|SHORT RESEARCH COMMUNICATION
|Year : 2018 | Volume
| Issue : 1 | Page : 66-67
Antibodies to West Nile virus in Mexican pigs
Teresa Merino-Ramos1, Elizabeth Loza-Rubio2, Edith Rojas-Anaya2, Miguel A Martín-Acebes1
1 Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain
2 Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias (CENID-Microbiología), México D.F, Mexico
|Date of Submission||07-Sep-2016|
|Date of Acceptance||21-Dec-2017|
|Date of Web Publication||18-Jun-2018|
Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Ctra. De la Coruña Km 7.5, CP 28040, Madrid
Source of Support: None, Conflict of Interest: None
Keywords: Epidemiology; Flavivirus; pigs; surveillance; West Nile virus; zoonotic diseases
|How to cite this article:|
Merino-Ramos T, Loza-Rubio E, Rojas-Anaya E, Martín-Acebes MA. Antibodies to West Nile virus in Mexican pigs. J Vector Borne Dis 2018;55:66-7
|How to cite this URL:|
Merino-Ramos T, Loza-Rubio E, Rojas-Anaya E, Martín-Acebes MA. Antibodies to West Nile virus in Mexican pigs. J Vector Borne Dis [serial online] 2018 [cited 2022 Aug 16];55:66-7. Available from: https://www.jvbd.org/text.asp?2018/55/1/66/234630
West Nile virus (WNV), a member of Flavivirus genus within the Flaviviridae family, is a mosquito-borne neurotropic viral pathogen maintained in an enzootic cycle between mosquitoes (vectors) and birds (natural hosts) with equids, humans, and other vertebrates acting as dead-end hosts. WNV was first detected in the Americas in New York in 1999, and since then, the virus has spread across the United States (US), north into Canada, and south into Mexico and central/south America. However, contrary to the high mortality among birds and horses, and the hundreds of human deaths reported in the US, very few veterinary or human cases have been described in Mexico.
The first evidence of WNV activity in Mexico, was reported in 2002, when antibodies to WNV were detected in horses in states border to the US, and, since then, viral activity has been observed in several domestic and wild fauna, and in humans across the country.The virus has been isolated from different birds, mosquitoes, and humans. Though, porcine production in the Mexico (with over 1.300 million tons of meat/yr) occupies the second place in central and south America, only behind Brazil, no serological studies have been conducted in pigs in Mexico. In fact, very few studies have addressed the worldwide prevalence of anti-WNV antibodies in swine. Here, data on the detection of antibodies against WNV in farmed pigs in Mexico are presented.
Swine serum samples (n = 683) were collected during 2010–13 from nine states in the central region of Mexico. Samples included healthy pigs (>1 to 48 months of age) grown in farms from 48 municipalities. Written permission was obtained from the farm’s owners for sample collection and the study was conducted in accordance to all the applicable guidelines related to animal welfare. The study was approved by the Institutional Animal Care and Use Committee (IACUC) of the Centro Nacional de Investigación Disciplinaria en Microbiología Animal (No. approval: 001-2012), Mexico.
Anti-WNV IgG was detected using an inactivated WNV-based enzyme linked immunosorbent assay (ELISA) as described by Cordoba et al. The positive/ negative (P/N) value of each sample was calculated as the mean absorbance of positive antigen-containing wells divided by the mean absorbance of the negative antigen-containing wells. Samples with a P/N value >2 were considered positive. All positive samples and an equal number of negative samples were retested to confirm the results. The detection of neutralizing antibodies was undertaken by virus neutralization test (VNT) on Vero cells using two-fold serial dilutions of serum (starting form 1/20) and a cell culture passaged New York/1999 (NY99) WNV strain (GenBank acc.: KC407666),. Titres were calculated as the serum dilution that completely inhibited cytopathic effect. All infectious virus manipulations were performed in biosafety level 3 (BSL-3) facilities. Statistical significance of the data was analyzed using the chi-square test.
In total, 4.5% (31/683) of the serum tested were positive for WNV antibodies by ELISA (average P/N = 3.13, range 2.10–5.98), of which 35.5% neutralized viral infectivity with VNT titres of 1/20. Although, similar studies are scarce, these figures are similar to that reported in Spain, where 3.4% swine serum samples were positive in ELISA, and India, where prevalence ranged from 2.13 to 7.7%, but lower than those from US, where 22.6% positive samples were recorded. Likewise, and although the reasons are not clear yet, a discrepancy between the number of ELISA and VNT positive samples as that observed in this study, has also been documented previously in pigs around the world,.
The proportion of anti-WNV IgG positive animals was significantly higher among animals older than six months of age (11.7%, 23/197, p <0.0001), than among pigs under six months of age (1.7%, 8/478). These data agree with those reported previously for pigs in USA and probably reflect a higher exposure of older animals to the mosquito bites. Additionally, WNV antibodies were more prevalent in females (6.97%, p <0.0057) than in males (1.8%). No relationship was found between the WNV seropositivity observed in this study and that reported earlier for other viral infections in the same cohort. The prevalence of anti-WNV antibodies varied widely between states and municipalities [Table 1]. Infected pigs were only found in four (San Luis Potosí, Puebla, Michoacán and Jalisco) of the nine states included in the study. Statistically significant differences were observed for the number of farms with positive animals (positive farms) among the states analyzed (p < 0.0008). The number of farms with positive animals was higher in Michoacán (50%) and Jalisco state (63.3%). Specifically, 19% of the total tested pigs resulted positive in Michoacán and 9.1% of the total tested pigs resulted positive in Jalisco. No appreciable geographical or climatic differences were observed with regard to the seroprevalence rates. For instance, farms from the same state showed uneven seroprevalence.
|Table 1: Number and percentages of WNV positive pigs (determined by ELISA and VNT) in municipalities and farms in the studied Mexican states|
Click here to view
Even though, the role of pigs in the life cycle of WNV still has to be elucidated, the virus has been shown to replicate at low levels in experimentally infected pigs without clinical signs. Thus, contrary to the WNV-related flavivirus Japanese encephalitis virus, pigs are unlikely to play a role in WNV amplification in nature. Although, some reports have described the seroconversion of pigs pointing to its possible usefulness as sentinels,, the experimental infection data and lower prevalence of anti-WNV antibodies found in this study, as well as in other regions of the world, suggests that pigs do not play significant role in WNV circulation, therefore, do not appear to be good sentinel candidates.
| References|| |
Martin-Acebes MA, Saiz JC. West Nile virus: A re-emerging pathogen revisited. World J Virol
2012; 1(2): 51-70.
Elizondo-Quiroga D, Elizondo-Quiroga A. West Nile virus and its theories, a big puzzle in Mexico and Latin America. J Glob Infect Dis
2013; 5(4): 168-75.
Merino-Ramos T, Martin-Acebes MA, Casal J, Saiz JC, Loza- Rubio E. Prevalence of Hepatitis E virus (hev) antibodies in mexican pigs. Food Environ Virol
2016; 8(2): 156-9.
Cordoba L, Escribano-Romero E, Garmendia A, Saiz JC. Pregnancy increases the risk of mortality in West Nile virus-infected mice. J Gen Virol
Martin-Acebes MA, Saiz JC. A West Nile virus mutant with increased resistance to acid-induced inactivation. J Gen Virol
2011; 92(pt IV): 831-40.
Gutierrez-Guzman AV, Vicente J, Sobrino R, Perez-Ramirez E, Llorente F, Hofle U. Antibodies to West Nile virus and related flaviviruses in wild boar, red foxes and other mesomammals from spain. Vet Microbiol
2012; 159(3-4): 291-7.
Ratho RK, Sethi S, Prasad SR. Prevalence of Japanese encephalitis and West Nile viral infections in pig population in and around Chandigarh. J Commun Dis
Gibbs SE, Marlenee NL, Romines J, Kavanaugh D, Corn JL, Stallknecht DE. Antibodies to West Nile virus in feral swine from Florida, Georgia, and Texas, USA. Vector Borne Zoonotic Dis
2006; 6(3): 261-5.
Teehee ML, Bunning ML, Stevens S, Bowen RA. Experimental infection of pigs with West Nile virus. Arch Virol
2005; 150(6): 1249-56.
Weaver SC, Reisen WK. Present and future arboviral threats. Antiviral Res
2010; 85(2): 328-45.