Seattle startup AttoDx wins NIH funds for ultrasensitive TB MDx
NEW YORK (GenomeWeb) – Start-up diagnostics firm AttoDx has been awarded National Institutes of Health funds to develop an ultrasensitive molecular diagnostic for difficult-to-detect cases of tuberculosis.
The one-year, Phase I Small Business Technology Transfer grant
from the National Institute of Allergy and Infectious Disease
totals $220,230. AttoDx will develop the assay in collaboration
with Claremont BioSolutions and researchers at the University of
Washington, initially for same-day diagnosis of smear-negative
and extrapulmonary Mycobacterium tuberculosis from
sputum and cerebrospinal fluid of HIV-coinfected patients.
The
core technology of the diagnostic is molecular viability
testing, or MVT, a technique licensed by AttoDx from UW. The
patent-pending method amplifies ribosomal RNA precursors
(pre-rRNA) which are rapidly upregulated when bacteria are
nutritionally supplemented.
"If they're alive,
they'll make pre-rRNA, and they'll make quite a large amount of
it — that makes it easier to detect the bacteria," Jerry
Cangelosi, consulting scientific director at AttoDx and a
professor in the Department of Environmental and Occupational
Health Sciences at UW told GenomeWeb in an interview.
The
MVT method measures increased pre-rRNA copy number in response
to nutritional stimulation. The ultimate product will consist of
a single-use pre-PCR cartridge which will partition the sample
and nutritionally stimulate half of it. From this, two cDNA
samples result, and then these go into a qPCR system already
present in a lab, Cangelosi explained.
MVT was
originally designed to reduce false-positive results by
estimating the proportion of living bacteria in a sample.
However, a report in
PLoS One
last year showed that, for a diverse range of bacteria,
stimulation-induced upregulation of pre-rRNA was so robust that
the test was actually 5- to 10-fold more sensitive than standard
PCR.
Moreover, the pre-rRNA are specific for
different species of bacteria.
The pre-PCR cartridge
will be spearheaded by Claremont BioSolutions, which "has a very
nice, low-cost, battery-powered, sample processing system that
can extract DNA and RNA very quickly and cheaply," Cangelosi
said, noting that this element was described in a
Journal of Clinical Microbiology
study.
Claremont's miniaturized cell lysis system is
also part of
a number of projects
at Keck Graduate Institute, and the firm has been
funded
in the past to develop it further for Clostridium difficile
— a bacterium with a notoriously rugged external shell.
Cangelosi
is also co-PI on a Keck grant to develop a point-of-care,
lateral flow TB assay, also in collaboration with Claremont.
That assay will be for adult, pulmonary TB, he said, while the
newly funded 'ultrasensitive' test is for more challenging
infections.
"There's plenty of cases, [such as]
pediatric and extrapulmonary TB, where a clinician is pretty
sure that a patient has tuberculosis but they're just not able
to culture it, or see it by PCR," Cangelosi said. "Our product
is designed for that situation — you would order this test
when you really want the highest possible sensitivity.
When
tuberculosis infects children or people with HIV, levels of
bacteria are sometimes too low to detect by standard methods,
and infections can also occur outside of the lungs.
Extrapulmonary
TB is more common in people with HIV coinfection, and is not
well detected by the commonly used Cepheid GeneXpert MTB/RIF
test, as
previously reported. That test has recently been shown to be
less sensitive
on samples from children.
There is also a
particularly high rate of HIV and TB co-infection in Swaziland,
and Cepheid's test was recently demonstrated to be unable to
detect
around 30 percent
of infections in that country.
However, because of
the estimated cost and technical complexity of the AttoDx
MVT-based test, Cangelosi said the firm intends to initially
market it in higher-income countries that also have high TB
rates, such as China and India.
Those two countries
account for almost 40 percent of the estimated global burden of
tuberculosis
according to the World Health Organization." These are countries that do have some clinical laboratory
infrastructure … [our assay] is not going to be the
cheapest possible TB test; it’s something that you order
when you need the maximum sensitivity," Cangelosi said.
However,
"AIDS-related, extrapulmonary, and pediatric TB — that's
when the disease is most life-threatening," he said. "We don't
envision stopping at tuberculosis, we envision going well beyond
that, but TB is a good place to start because the need is so
acute."
Source:
GenomeWeb