February 15, 2022 5 min read
Although the existence of different blood types is common knowledge, what constitutes these blood types and the physiological differences between individuals with varying blood types is a much less discussed topic.
An individual’s blood type is conferred by what are known as AB O histo-blood group antigens. Antigens are generally proteins or complex sugars but can also be glycoproteins (sugar-bound proteins) or glycolipids (sugar-bound fats) that are recognizable by the immune system. In this case, the three ABO antigens (A, B, and H) are polysaccharides (multiple sugar molecules bound together).
H-antigen
Irrespective of blood type, the vast majority of people have red blood cells that express the H antigen. People that lack the H antigen are said to have the Bombay phenotype, named after the location where this blood type was first identified. Then, depending on an individual’s genetic make-up, someone can either express the A antigen, B antigen, both the A and B antigen, or neither the A nor B antigen on the surface of their red blood cells. For example, individuals expressing the type A antigen have type A blood, whereas individuals expressing neither A nor B antigen have type O blood. In addition, an individual is said to have a positive or negative blood type depending on the presence or absence of the genetically-inherited Rhesus (Rh) factor. If someone has Rh factor on their red blood cells, they are said to have a positive blood type, whereas someone lacking the Rh factor on their red blood cells is said to have a negative blood type (e.g., if you have red blood cells that express both A and B antigens as well as Rh factor, then your blood type is AB+; if your red blood cells possess neither A nor B antigen and also lack Rh factor, then your blood type is O-).
What is FUT1?
Galactoside 2-L-fucosyltransferase 1 (FUT1) is the enzyme that facilitates the transport of ABO histo-blood group antigens onto the surface of red blood cells. However, contrary to what most of us learned in basic biology classes, blood isn’t the only bodily fluid that contains ABO antigens thanks to a variant of FUT1 known as FUT2.
What is FUT2?
FUT2 is expressed by all secretory cells and facilitates the excretion of ABO histo-blood group antigens into mucosal secretions. For example, if you have type A blood, then FUT2 allows cells to excrete type A antigen into your saliva, tears, gut mucosa, lung mucosa, and all other major bodily fluids except cerebrospinal fluid.
Are you an FUT2 non-secretor? (20% chance you are)
About 80% of the population has one or two functional copies of FUT2and are classified as “secretors”. Interestingly, however, the other 20% of the population possesses loss-of-function mutations in both copies of FUT2. Thus, although these individuals express ABO antigens on their red blood cells, they lack the ability to excrete ABO antigens into any other bodily fluids and are deemed “non-secretors”.
What you can do to optimize your health as the FUT2 non-secretors?
There are a few important considerations for non-secretor individuals looking to optimize their health.
Interestingly, in addition to the impact of secretor status on microbiota composition, ABO antigen expression also influences the bacteria found in the gut. For example, different strains of Lactobacillus have diverse preferences for A, B, and H antigens as nutrient sources. Additionally, secretors with type A blood have the highest diversity of Bifidobacteria, as bacteria within this genus prefer to directly feast on type A antigen as a nutrient source.
Is there a silver lining for FUT2 non-secretors?
Although there are many drawbacks to the non-secretor phenotype, evidence suggests that non-secretors do exhibit resistance to infection by certain viruses that cause diarrheal diseases including norovirus and rotavirus. These viruses use blood group antigens in the mucosa to bind to and infect cells. Thus, the absence of these antigens helps to prevent the pathogens from getting a foothold in the body. In secretors, supplementation with 2’FL may help to prevent viral infection in the gut by binding to the surface of viral particles and blocking their ability to bind to human cells. Additionally, non-secretors also appear to exhibit some protection against severe COVID-19 symptoms and were significantly less hospitalized than secretors since the beginning of the COVID-19 pandemic.
How to determine if you are a FUT2 non-secretor?
The easiest way to determine your secretor status is to reference your genome sequencing data such as those provided by 23andMe. The FUT2 genetic locus can be found under the name rs601338. A genotype of “GA” or “GG” at this locus indicates that you are a secretor, whereas a genotype of “AA” indicates that you are a non-secretor. Regardless of the result, the simple, actionable steps outlined above can help all of us to leverage our secretor status and not only optimize gut health and digestion but also improve immune function and decrease disease susceptibility.
Written by: Dr. Alexis Cowan, a Princeton-trained PhD specializing in the metabolic physiology of nutritional and exercise interventions. Follow Dr. Cowan on Instagram: @dralexisjazmyn
REFERENCES
Castillo, Brian (2018). Transfusion Medicine for Pathologists || Red cell antigens and antibody, 69–112. doi:10.1016/B978-0-12-814313-1.00005-8
Rausch P, Rehman A, Künzel S, et al. Colonic mucosa-associated microbiota is influenced by an interaction of Crohn disease and FUT2 (Secretor) genotype. Proc Natl Acad Sci U S A. 2011;108(47):19030-19035.
Taylor SL, McGuckin MA, Wesselingh S, Rogers GB. Infection's Sweet Tooth: How Glycans Mediate Infection and Disease Susceptibility. Trends Microbiol. 2018 Feb;26(2):92-101.
Wacklin P, Mäkivuokko H, Alakulppi N, Nikkilä J, Tenkanen H, Räbinä J, Partanen J, Aranko K, Mättö J. Secretor genotype (FUT2 gene) is strongly associated with the composition of Bifidobacteria in the human intestine. PLoS One. 2011;6(5):e20113.
Giampaoli O, Conta G, Calvani R, Miccheli A. Can the FUT2 Non-secretor Phenotype Associated With Gut Microbiota Increase the Children Susceptibility for Type 1 Diabetes? A Mini Review. Front Nutr. 2020 Dec 23;7:606171.
March 08, 2024
Hello! If we add these bacteria back in- will our child then get it through breast milk or no? My 15 month old still really only consistently nurses and doesn’t take much liquid from a cup/bottle
June 12, 2022
Re: Amy
Hi Amy, we found only 1 non peer-reviewed article about FUT2 and COVID. Please see below:
FUT2 “non-secretor” status reduces the risk of severe COVID-19 outcomes in patients with blood group A
https://www.medrxiv.org/content/10.1101/2020.12.19.20248172v1.full.pdf
June 11, 2022
Thank you for this article. Has anyone made an association of the occurrence of Long Haul Covid cases associated in secretors vs non-secreters?
May 08, 2022
Hi Susan, Thank you for your question. Dr Alexis will reply to your question by email. Thank you.
May 05, 2022
Wonderful article, thank you Dr. Alexis! What are your thoughts on compounded heterogeneous FUT2 rs601338, rs492602, rs1800028.
December 21, 2024 7 min read
Discover the unique benefits of our brand new MitiAging product. It restores the gut microbiome to kickstart it into naturally producing urolithin A, a postbiotic hailed for its anti-aging properties.
December 15, 2024 8 min read
December 08, 2024 7 min read
Autumn
September 01, 2024
I found out I’m a non-secretor by submitting saliva to various DNA testing companies (including 23&Me) & not one of them could get DNA. How on earth can a mutation on the FUT2 gene be detected if they don’t secrete DNA via bodily fluids? Blood. But I cannot find a 23&Me type of DNA testing company that will test a person’s blood to extract DNA & get all the same interesting information that secretors get? 20% of the population is excluded from this. Or, if a company is found, us non secretors will have to pay much more.