SBIR/STTR Research Award
Point-of-care microdevices for simultaneous detection of multiple pertussis-like respiratory diseases from Bordetella species
Award amount
$390,952Program and phase
STTR · Phase IAward year
2022Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- MICROBIOCHIP DIAGNOSTICS LLC
- Proposal award date
- 2022-08-19
- Contract end date
- 2024-01-31
- UEI
- NTJWKBC6YJA7
- Solicitation number
- PA20-265
- Topic code
- NIAID
Research abstract
ABSTRACT
Pertussis, also known as whooping cough, caused by B. pertussis and B. parapertussis, is the
only vaccine-preventable infection that remains endemic in the U.S. Since pertussis vaccine-
induced immunity is not permanent, the immunized host is vulnerable to re-infection later in life.
Worldwide, there are an estimated 24.1 million cases of pertussis, and about 160,700 deaths per
year from pertussis in children, most of which are from developing nations. These two Bordetella
species are highly contagious and cause similar clinical symptoms, making them difficult to
diagnose. Although B. parapertussis infection manifests in milder symptoms to B. pertussis-
derived infection, both infections can be deadly, especially to children, the elderly, and
immunocompromised patients. Current diagnostic methods are either slow or require costly
instruments. Low-cost point-of-care (POC) detection of these two whooping cough-causing
pathogens is greatly needed to meet the unmet demand for rapid diagnosis of whooping cough
in resource-limited settings. During our recent preliminary study, we, for the first time, developed
a low-cost microfluidic technology integrated with the loop-mediated isothermal DNA amplification
(LAMP) for rapid POC detection of B. pertussis. Herein, the goal of this proposal is to develop
a new low-cost paper/polymer hybrid microfluidic POC device integrated with LAMP for rapid,
specific, and sensitive diagnosis of two major whooping cough-causing Bordetella species (B.
pertussis and B. parapertussis) that can be used in various venues such as physicians’ offices,
schools, and other low-resource settings. Our central hypothesis is that the integration of a low-
cost portable paper-based microfluidic technology with specific DNA testing assays can provide
a fast, accurate, and rapid diagnosis in resource-poor settings (US patent # 10,875,024). To
accomplish our goal, we have developed three specific aims: (1) Develop and optimize LAMP
assays for simultaneous detection of B. pertussis and B. parapertussis; (2) Develop a low-cost
paper/polymer hybrid microfluidic POC device for the simultaneous instrument-free detection of
B. pertussis and B. parapertussis; and (3) Verify the POC device for rapid detection of Bordetella
species using clinical samples. The proposed methodology will allow for the confirmation of
suspected cases of whooping cough caused by different Bordetella species at the point of care,
filling a gap of current diagnostic methods in whooping cough. Furthermore, our biochip has great
potential for the rapid detection of a variety of other respiratory infectious diseases such as
COVID-19 in resource-poor settings.
Technology keywords
Not reported
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