Next Article in Journal / Special Issue
Genetic, but Not Behavioral, Evidence Supports the Distinctiveness of the Mealy Amazon Parrot in the Brazilian Atlantic Forest
Previous Article in Journal
Postojna-Planina Cave System in Slovenia, a Hotspot of Subterranean Biodiversity and a Cradle of Speleobiology
Previous Article in Special Issue
Parrot Free-Flight as a Conservation Tool
 
 
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Communication

Molecular Survey of Pathogens in Wild Amazon Parrot Nestlings: Implications for Conservation

1
Avian Ecopathology Laboratory, School of Veterinary Medicine and Animal Science, University of São Paulo, 05508-270 São Paulo, Brazil
2
Society for Wildlife Research and Environmental Education, 80520-310 Curitiba, Brazil
3
Parque das Aves, 85855-750 Foz do Iguaçu, Brazil
4
Neotropical Foundation of Brazil, 79290-000 Bonito, Brazil
5
Institute of Biological Sciences, University of Passo Fundo, 99042-800 Passo Fundo, Brazil
*
Author to whom correspondence should be addressed.
Diversity 2021, 13(6), 272; https://doi.org/10.3390/d13060272
Received: 26 April 2021 / Revised: 11 June 2021 / Accepted: 12 June 2021 / Published: 16 June 2021

Abstract

:
South America presents the greatest Psittacidae diversity in the world, but also has the highest numbers of threatened parrot species. Recently, exotic viruses have been detected in captive native psittacine birds in Brazil, however, their impacts on the health of wild parrots are still unknown. We evaluated the presence of Chlamydia psittaci, Psittacid alphaherpesvirus 1 (PsHV-1), avipoxvirus and beak and feather disease virus (BFDV) in wild Amazona aestiva, A. brasiliensis and A. pretrei nestlings and in wild caught A. aestiva nestlings seized from illegal trade. Samples were collected from 205 wild nestlings and 90 nestlings from illegal trade and pathogen-specific PCR was performed for each sample. Chlamydia DNA prevalence was 4.7% in A. aestiva and 2.5% in A. brasiliensis sampled from the wild. Sequencing revealed that the C. psittaci sample belonged to the genotype A. PsHV-1, avipoxvirus and BFDV DNA was not detected. These results have conservation implications since they suggest that wild parrot populations have a low prevalence of the selected pathogens and, apparently, they were not reached by the exotic BFDV. Stricter health protocols should be established as condition to reintroduction of birds to the wild to guarantee the protection of Neotropical parrots.

1. Introduction

Psittacidae diversity in South America is the greatest in the world and Brazil is the country with the largest number of species. Among the 411 known species, 86 occur in the national territory [1]. Unfortunately, Brazil is also in the first position when it comes to threatened species, with Psittaciformes being one of the most threatened, containing 25 native species in the Global International Union for Conservation of Nature (IUCN) Red List [2].
Amazon parrots are prominent among the national species, being the first among the most trafficked psittacine birds in Brazil. Amazona genus comprises 12 species in Brazil and these birds are threatened mainly by the illegal trade and loss of their habitat. Currently, one third of the native Amazon species is threatened [2].
Among these species, the red-spectacled Amazon parrot (Amazona pretrei) is threatened within the vulnerable category. The red-tailed Amazon parrot (Amazona brasiliensis) has left the IUCN Red List, entering the near-threatened status. Both species have a restricted distribution and exist only in Brazilian territory. The blue-fronted Amazon parrot (Amazona aestiva) is also in the near-threatened category and has a wide distribution, including Brazil, Argentina, Bolivia, and Paraguay territories. However, there is a special interest in this species because it is the main target of the illegal trade [2,3].
Nonetheless, another current challenge to wildlife conservation efforts is the dissemination of infectious diseases. As parrots are extremely popular pets, the demand created around the world has led to an international movement of over 19 million birds since 1975 [4], which triggers the spread of pathogens. Disease emergence can be triggered by translocation; introduction of infected animals, pathogens or vectors to new geographic regions; human or domestic animals’ encroachment, spill-over, ex situ contact and ecological manipulation [5]. Amazon parrots are subjected to at least three of these situations [6], therefore, their health assessment in the wild is an important addition to their conservation efforts.
The illegal trade of wild birds is still a reality in Brazil, and only a small part of the nestlings removed from nature is apprehended by environmental authorities. These birds are mixed in rehabilitation centres with resident or pet birds and are often released into the wild without any health criteria [7]. In addition, national and international cross border movement of birds continues as the result of smuggling and legal trade of domestically raised birds [8], creating the perfect scenario for disease dissemination in wild and captive animals, as trafficked and imported birds are fed with improper diets, housed in crowded unhygienic conditions, and mixed with other species [9,10]. The global spread of diseases has caused a significantly negative conservation impact on captive and wild populations [11,12]. Highly resistant viruses in the environment and persistent subclinical infections make controlling these pathogens a challenge [8].
Chlamydia psittaci and the Psittacid herpesvirus 1 (PsHV-1) are relevant pathogens that affect parrots and have been observed in captive psittacine in Brazil [13,14], including occasional outbreaks [10]. A neglected virus in wild birds, the avipoxvirus, has also caused an outbreak in psittacine species located in a facility in Brazil [15]. In addition, the Psittacine Beak and Feather Disease (PBFD) caused by a circovirus, is an exotic pathogen introduced in the country [16], that has been reported in exotic and native pet birds [17,18].
The results of all the negative anthropogenic actions for the health of wild Amazon parrots in Brazil are unknown and information is scarce in the literature [19,20,21]. The aim of the present study was to investigate the presence of C. psittaci and viral pathogens DNA in wild Amazon parrot nestlings and in wild caught nestlings recently apprehended from illegal trade in Brazil, and to discuss the implications of the results for the conservation of psittacine birds.

2. Materials and Methods

The study comprised three species of parrots in four states of Brazil (Figure 1). Amazona pretrei nestlings were sampled in a fragmented area of the southern fields, in the municipality of Pontão, state of Rio Grande do Sul. Amazona brasiliensis parrots were studied on three islands (Ilha Rasa, Ilha Gamela and Ilha Chica), in the state of Paraná, located in the Guaraqueçaba Environmental Protection Area, which has an extensive area of Atlantic Forest. This species was also sampled in Comprida Island, state of São Paulo, another Atlantic Forest area within the Ilha Comprida Environmental Protection Area. Amazona aestiva parrots were sampled in Miranda, state of Mato Grosso do Sul, located in the Brazilian Pantanal wetlands.
Oropharyngeal and cloacal swab samples and/or blood samples were collected from Amazon parrot nestlings in field expeditions during the breeding seasons (October to January) from 2013 to 2018. All samples were collected by trained professionals. Natural and artificial nests were accessed using ladders or climbing equipment. The birds were removed from the nests, examined, sampled, and then placed back in the nests. Swab samples were kept frozen in microtubes containing viral transport media, and blood samples were kept frozen in microtubes until the analyses. One A. brasiliensis was found recently dead inside a nest and was necropsied for sample collection. Liver and spleen fragments were collected and kept frozen until laboratory analysis.
Additionally, in 2015, 413 wild caught A. aestiva nestlings were seized from the illegal trade by environmental officials in three different locations (A—262 birds, B—116 birds, C—35 birds) in two states of Brazil (Mato Grosso do Sul and Paraná). The nestlings apprehended were submitted to the Wildlife Rehabilitation Center (WRC) located in the city of Campo Grande, Mato Grosso do Sul. Birds were different ages, ranging from recently hatched to fully fledged nestlings (about 5 to 50 days). They were housed inside boxes in a proper room, separated by bird size and by origin. Biological samples were collected in the first 72 h after the birds were seized. Cloacal swab samples were randomly collected from approximately 20% of the nestlings from each box, totalizing 90 nestlings, 21.6% of the nestlings received in that year. Blood was collected from the brachial vein in 30 of these parrots and all samples were kept frozen until analysis.
Genomic DNA extraction was performed using the NucleoSpin Tissue kit® (Macherey-Nagel, Germany) according to manufacturer’s instructions. Each sample was digested in 200 µL of lysis buffer and proteinase K (20 mg/mL) at 56 °C for 12 h prior extraction. DNA was extracted from 326 samples (swab/blood samples and a fragment of liver/spleen) from 205 birds. All samples were screened for the presence of chlamydial DNA using a conventional PCR targeting 111bp of the Chlamydiaceae 23S rRNA gene with primers from Enrich et al. [22]. A 25 μL reaction mix containing 3 μL of genomic DNA, 10 pmol of each primer, 12.5 μL of buffer (DreamTaq Green PCR Master Mix, Thermo Fisher Scientific, Waltham, MA, USA) and nuclease-free water qsp was used in the reaction. Target DNA was amplified performing a conventional PCR using an initial denaturation of 60 s at 96 °C, then 40 cycles of 30 s at 94 °C, 60 s at 50 °C and 30 s at 72 °C, followed by a final extension of 4 min at 72 °C. The samples were also screened for the presence of viruses using conventional PCRs for PsHV-1 [23], avipoxvirus [24] and BFDV [25]. Following this, positive samples in the Chlamydiaceae PCR were evaluated using a second PCR assay to amplify a fragment of C. psittaci ompA gene [26]. The primer sequences used for all agents can be found in the Table S1.
Negative and positive standard controls were used in all PCR reactions for each agent. Nuclease-free water was used as negative control. The C. psittaci genotype A, Cpsi/Mm/BR01 DNA was used as positive control (GenBank accession number JQ926183) for Chlamydiacea and ompA PCR assays. BFDV (strain from a Psittacus erithacus), herpesvirus (PsHV-1 genotype 3 from an Ara ararauna) and Pox vaccine (Pox pigeon, Biovet, Brazil) DNA were used as positive controls for the other PCR assays. All reactions were carried out using the thermal cycler Axygen® Maxygene (Axygen, Union City, CA, USA). The products were analysed by electrophoresis in a 1.5% agarose gel stained with GelRed® (Biotium, Fremont, CA, USA) nucleic acid stain.
Amplified products from the ompA PCR assays were purified from the agarose gel using a commercial kit (NucleoSpin Gel and PCR Clean-Up, Macherey Nagel, Düren, North Rhine-Westphalia, Germany) according to the manufacturer’s instructions and sequenced in dual-direction by Sanger sequencing (Genome Research Center, University of São Paulo, São Paulo, Brazil). The chromatograms were analysed for quality using MEGA X software, and sequences were compared with data available on GenBank through a BLAST search. The nucleotide alignment was performed using MAFFT version 7 with the FFT-NS-I algorithm [27]. A neighbor joining tree was constructed using Mega X [28]. The Tamura-Nei model was chosen to create the tree tested by bootstrapping with 1000 replicates.

3. Results

A total of 205 Amazon parrot nestlings from wildlife were sampled as shown in Table 1. All the birds showed no clinical signs that could suggest infection by any of the pathogens here investigated. Liver and spleen fragments were collected from one wild A. brasiliensis nestling that was found recently dead inside one nest at Rasa Island, but pathogens DNA were not detected in those samples. None of the nestling samples tested yielded positive PCR results for PsHV-1, avipoxvirus or BFDV.
Chlamydia prevalence found for all the parrots evaluated was 3.4% (5/147); these samples were from parrots sampled between 2015–2018. From the Chlamydia-positive samples, 4.8% (3/63) were collected from A. aestiva (cloacal swab samples), and 2.5% (2/80) were collected from A. brasiliensis (one cloacal/oropharyngeal swab sample and one blood sample). The A. pretrei nestlings evaluated were negative (0/4, 0%). Chlamydia psittaci nucleotide sequencing was possible only in the blood sample from an A. brasiliensis nestling (Cpsi/Ab/BR02; GenBank accession number MT741095). This partial ompA gene sequence was analysed and aligned with reference sequences available on GenBank (Table S2). The phylogenetic tree is presented in Figure 2. The sequence obtained was confirmed as C. psittaci as it had a high percentage of identity (99.25%) with other C. psittaci sequences, clustering within the Genotype A.
Regarding the nestlings from illegal trade, all samples (90 swabs and 30 blood samples) collected in the first 72 h after apprehension of the birds were negative for the agents analysed (Chlamydia psittaci, PsHV-1, avipoxvirus and BFDV).

4. Discussion

Anthropogenic activities have been a trigger for dissemination of diseases in psittacine birds as shown in previous studies around the world [5], including the international introduction of pathogens to wild and captive naïve populations [11], and outbreaks in wild and captive birds [29]. Nevertheless, the impact of these actions on the health of wild Brazilian parrots is unknown, as a large-scale assessment has never been performed. The results of this study showed low prevalence of C. psittaci and no viral detection in the wild Amazon parrot nestlings sampled, which apparently have not yet been reached by the global spread of relevant psittacine pathogens, which is not the case of BFDV in other countries [30].
C. psittaci is a bacterium considered endemic in Brazilian psittacine birds. It was first detected in wild A. aestiva (2/32, 6.3%) in Pantanal, Mato Grosso do Sul, in 2006, using a semi-nested PCR and complement fixation test [19]. This prevalence is in accordance with our results (3/63, 4.8%) in A. aestiva nestlings evaluated from the same region of Pantanal. Other studies in A. brasiliensis nestlings in Rasa Island, Paraná, showed 0.8% [20] and 0% [21] of C. psittaci prevalence which are in accordance with our results for this species (2/80, 2.5%). Unfortunately, no C. psittaci sequences from these previous studies are available for comparison. Therefore, even though some parrot populations have the bacteria circulating, the overall prevalence seems to be stable over the years and, in some of them, the circulating genotypes are unknown. Conventional PCR is widely used in research of pathogens in captive birds; however, a minor limitation is that this assay can have less sensitivity than real time PCR and maybe low copy number samples can be missed. The sampled birds here were very young fledglings and possibly were not even infected. This fact was demonstrated in a previous study [21], in which the combined serology and PCR results were negative for Chlamydia, demonstrating that the nestlings were not infected in the sample collection time. Therefore, we believe that the chlamydial prevalence in these populations is indeed low. In other Latin American countries, only serologic surveys are available for C. psittaci in the wild: A. aestiva in Bolivia [31] and Aratinga weddelli and Brotogeris sanctithomae in Peru [32]. However, no antibodies against C. psittaci were detected.
The amplified C. psittaci ompA fragment clustered with previously described ompA Genotype A. Based on BLAST analyses, our sequence had 99% identity with the reference sequence 6BC (NC_017287) and with two Brazilian C. psittaci sequences: one from a long-term captive A. aestiva (Genbank MH138296) and one from a wild caught monk parakeet (Myiopsitta monachus) sampled after being seized from poachers in Southern Brazil (Genbank JQ926183) [33]. Furthermore, the highest percentage of nucleotide identity (99.25%) was observed with C. psittaci found in birds and humans from Europe and Asia (Genbank CP033059, KP893667 and AB468956). The sequence obtained here and from previous studies in Brazil suggest that Genotype A can be the main circulating genotype in wild psittacine birds in the country. Moreover, Genotype A is most frequently associated with psittacosis cases in humans. In Brazil, the potential of monk parakeets (Myiopsitta monachus) in transmitting C. psittaci to humans has already been documented [34].
In the present study, no BFDV, PsHV and avipoxvirus DNA was detected in wild and in smuggled nestlings. Nevertheless, the wild caught nestlings seized from the illegal trade were not sampled later to evaluate housing long term effects on their health.
Pacheco's disease (PD) is caused by PsHV-1 and it was first recognized in parrots in Brazil [35], and only later it was seen in many psittacine birds exported from South America to Europe and North America [36]. Even so, there are only sporadic reports on PD occurrence in parrots in Brazil [14] and there is no information on the genotypes circulating in the country. So far, in captive birds, only Genotype 1 was found in 18 Amazon individuals [37]. Negative results for avipoxvirus were also reported in 29 captive A. vinacea using the same primers in a conventional PCR [38]. However, avipoxvirus outbreaks have been reported in captive native [15] and exotic [39] Psittaciformes in Brazil, showing low and high mortality rates, respectively. BFDV has been recently detected in captive exotic and native species [17,18] in Brazil. Based on the initial findings of the present study, it is likely that wild parrot populations can still be unreached by the global spread of BFDV [40]. Because of the high dissemination capacity and the immunosuppressive effects, BFDV has worried avian veterinarians around the world [41]. Hence, further research must be done to provide more detailed data on prevalence, diversity of genotypes and host range of these viruses in wild and captive psittacine birds in the South America.
Wildlife rehabilitation centers are responsible for receiving injured or apprehended wild animals, which are mainly represented by native species seized from illegal trade or illegally maintained as pets by owners or by irregular breeders and, occasionally, exotic species from irregular captivity. Frequently, these places release native birds to the wild after being recovered. This situation is concerning and there is an imminent risk of introduction of pathogens to wild Brazilian psittacine populations, as thousands of birds are released to the wild every year without any health criteria/quarantine. Considering these data and the negative results for BFDV reported here in wild parrots, little has been done in mitigating health threats and to improve the protection of the Brazilian parrot fauna. Therefore, the elaboration of a national health program for relevant pathogens that affects psittacine birds is extremely urgent. Once introduced in a captive or wild population, it is difficult or even impossible to eradicate the BFDV, and many birds would have to be euthanized to achieve this. Thus, there is no doubt that prevention methods are the best approach to control the spread of this virus [41].

5. Conclusions

Our study reveals a longitudinal pathogens assessment of wild psittacine fledglings showing low chlamydial prevalence and no detection of some important parrot viruses. Even though the incidence of exotic viral diseases is increasing in captive psittacine in Brazil, it is still early to assess the real impact in wildlife parrots. Unfortunately, the capture and sampling of adult Amazon parrots is not an easy procedure in natural conditions, which could provide more robust data about the health status of these populations. Further, the infectious diseases control in psittacine from captivity or from illegal trade must be carried out carefully before releasing the birds into the wild avoiding the dissemination of pathogens that have the potential to negatively impact the conservation of Neotropical parrots.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/d13060272/s1, Table S1: primer sequences used for detection of viruses and Chlamydia psittaci in wild Amazon parrot from Brazil. Table S2: GenBank accessions, host species, origins, and Chlamydia psittaci strains used for comparation in this study.

Author Contributions

Conceptualization: T.F.R., F.F.V. Formal analysis: T.F.R., F.F.V. Funding acquisition: T.F.R., F.F.V. Investigation: F.F.V., E.A.B.S., G.H.F.S., N.P.P., J.M., T.F.R. Methodology: F.F.V., E.A.B.S., G.H.F.S., N.P.P., J.M., T.F.R. Project administration: T.F.R. Supervision: T.F.R. Writing—original draft: F.F.V., T.F.R. Writing—Review and Editing: F.F.V., E.A.B.S., G.H.F.S., N.P.P., J.M., T.F.R. All authors have read and agreed to the published version of the manuscript.

Funding

FFV was recipient of PhD fellowship by the FAPESP (2016/03928-2).

Institutional Review Board Statement

Captures and all sampling collection in this study were approved by the Brazilian Ministry of Environment (SISBIO 43876-1, 4993-6, 35621-4) and by the Ethics Committee on Animal Use of the School of Veterinary Medicine and Animal Science of the University of São Paulo (CEUA 9545290116).

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We thank Nara Pontes and the staff of the Wildlife Rehabilitation Centre (CRAS, IMASUL) in Campo Grande/MS for assistance in the collection of samples in smuggled nestlings.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Piacentini, V.Q.; Aleixo, A.; Agne, C.E.; Mauricio, G.N.; Pacheco, J.F.; Bravo, G.A.; Brito, G.R.R.; Naka, N.L.; Olmos, F.; Posso, S.; et al. Annotated checklist of the birds of Brazil by the Brazilian Ornithological Records Committee. Rev. Bras. Ornitol. 2015, 23, 91–298. [Google Scholar] [CrossRef]
  2. IUCN—International Union for Conservation of Nature. Red List of Threatened Species, Version 2010-2; 2020. Available online: http://www.iucnredlist.org (accessed on 15 March 2021).
  3. Seixas, G.H.F.; Mourão, G. Communal roosts of the Blue-fronted Amazons (Amazona aestiva) in a large tropical wetland: Are they of different types? PLoS ONE. 2018, 13, e0204824. [Google Scholar] [CrossRef]
  4. CITES—Convention on International Trade in Endangered Species of Wild Fauna and Flora. CITES Trade Database—1975–2018. 2018. Available online: https://trade.cites.org/ (accessed on 15 March 2021).
  5. Daszak, P.; Cunningham, A.A.; Hyatt, A.D. Emerging infectious diseases of wildlife—threats to biodiversity and human health. Science 2000, 28, 443–449. [Google Scholar] [CrossRef] [PubMed]
  6. Berkunsky, I.; Quillfeldt, P.; Brightsmith, D.J.; Abbud, M.C.; Aguilar, J.M.R.E.; Alemán-Zelaya, U.; Aramburú, R.M.; Arce Arias, A.; Balas McNab, R.; Balsby, T.J.S.; et al. Current threats faced by Neotropical parrot populations. Biol. Cons. 2017, 214, 278–287. [Google Scholar] [CrossRef][Green Version]
  7. Marini, M.A.; Garcia, F.I. Bird conservation in Brazil. Cons. Biol. 2005, 19, 665–671. [Google Scholar] [CrossRef]
  8. Phalen, D.N. The globalization of parrot viruses as the result of the trade in wild caught parrots and its potential conservation implications. In Proceedings of the Wildlife Diseases Association International Conference, Sunshine Coast, Australia, 26–30 July 2015; p. 24. [Google Scholar]
  9. Gaskin, J.M.; Robbins, C.M.; Jacobson, E.R. An explosive outbreak of Pacheco’s parrot disease and preliminary experimental findings. In Proceedings of the American Association of Zoo Veterinarians, Knoxville, TN, USA, 7–9 November 2019; pp. 365–374. [Google Scholar]
  10. Raso, T.F.; Godoy, S.N.; Milanelo, L.; Souza, C.A.I.; Matushima, E.R.; Araújo Júnior, J.P.; Pinto, A.A. An outbreak of chlamydiosis in captive Blue-fronted Amazon parrots (Amazona aestiva) in Brazil. J. Zoo Wildl. Med. 2004, 35, 94–96. [Google Scholar] [CrossRef] [PubMed]
  11. Kundu, S.; Faulkes, C.G.; Greenwood, A.G.; Jones, C.G.; Kaiser, P.; Lyne, O.D.; Black, S.A.; Chowrimootoo, A.; Groombridge, J.J. Tracking viral evolution during a disease outbreak: The rapid and complete selective sweep of a circovirus in the endangered Echo parakeet. J. Virol. 2012, 86, 5221–5229. [Google Scholar] [CrossRef][Green Version]
  12. Olsen, G.H.; Crosta, L.; Gartrell, B.D.; Marsh, P.M.; Stringfield, C.E. Conservation of avian species. In Current Therapy in Avian Medicine and Surgery; Speer, B.L., Ed.; Elsevier: St.Louis, MO, USA, 2016; pp. 719–748. [Google Scholar]
  13. Raso, T.F.; Teixeira, R.H.F.; Carrasco, A.O.T.; Araújo, J.P., Jr.; Pinto, A.A. Chlamydophila psittaci infections in hyacinth macaws (Anodohynchus hyacinthinus) confiscated in Brazil. J. Zoo Wildl. Med. 2013, 44, 169–172. [Google Scholar] [CrossRef]
  14. Luppi, M.M.; Luiz, A.P.M.F.; Coelho, F.M.; Malta, M.C.C.; Preis, I.S.; Ecco, R.; Fonseca, F.G.; Resende, M. Identification and isolation of psittacid herpesvirus from psittacids in Brazil. Vet. Microbiol. 2011, 154, 69–77. [Google Scholar] [CrossRef] [PubMed]
  15. Esteves, F.C.B.; Marín, S.Y.; Resende, M.; Silva, A.S.G.; Coelho, H.L.G.; Barbosa, M.B.; D’Aparecida, N.S.D.; Resende, J.S.; Torres, A.C.D.; Martins, N.R.S. Avian pox in native captive psittacines, Brazil. Emerg. Infect. Dis. 2015, 23, 154–156. [Google Scholar] [CrossRef][Green Version]
  16. Werther, K.; Raso, T.F.; Durigon, E.L.; Latimer, K.S.; Campagnoli, R.P. Psittacine Beak and Feather Disease in Brazil: Case report. Braz. J. Poult. Sci. 1999, 1, 85–88. [Google Scholar]
  17. Araújo, A.V.; Andery, D.A.; Ferreira, F.C., Jr.; Ortiz, M.C.; Marques, M.V.R.; Marin, S.Y.; Vilela, D.A.R.; Resende, J.S.; Resende, M.; Donatti, R.V.; et al. Molecular diagnosis of beak and feather disease in native psittacine species. Brazil. J. Poult. Sci. 2015, 17, 451–458. [Google Scholar] [CrossRef][Green Version]
  18. Azevedo, N.P. Detecção de bornavírus, poliomavírus e circovírus em amostras biológicas, utilizando PCR e RT-PCR, de psitacídeos com diferentes aspectos clínicos. Master’s Thesis, University of São Paulo, São Paulo, 2014. Available online: https://teses.usp.br/teses/disponiveis/10/10133/tde-07102014-152516/pt-br.php (accessed on 8 January 2021).
  19. Raso, T.F.; Seixas, G.H.F.; Guedes, N.M.R.; Pinto, A.A. Chlamydophila psittaci in free-living Blue-fronted Amazon parrots (Amazona aestiva) and Hyacinth macaws (Anodorhynchus hyacinthinus) in the Pantanal of Mato Grosso do Sul, Brazil. Vet. Microbiol. 2006, 117, 235–241. [Google Scholar] [CrossRef]
  20. Ribas, J.M.; Sipinski, E.A.B.; Serafini, P.P.; Ferreira, V.L.; Raso, T.F.; Pinto, A.A. Chlamydophila psittaci assessment in threatened Red-tailed Amazon (Amazona brasiliensis) parrots in Paraná, Brazil. Ornithologia 2014, 6, 144–147. [Google Scholar]
  21. Vaz, F.F.; Serafini, P.P.; Locatelli-Dittrich, R.; Meurer, R.; Durigon, E.L.; Araújo, J.; Thomazelli, L.M.; Ometto, T.; Spinski, E.A.B.; Sezerban, R.M.; et al. Survey of pathogens in threatened wild red-tailed Amazon parrot (Amazona brasiliensis) nestlings in Rasa Island, Brazil. Brazil J. Microbiol. 2017, 48, 747–753. [Google Scholar] [CrossRef]
  22. Ehricht, R.; Slickers, P.; Goellner, S.; Hotzel, H.; Sachse, K. Optimized DNA microarray assay allows detection and genotyping of single PCR-amplifiable target copies. Mol. Cell Probes. 2006, 20, 60–63. [Google Scholar] [CrossRef]
  23. Tomaszewski, E.K.; Kaleta, E.F.; Phalen, D.N. Molecular phylogeny of the psittacid herpesviruses causing Pacheco’s disease: Correlation of genotype and phenotypic expression. J. Virol. 2003, 77, 11260–11267. [Google Scholar] [CrossRef] [PubMed][Green Version]
  24. Lee, L.H.; Lee, K.H. Application of the polymerase chain reaction for the diagnosis of fowl poxvirus infection. J. Virol. Meth. 1997, 63, 113–119. [Google Scholar] [CrossRef]
  25. Ypelaar, I.; Bassami, M.R.; Wilcox, G.E.; Raidal, S.R. A universal polymerase chain reaction for the detection of psittacine beak and feather disease virus. Vet. Microbiol. 1999, 16, 141–148. [Google Scholar] [CrossRef]
  26. Sachse, K.; Laroucau, K.; Vorimore, F.; Magnino, S.; Feige, J.; Müller, W.; Kube, S.; Hotzel, H.; Schubert, E.; Slickers, S.; et al. DNA microarray-based genotyping of Chlamydophila psittaci strains from culture and clinical samples. Vet. Microbiol. 2009, 135, 22–30. [Google Scholar] [CrossRef]
  27. Katoh, K.; Standley, D.M. MAFFT multiple sequence alignment software version 7: Improvements in performance and usability. Mol. Biol. Evol. 2013, 30, 772–780. [Google Scholar] [CrossRef] [PubMed][Green Version]
  28. 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, 28, 2731–2739. [Google Scholar] [CrossRef][Green Version]
  29. Regnard, G.L.; Boyes, R.S.; Martin, R.O.; Hitzeroth, I.I.; Rybicki, E.P. Beak and feather disease viruses circulating in Cape parrots (Poicepahlus robustus) in South Africa. Arch. Virol. 2015, 160, 47–54. [Google Scholar] [CrossRef]
  30. Fogell, D.J.; Martin, R.O.; Bunbury, N.; Lawson, B.; Sells, J.; McKeand, A.M. Trade and conservation implications of new beak and feather disease virus detection in native and introduced parrots. Cons Biol. 2018, 32, 1325–1335. [Google Scholar] [CrossRef][Green Version]
  31. Deem, S.L.; Noss, A.J.; Cuellar, R.L.; Karesh, W.B. Health evaluation of free-ranging and captive blue-fronted amazon parrots (Amazona aestiva) in the Gran Chaco, Bolivia. J. Zoo Wildl. Med. 2005, 36, 598–605. [Google Scholar] [CrossRef]
  32. Gilardi, K.V.K.; Lowentime, L.J.; Gilardi, J.D.; Munn, C.A.A. A survey for selected viral, chlamydial, and parasitic diseases in wild dusky-headed parakeets (Aratinga weddelli) and tui parakeets (Brotogeris sanctithomae) in Peru. J. Wildl. Dis. 1995, 31, 523–528. [Google Scholar] [CrossRef] [PubMed][Green Version]
  33. Raso, T.F.; Almeida, M.A.B.; Santos, E.; Bercini, M.; Barbosa, M. Genetic characterization of Chlamydophila psittaci from monk parakeet (Myiopsitta monachus). In Proceedings of the Congresso Latinoamericano de Microbiologia, Santos, Brazil, 28–31 October 2012; p. 152. [Google Scholar]
  34. Raso, T.F.; Ferreira, V.L.; TIMM, L.N.; Abreu, M.F.T. Psittacosis domiciliary outbreak associated with monk parakeets (Myiopsitta monachus) in Brazil: Need for surveillance and control. JMM Case Rep. 2014, 1, e003343. [Google Scholar] [CrossRef][Green Version]
  35. Pacheco, G.; Bier, O. Epizootie chex les perroquets du Brésil. Relations avec le psittacose. CR Soc. Biol. 1930, 105, 109–111. [Google Scholar]
  36. Miller, T.D.; Millar, D.L.; Naqi, S.A. Isolation of Pacheco’s disease herpesvirus in Texas. Avian Dis. 1979, 23, 753–756. [Google Scholar] [CrossRef]
  37. Luppi, M.M.; Luiz, A.P.M.F.; Coelho, F.M.; Ecco, R.; Fonseca, F.G.; Resende, M. Genotypic characterization of psittacid herpesvirus isolates from Brazil. Braz. J. Microbiol. 2016, 47, 217–224. [Google Scholar] [CrossRef] [PubMed][Green Version]
  38. Saidenberg, A.B.S.; Zuniga, E.; Melville, P.A.; Salaberry, S.; Benites, N.R. Health-screening protocols for vinaceous amazons (Amazona vinacea) in a reintroduction project. J. Zoo Wildl. Med. 2015, 46, 704–712. [Google Scholar] [CrossRef] [PubMed][Green Version]
  39. Murer, L.; Westenhofen, M.; Kommers, G.D.; Furian, T.Q.; Borges, K.A.; Kunert-Filho, H.C.; Streck, A.F.; Lovato, M. Identification and phylogenetic analysis of clade C Avipoxvirus in a fowlpox outbreak in exotic psittacines in southern Brazil. J. Vet. Diagn. Investig. 2018, 30, 946–950. [Google Scholar] [CrossRef][Green Version]
  40. Fogell, D.J.; Martin, R.O.; Groombridge, J.J. Beak and feather disease virus in wild and captive parrots: An analysis of geographic and taxonomic distribution and methodological trends. Arch. Virol. 2016, 161, 2059–2074. [Google Scholar] [CrossRef][Green Version]
  41. Raidal, S.R.; Peters, A. Psittacine beak and feather disease: Ecology and implications for conservation. Emu—Austral Ornithol. 2018, 118, 80–93. [Google Scholar] [CrossRef]
Figure 1. Distribution of Amazona pretrei, Amazona brasiliensis and Amazona aestiva in Brazil and South America and sampling areas.
Figure 1. Distribution of Amazona pretrei, Amazona brasiliensis and Amazona aestiva in Brazil and South America and sampling areas.
Diversity 13 00272 g001
Figure 2. A mid-point rooted, neighbor joining phylogeny of the partial DNA sequences of the Chlamydia psittaci outer membrane protein gene alignment (1000 bootstrap replicates). Bootstrap support of nodes is shown if it exceeds 60%. (Cpsi/Ab/BR02, GenBank accession number MT741095).
Figure 2. A mid-point rooted, neighbor joining phylogeny of the partial DNA sequences of the Chlamydia psittaci outer membrane protein gene alignment (1000 bootstrap replicates). Bootstrap support of nodes is shown if it exceeds 60%. (Cpsi/Ab/BR02, GenBank accession number MT741095).
Diversity 13 00272 g002
Table 1. Number of wild Amazon parrot nestlings sampled according to breeding season in the states of Rio Grande do Sul (RS), Paraná (PR), Mato Grosso do Sul (MS) and São Paulo (SP), Brazil.
Table 1. Number of wild Amazon parrot nestlings sampled according to breeding season in the states of Rio Grande do Sul (RS), Paraná (PR), Mato Grosso do Sul (MS) and São Paulo (SP), Brazil.
Amazon SpeciesState2013/
2014
2015201620172018Total Samples
(Swab and/or Blood)
Number of Birds Sampled for Selected Virus **/Positive (%)Number of Chlamydia Positive/Total Birds (%)
A. pretreiRS0040084 (0%)0/4 (0%)
A. brasiliensisPR/SP74 *028 #1521 230138 (0%)2/80 (2.5%)
A. aestivaMS1717233 08963 (0%)3/63 (4.8%)
Total 327205 (0%)5/147 (3.4%)
* Just 16 swabs were tested for Chlamydia in this period. Total number of birds tested for Chlamydia = 147. # Liver and spleen fragments sampled from one carcass. ** PsHV-1, avipoxvirus and BFDV.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Vaz, F.F.; Sipinski, E.A.B.; Seixas, G.H.F.; Prestes, N.P.; Martinez, J.; Raso, T.F. Molecular Survey of Pathogens in Wild Amazon Parrot Nestlings: Implications for Conservation. Diversity 2021, 13, 272. https://doi.org/10.3390/d13060272

AMA Style

Vaz FF, Sipinski EAB, Seixas GHF, Prestes NP, Martinez J, Raso TF. Molecular Survey of Pathogens in Wild Amazon Parrot Nestlings: Implications for Conservation. Diversity. 2021; 13(6):272. https://doi.org/10.3390/d13060272

Chicago/Turabian Style

Vaz, Frederico Fontanelli, Elenise Angelotti Bastos Sipinski, Gláucia Helena Fernandes Seixas, Nêmora Pauletti Prestes, Jaime Martinez, and Tânia Freitas Raso. 2021. "Molecular Survey of Pathogens in Wild Amazon Parrot Nestlings: Implications for Conservation" Diversity 13, no. 6: 272. https://doi.org/10.3390/d13060272

Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop