the phytopathogenic fungus Fusarium equiseti. Chitinase enzymes would also be useful for digesting the cell wall of yeast.(Source)
Just so you know, Chitinase activity is quite often found in the enzymes Cellulase and Hemicellulase.
There are a few ways to take this and I usually suggest it be taken with an enzyme for yeast at the least. However, the best way to take it would be like this:
For the first three days take 5 capsules four times a day at least 30 minutes away from food with the enzyme twice a day. After those three days drop the dose to 5 capsules two times per day and use the enzyme formula one hour before breakfast and 30 minutes before bedtime.
At the end of those two weeks, go back to taking B. Laterosporus BOD at the 5 capsules four times a day for three days. After those three days go back to the lower dose for another two weeks. Then back to the three days at 20 capsules a day and so on as long as needed.
I do suggest you keep doing this for at least 30 days after all symptoms have disappeared. You might also want to consider using it for maintenance for a while but that is ultimately your choice.
You can take less than what I have suggested above if you wish, you are the doctor and only you know how you feel. However, it could take longer to get well at lower doses, it just depends upon how bad your infection is.
Any of these Bacillus Laterosporus BOD products at Amazon will work.
This probiotic is not meant to build up good bacterial colonies if you are low on good bacteria. It works best as a yeast and bad bacteria killer. CP-1 or the 11-Strain are what you should use for building good bacteria levels during the two week cycle or after on a long term basis.
Like all probiotics if you are not used to taking them it is possible during the first five to seven days to have a slight bloating, or a feeling of being plugged up, effect. It could possibly be a little harder to have a bowel movement as well. For some people it has the opposite effect and they develop very loose stools, this usually subsides in five to seven days as well.
These problems tend to clear up after that first week as the probiotic cleans you out. From there, no more problems are felt.
I am not endorsing any specific product, however, based on several scientific studies performed on Brevibacillus laterosporus (as referred in the article and below), the information provided about the biological activity of B. laterosporus is correct. B. laterosporus is relatively well-studied bacteria with more than 100 published articles from a diverse group of researchers.
Whole genome sequence and analysis has shown this species has an ability to produce various bioactive secondary metabolites (1). In line with this, B. laterosporus strains have been found to produce anti-tumor compound - spergualine (2), antibiotic laterosporamine (3), laterocidin (4), bacteriocin-laterosporulin (5), and antimicrobial peptide-BL-A60 (6), peptide-tupuseleiamides and antifungal polyketide-basiliskamides (7), lipopeptide antibiotics-tauramamide (8), thrombin inhibitors-bacithrocins (9), some of which are stable at high temperatures and wide range of pH.
The crude extracts of the cultures of B. laterosporus along with the secondary metabolites produced have diverse in vitro antibacterial and antifungal activities against various pathogenic microorganisms such-as Staphylococcus aureus, Serratia marcescens, Mycobacterium spp, Klebsiella, and fungi such as Penicillium funiculosum and Aspergillus unilateralis (10), and (11).
The use of B. laterosporus in poultry food has been reported in scientific literatures (12).
In general, B. laterosporus is found in the natural environment and has been isolated from various sources such as- soil, water, and plants. It has been shown to be pathogenic to insects, however, no case with human infection has been reported so far.
Last updated 12/14/2019
Dr. Atmika Paudel received her Bachelors in Pharmacy in 2005 from Tribhuvan University in Nepal, which is the 10th largest University in the world. She completed her Masters in Pharmaceutical Biology in 2010 and went on to complete her PhD in Pharmaceutical Biology from The University of Tokyo in 2013.
Since graduation, Dr. Paudel has been a Research Fellow at the University of Tokyo and is currently a Research Scientist at Teikyo University in Japan.
Dr. Paudel has many published research papers in the use of antimicrobial agents, both pharmaceutical and natural. She was part of a research team that studied the genome sequence of Candida albicans TIMM1768, including studies of its virulence mechanisms to help in the development of treatment strategies for severe candidiasis.
Because of Dr. Paudel's hands on research of the yeast Candida albicans, she is more than qualified to fact check, edit and revise any article on this website.
Probiotics for Yeast & Bacillus Laterosporus BOD Home
If you have any questions about Brevibacillus Laterosporus or yeast infections in general, please feel free to contact us through the contact page of this website.
Dr. Paudel's References
1. JOURNAL OF BACTERIOLOGY, Oct. 2011, p. 5535–5536 Vol. 193, No. 19
0021-9193. American Society for Microbiology. Genome Sequence of
Brevibacillus laterosporus LMG 15441, a Pathogen of Invertebrates
2. UMEZAWA, H.; S. KONDO, H. IINUMA, S. KUNIMOTO,Y. IKEDA, H. IWASAWA, D. IKEDA & T. TAKEUCHI: Structure of an antitumor antibiotic, spergualin. J. Antibiotics 34: 1622. 1624, 1981
3.THE JOURNAL OF ANTIBIOTICS APR. 1976. ISOLATION OF A NEW ANTIBIOTIC, LATEROSPORAMINE (STUDIES ON ANTIBIOTICS FROM THE GENUS BACILLUS. XIIV) Shionogi Research Laboratory, Shionogi & Co., Ltd., Fukushima-ku, Osaka 553, Japan
4. Chuanguang Qin, Chunlan Xu, Ruijie Zhang, Weining Niu, Xiaoya Shang. Corrigendum to “On-resin cyclization and antimicrobial activity of Laterocidin and its analogues” [Tetrahedron Lett. 51 (2010) 1257]. Tetrahedron Letters, Volume 51, Issue 18, 5 May 2010, Pages 2557
5. Identification, Purification and Characterization of Laterosporulin, a Novel Bacteriocin Produced by Brevibacillus sp. Strain GI-9. Published: March 5, 2012
6. Corrigendum to “Purification and characterization of a novel antimicrobial peptide from Brevibacillus laterosporus strain A60” [Peptides 33(2) (2012) 206–211] Peptides, Volume 36, Issue 2, August 2012, Pages 340.
7. J. Nat. Prod. 2002, 65, 10, 1447-1451. Publication Date:August 29, 2002. American Chemical Society and American Society of Pharmacognosy
8. J. Nat. Prod. 2007, 70, 12, 1850-1853. Publication Date:November 29, 2007. The American Chemical Society and American Society of Pharmacognosy
9. THE JOURNAL OF ANTIBIOTICS 959. BACITHROCINS A, B AND C, NOVEL THROMBIN INHIBITORS. Nippon Roche Research Center, 200 Kajiwara, Kamakura, Kanagawa 247, Japan(Received for publication April 14, 1994)
10. Microbial Depository Center of Scientific and Production Center, “Armbiotechnology” NAS of Armenia, 14, Gyurjyan Str., Yerevan, 0056, Armenia. Available online 11 July 2018.
11. Microbial Control of Insect and Mite Pests Theory to Practice2017, Pages 47-67, Chapter 4 - Basic and Applied Research: Entomopathogenic Bacteria. T.R.Glare J.-L.Jurat-Fuentes, M.O’Callaghan. Lincoln University, Christchurch, New Zealand2University of Tennessee, Knoxville, TN, United States3AgResearch, Christchurch, New Zealand. Available online 9 September 2016.
12. Evaluation of selected direct-fed microbial candidates on live performance and Salmonella reduction in commercial turkey brooding houses 
1. Isolation and Identification of Brevibacillus lactosporum From Soil and Evaluation of their Antibiotic Properties. International Journal of Advanced Research in Biological Sciences. Volume 4, Issue 6 - 2017
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