Volume 16, Number 4—April 2010
Sympatric Occurrence of 3 Arenaviruses, Tanzania
To determine the specificity of Morogoro virus for its reservoir host, we studied its host range and genetic diversity in Tanzania. We found that 2 rodent species other than Mastomys natalensis mice carry arenaviruses. Analysis of 340 nt of the viral RNA polymerase gene showed sympatric occurrence of 3 distinct arenaviruses.
Arenaviruses are RNA viruses, primarily rodent borne, that include the etiologic agents of lymphocytic choriomeningitis and hemorrhagic fevers in humans. On the basis of their antigenic properties, arenaviruses have been divided in 2 groups: New World and Old World (1). In Africa, 2 arenaviruses are known to be highly pathogenic to humans: Lassa virus in West Africa and the recently described Lujo virus from southern Africa (2). Rodents from the subfamily Murinae are the principal hosts of the Old World arenaviruses. The multimammate mouse, Mastomys natalensis, is the reservoir host of Lassa virus in western Africa (3) and Mopeia virus, for which human pathogenicity has not been reported, in eastern Africa (4,5).
Previously, a serosurvey of small mammals from Tanzania identified a hot spot of arenavirus circulation in Morogoro (6). Molecular screening detected a new arenavirus in M. natalensis mice: Morogoro virus, closely related to Mopeia virus (6). This virus seems a promising model for studying virus–host dynamics and testing rodent control measures for arenaviruses for which M. natalensis mice are host. However, before being used as a model, the degree of specificity of Morogoro virus for its reservoir host must be assessed because secondary reservoir species may play a role in the transmission and maintenance of the virus in natural habitats. Our objective, therefore, was to determine the limit of specificity of the Morogoro virus.
From October 13 through December 3, 2008, a total of 555 small mammals were trapped in Morogoro, Tanzania (6.84°S, 37.65°E). This period corresponds to the end of the dry season, when the density of M. natalensis mice is usually high (7). Sherman traps were set in habitats where these mice were expected to occur in high density (7). Dried blood samples were preserved on calibrated, prepunched filter papers. Blood samples (1 punch ≈15µL/rodent) were eluted in 300 µL of phosphate-buffered saline and tested for antibodies to arenaviruses by indirect immunofluorescence antibody (IFA) testing using Morogoro virus as antigen. In addition, total RNA was extracted from another punch of blood by using 300 µL of AVL buffer (QIAGEN, Venlo, the Netherlands). The lysate, plus 300 µL of ethanol, was centrifuged in a silica column (Zymo Research, Orange, CA, USA). The column was washed with 400 µL of AW1 and AW2 buffers (QIAGEN). RNA was eluted with 15 µL of water. A 1-step reverse transcription–PCR (RT-PCR) selective for the Morogoro virus RNA polymerase (large [L]) gene was performed as described (6); it was based on a pan–Old World arenavirus RT-PCR approach (8), but primers were adjusted to detect the Morogoro virus (6). Products were shown by agarose gel electrophoresis. A subset of the amplicons was purified and unidirectionally sequenced by using MoroL3359-fwd primer (6). Amplicons derived from Lemniscomys rosalia and Mus minutoides mouse blood samples were bidirectionally sequenced. Nucleotide and amino acid sequences were aligned by using BioEdit software (9). Old World arenaviruses and 2 representatives of New World arenaviruses were used to estimate nucleotide and amino acid pairwise divergence (p-distance) with MEGA 4 (10). A phylogram was reconstructed by using the neighbor-joining algorithm in MEGA 4.
We trapped 511 M. natalensis mice and 44 individuals from 7 other small mammal species (Table 1). IFA results were positive for 58 blood samples from M. natalensis, 1 from L. rosalia, and 1 from M. minutoides mice (Table 1). M. rosalia mice were trapped in woodlands, whereas M. minutoides mice were trapped in vegetable gardens and fallow fields. These results are consistent with recently reported results from a study in the same locality 20 years ago, in which mice from the genera Lemniscomys and Mus were seropositive for arenaviruses according to IFA with Lassa virus as antigen (6). In our 2008 study, the antibody prevalence for M. natalensis mice was 12.1%, which is low compared with 50% antibody prevalence reported for 2004 and 2007 (6), suggesting high fluctuation of interannual or seasonal prevalence of Morogoro virus in its host.
Using RT-PCR selective for the arenavirus L gene, we obtained positive results for 43 mice: 41 M. natalensis, 1 L. rosalia, and 1 M. minutoides. In total, 6 samples were positive according to IFA and RT-PCR. We sequenced 33 RT-PCR amplicons. The sequences derived from M. natalensis mice (286 bp used for the analysis) showed 97.1%–100% amino acid homology with the Morogoro prototype L sequence (GenBank accession no. EU914104). In contrast, the 2 sequences derived from the blood samples of L. rosalia and M. minutoides mice showed only 69.3% and 65.2% aa homology with the Morogoro prototype L sequence. These sequences (320 bp) were compared with sequences of the Old World arenaviruses (Table 2). The virus amino acid sequence from M. minutoides mice clustered at 93.7% homology with that of the Kodoko virus, in the lymphocytic choriomeningitis clade (Figure; Table 2): thus, the arenavirus of M. minutoides mice seems to be a strain of the Kodoko virus originally isolated from 2 M. minutoides mice in Guinea (11). Our finding supports M. minutoides mice as the true reservoir of Kodoko virus in Africa.
The amino acid sequence of the virus isolated from L. rosalia mice clusters with the Ippy virus sequence (Figure). Ippy virus was isolated in the Central African Republic from Arvicanthis niloticus rodents (12). For the portion of L gene sequenced (320 bp), the level of amino acid divergence between the 2 is 17.3%, higher than the level of divergence between other Old World arenavirus species (e.g., 14.5% aa divergence between Mobala and Lassa viruses; Table 2). Thus, the arenavirus found in L. rosalia mice appears to be a new species of Old World arenavirus. The genus Lemniscomys is more closely related to the genus Arvicanthis than to the genera Mus and Mastomys.
In high-density habitats of M. natalensis mice, where Morogoro arenavirus transmission occurs, sympatric murine species do not seem to be secondary reservoirs for the virus. In contrast, 2 mouse species, L. rosalia and M. minutoides, seem to be reservoirs of 2 other Old World arenaviruses, 1 of which may be a new species. Our study emphasizes the complementary nature of serologic and genetic-based approaches for arenavirus detection. Because of the cross-reactivity of Morogoro antigens with immune serum from individuals infected with other arenaviruses, a serology-only approach might have led to the conclusion that an extended set of hosts exists for the Morogoro virus. Because of its high cost, a genetics-only approach might never have indicated the hot spot of arenavirus around Morogoro that was shown by IFA (6). However, critically, genetics then allow cross-reactivity to be decomposed.
Our study demonstrates the presence of 3 Old World arenaviruses in a single location. To date, only 5 Old World arenavirus species and 17 New World arenaviruses have been recognized by the International Committee for Taxonomy of Viruses (13). Although the likely presence of additional arenaviruses in Africa has long been suggested (14,15), the discovery of new Old World arenaviruses is rare. Our study illustrates that arenaviruses in Africa may be highly diverse and demonstrates the efficiency of the recently developed pan–Old World arenavirus RT-PCR for identifying new Old World arenaviruses (8). To isolate and describe the new arenavirus of L. rosalia mice and the strain of Kodoko virus, additional sampling and genotyping are being conducted. In particular, determining the sequence of the S segment will further clarify evolutionary relationships within the Old World group.
Dr Goüy de Bellocq is a postdoctoral researcher at the Fund for Scientific Research-Flanders. Her research interests are the evolutionary ecology and epidemiology of arenaviruses and macroparasites in rodents.
We thank the academic authorities of the Sokoine University of Agriculture, Morogoro, who provided us with the necessary permits and working facilities. We are also grateful to our colleagues Khalid Kibwana and Shabani Lutea for their help with field work.
Financial support was provided by the University of Antwerp (grant no. 2964 to J.G.B.) and the Fund for Scientific Research-Flanders (grant no. 1.5.180.09 to J.G.B.).
- Charrel RN, De Lamballerie X, Emonet S. Phylogeny of the genus Arenavirus. Curr Opin Microbiol. 2008;11:362–8.
- Briese T, Paweska JT, McMullan LK, Hutchison SK, Street C, Palacios G, Genetic detection and characterization of Lujo virus, a new hemorrhagic fever–associated arenavirus from southern Africa. PLoS Pathog. 2009;5:e1000455.5556.
- Lecompte E, Fichet-Calvet E, Daffis S, Koulémou K, Sylla O, Kourouma F, Mastomys natalensis and Lassa fever, West Africa. Emerg Infect Dis. 2006;12:1971–4.
- Johnson KM, Taylor P, Elliott LH, Tomori O. Recovery of a Lassa-related arenavirus in Zimbabwe. Am J Trop Med Hyg. 1981;30:1291–3.
- Wulff H, McIntosh BM, Hamner DB, Johnson KM. Isolation of an arenavirus closely related to Lassa virus from Mastomys natalensis in south-east Africa. Bull World Health Organ. 1977;55:441–4.
- Günther S, Hoofd G, Charrel R, Röser C, Becker-Ziaja B, Lloyd G, Mopeia virus–related arenavirus in natal multimammate mice, Morogoro, Tanzania. Emerg Infect Dis. 2009;15:2008–12.
- Leirs H. Population ecology of Mastomys natalensis (Smith, 1834). Implications for rodent control in Africa. Agricultural ed. no. 35. Brussels: Belgian Administration for Development Cooperation; 1994.
- Vieth S, Drosten C, Lenz O, Vincent M, Omilabu S, Hass M, RT-PCR assay for detection of Lassa virus and related Old World arenaviruses targeting the L gene. Trans R Soc Trop Med Hyg. 2007;101:1253–64.
- Hall TA. Bioedit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 1999;41:95–8.
- Tamura K, Dudley J, Nei M, Kumar S. MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol. 2007;24:1596–9.
- Lecompte E, ter Meulen J, Emonet S, Daffis S, Charrel RN. Genetic identification of Kodoko virus, a novel arenavirus of the African pigmy mouse (Mus Nannomys minutoides) in West Africa. Virology. 2007;364:178–83.
- Swanepoel R, Leman PA, Shepherd AJ, Shepherd SP, Kiley MP, McCormick JB. Identification of Ippy as a Lassa fever–related virus. Lancet. 1985;1:639.
- Salvato MS, Clegg JCS, Buchmeier MJ, Charrel RN, Gonzales JP, Lukashevich IS, V: Family Arenaviridae. In: Van Regenmortel MHV, Fauquet CM, Mayo MA, Maniloff J, Desselberger U, Ball LA, editors. Virus taxonomy. Eighth report of the International Committee on Taxonomy of Viruses. San Diego (CA): Elsevier Academic Press;2005;725–38.
- Gonzalez JP. Les arenavirus d’Afrique: un nouveau paradigme d’evolution. Bull Inst Pasteur. 1986;84:67–85.
- Kiley MP, Swanepoel R, Mitchell SW, Lange JV, Gonzalez JP, McCormick JB. Serological and biological evidence that Lassa-complex arenaviruses are widely distributed in Africa. Med Microbiol Immunol (Berl). 1986;175:161–3.
Suggested citation for this article: Goüy de Bellocq J, Borremans B, Katakweba A, Makundi R, Baird SJE, Becker-Ziaja B, et al. Sympatric occurrence of 3 arenaviruses, Tanzania. Emerg Infect Dis [serial on the Internet]. 2010 Apr [date cited]. http://wwwnc.cdc.gov/eid/article/16/4/09-1721
- Page created: December 28, 2010
- Page last updated: December 28, 2010
- Page last reviewed: December 28, 2010
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)