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Emerg Microbes Infect. 2012 Oct;1(10):e31. doi: 10.1038/emi.2012.32. Epub 2012 Oct 24.

In memory of Patrick Manson, founding father of tropical medicine and the discovery of vector-borne infections.

Emerging microbes & infections

Kelvin Kw To, Kwok-Yung Yuen

Affiliations

  1. Department of Microbiology, State Key Laboratory for Emerging Infectious Diseases, Research Centre for Infection and Immunology, The University of Hong Kong , Hong Kong, China.

PMID: 26038403 PMCID: PMC3630944 DOI: 10.1038/emi.2012.32

Abstract

Patrick Manson, a clinician-scientist serving in China (1866-1889), discovered that many tropical infectious diseases require a vector peculiar to warm climate for person to person transmission. He demonstrated the nocturnal periodicity of microfilariae in the blood of patients with elephantiasis. These microfilariae undergo metamorphosis when ingested by the mosquito acting as the vector for the completion of their life cycle. Furthermore, he demonstrated the linkage between the lung fluke and endemic haemoptysis by finding operculated eggs in patients' sputa. He predicted that the miracidium from hatched eggs uses crustaceans, such as fresh-water snails found at tropical conditions, as the intermediate hosts in the life cycle of many trematodes. His vector hypothesis leads to vector control which is now the cornerstone for the World Health Organization's programme for the elimination/control of lymphatic filariasis, dracunculiasis and malaria. Before leaving China, he established the Alice Memorial Hospital, the Hong Kong College of Medicine for Chinese (the forerunner of the University of Hong Kong), and the Hong Kong Medical Society for medical service and education. He also incepted the Hong Kong Dairy Farm for supplying hygienic milk affordable by pregnant women, children and patients.

Keywords: Patrick Manson; tropical disease; vector

References

  1. Science. 2002 Oct 4;298(5591):119-21 - PubMed
  2. J Virol. 2012 May;86(10):5481-96 - PubMed
  3. J Virol. 2012 Mar;86(6):3402-3 - PubMed
  4. Proc Natl Acad Sci U S A. 2005 Sep 27;102(39):14040-5 - PubMed
  5. Br Med J. 1902 Dec 20;2(2190):1894-5 - PubMed
  6. Br Med J. 1892 Jan 23;1(1621):163-7 - PubMed
  7. Lancet. 1998 Feb 14;351(9101):467-71 - PubMed
  8. Clin Infect Dis. 2008 May 15;46(10):1582-8 - PubMed
  9. Curr Opin Infect Dis. 2011 Oct;24(5):496-502 - PubMed
  10. J Exp Med. 1917 Sep 1;26(3):297-323 - PubMed
  11. Lancet. 2003 Apr 19;361(9366):1319-25 - PubMed
  12. Arch Pathol Lab Med. 2000 Nov;124(11):1594-5 - PubMed
  13. J Virol. 2012 Jan;86(1):395-405 - PubMed
  14. J Virol. 2012 Mar;86(5):2797-808 - PubMed
  15. Soc Hist Med. 2000 Dec;13(3):467-93 - PubMed
  16. N Engl J Med. 2009 Jan 8;360(2):121-8 - PubMed
  17. Lancet. 2012 Feb 18;379(9816):662-71 - PubMed
  18. Med Hist. 2010 Jul;54(3):295-314 - PubMed
  19. Mem Inst Oswaldo Cruz. 2011 Aug;106 Suppl 1:212-7 - PubMed
  20. N Engl J Med. 2011 Aug 4;365(5):422-9 - PubMed
  21. Proc R Soc Med. 1913;6(Dermatol Sect):31-9 - PubMed
  22. Proc Natl Acad Sci U S A. 2009 Oct 13;106(41):17443-7 - PubMed
  23. J Pathol Bacteriol. 1956 Jul;72(1):239-46 - PubMed
  24. N Engl J Med. 2011 Apr 21;364(16):1523-32 - PubMed
  25. Nature. 2008 Feb 21;451(7181):990-3 - PubMed
  26. Lancet. 2006 Mar 11;367(9513):859-69 - PubMed
  27. N Engl J Med. 2012 Aug 30;367(9):834-41 - PubMed
  28. Proc Natl Acad Sci U S A. 2012 Apr 3;109(14):5435-40 - PubMed
  29. Lancet. 2003 Jun 28;361(9376):2226-34 - PubMed

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