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Bagaza virus in partridges and pheasants, Spain, 2010.

An essential feature of certain emerging pathogens is their ability to expand their geographic ranges. Several arboviral diseases, particularly those caused by flaviviruses, have been found in new areas beyond their usual ranges. The best example of this phenomenon was introduction of West Nile virus into the Americas in 1999 (1). Other recent expansions of flaviviruses were the introductions of Japanese encephalitis virus into Australia in 1995-1998 (2) and Usutu virus into Europe in 2001 (3).

We report an outbreak of disease in wild birds (partridges and pheasants) in Spain that was caused by a flavivirus, Bagaza virus (BAGV). This virus was first isolated in Bagaza, Central African Republic, in 1966, from a pool of mixed-species female Culex spp. mosquitoes (4). It has subsequently been found in mosquitoes in other countries in western Africa (5,6) and in India, where serologic evidence suggests that this virus may infect humans (7), although its pathogenicity in humans is uncertain. BAGV has been shown to be synonymous with Israel turkey meningoencephalitis virus, a pathogen affecting poultry (turkeys) and reported only in Israel and South Africa (8).

The Study

In September, 2010, an unusually high number of red-legged partridges (Alectoris rufa) died on several hunting properties in southwestern Cadiz, the southernmost province in Andalusia, Spain. Clinical signs included weakness, prostration, lack of motor coordination, weight loss, and white diarrhea. Some common pheasants (Phasianus colchicus) were also affected. These findings coincided in time with the first cases of West Nile virus (WNV) infection in horses detected in Spain (9).

Because red-legged partridges have recently been shown to be susceptible to WNV disease (10), it immediately raised suspicions that WNV could be responsible for these deaths. Therefore, samples were obtained from dead partridges (n = 11) and pheasants (n = 2) and sent to the Spanish Central Veterinary Laboratory in Algete for diagnostic analysis. The carcass of 1 of the affected partridges was also subjected to necroscopic analysis of different tissues, including heart, intestine, lung, liver, kidney, brain, and feathers (Table).

Analysis by real-time reverse transcription PCR (RT-PCR) specific for lineage 1 and lineage 2 WNV (11) showed negative results for all samples tested. However, a heminested RT-PCR specific for a broad range of flaviviruses (12) showed positive results for all samples (Table), indicating that a non-WNV flavivirus was present in samples from different tissues of diseased birds.

cDNA obtained after real-time RT-PCR (252-bp fragment) or heminested RT-PCR (214-bp fragment) amplification of samples was subjected to nucleotide sequencing. Resulting nucleotide sequences were compared with those in GenBank by using BLAST analysis (www. ncbi.nlm.nih.gov). Our isolates had >90% homology with 2 BAGV strains in GenBank (strain DakAr B209 from Africa, GenBank accession no. AY632545, and strain 96363 from India, GenBank accession no. EU684972).

Virus isolation was performed by infection of embyonated chicken eggs with tissue homogenates from an infected partridge and confirmed by pan-flaviviral RT-PCR and nucleotide sequencing (Table). Virus was detected more frequently in allantoic fluid of infected eggs than in other egg tissues (Table). Further propagation was accomplished in BSR cells, a clone of baby hamster kidney-21 cells.

Genomic characterization of virus was performed by bidirectional sequencing of real-time RT-PCR fragments amplified from heart and brain samples from 1 of the affected partridges. We used 27 primer sets designed for this study on the basis of sequences for BAGV in GenBank. Full-length genome sequences were obtained by assembling overlapping nucleotide sequences and using the SeqScape program (Applied Biosystems, Foster City, CA, USA). Two full-length genome sequences obtained from heart (BAGV Spain H/2010, GenBank accession no. HQ644143) and brain (BAGV Spain B/2010, accession no. HQ644144), were identical.

To assess phylogenetic relationships between these new BAGVs and other flaviviruses, the complete BAGV sequence obtained in this study (accession no. HQ644143) or a partial envelope (E) protein-coding gene subregion were aligned with other complete flaviviral genomes in GenBank by using the ClustalW algorithm in MEGA5 (13). Phylogenetic trees were constructed by using the complete BAGV genomic sequence or the partial E region (the E region is a well-known variable region in flaviviruses, and additional relevant nucleotide sequences are available in GenBank). Maximum-likelihood, neighbor-joining, or maximum-parsimony algorithms were used, and bootstrap tests with 500 replicates were performed to support each tree grouping. All generated trees showed similar topology and clustered the genomic sequence obtained in this study within the BAGV branch. Maximum likelihood trees are shown in Figures 1 and 2.

[FIGURE 1 OMITTED]

Sequence of BAGV from Spain was closely related to the 2 unique full-length BAGV sequences available in GenBank and showed greater similarity with the strain from Africa (94.1% nt identity) than with the strain from India (92.8% nt identity). Identity between the isolates from Africa and India was 95.0%, indicating that they are more related to each other than to BAGV from Spain. A total of 742 nt and 637 nt differences (70 nt and 47 aa differences) were observed between BAGV from Spain and the isolates from India and Africa, respectively. Genetic relatedness between all 3 viruses was high (>92%), which indicates that they belong to the same Flavivirus species (Bagaza virus). The tree based on the E region grouped Israel turkey meningoencephalitis virus and BAGV within the same cluster and showed that both viruses are closely related to Ntaya virus (Figure 2).

[FIGURE 2 OMITTED]

Conclusions

BAGV has been detected and isolated in Cadiz, Spain. It appeared to seriously affect partridges and, to a lesser extent, pheasants, and caused an unusually high number of deaths in these birds. No signs of infection and no deaths were observed for other bird species. However, whether other bird species are susceptible to disease caused by BAGV should be determined because this virus is similar to Israel turkey meningoencephalitis virus, a relevant pathogen for turkeys. Also, other vertebrates could be at risk for infection with this virus. Thus, experimental studies on the pathogenicity of this virus in specific vertebrates should be conducted.

Transcontinental spread of flaviviruses has been often associated with bird migrations (14,15). Thus, infected birds migrating between Africa and Europe could have introduced BAGV into Spain. However, there is no evidence of transmission of this virus by migratory birds, and alternative explanations (poultry industry or trading of exotic birds for commercial or hunting purposes) should not be overlooked.

DOI: 10.3201/eid1708.110077

Acknowledgments

We thank A. Robles, C. Gomez, A. Villalba, and other personnel for excellent technical work, and personnel from the Junta de Andalucia for skillful field work.

This study was supported in part by the Instituto Nacional de Investigacion y Tecnologia Agraria y Alimentaria-Ministerio de Medio Ambiente, Medio Rural y Marino (agreement CC08-020) and the Instituto Nacional de Investigacion y Tecnologia Agraria y Alimenteria (grant FAU 2008-00002-00-00).

Dr Aguero is a research scientist at and deputy director of the Central Veterinary Laboratory, Algete, Spain. Her research interests are virology, veterinary diagnosis, and animal health.

References

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(2.) Mackenzie JS, Johansen CA, Ritchie SA, van Den Hurk AF, Hall RA. Japanese encephalitis as an emerging virus: the emergence and spread of Japanese encephalitis virus in Australasia. Curr Top Mi crobiol Immunol. 2002;267:49-73.

(3.) Weissenbock H, Kolodziejek J, Url A, Lussy H, Rebel-Bauder B, Nowotny N. Emergence of Usutu virus, an African mosquito-borne flavivirus of the Japanese encephalitis virus group, central Europe. Emerg Infect Dis. 2002;8:652-6.

(4.) Digoutte JP. Bagaza (BAG) strain: Dak Ar B 209. Am J Trop Med Hyg. 1978;27:376-7.

(5.) Diallo M, Nabeth P, Ba K, Sall AA, Ba Y, Mondo M, et al. Mosquito vectors of the 1998-1999 outbreak of Rift Valley fever and other arboviruses (Bagaza, Sanar, Wesselsbron and West Nile) in Mauritania and Senegal. Med Vet Entomol. 2005;19:119-26. doi:10.1111/ j.0269-283X.2005.00564.x

(6.) Traore-Lamizana M, Zeller HG, Mondo M, Hervy JP, Adam F, DiGoutte JP. Isolations of West Nile and Bagaza viruses from mosquitoes (Diptera: Culicidae) in central Senegal (Ferlo). J Med Entomol. 1994;31:934-8.

(7.) Bondre VP, Sapkal GN, Yergolkar PN, Fulmali PV, Sankararaman V, Ayachit VM, et al. Genetic characterization of Bagaza virus (BAGV) isolated in India and evidence of anti-BAGV antibodies in sera collected from encephalitis patients. J Gen Virol. 2009;90:2644-9. doi:10.1099/vir.0.012336-0

(8.) Kuno G, Chang GJ. Full-length sequencing and genomic characterization of Bagaza, Kedougou, and Zika viruses. Arch Virol. 2007;152:687-96. doi:10.1007/s00705-006-0903-z

(9.) World Organisation for Animal Health. West Nile fever, Spain (immediate notification: 10/09/2010). The Organisation; 2010 [cited 2011 Mar 29]. http://web.oie.int/wahis/public.php?page=home

(10.) Sotelo E, Gutierrez-Guzman AV, Del Amo J, Llorente F, El-Harrak M, Perez-Ramirez E, et al. Pathogenicity of two recent western Mediterranean West Nile virus isolates in a wild bird species indigenous to southern Europe: the red-legged partridge. Vet Res. 2011;42:11. doi:10.1186/1297-9716-42-11

(11.) Jimenez-Clavero MA, Aguero M, Rojo G, Gomez-Tejedor C. A new fluorogenic real-time RT-PCR assay for detection of lineage 1 and lineage 2 West Nile viruses. J Vet Diagn Invest. 2006;18:459-62. doi:10.1177/104063870601800505

(12.) Scaramozzino N, Crance JM, Jouan A, DeBriel DA, Stoll F, Garin D. Comparison of flavivirus universal primer pairs and development of a rapid, highly sensitive heminested reverse transcription-PCR assay for detection of flaviviruses targeted to a conserved region ofthe NS5 gene sequences. J Clin Microbiol. 2001;39:1922-7. doi:10.1128/JCM.39.5.1922-1927.2001

(13.) Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011; [Epub ahead of print].

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(15.) Gould EA, de Lamballerie X, Zanotto PM, Holmes EC. Evolution, epidemiology, and dispersal of flaviviruses revealed by molecular phylogenies. Adv Virus Res. 2001;57:71-103. doi:10.1016/S0065 3527(01)57001-3

Address for correspondence: Miguel A. Jimenez-Clavero, Centro del Investigacion en Sanidad Animal, Instituto Nacional de Investigacion y Tecnologia Agraria y Alimentaria, Ctra. Algete, El Casar s/n, 28130, Valdeolmos, Spain; email: majimenez@inia.es

The opinions expressed by authors contributing to this journal do not necessarily reflect the opinions of the Centers for Disease Control and Prevention or the institutions with which the authors are affiliated.

Author affiliations: Laboratorio Central de Veterinaria, Algete, Spain (M. Aguero, D. Buitrago, A. Sanchez, E. San Miguel, R. Villalba); and Centro de Investigacion en Sanidad Animal, Valdeolmos, Spain (J. Fernandez-Pinero, M. Elizalde, F. Llorente, M.A. Jimenez-Clavero)
Table. Analysis of red-legged partridges (Alectoris rufa) and
common pheasants (Phasianus colchicus) for WNV and BAGV, Cadiz,
Spain, 2010 *

                                                            Virus
                                         No. positive/    isolation
            No. animals                  no. tested      in ECE, no.
Species      analyzed     Sample type    WNV    BAGV       samples
                                                          positive/
                                                         no. tested
                                                         ([dagger])

A. rufa         11           Brain       0/11   11/11     1/3 (AF)
                          Cloacal swab   0/2     1/2         NA
                           Oral swab     0/2     1/2         NA
                              Gut        0/1     1/1         NA
                             Heart       0/1     1/1      1/3 (AF)
                           ([dagger])
                            Kidney       0/1     1/1    2/3 (AF, CM,
                            ([double                       and VS)
                            dagger])
                              Lung       0/1     1/1         NA
                             Liver       0/1     1/1         NA
                             Blood       0/1     1/1         NA
                           Featherss.     0/3     3/3         NA
P.               2           Brain       0/2     2/2         NA
colchicus

* West Nile virus (WNV) or Bagaza virus (BAGV) nucleic acids were
identified by using real-time reverse transcription PCR (RT-PCR) or
panflaviviral heminested RT-PCR, respectively, and amplicon (214 bp)
sequencing. ECE, embryonated chicken egg; AF, allantoic fluid; NA,
not analyzed; CM, chorioallantoic fluid; VS, viscera.

([dagger]) ECEs were infected with homogenates of various samples.

([double dagger]) Samples from which full-length sequence of BAGV was
obtained.

([section] Tail, breast, and wing feathers from 1 partridge were
analyzed.
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Title Annotation:DISPATCHES
Author:Aguero, Montserrat; Fernandez-Pinero, Jovita; Buitrago, Dolores; Sanchez, Azucena; Elizalde, Maia; S
Publication:Emerging Infectious Diseases
Article Type:Report
Geographic Code:4EUSP
Date:Aug 1, 2011
Words:2027
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