John Mekalanos

John Mekalanos is a microbiologist who is primarily known for leading one of the first teams that reported the discovery of the type VI secretion system as well as his work on the pathogenicity of the bacterial species Vibrio cholerae, its toxin, and its secretion systems. Since 1998, he has been a member of the National Academy of Sciences.[1]

Education

He started his research studies as a graduate student in the labs of R. John Collier and William Robert Romig at UCLA where his research was focused on studying the genetic and biochemical analysis of the cholera toxin secreted by the bacterium Vibrio cholerae.[2] Highlights of his career during this time was, along with Romig, the development of a screening assay designed to isolate the tox mutants of Vibrio cholerae (strains with altered toxin production ability)[3] which led to the genetic mapping of the toxin-regulatory mutants in this bacterial species.[4]

He continued his work on cholera toxin as a post-doc at the Department of Microbiology and Molecular Genetics at Harvard Medical School with John R. Murphy, which was followed by his appointment as an assistant professor there.[5]

Career and Research

Early Research

His early work as an independent researcher led to the identification of toxR, a gene that affects the expression of the cholera toxin operon ctxAB,[6] the discovery that the Staphylococcus aureus enterotoxin A (entA) is a phage-encoded protein,[7] and finally, the demonstration of the presence of duplications of the toxin operon in different strains of Vibrio cholerae that could account for the variable toxinogenicity of the strains[8] which led to his promotion to Professor in 1986.[5] His continued strong research output led to his appointment as Chairman of the then Department of Microbiology and Molecular Genetics (now Microbiology and Immunobiology) ten years later in 1996 and his election to the National Academy of Sciences in 1998.[5]

T6SS Discovery

In 2006, his group published the first account of the identification of a novel secretion system that they named the type VI secretion system, a system initially found to be capable of conferring increased virulence in non-O1/non-O139 strain strains of V. cholerae,[9] which was later however shown to be primarily responsible for interbacterial competition.[10]

Awards and honors

References
  1. "John J. Mekalanos".
  2. "William Robert Romig".
  3. Mekalanos JJ, Collier RJ, Romig WR (1978). "Affinity filters, a new approach to the isolation of tox mutants of Vibrio cholerae". Proc Natl Acad Sci U S A. 75 (2): 941–5. doi:10.1073/pnas.75.2.941. PMC 411374. PMID 345281.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. Mekalanos JJ, Sublett RD, Romig WR (1979). "Genetic mapping of toxin regulatory mutations in Vibrio cholerae". J Bacteriol. 139 (3): 859–65. doi:10.1128/jb.139.3.859-865.1979. PMC 218032. PMID 479110.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. "John J. Mekalanos, PHD".
  6. Miller VL, Mekalanos JJ (1984). "Synthesis of cholera toxin is positively regulated at the transcriptional level by toxR". Proc Natl Acad Sci U S A. 81 (11): 3471–5. doi:10.1073/pnas.81.11.3471. PMC 345530. PMID 6374658.
  7. Betley MJ, Mekalanos JJ (1985). "Staphylococcal enterotoxin A is encoded by phage". Science. 229 (4709): 185–7. doi:10.1126/science.3160112. PMID 3160112.
  8. Mekalanos JJ (1983). "Duplication and amplification of toxin genes in Vibrio cholerae". Cell. 35 (1): 253–63. doi:10.1016/0092-8674(83)90228-3. PMID 6627396.
  9. Pukatzki S, Ma AT, Sturtevant D, Krastins B, Sarracino D, Nelson WC; et al. (2006). "Identification of a conserved bacterial protein secretion system in Vibrio cholerae using the Dictyostelium host model system". Proc Natl Acad Sci U S A. 103 (5): 1528–33. doi:10.1073/pnas.0510322103. PMC 1345711. PMID 16432199.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  10. Hood RD, Peterson SB, Mougous JD (2017). "From Striking Out to Striking Gold: Discovering that Type VI Secretion Targets Bacteria". Cell Host Microbe. 21 (3): 286–289. doi:10.1016/j.chom.2017.02.001. PMC 6404758. PMID 28279332.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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