Diagnosing Bacterial Infections in Blood Samples
News Aug 24, 2016
Researchers supported by the National Institutes of Health have shown that it’s possible to diagnose a bacterial infection from a small sample of blood — based on the immune system’s response to the bacteria — in infants with fevers who are 2 months of age or younger. With additional research, the new technique could be an improvement over the standard method, which requires isolating live bacteria from blood, urine or spinal fluid and growing them in a laboratory culture. The study, funded in part by NIH’s Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), appears in the Aug. 23, 2016, issue of the Journal of the American Medical Association.
Health care providers who evaluate young infants with fevers have limited means to quickly and accurately diagnose whether or not an illness results from a bacterial infection. Determining if the illness is caused by bacteria may involve complicated medical procedures, such as a lumbar puncture (spinal tap). While they wait for the test results, physicians also may need to admit the infant for a lengthy hospital stay or prescribe antibiotics, which may later turn out to be unnecessary.
“The development of a fast and non-invasive diagnostic tool holds promise for better outcomes and lower treatment costs for young infants with fevers of unknown cause,” said Valerie Maholmes, Ph.D., chief of NICHD’s Pediatric Trauma and Critical Illness Branch.
With advances in genetic sequencing technology, researchers have explored alternative approaches to diagnosing infections, such as assessing the body’s immune response. When the immune system wards off an infection, immune cells activate certain genes, depending on whether the infection results from bacteria or viruses. Collectively, these distinct genes form what is called a “biosignature.”
“Previous studies have suggested that analyzing immune cell biosignatures can distinguish between bacterial and viral infections in children and adults,” said Ruth Brenner, M.D., M.P.H., an NICHD program officer. “However, scientists were uncertain if this approach would work in young infants because of their immature immune systems.”
In the current study, researchers in the Pediatric Emergency Care Applied Research Network (PECARN) sought to define a group of genes that could serve as a biosignature in infants. The study team enrolled infants 2 months of age or younger from 22 emergency rooms. More than 1,800 infants with fevers were enrolled. For this preliminary study, the researchers tested samples from 279 randomly selected infants (89 with bacterial infections, 190 without bacterial infections), along with samples from 19 healthy infants without fevers.
The PECARN team identified a biosignature of 66 genes, measured in a small blood sample, from which they could distinguish between newborns with or without bacterial infections. These serious bacterial infections included urinary tract infections, brain or spinal fluid infections (bacterial meningitis) and blood infections (bacteremia), all of which are typically diagnosed by growing bacteria from samples of body fluids. In their study, the biosignature was 87 percent sensitive — correctly identifying a sample as positive. The researchers also found a group of 10 genes signifying bacteremia, a very serious condition. This biosignature correctly identified a positive sample 94 percent of the time.
When compared to the traditional culture method, these preliminary findings indicate that biosignatures could ultimately lead to a fast and non-invasive test for diagnosing bacterial infections in infants with fevers. More work is needed, however, to optimize this diagnostic approach.
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