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Volume 15, Number 12—December 2009

Dispatch

Sympatry of 2 Hantavirus Strains, Paraguay, 2003–2007

Yong-Kyu Chu, Douglas Goodin, Robert D. Owen1, David Koch, and Colleen B. JonssonComments to Author 
Author affiliations: Southern Research Institute, Birmingham, Alabama, USA (Y.-K. Chu, C.B. Jonsson); Kansas State University, Manhattan, Kansas, USA (D. Goodin, D. Koch); Texas Tech University, Lubbock, Texas, USA (R.D. Owen); University of Louisville, Louisville, Kentucky, USA (C.B. Jonsson)

Suggested citation for this article

Abstract

To explore geographic and host-taxonomic patterns of hantaviruses in Paraguay, we established sampling sites in the Mbaracayú Biosphere Reserve. We detected Jaborá virus and Itapúa37/Juquitiba–related virus in locations ≈20 m apart in different years, which suggested sympatry of 2 distinct hantaviruses.

Hantaviruses are rodent-borne viruses that may cause hemorrhagic fever with renal syndrome or hantavirus pulmonary syndrome in humans, although some strains do not cause disease (1,2). In Paraguay in 1995, Laguna Negra virus carried by Calomys laucha (little laucha) caused an outbreak of hantavirus pulmonary syndrome in western Paraguay (3).

Figure 1

Thumbnail of Satellite image of collection sites of hantavirus RNA–positive rodents, including selected Juquitiba virus (circles) and Jaborá virus (triangles) samples, Paraguay, 2003–2007. Inset shows location of showing the study site in Paraguay. OLFO, Oligoryzomys fornesi; OLNI, O. nigripes; OLSP, Oligoryzomys sp.; AKMO, Akodon montensis.

Figure 1. Satellite image of collection sites of hantavirus RNA–positive rodents, including selected Juquitiba virus (circles) and Jaborá virus (triangles) samples, Paraguay, 2003–2007. Inset shows location of showing the study site in Paraguay....

We have identified 4 additional strains in Paraguay: Alto Paraguay virus harbored by Holochilus chacarius (Chacoan marsh rat) in western Paraguay; and Ape Aime virus (AAIV) harbored by Akodon montensis (Montane akodont), Itapúa virus strain 37 (IPV37) harbored by Oligoryzomys nigripes (black-footed colilargo), and Bermejo virus strain Ñeembucu harbored by O. chacoensis (Chacoan colilargo) in eastern Paraguay (4,5). We have continued our surveillance of hantaviruses in the interior Atlantic forests within and near Reserva Natural del Bosque Mbaracayú (RNBM), a World Biosphere Reserve located within Departamento Canindeyú in eastern Paraguay (Figure 1).

The Study

We established and sampled 10 mark-recapture sites within and adjacent to RNBM during 2003–2007. Sampling of grids depended upon weather conditions, the purpose of the grid, and transitory human settlements. Each mark-recapture grid consisted of an 11 × 11 array of trap stations spaced 10 m apart, each of which had 1 standard live trap (H.B. Sherman Traps, Tallahassee, FL, USA) placed on the ground, and another in branches or vines 2–3 m above ground to capture arboreal species. Grids were sampled for 8 nights, with at least 2 months between sampling sessions. Rodents captured in the mark-recapture grids were individually marked with passive integrated transponder tags, and ≈100 μL of blood was collected from the retroorbital sinus (once per trapping session). Animals were identified to species, age class, reproductive condition, sex, and weight and released.

Rodents were also collected in a series of traplines, each of which contained 50 traps placed ≈10 m apart. Animals collected in traplines were killed, standard collecting information was recorded, and liver, lung, heart, kidney, muscle tissues, and blood specimens were collected. All samples were snap-frozen in liquid nitrogen, transported to the Museum of Texas Tech University (TTU), and stored at –80°C. Standard voucher specimens were prepared from these animals, and have or will be deposited in the Museum of TTU or the Museo Nacional de Historia Natural del Paraguay. All field protocols followed American Society of Mammologists guidelines for the use of wild mammals in research (6), and were reviewed and approved by the TTU Animal Care and Use Committee.

A total of 1,150 small mammals from >20 species were captured, including 13 sigmodontine rodent species (1,140 animals) (Technical Appendix [PDF - 118 KB - 1 page]). The dominant rodent species in Mbaracayú were A. montensis (55.7%), Necromys lasiurus (hairy-tailed akodont) (10.8%), C. callosus (big laucha) (6.5%), and O. fornesi (Fornes’ colilargo) (6.3%).

Antibodies to hantavirus antigens were detected in blood specimens by using an indirect immunofluorescent antibody assay and irradiation-sterilized slides of Vero E6 cells infected with Andes virus as described (4). Seven species were antibody positive: A. montensis, N. lasiurus, O. fornesi, O. nigripes, Oligoryzomys sp., Oryzomys megacephalus (Azara’s broad-headed Oryzomys sp.), and Oxymycterus delator (Paraguayan hocicudo). Antibodies to hantavirus antigens were 3× more abundant in blood samples from males than females (Technical Appendix [PDF - 118 KB - 1 page]).

Total RNA was extracted from antibody-positive blood clots from mark-recapture samples or lung tissue from killed animals. Nested reverse transcription–PCR was performed to amplify a 371-nt small (S) hantavirus RNA segment (4). Hantavirus RNA was detected in 23 A. montensis, 5 O. fornesi, 1 O. nigripes, and 1 Oligoryzomys sp. Of these animals, all but 2 A. montensis were males, which indicated that male rodents play the primary role in maintenance and transmission of hantavirus.

Figure 2

Thumbnail of Phylogenetic tree based on Bayesian analysis of the small (S) segment of American hantaviruses, Paraguay, 2003–2007. The tree is based on 1,014 nucleotides of partial S segment of North and South American hantaviruses. Clades (upper case letters), subclades (numbers), and groups (lower case letters) are indicated on the left. Numerical values at the nodes indicate posterior probabilities that supported each interior branch. Scale bar indicates mean number of nucleotide substitutions

Figure 2. Phylogenetic tree based on Bayesian analysis of the small (S) segment of American hantaviruses, Paraguay, 2003–2007. The tree is based on 1,014 nucleotides of partial S segment of North and South...

A representative sample (15 A. montensis, 3 O. fornesi, 1 O. nigripes, and 1 Oligoryzomys sp.) were selected for additional PCR, sequencing, and phylogenetic analysis. PCR-amplified cDNAs of a 1,014-nt amino terminus region of the S segment were purified by agarose gel electrophoresis and cloned into pCRII (Invitrogen, Carlsbad, CA, USA) (4,5). M13 forward and reverse primers were used for sequencing. For sequence comparison and phylogenetic analysis, sequences of representative New and Old World hantaviruses were obtained from GenBank. Phylogeny reconstruction was conducted by using Modeltest version 3.6 analysis (http://darwin.uvigo.es/software/modeltest.html.), maximum-likelihood estimation, and Bayesian inference (Figure 2).

Bayesian analysis based on the 1,014-nt sequence showed that all sequences from A. montensis formed a strongly supported clade, which included AAIV-related hantaviruses from Itapúa Department, Jaborá virus (JABV) from southern Brazil, and strains from RNBM in Paraguay (Figure 2, clade C1). Phylogenetic analyses identified 3 subclades representing virus sequences from animals in the RNBM, Itapúa, and southern Brazil. This type of geographic clustering is similar to Sin Nombre–related viruses in deer mice in North America (7). All S segment sequences from A. montensis were closely related, with nucleotide sequence differences between RNBM strains and AAIV and JABV of 4% and 12%, respectively, and derived amino acid differences of 0% or 1%, respectively (Table 1).

In contrast, all virus sequences from O. fornesi, O. nigripes, and Oryzomys sp. at RNBM formed a strongly supported clade with viruses related to Juquitiba virus (JUQV) from Brazil and Itapúa virus strain 37, which was originally detected in O. nigripes from Itapúa Department in eastern Paraguay (Figure 2, clade C2d). Nucleotide sequence differences between JUQV strains from RNBM were 0%–2%. Nucleotide sequence differences between JUQV strains from RNBM and Itapúa virus strain 37 or JUQV (Brazil) were 5% or 4%, respectively, and derived amino acid differences were 0% (Table 1). This clade is phylogenetically distinct from viruses that form the Akodon montensis clade at RNBM and more closely related to Andes (clade C2b) and Bermejo-Ñeembucú (clade C2a) viruses. This finding suggests that spillover infection of JUQV-related viruses is actively occurring among oryzomyine rodent species at RNBM, as reported for other hantaviruses in oryzomyines (8) and other rodent hosts of Old World hantaviruses (9,10). Additional data are needed to determine the primary oryzomyine reservoir of JUQV and to better understand mechanisms by which spillover occurs.

In addition to spillover infection of JUQV among oryzomyine rodents, we identified 2 virus strains (JUQV and JABV) in close proximity (collected ≈20 m apart on the same grid in the same sampling session) on 2 occasions, in sites separated by ≈30 km (Figure 1; Table 2). Thus, these 2 distinct hantaviruses appear to be maintaining a sympatric status across a considerable expanse of landscape, rather than reflecting a temporary or localized phenomenon. We use the term sympatric to underscore that these viruses are in the same community and are near enough (their rodent reservoirs) to interact.

Conclusions

Coexistence of hantaviruses in 2 rodent species at mark-recapture sites has been observed (1113). Serologic analyses in these studies would not have differentiated whether distinct strains of hantaviruses were co-circulating or active spillover infection was occurring among sympatric rodents at collection sites. Recently, Raboni et al. reported JUQV circulating in 3 sympatric rodent species in southern Brazil and 2 distinct hantaviruses (Jabora and JUQV) in 1 rodent species (A. montensis) (14). We have not detected JUQV in A. montensis in Paraguay. To address host-jumping of hantaviruses among sympatric rodent species in RNBM and other regions in South America, future longitudinal studies are warranted. Such studies are critical to understanding evolutionary adaptation of hantaviruses in rodents in South America, the ability of these viruses to adapt to new rodent reservoirs, and their emergence and maintenance in the environment.

Dr Chu is a research scientist at Southern Research Institute. His research interests include the ecology and evolution of hantaviruses.

Acknowledgments

We thank Robert J. Baker and Heath Garner for approving and facilitating loans of rodent tissues; the Secretaría del Ambiente (Paraguay) for providing permits to collect and export rodents and tissues; and the field crew, led by Ismael Mora, for dedication to their work, regardless of circumstances.

This work was supported by a grant from the Fogarty International Center (1 R01 TW006986-01) to C.B.J. under the National Institutes of Health–National Science Foundation Ecology of Infectious Diseases initiative.

References

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Figures

Tables

Technical Appendix

Suggested citation for this article: Chu Y-K, Goodin D, Owen RD, Koch D, Jonsson CB. Sympatry of 2 hantavirus strains, Paraguay, 2003–2007. Emerg Infect Dis [serial on the Internet]. 2009 Dec [date cited]. Available from http://wwwnc.cdc.gov/eid/article/15/12/09-0338.htm

DOI: 10.3201/eid1512.090338

1Current affiliation: Martín Barrios 2230 c/ Pizarro, Barrio Republicano, Asunción, Paraguay.

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Table of Contents – Volume 15, Number 12—December 2009

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