EN PL
ORIGINAL PAPER
Antibody profile to Borrelia burgdorferi in veterinarians from Nuevo León, Mexico, a non-endemic area of this zoonosis
 
More details
Hide details
 
Submission date: 2016-05-04
 
 
Final revision date: 2016-06-30
 
 
Acceptance date: 2016-07-02
 
 
Online publication date: 2016-07-18
 
 
Publication date: 2016-06-30
 
 
Reumatologia 2016;54(3):97-102
 
KEYWORDS
TOPICS
ABSTRACT
Objectives: Lyme disease is a tick-borne disease caused by infections with Borrelia. Persons infected with Borrelia can be asymptomatic or can develop disseminated disease. Diagnosis and recognition of groups at risk of infection with Borrelia burgdorferi is of great interest to contemporary rheumatology. There are a few reports about Borrelia infection in Mexico, including lymphocytoma cases positive to B. burgdorferi sensu stricto by PCR and a patient with acrodermatitis chronica atrophicans. Veterinarians have an occupational risk due to high rates of tick contact.
The aim of this work was to investigate antibodies to Borrelia in students at the Faculty of Veterinary Medicine and Zootechnics, at Nuevo León, Mexico, and determine the antibody profile to B. burgdorferi antigens.
Material and methods: Sera were screened using a C6 ELISA, IgG and IgM ELISA using recombinant proteins from B. burgdorferi, B. gariniii and B. afzelii. Sera with positive or grey-zone values were tested by IgG Western blot to B. burgdorferi sensu stricto.
Results: All volunteers reported tick exposures and 72.5% remembered tick bites. Only nine persons described mild Lyme disease related symptoms, including headaches, paresthesias, myalgias and arthralgias. None of the volunteers reported erythema migrans. Nine samples were confirmed by IgG Western blot. The profile showed 89% reactivity to OspA, 67% to p83, and 45% to BmpA.
Conclusions: Positive sera samples shared antibody reactivity to the markers of late immune response p83 and BmpA, even if individuals did not present symptoms of Lyme arthritis or post-Lyme disease. The best criterion to diagnose Lyme disease in our country remains to be established, because it is probable that different strains coexist in Mexico. This is the first report of antibodies to B. burgdorferi in Latin American veterinarians. Veterinarians and high-risk people should be alert to take precautionary measures to prevent tick-borne diseases.
 
REFERENCES (33)
1.
Castro LR, Gabrielli S, Lori A, Cancrini G. Molecular detection of Rickettsia, Borrelia, and Babesia species in Ixodes ricinus sampled in northeastern, central, and insular areas of Italy. Exp Appl Acarol 2015; 66: 443-452.
 
2.
Adelson ME, Rao RV, Tilton RC, et al. Prevalence of Borrelia burgdorferi, Bartonella spp., Babesia microti, and Anaplasma phagocytophila in Ixodes scapularis ticks collected in Northern New Jersey. E J Clin Microbio 2004; 42: 2799-2801.
 
3.
Steere AC, Coburn J, Glickstein L. The emergence of Lyme disease. J Clin Invest 2004; 113: 1093-1101.
 
4.
Aguero-Rosenfeld ME, Wang G, Schwartz I, Wormser GP. Diagnosis of Lyme borreliosis. Clin Microbiol Rev 2005; 18: 484-509.
 
5.
Ścieszka J, Dąbek J, Cieślik P. Post-Lyme disease syndrome. Reumatologia 2015; 53: 46-48.
 
6.
Harvey WT, Salvato P. ‘Lyme disease’: Ancient engine of an unrecognized borreliosis pandemic? Med Hypotheses 2003; 60: 742-759.
 
7.
Burgess EC, Windberg LA. Borrelia sp. infection in coyotes, black-tailed jack rabbits and desert cottontails in southern Texas. J Wildl Dis 1989; 25: 47-51.
 
8.
Lin T, Oliver JH Jr, Gao L, et al. Genetic heterogeneity of Borrelia burgdorferi sensu lato in the Southern United States based on restriction fragment length polymorphism and sequence analysis. J Clin Microbiol 2001; 39: 2500-2507.
 
9.
Williamson PC, Billingsley PM, Teltow GJ, et al. Borrelia, Ehrlichia, and Rickettsia spp. in ticks removed from persons, Texas, USA. Emerg Infect Dis 2010; 16: 441-446.
 
10.
Cohen ND, Carter CN, Thomas MA Jr, et al. Clinical and epizootiologic characteristics of dogs seropositive for Borrelia burgdorferi in Texas: 110 cases (1988). J Am Vet Med Assoc 1990; 197: 893-898.
 
11.
Mead P, Goel R, Kugeler K. Canine serology as adjunct to human Lyme disease surveillance. Emerg Infect Dis 2011; 17: 1710-1712.
 
12.
Guzmán C, Robbins R. The genus Ixodes (Acari: Ixodidae) in Mexico: adult identifcation keys, diagnoses, hosts, and distribution. Rev Mex Biodivers 2010; 81: 289-298.
 
13.
Vargas MH. Lyme disease in Mexico City. Salud Publica Mex 1993; 35: 435-436 [in Spanish].
 
14.
Galaviz-Silva L, Pérez-Trevińo KC, Molina-Garza ZJ. Distribution of ixodid ticks on dogs in Nuevo León, Mexico, and their association with Borrelia burgdorferi sensu lato. Exp Appl Acarol 2013; 61: 491-501.
 
15.
Salinas-Meléndez JA, Tamez-González R, Welsh-Lozano O, Barrera-Saldańa HA. Detection of Borrelia burgdorferi DNA in human skin biopsies and dog synovial fluid by the polymerase chain reaction. Rev Latinoam Microbiol 1995; 37: 7-10.
 
16.
Salinas-Meléndez JA, Avalos-Ramírez R, Riojas-Valdez VM, Martínez-Muńoz A. Serological survey of canine borreliosis. Rev Latinoam Microbiol 1999; 41: 1-3.
 
17.
Salinas-Mélendez JA, Galván de la Garza S, Riojas-Valdés VM, et al. Antibody detection against Borrelia burgdorferi in horses located in the suburban areas of Monterrey, Nuevo Leon. Rev Latinoam Microbiol 2001; 43: 161-164.
 
18.
Gordillo-Pérez Torres J, Solórzano-Santos F, et al. Seroepidemiologic study of Lyme’s borreliosis in Mexico City and the northeast of the Mexican republic. Salud Publica Mex 2003; 45: 351-355.
 
19.
Gordillo-Pérez G, Torres J, Solórzano-Santos F, et al. Borrelia burgdorferi infection and cutaneous Lyme disease, Mexico. Emerg Infect Dis 2007; 13: 1556-1558.
 
20.
Feria-Arroyo TP, Castro-Arellano I, Gordillo-Perez G, et al. Implications of climate change on distribution of tick vector Ixodes scapularis and risk for Lyme Disease in Texas-Mexico transboundary region. Parasit Vectors 2014; 7: 199.
 
21.
Jackson J, Villarroel A. A survey of the risk of zoonoses for veterinarians. Zoonoses Public Health 2012; 59: 193-201.
 
22.
McDaniel CJ, Cardwell DM, Moeller RB Jr, Gray GC. Humans and cattle: a review of bovine zoonoses. Vector Borne Zoonotic Dis 2014; 14: 11-19.
 
23.
Magnarelli LA, Ijdo JW, Padula SJ, et al. Serologic diagnosis of Lyme borreliosis by using enzyme-linked immunosorbent assays with recombinant antigens. J Clin Microbiol 2000; 38: 1735-1739.
 
24.
Cisak EJ, Chmielewska-Badora J, Zwolinski A, et al. Risk of tick-borne bacterial diseases among workers of Roztocze national park (southeastern Poland). Ann Agric Environ Med 2005; 12: 127-132 .
 
25.
Fahrer H, Van der Linden SM, Sauvain MJ, et al. The prevalence and incidence of clinical and asymptomatic Lyme borreliosis in a population at risk. J Infect Dis 1991; 163: 305-310.
 
26.
Lin T, Gao L, Seyfang A, Oliver JH Jr. ‘Candidatus Borrelia texasensis’, from the American dog tick Dermacentor variabilis. Int J Syst Evol Microbiol 2005; 55: 685-693.
 
27.
Pritt BS, Mead PS, Johnson DK, et al. Identification of a novel pathogenic Borrelia species causing Lyme borreliosis with unusually high spirochaetaemia: a descriptive study. Lancet Infect Dis 2016; pii: S1473-3099(15)00464-8.
 
28.
Escalier-Palmer MG, Meza-Nava AI. Borreliosis. A. Clinic case. Rev Sanid Milit Mex 2006; 60: 346-351 [in Spanish].
 
29.
Wormser GP, Tang AT, Schimmoeller NR, et al. Utility of serodiagnostic designed for use in the United States for detection of Lyme borreliosis acquired in Europe and vice versa. Med Microbiol Immunol 2014; 203: 65-71.
 
30.
Kalish RA, Leong JL,Steere AC. Association of treatment-resistant chronic Lyme arthritis with HLA-DR4 and antibody reactivity to Osp A and Osp B of Borrelia burgdorferi. Infect Immun 1993; 61: 2774-2779.
 
31.
Montgomery RR, Malawista SE, Feen KJ, Bockenstedt LK. Direct demonstration of antigenic substitution of Borrelia burgdorferi ex vivo: Exploration of the paradox of the early immune response to outer surface proteins A and C in Lyme disease. Exp Med 1996; 183: 261-269.
 
32.
Steere AC, Drouin E E, Glickstein LJ. Relationship between Immunity to Borrelia burgdorferi Outer-surface Protein A (OspA) and Lyme Arthritis. Clin Infect Dis 2011; 52: 259-265.
 
33.
Malawista SE, Montgomery RR, Wang XM, et al. Geographic clustering of an outer surface protein A mutant of Borrelia burgdorferi. Possible implications of multiple variants for Lyme disease persistence. Rheumatology 2000; 39: 537-541.
 
Copyright: © Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie. This is an Open Access journal, all articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (https://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
eISSN:2084-9834
ISSN:0034-6233
Journals System - logo
Scroll to top