Evaluation of the diagnostic potential of recombinant leptospiral OMP A-like protein (Loa22) and transmembrane (OmpL37) protein in latex agglutination test for serodiagnosis of leptospirosis in animals.


Journal

Letters in applied microbiology
ISSN: 1472-765X
Titre abrégé: Lett Appl Microbiol
Pays: England
ID NLM: 8510094

Informations de publication

Date de publication:
Jun 2021
Historique:
revised: 02 02 2021
received: 05 10 2020
accepted: 11 02 2021
pubmed: 17 2 2021
medline: 28 5 2021
entrez: 16 2 2021
Statut: ppublish

Résumé

Leptospirosis is a re-emerging zoonotic disease of animals and humans caused by pathogenic Leptospira, which has major public health concerns. The study is aimed to express the recombinant outer membrane protein (OMP) A-like protein (rLoa22) and transmembrane (rOmpL37) protein of Leptospira interrogans serovar Hardjo in the Escherichia coli and their evaluation as a diagnostic antigen in the latex agglutination test (LAT) to detect anti-leptospiral antibodies in the sera of animals. The Loa22 and OmpL37 genes lacking signal peptide coding sequences were individually amplified (522 and 963 bp), by polymerase chain reaction, and directionally cloned into a pETite N-His Kan vector for expression. The expressed purified proteins were characterized by sodium dodecyl sulphate-polyacrylamide gel electrophoresis and immunoblot, which confirmed leptospiral specific reactive protein with a molecular weight of ~19 and 36 kDa, respectively. The sensitized latex beads coated with these OM proteins separately were evaluated in LAT using cattle sera of microscopic agglutination test (MAT) confirmed positive (n = 53) and negative (n = 52) cases of leptospirosis. The rLoa22 LAT and rOmpL37 LAT revealed the relative diagnostic sensitivity of 94·34 and 96·23%, diagnostic specificity of 92·31 and 96·15% and accuracy of 93·33 and 96·19%, with the excellent agreement of Cohen's kappa value of 0·87 and 0·92, respectively. After extensive evaluation, this rapid recombinant protein-based field diagnostic test can be applied as a screening test for the detection of anti-leptospiral antibodies in the sera of animals in the field conditions.

Identifiants

pubmed: 33590504
doi: 10.1111/lam.13461
doi:

Substances chimiques

Antibodies, Bacterial 0
Antibodies, Protozoan 0
Antigens, Bacterial 0
Bacterial Outer Membrane Proteins 0
Recombinant Proteins 0
OMPA outer membrane proteins 149024-69-1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

730-740

Subventions

Organisme : Indian Council of Medical Research
ID : Leptos/7/2013-ECD-I
Organisme : Indian Council of Medical Research
ID : 80/820/2013-ECD-I

Informations de copyright

© 2021 The Society for Applied Microbiology.

Références

Alamuri, S., Kumar, K.V., SowjanyaKumari, S., Linshamol, L., Sridevi, R., Nagalingam, M., Roy, P. and Balamurugan, V. (2020) Expression of recombinant leptospiral surface lipoprotein-Lsa27 in E. coli and its evaluation for serodiagnosis of bovine leptospirosis by latex agglutination test. Mol Biotechnol 62, 598-610.
Alizadeh, S.A., Abdolahpour, G., Pourmand, M.R., Naserpour, T., Najafipour, R. and Eshraghi, S.S. (2014) Evaluation of New ELISA based on rLsa63 - rLipL32 antigens for serodiagnosis of human leptospirosis. Iran J Microbiol 6, 184-189.
Altschul, S.F., Madden, T.L., Schaffer, A.A., Zhang, J., Zhang, Z., Miller, W. and Lipman, D.J. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25, 3389-3402.
Balamurugan, V., Alamuri, A., Bharathkumar, K., Patil, S.S., Govindaraj, G.N., Nagalingam, M., Krishnamoorthy, P., Rahman, H. et al. (2018) Prevalence of Leptospira serogroup-specific antibodies in cattle associated with reproductive problems in endemic states of India. Trop Anim Health Prod 50, 1131-1138.
Balamurugan, V., Thirumalesh, S.R.A., Sridevi, R., Govindaraj, G., Nagalingam, M., Hemadri, D., Gajendragad, M.R. and Rahman, H. (2016) Microscopic agglutination test analysis identifies prevalence of intermediate species serovars in ruminants in endemic states of India. Proc Natl Acad Sci India Sect B Biol Sci 86, 469-475.
Balamurugan, V., Veena, S., Thirumalesh, S.R.A., Alamuri, A., Sridevi, R., Sengupta, P.P., Govindaraj, G., Nagalingam, M. et al. (2017) Distribution of serogroup specific antibodies against leptospirosis in livestock in Odisha. Indian J Anim Sci 87, 546-551.
Chalayon, P., Chanket, P., Boonchawalit, T., Chattanadee, S., Srimanote, P. and Kalambaheti, T. (2011) Leptospirosis serodiagnosis by ELISA based on recombinant outer membrane protein. Trans R Soc Trop Med Hyg 105, 289-297.
Delooz, L., Czaplicki, G., Gregoire, F., Dal Pozzo, F., Pez, F., Kodjo, A. and Saegerman, C. (2018) Serogroups and genotypes of Leptospira spp. strains from bovine aborted foetuses. Transbound Emerg Dis 65, 158-165.
Deneke, Y., Sabarinath, T., Gogia, N., Lalsiamthara, J., Viswas, K.N. and Chaudhuri, P. (2014) Evaluation of recombinant LigB antigen-based indirect ELISA and latex agglutination test for the serodiagnosis of bovine leptospirosis in India. Mol Cell Probes 28, 141-146.
Costa, F., Hagan, J. E., Calcagno, J., Kane, M., Torgerson, P., Martinez-Silveira, M. S., Stein, C., Abela-Ridder, B., and Ko, A. I. (2015) Global Morbidity and Mortality of Leptospirosis: A Systematic Review. PLOS Neglected Tropical Diseases 9, e0003898. https://doi.org/10.1371/journal.pntd.0003898
Dey, S., Madhan Mohan, C., Ramadass, P., and Nachimuthu, K. (2007) Recombinant Antigen-based Latex Agglutination Test for Rapid Serodiagnosis of Leptospirosis. Veterinary Research Communications 31, 9-15. https://doi.org/10.1007/s11259-006-3364-7
Ellis, W.A. (2015) Animal leptospirosis. Curr Top Microbiol Immunol 387, 99-137.
Ghosh, K.K., Prakash, A., Shrivastav, P., Balamurugan, V. and Kumar, M. (2018) Evaluation of a novel outer membrane surface-exposed protein, LIC13341 of Leptospira, as an adhesin and serodiagnostic candidate marker for leptospirosis. Microbiology 164, 1023-1037.
Haake, D.A. and Zuckert, W.R. (2015) The leptospiral outer membrane. Curr Top Microbiol Immunol 387, 187-221.
Hull-Jackson, C., Glass, M.B., Ari, M.D., Bragg, S.L., Branch, S.L., Whittington, C.U., Edwards, C.N. and Levett, P.N. (2006) Evaluation of a commercial latex agglutination assay for serological diagnosis of leptospirosis. J Clin Microbiol 44, 1853-1855.
Libonati, H.A., Santos, G.B., Souza, G.N., Brandao, F.Z. and Lilenbaum, W. (2018) Leptospirosis is strongly associated to estrus repetition on cattle. Trop Anim Health Prod 50, 1625-1629.
Limmathurotsakul, D., Turner, E.L., Wuthiekanun, V., Thaipadungpanit, J., Suputtamongkol, Y., Chierakul, W., Smythe, L.D., Day, N.P. et al. (2012) Fool's gold: why imperfect reference tests are undermining the evaluation of novel diagnostics: a reevaluation of 5 diagnostic tests for leptospirosis. Clin Infect Dis 55, 322-331.
Nagalingam, M., Thirumalesh, S.R., Kalleshamurthy, T., Niharika, N., Balamurugan, V., Shome, R., Sengupta, P.P., Shome, B.R. et al. (2015) Comparative evaluation of recombinant LigB protein and heat-killed antigen-based latex agglutination test with microscopic agglutination test for diagnosis of bovine leptospirosis. Trop Anim Health Prod 47, 1329-1335.
OIE (2018) Chapter 3.1.12. Leptospirosis. Manual of diagnostic tests and vaccines for terrestrial animals 2019 pp. 503-5016. Terrestrial Manual. 1, 2, 3, 8. OIE. https://www.oie.int/fileadmin/Home/eng/Health_standards/tahm/3.01.12_LEPTO.pdf
Picardeau, M. (2015) Leptospirosis: updating the global picture of an emerging neglected disease. PLoS Negl Trop Dis 9, e0004039. https://doi.org/10.1371/journal.pntd.0004039.
Pinne, M., Choy, H.A. and Haake, D.A. (2010) The OmpL37 surface-exposed protein is expressed by pathogenic Leptospira during infection and binds skin and vascular elastin. PLoS Negl Trop Dis 4, e815.
Raja, V. and Natarajaseenivasan, K. (2015) Pathogenic, diagnostic and vaccine potential of leptospiral outer membrane proteins (OMPs). Crit Rev Microbiol 41, 1-17.
Senthilkumar, T., Subathra, M., Phil, M., Ramadass, P. and Ramaswamy, V. (2008a) Rapid serodiagnosis of leptospirosis by latex agglutination test and flow-through assay. Indian J Med Microbiol 26, 45-49.
Senthilkumar, T., Subathra, M. and Ramadass, P. (2008b) Latex agglutination test for the detection of canine leptospiral antibodies using recombinant OmpL1 antigen. Veternarski Arhiv 78, 393-399.
Senthilkumar, T.M., Subathra, M., Ramadass, P. and Ramaswamy, V. (2010) Serodiagnosis of bovine leptospirosis by IgG-enzyme-linked immunosorbent assay and latex agglutination test. Trop Anim Health Prod 42, 217-222.
Shekatkar, S., Acharya, N., Harish, B. and Parija, S. (2010) Comparison of an in-house latex agglutination test with IgM ELISA and MAT in the diagnosis of leptospirosis. Indian J Med Microbiol 28, 238-240.
Smits, H.L., Chee, H.D., Eapen, C.K., Kuriakose, M., Sugathan, S., Gasem, M.H., Yersin, C., Sakasi, D. et al. (2001) Latex based, rapid and easy assay for human leptospirosis in a single test format. Trop Med Int Health 6, 114-118.
Thome, S., Lessa-Aquino, C., Ko, A., Lilenbaum, W. and Medeiros, M. (2014) Identification of immunodominant antigens in canine leptospirosis by Multi-Antigen Print ImmunoAssay (MAPIA). BMC Vety Res 10, 288.
Ye, C., Yan, W., Xiang, H., He, H., Yang, M., Ijaz, M., Useh, N., Hsieh, C.-L. et al. (2014) Recombinant antigens rLipL21, rLoa22, rLipL32, and rLigACon4-8 for serological diagnosis of leptospirosis by enzyme-linked immunosorbent assays in dogs. PLoS One 9, e111367.

Auteurs

V Balamurugan (V)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.

S R A Thirumalesh (SRA)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.
Jain University, Bengaluru, Karnataka, India.

A Alamuri (A)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.

S SowjanyaKumari (S)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.

K Vinod Kumar (K)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.

L Linshamol (L)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.

V Bharath (V)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.

M Nagalingam (M)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.

P Roy (P)

ICAR-National Institute of Veterinary Epidemiology and Disease informatics (NIVEDI), Yelahanka, Bengaluru, Karnataka, India.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH