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Pathogen Detection History

Edward Jenner

1796

Created one of the first vaccinations for smallpox through scientific ways. He inoculated his patients by scratching their skin with matter infected with the smallpox virus. His practices were soon used by others. 

Anton Leeuwenhoek

1677

Discovered protozoa under his improved microscope to look at single celled organisms. He called them "animalcules", but is what we now know as microorganisms. He is considered the father of microbiology.

Anton Leeuwenhoek
Edward Jenner

Louis Pasteur

1862

Developed the Germ Theory that states how particular diseases are caused by microorganisms, too small to see with the naked eye, infecting the body. He proved this by showing fermentation and decomposition is caused by organisms in the air. His use of carbolic acid in surgery stopped the infection of bones.

Louis Pasteur

Robert Koch

1876

Discovered the anthrax bacillus to prove it causes the bacterial disease, anthrax. He did this by being the first to grow the bacteria on solid material, an ox eye. With a concentrated source of bacteria, he was able to use it to inoculate other animals.

Robert Koch

Peter Perlmann & Eva Engvall 1971

Developed the ELISA (enzyme-linked immunosorbent assay) at Stockholm University of Sweden that uses antibodies to detect any hormones or viruses. This technology and technique allowed for results to be done faster within hours or minutes. It is now used worldwide from detecting malaria to pregnancies. 

Perlmann & Engvall

Kary Mullis 1983

Invented PCR (polymerase chain reaction) that allowed for millions of copies of a DNA sample to be made from a small sample. He created this while he was a chemist at the Cetus Corporation, a biotechnology firm. It is used to help with detecting diseases by having a concentrated sample of DNA of bacteria and viruses. PCR is especially used in the detection of HIV and AIDS.

Kary Mullis

Jennifer Doudna

2012

Discovered CRISPR-Cas9  (clustered regularly interspaced short palindromic repeats) with Emmanuelle Charpentier at UC Berkley. This enzyme allows for gene editing by cutting specific codons. She is also a part of developing Cas13, a highly sensitive variety of Cas9 enzyme. It has the potential to be 1 million times more sensitive than ELISA for specific DNA or RNA. 

Jennifer Doudna
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