Volume 16, Number 6—June 2010
Genetic Evidence for a Tacaribe Serocomplex Virus, Mexico
We isolated arenavirus RNA from white-toothed woodrats (Neotoma leucodon) captured in a region of Mexico in which woodrats are food for humans. Analyses of nucleotide and amino acid sequence data indicated that the woodrats were infected with a novel Tacaribe serocomplex virus, proposed name Real de Catorce virus.
The Tacaribe serocomplex (family Arenaviridae, genus Arenavirus) comprises 7 North American viruses (Table 1) and 15 South American viruses (9). The South American viruses include Guanarito virus, 4 other agents of hemorrhagic fever, and Pirital virus. Members of the rodent family Cricetidae are the principal hosts of the Tacaribe serocomplex viruses for which natural host relationships have been well characterized. For example, the southern plains woodrat (Neotoma micropus) in southern Texas is the principal host of Catarina virus (4), and the hispid cotton rat (Sigmodon hispidus) in southern Florida is the principal host of Tamiami virus (6).
A recent study found antibody to a Tacaribe serocomplex virus in white-toothed woodrats (N. leucodon) captured in Mexico (M.L. Milazzo, unpub. data). We report the determination of the nucleotide sequence of a 3352-nt fragment of the small (S) genomic segment of arenavirus AV H0030026 from RNA isolated from a white-toothed woodrat captured in 2005 in northeastern Mexico.
Rodents were captured in a rural area 22.8 km north of the town of Real de Catorce in the municipality of Catorce, San Luis Potosí, Mexico (Figure 1). A total of 400 live-capture traps were set each night on 2 consecutive nights in the first week of August 2005. Each rodent caught was assigned a unique identification number. Samples of whole blood, samples of kidney and other solid tissues, and the skins and skeletons of the rodents were deposited into the Museum of Texas Tech University.
The blood samples were tested by ELISA (10) for antibody (immunoglobulin [Ig] G) to Whitewater Arroyo virus strain AV 9310135 (7). Samples of spleen and kidney from white-toothed woodrats TK133448 and TK133451, 7 other white-toothed woodrats, 2 antibody-positive Nelson’s pocket mice (Chaetodipus nelsoni), and an antibody-positive Merriam’s kangaroo rat (Dipodomys merriami) were tested for arenavirus by cultivation in monolayers of Vero E6 cells (11). Samples of kidney from the antibody-positive rodents were tested for arenavirus RNA by using heminested PCR assays. The first-strand cDNA for the PCR was synthesized by using SuperScript II Reverse Transcriptase (Invitrogen Life Technologies, Inc., Carlsbad, CA, USA) in conjunction with oligont 19C-cons (2). The nucleotide sequence alignments were analyzed by using MRBAYES 3.1.2 (12) in the computer software package PAUP*, version 4.0b10 (http://paup.csit.fsu.edu). (Details of the assays for IgG, arenavirus, and arenavirus RNA and the analyses of the amino acid sequence data and nucleotide sequence data are available from C.F.F.)
Nine white-toothed woodrats, 3 northern grasshopper mice (Onychomys leucogaster), 19 deer mice (Peromyscus spp.), 11 harvest mice (Reithrodontomys spp.), 13 Nelson’s pocket mice, 45 Merriam’s kangaroo rats, and 16 other kangaroo rats (Dipodomys spp.) were captured during 800 trap-nights; overall trap success rate was 116/800 (14.5%). IgG against Whitewater Arroyo virus was found in 2 (22.2%) of the white-toothed woodrats, 2 (15.4%) of the Nelson’s pocket mice, 1 (2.2%) of the Merriam’s kangaroo rats, and none of the 49 other rodents. Arenavirus was isolated from none of the 12 animals included in the virus assays.
The sequence of the 3,352-nt fragment of the S genomic segment of arenavirus AV H0030026 (GenBank accession no. GQ903697) was determined from RNA isolated from white-toothed woodrat TK133448. The 3,352-nt fragment included the complete glycoprotein precursor (GPC) gene and complete nucleocapsid (N) protein gene of AV H0030026. Nonidentities between the amino acid sequences of the GPC and N protein of AV H0030026 and the amino acid sequences of the GPC and N proteins of the 10 other North American viruses included in the analyses of amino acid sequence data ranged from 28.3% to 35.2% and from 11.6% to 21.0%, respectively (Table 2). The results of the Bayesian analyses of complete GPC gene sequences (Figure 2, panel A) and complete N protein gene sequences (Figure 2, panel B) indicated that AV H0030026 represents a unique phylogenetic lineage but failed to resolve the relationship of AV H0030026 to the other North American viruses analyzed.
The nucleotide sequence of a 687-nt fragment of the S genomic segment of arenavirus AV H0030028 was determined from RNA isolated from a kidney of white-toothed woodrat TK133451. The sequence of this fragment (GenBank accession no. GU137350) was 99.9% identical to the sequence of the homologous region of the N protein gene AV H0030026. Results of assays for arenavirus RNA in the kidneys of the antibody-positive Nelson’s pocket mice and the antibody-positive kangaroo rat were negative.
Tacaribe serocomplex viruses have been isolated from white-throated woodrats (N. albigula), large-eared woodrats (N. macrotis), Mexican woodrats (N. mexicana), southern plains woodrats (N. micropus), and a bushy-tailed woodrat (N. cinerea) captured in the western United States (2–5,7,8), and antibody to Whitewater Arroyo virus has been found in woodrats captured in San Luis Potosí (M.L. Milazzo, unpub. data). Our results indicate that an arenavirus is naturally associated with the white-toothed woodrat (N. leucodon) and that Tacaribe serocomplex viruses are enzootic to Mexico.
The results of the Bayesian analyses indicated that AV H0030026 is phylogenetically distinct from other North American arenaviruses. Sequence nonidentities between the GPC of AV H0030026 and the GPC of the other North America arenaviruses (Table 2) were substantively greater than sequence nonidentities between the GPC of strains of phylogenetically closely related South American arenavirus species (3). Furthermore, sequence nonidentities between the N protein of AV H0030026 and the N proteins of the other North American arenaviruses (Table 2) were comparable to the amino acid sequence nonidentities between the N proteins of strains of phylogenetically closely related South American arenavirus species (3). Thus, AV H0030026 may represent a novel species (proposed name Real de Catorce) in the family Arenaviridae, genus Arenavirus (9).
Nelson’s pocket mouse (C. nelsoni) and Merriam’s kangaroo rat (D. merriami) are members of the rodent family Heteromyidae. No accounts of arenavirus infections in these or other heteromyid rodents have been published. The anti-arenavirus antibody in the pocket mice and kangaroo rat in this study may be a consequence of infection with an arenavirus other than Real de Catorce virus. Alternatively, the results of the ELISA on these rodents are inaccurate (i.e., falsely positive).
Five Tacaribe serocomplex viruses are known to naturally cause severe febrile disease in humans: GTOV, Junín, Machupo, Sabiá, and Chapare viruses. The diseases caused by these viruses range from sporadic cases to small outbreaks to hyperendemic episodes. Humans usually become infected with arenaviruses by inhalation of virus in aerosolized droplets of secretions or excretions from infected rodents. Other means of infection may include ingestion of infected rodents (13).
Human consumption of woodrats is common in rural regions in the highlands of Mexico. For example, white-throated woodrats are consumed by humans in the Potosí-Zacatecan Mexican Plateau (14), and Mexican woodrats (N. mexicana), Mexican deer mice (Peromyscus mexicanus), and other cricetid rodents are consumed by the Tzeltzal Indians in Chiapas (15). Future studies on arenaviruses native to North America should include assessments of whether humans who consume woodrats or live or work in close association with woodrats are infected by the Tacaribe serocomplex viruses associated with these rodents.
Ms Inizan is a master’s degree student in physiopathology at the École Normale Supérieure de Cachan, Cachan, France. Her research interests include early events in the immune response in infectious diseases of humans and other vertebrate animals.
Ildefonso Fernández-Salas facilitated the work at the study site. Ryan Chambers, Nevin Durish, Michelle Knapp, Vicki Swier, and J. Delton Hanson assisted with the collection of rodents. J. Delton Hanson also provided the map in Figure 1. Mary J. Wilson assisted with development of the assays for arenavirus RNA in rodent TK133448.
Financial support for this study came from National Institutes of Health grants AI-41435 and AI-67947. Patricia Repik and Christina Cassetti facilitated the grant support for this study.
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- Figure 1. Southern Texas and 4 states in northeastern Mexico. The filled circle in southern Texas indicates the locality in which Catarina virus is enzootic. The star in San Luis Potosí...
- Figure 2. Phylogenetic relationships among 11 North American arenaviruses based on Bayesian analyses of A) glycoprotein precursor gene sequences and B) nucleocapsid protein gene sequences. The number(s) at the nodes are...
- Table 1. Natural hosts and geographic distribution of the North American Tacaribe serocomplex viruses
- Table 2. Nonidentities among the predicted amino acid sequences of the glycoprotein precursors and among the predicted amino acid sequences of the nucleocapsid proteins of the North American arenaviruses
Suggested citation for this article: Inizan CC, Cajimat MNB, Milazzo ML, Barragán-Gomez A, Bradley RD, Fulhorst CF. Genetic evidence for a Tacaribe serocomplex virus, Mexico. Emerg Infect Dis [serial on the Internet]. 2010 Jun [date cited]. http://wwwnc.cdc.gov/eid/article/16/6/09-1648
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Charles F. Fulhorst, Department of Pathology, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555-0609, USA
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