Gerald Domingue

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Gerald Domingue (born 2 March 1937) is an American medical researcher (bacteriology, immunology, experimental urology) and academic who served as Professor of Urology, Microbiology and Immunology in the Tulane University School of Medicine and Graduate School for thirty years and also as Director of Research in Urology. He is currently retired and resides in Zurich, Switzerland, where he is engaged in painting and creative writing (www.dlareg-arts.com). At retirement he was honored with the title of Professor Emeritus at Tulane (1967–1997). Prior to Tulane, he served on the faculty of St. Louis University (school of medicine); was a lecturer at Washington University (school of dentistry) and director of clinical microbiology in St. Louis City Hospital (Snodgrass Laboratory of Pathology and Bacteriology), St. Louis, Missouri.

Over the course of his thirty-nine-year career, Domingue received funding from the National Institutes of Health, Veterans Administration, and a variety of national and international research foundations; served on grant review committees of these agencies as well as consultant to various journal review boards. He also served as clinical microbiology and research consultant to hospital clinical laboratories and to industry. He enjoys international recognition as an authority on the basic biology and medical significance of atypical bacterial organisms and is considered a pioneer and an expert on the role of these unusual bacteria in the persistence and expression of kidney and urological infectious diseases.

Domingue was named a Fellow of the American Academy for Microbiology (1973) and a Fellow of the Infectious Diseases Society of America (1975).[1][2] In 1995, he received the prestigious Palmes Academiques Medal (Chevalier) from the country of France.

Education and early work[edit]

Domingue was born in 1937 in Lafayette, Louisiana. He was educated at Southwestern Louisiana Institute (presently University of Louisiana at Lafayette, LA), receiving the Bachelor of Science degree in three years (bacteriology with minors in chemistry and French); matriculating to graduate school at the University of Southwestern Louisiana (presently University of Louisiana at Lafayette)(graduate courses in bacteriology, atomic physics and advanced qualitative organic chemistry; served as instructor of laboratory courses in bacteriology and immunology in university); Louisiana State University(basic medical sciences) and Tulane University where he earned the doctorate (1964); holds the Ph.D. degree in medical microbiology and immunology; followed by a postdoctoral research fellowship in microbiology/infectious diseases and a residency in clinical microbiology under the mentorship of the late distinguished bacteriologist/immunologist, Erwin Neter at The Children's Hospital of the State University of New York, Buffalo, New York.

He first became interested in the role of atypical bacterial forms after noting that a large number of patients with urinary tract infections suffer from continual relapsing illness. Using a direct phase microscope, he examined the urine specimens of several patients with urinary tract infections and found atypical bacteria in his samples.

He began to investigate atypical bacteria (cell wall-defective, L-forms and difficult-to-culture bacteria) striving to better understand their biology and the role they play in causing disease. Over the course of the next 30 years, he was able to explain much of the mystery behind how the bacteria are able to persist in the body, and published a wide array of clinical and experimental studies on the subject.

L-form bacteria – electron dense bodies[edit]

Domingue worked with a team that included pre and post-doctoral students and fellows along with faculty colleagues and laboratory assistants. Together they discovered that L-form bacteria are able to form tiny dense bodies within parent cells that already lack cell walls. They noted that the forms, which they called electron dense bodies were so small that they could pass through bacterial filters that normally withheld ordinary bacteria with cell walls.[3][4]

The electron dense bodies could persist inside tissue culture cells in the laboratory. After applying these data to the human condition, Domingue reasoned that in some patients who suffer from chronic bacterial infections, the disease process could be related to the fact that bacteria are able to differentiate into the resistant electron dense bodies that he observed in tissue cultures.[5]

Significant papers[edit]

In 1974, he and his graduate student, Mary Green, along with Paul Heidger, a faculty collaborator, published two landmark companion papers in the journal Infection and Immunity.[3][4] The papers detail how L-form bacteria inside an experimental human embryonic kidney tissue culture system are able to persist in cells and explains how they are able to revert into the cell wall-containing parent bacterial form. They also proposed a detailed reproductive cycle for L-form bacteria, followed by electron microscopy of the microorganisms.

These papers set the stage for Domingue and his team to delve even further into the role that cryptic atypical bacteria play in causing persistent and recurrent infections. In 1997, he and a colleague, the late Hannah Woody published an invited extensive review article on chronic bacterial infection in Clinical Microbiological Reviews.[5] Among their conclusions was the claim that "difficult to culture and dormant bacteria are involved in the latency of infection and that these persistent bacteria may be pathogenic."

He implicated atypical bacteria in several kidney-related diseases including pyelonephritis,[6][7] glomerulonephritis, idiopathic hematuria,[8] and interstitial cystitis.[9] He also speculated about their role in other diseases such as rheumatic fever, tuberculosis, syphilis, and rheumatoid arthritis.

In the review Domingue stated, "Clearly, any patient with a history of recurrent infection and persistent disability is sending the signal that the phenomenon (infection with atypical bacteria) could be occurring. The so-called autoimmune diseases in which no organism can be identified by routine testing techniques are particularly suspect."[5] He went on to conclude, "Bacteriologic advances, which include special culture media and stains, electron microscopy and molecular techniques such as PCR (polymerase chain reaction), have revealed an increasing number of previously unidentifiable organisms in a variety of pathologic conditions. It is unwise to dismiss the pathogenic capacities of any microbe in a patient with a mysterious disease."[5] Over the course of his thirty-nine-year career Domingue published numerous papers, monographs, and book chapters devoted to atypical bacterial research. He delivered many invited international and national lectures about bacterial persistence and expression of disease and wrote a book on the subject, Cell Wall-Deficient Bacteria: Basic Principles and Clinical Significance.[10]

Other research[edit]

Although Domingue's primary research focus was on bacterial L-forms, he also published extensively on the biological significance of the enterobacterial common antigen of gram negative bacteria– its antigenicity, immunogenicity, and vaccine potential against urinary tract infections.[11][12]

He studied the immunological consequences of a vasectomy, as well as the role of various gram negative pathogens in the host-pathogen interaction in pyelonephritis, and the effects of antibiotics and chemotherapy on urinary tract infections.[13][14]

He also published microbiological and immunological studies on bacteria that produce chorionic gonadotropin-like hormone and their role in an experimental tumor model.[15]

He was even the co-author of a publication that characterized the oral microbial flora of alligators in order to develop better therapy for alligator bites. [ref]Flandry,F.,Lisecki,E.J.,Domingue,G.J.,Nichols,R.L.,Greer,D.L.,Haddad, R.J. Initial Therapy for Alligator Bites. Characterization of the Oral Flora of Alligator mississippiens. Southern Medical Journal, volume 82, pages 262-266, 1989.

References[edit]

  1. ^ Marquis Who's Who, Inc. (2000). Who's who in medicine and healthcare. New Providence NJ: Marquis Who's Who[page needed]
  2. ^ Marquis Who's Who, Inc. (1993). Who's who in science and engineering. Wilmette, Ill: Marquis Who's Who.[page needed]
  3. ^ a b Green MT, Heidger PM, Domingue G (1 October 1974). "Proposed Reproductive Cycle for a Relatively Stable L-Phase Variant of Streptococcus faecalis". Infection and Immunity 10 (4): 915–27. PMC 423038. PMID 4214786. 
  4. ^ a b Green MT, Heidger PM, Domingue G (1 October 1974). "Demonstration of the Phenomena of Microbial Persistence and Reversion with Bacterial L-Forms in Human Embryonic Kidney Cells". Infection and Immunity 10 (4): 889–914. PMC 423037. PMID 4214785. 
  5. ^ a b c d Domingue GJ, Woody HB (1 April 1997). "Bacterial persistence and expression of disease". Clinical Microbiology Reviews 10 (2): 320–44. PMC 172922. PMID 9105757. 
  6. ^ Domingue GJ, Schlegel JU (December 1970). "The possible role of microbial L-forms in pyelonephritis". The Journal of Urology 104 (6): 790–8. PMID 5499826. 
  7. ^ Ponig B, Domingue G, Schlegel J (January 1972). "The role of in vitro induced microbial L-forms in experimental hematogenous pyelonephritis". Investigative Urology 9 (4): 282–5. PMID 4550878. 
  8. ^ Domingue GJ, Schlegel JU (December 1978). "Novel bacterial structures in human blood. II. Bacterial variants as etiologic agents in idiopathic hematuria". The Journal of Urology 120 (6): 708–11. PMID 731811. 
  9. ^ Domingue GJ, Ghoniem GM, Bost KL, Fermin C, Human LG (April 1995). "Dormant microbes in interstitial cystitis". The Journal of Urology 153 (4): 1321–6. doi:10.1016/S0022-5347(01)67594-3. PMID 7869536. 
  10. ^ Domingue, Gerald J. (1982). Cell wall-deficient bacteria: basic principles and clinical significance. Reading, Massachusetts: Addison–Wesley. ISBN 978-0-201-10162-1. OCLC 8284964. 
  11. ^ Domingue GJ, Neter E (1 January 1966). "Opsonizing and Bactericidal Activity of Antibodies Against Common Antigen of Enterobacteriaceae". Journal of Bacteriology 91 (1): 129–33. PMC 315921. PMID 4955466. 
  12. ^ Domingue, G. J. and Johnson, E.J. (1975). "The Common Antigen of Enterobacteriaceae and its Biologic Significance". In Erwin Neter and Felix Milgrom. The immune system and infectious diseases. Basel: Karger. pp. 242–262. ISBN 3-8055-2177-4. OCLC 1823430. 
  13. ^ Kawahara M, Human LG, Winningham JS, Domingue GJ (December 1994). "Antibodies to Escherichia coli 06 porins cross-react with urinary pathogens". Immunobiology 192 (1–2): 65–76. doi:10.1016/S0171-2985(11)80408-0. PMID 7538488. 
  14. ^ Domingue GJ, Roberts JA, Laucirica R, et al. (June 1985). "Pathogenic significance of P-fimbriated Escherichia coli in urinary tract infections". The Journal of Urology 133 (6): 983–9. PMID 2860251. 
  15. ^ Domingue GJ, Acevedo HF, Powell JE, Stevens VC (1 July 1986). "Antibodies to bacterial vaccines demonstrating specificity for human choriogonadotropin (hCG) and immunochemical detection of hCG-like factor in subcellular bacterial fractions". Infection and Immunity 53 (1): 95–8. PMC 260080. PMID 3721581. 

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