1. A customizable multiplex protein microarray for antibody testing and its application for tick-borne and other infectious diseases.
- Author
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Krishnamurthy HK, Jayaraman V, Krishna K, Wang T, Bei K, Changalath C, Matilda S, Rai AJ, Welc-Falęciak R, Pawełczyk A, Blanton LS, Chrdle A, Fořtová A, Růžek D, Nasrallah GK, Abu-Raddadi LJ, Al-Sadeq DW, Abdallah MAA, Lilleri D, Fornara C, D'Angelo P, Furione M, Söderlund-Venermo M, Hedman K, Chochlakis D, Makridaki E, Ntoula A, Psaroulaki A, Escárcega-Ávila A, and Rajasekaran JJ
- Subjects
- Humans, Lyme Disease diagnosis, Lyme Disease immunology, Immunoglobulin M blood, Immunoglobulin M immunology, Immunoglobulin G immunology, Immunoglobulin G blood, Animals, Antigens, Bacterial immunology, Ticks microbiology, Protein Array Analysis methods, Tick-Borne Diseases diagnosis, Tick-Borne Diseases immunology, Antibodies, Bacterial immunology, Antibodies, Bacterial blood, Borrelia burgdorferi immunology
- Abstract
Tick-borne infections are the most common vector-borne diseases in the USA. Ticks harbor and transmit several infections with Lyme disease being the most common tickborne infection in the US and Europe. Lack of awareness about tick populations, specific diagnostic tests, and overlapping signs and symptoms of tick-borne infections can often lead to misdiagnosis affecting treatment and the prevalence data reported especially for non-Lyme tick-borne infections. The diagnostic tests currently available for tick-borne diseases are severely limited in their ability to provide accurate results and cannot detect multiple pathogens in a single run. The multiplex protein microarray developed at Vibrant was designed to detect multiple serological antibodies thereby detecting exposure to multiple pathogens simultaneously. Our microarray in its present form can accommodate 400 antigens (molecules that can bind to specific antibodies) and can multiplex across antigen types, whole cell lysates, recombinant proteins, and peptides. A designed array containing multiple antigens of several microbes including Borrelia burgdorferi, the Lyme disease spirochete, was manufactured and evaluated. The immunoglobulin M (IgM) and G (IgG) responses against several tick-borne microbes and other infectious agents were analyzed for analytical and clinical performance. The microarray improved IgM and IgG sensitivities and specificities of individual microbes when compared with the respective gold standards. The testing was also performed in a single run in comparison to multiple runs needed for comparable testing standards. In summary, our study presents a flexible multiplex microarray platform that can provide quick results with high sensitivity and specificity for evaluating exposure to varied infectious agents especially tick-borne pathogens., Competing Interests: Declarations. Competing interests: The authors have read the journal’s policy and the authors of this manuscript have the following competing interests: CC and SM are paid employees of Vibrant America LLC. KK, VJ, TW, KB, HKK, and JJR are paid employees of Vibrant Sciences LLC. RWF, AP, LSB, AC, AF, DR, GKN, LJA, DWA, MAA, DL, CF, PD, MF, MSV, KH, DC, EM, AN, AP, and AE are academic collaborators who provided samples and assisted in the review and editing of the manuscript. AJR is a paid consultant of Vibrant America LLC. Vibrant America offers commercial testing for Lyme disease and other infectious diseases and could benefit from increased testing., (© 2025. The Author(s).)
- Published
- 2025
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