A 475 years-old founder effect involving IL12RB1: A highly prevalent mutation conferring Mendelian Susceptibility to Mycobacterial Diseases in European descendants

• Published in: Infection, genetics and evolution genetics and evolution, 2009-07, Vol.9 (4), p.574-580
• Main Authors: Yancoski, J., Rocco, C., Bernasconi, A., Oleastro, M., Bezrodnik, L., Vrátnica, C., Haerynck, F., Rosenzweig, S.D.
• Format: Article
• Language: English
• Subjects: Animals; Argentina; Bacillus Calmette Guerin; BCG Vaccine - administration & dosage; BCG Vaccine - adverse effects; European Continental Ancestry Group - genetics; Founder Effect; Genetic Predisposition to Disease; Hot spot; Humans; Interferon gamma; Linkage Disequilibrium; Models, Genetic; Mutation; Mycobacterium; Mycobacterium bovis - isolation & purification; Mycobacterium Infections - genetics; Receptors, Interleukin-12 - genetics; Salmonella
• ISSN: 1567-1348; 1567-7257
• DOI: 10.1016/j.meegid.2009.02.010

Mutations in IFNGR1, IFNGR2, IL12RB1, IL12B, STAT1 and NEMO result in a common clinical phenotype known as Mendelian Susceptibility to Mycobacterial Diseases (MSMD). Interleukin-12 receptor β1 (IL-12Rβ1) deficiency is the most common genetic etiology for MSMD. Known mutations affecting IL12RB1 are recessively inherited and are associated with null response to both IL-12 and IL-23. Mutation IL12RB1 1623_1624delinsTT was originally described in 5 families from European origin (2 from Germany; 1 from Cyprus, France and Belgium). Interestingly, this same mutation was found in an unexpectedly high prevalence among IL-12Rβ1 deficient patients in Argentina: 5-out-of-6 individuals born to unrelated families carried this particular change. To determine whether mutation 1623_1624delinsTT represents a DNA mutational hotspot or a founder effect, 34 polymorphic markers internal or proximal to IL12RB1 were studied in the Argentinean and the Belgian patients. A common haplotype spanning 1.45–3.51 Mb was shared by all chromosomes carrying mutation 1623_1624delinsTT, and was not detected on 100 control chromosomes. Applying a modified likelihood-based method the age of the most recent common ancestor carrying mutation 1623_1624delinsTT was estimated in 475 years (95% CI, 175–1275), which is the time when the Spaniards initiated the colonization of the Americas. Mutation 1623_1624delinsTT represents the first founder effect described on IL-12Rβ1, the most frequently affected gene in MSMD, and affecting patients with European ancestors. The reason(s) behind the persistency of this mutation across multiple generations, its relative high prevalence, and any potential selective advantage are yet to be established.