Age, Biography and Wiki

Robert Guthrie was born on 28 June, 1916 in Marionville, MO, is an An american microbiologist. Discover Robert Guthrie's Biography, Age, Height, Physical Stats, Dating/Affairs, Family and career updates. Learn How rich is he in this year and how he spends money? Also learn how he earned most of networth at the age of 78 years old?

Popular As N/A
Occupation N/A
Age 78 years old
Zodiac Sign Cancer
Born 28 June, 1916
Birthday 28 June
Birthplace Marionville, MO
Date of death 24 June, 1995
Died Place Seattle, WA
Nationality

We recommend you to check the complete list of Famous People born on 28 June. He is a member of famous with the age 78 years old group.

Robert Guthrie Height, Weight & Measurements

At 78 years old, Robert Guthrie height not available right now. We will update Robert Guthrie's Height, weight, Body Measurements, Eye Color, Hair Color, Shoe & Dress size soon as possible.

Physical Status
Height Not Available
Weight Not Available
Body Measurements Not Available
Eye Color Not Available
Hair Color Not Available

Dating & Relationship status

He is currently single. He is not dating anyone. We don't have much information about He's past relationship and any previous engaged. According to our Database, He has no children.

Family
Parents Not Available
Wife Not Available
Sibling Not Available
Children Not Available

Robert Guthrie Net Worth

His net worth has been growing significantly in 2023-2024. So, how much is Robert Guthrie worth at the age of 78 years old? Robert Guthrie’s income source is mostly from being a successful . He is from . We have estimated Robert Guthrie's net worth, money, salary, income, and assets.

Net Worth in 2024 $1 Million - $5 Million
Salary in 2024 Under Review
Net Worth in 2023 Pending
Salary in 2023 Under Review
House Not Available
Cars Not Available
Source of Income

Robert Guthrie Social Network

Instagram
Linkedin
Twitter
Facebook
Wikipedia
Imdb

Timeline

1916

Robert Guthrie, MD, Ph.D. (June 28, 1916 – June 24, 1995) was an American microbiologist, best known for developing the bacterial inhibition assay used to screen infants for phenylketonuria at birth, before the development of irreversible neurological damage.

Guthrie also pioneered the collection of whole blood on specially designed filter paper, commonly known as "Guthrie cards" as a sample medium that could be easily collected, transported and tested.

Although Guthrie is best known for developing the test for phenylketonuria, he worked tirelessly to raise awareness of the need to screen for treatable conditions and adapted his method to early screening tests for galactosemia and maple syrup urine disease.

Guthrie received his doctorate from the University of Minnesota, although his education took a circuitous route, as he eventually earned six degrees in six years, including both a medical doctorate and a doctor of philosophy.

While in school, Guthrie married Margaret, a fellow student, and they eventually had six children together.

His early research into bacterial inhibition assays came while he was employed by the Staten Island Public Health Hospital, testing antibiotic sensitivity.

1947

Guthrie became interested in causes and prevention of mental retardation after his son, John, was born disabled in 1947.

Despite his work in the field, the cause of his son's disability was never diagnosed.

1958

In 1958, Guthrie's 15-month-old niece was diagnosed with phenylketonuria (PKU), a condition in which the body cannot metabolize phenylalanine.

Untreated PKU results in irreversible neurological damage.

After the discovery of PKU as a cause of mental retardation, Horst Bickel and colleagues discovered that it could be treated successfully with a diet low in phenylalanine.

The main drawback in successful treatment of PKU was the delay in identifying affected individuals.

The common test for PKU at the time was mixing urine with ferric chloride.

The excess phenylpyruvic acid in the urine of an individual with PKU would produce a bright green colour when reacting with the ferric chloride.

Infants do not excrete high enough concentrations of this compound to give a positive test result, thus delaying their diagnosis, and allowing irreversible damage to take place.

Guthrie's disabled son had driven his interest in causes of mental retardation, the diagnosis of his niece with PKU turned his attention to preventable causes.

Others working with children who had PKU asked Guthrie to focus on a test that would allow for earlier identification, before irreversible damage had taken place.

Guthrie developed a simple method to screen for elevated phenylalanine levels using a bacterial inhibition assay.

He cultured Bacillus subtilis on agar in the presence of a phenylalanine antagonist, inhibiting the growth.

When exposed to blood from patients affected with PKU, the high levels of phenylalanine overcame the inhibition, and bacterial growth was visible.

This assay was initially developed to allow monitoring of phenylalanine concentrations in known patients on dietary treatment using serum spotted onto filter paper.

Guthrie recognized both the utility of this method as a screening test, and the need to eliminate serum as the sample type to minimize processing.

He tested the assay using whole blood collected on filter paper from a heel stick.

The collection of whole blood on special filter paper developed by Guthrie is still used in newborn screening programs around the world, allowing babies to be screened shortly after birth for a number of treatable conditions.

After establishing a test that could identify PKU in whole blood spots, Guthrie set out to test his method, starting in an institution in New York.

Here, his test correctly identified all patients known to have PKU and also four who had previously been undiagnosed.

1960

Throughout the 1960s, PKU testing expanded in the United States and around the world, eventually becoming required by law in many jurisdictions.

With the success of PKU testing, Guthrie and his colleagues focused on screening tests for other diseases that can affect newborns.

They developed bacterial inhibition assays for galactosemia and maple syrup urine disease that could be run using the same sample collection as the PKU test.

Guthrie decided that commercial production would be the most efficient way to manufacture 400,000 test kits, so he approached the Ames Company, a division of Miles Laboratories, which manufactured the older PKU tests.

1961

In 1961, Guthrie and his lab started screening infants for PKU, a project that quickly expanded.

In two years, they had tested 400,000 American newborns, and diagnosed 39 with PKU.

This early diagnosis allowed for early treatment and avoidance of the most severe consequences of the disease.

1962

Ames said it would only manufacture the kits if a patent was issued, so Guthrie filed a patent application in 1962 and signed an exclusive licensing agreement with Miles, under which he would receive no royalties and 5% of the proceeds would be divided among the National Association for Retarded Children Research Fund, the Association for Aid of Crippled Children, and the University of Buffalo Foundation.

Miles couldn't produce the kits fast enough, so Guthrie produced his own kits for 500 tests at a cost of $6 each.

1963

But in 1963, he found out that Ames planned to charge $262 for the same kit.

Guthrie was appalled, but Ames wouldn't lower their price.

Guthrie appealed to the U.S. Children's Bureau, which sponsored the field trial, and the Children's Bureau recommended that Miles not be granted exclusive commercial rights.

Most of the funding to develop the tests had come from the Children's Bureau ($742,0000) and the Public Health Service ($251,700).

The surgeon general determined that the invention belonged to the United States and abrogated the exclusive licensing agreement.