Printer Friendly

High diversity of RNA viruses in Rodents, Ethiopia.

Most emerging infectious diseases of humans or domestic animals are zoonoses, and among emerging pathogens, RNA viruses are highly represented (1). The synanthropic nature of some rodent species makes them important reservoirs of RNA viruses pathogenic to humans, such as hantaviruses (e.g., Seoul virus in black and Norway rats worldwide) and arenaviruses (e.g., Lassa virus in the multimammate mouse in western Africa or lymphocytic choriomeningitis virus in the house mouse worldwide). In Africa, members of the rodent genera Mastomys and Arvicanthis are linked to human activity; these rodents are widespread throughout sub-Saharan Africa and are crop pests and zoonotic reservoirs for human pathogens. Histories of synanthropy are likely longest for rodents in areas of early human sedentism, making RNA virus richness in early centers of domestication such as the Ethiopian Highlands of particular interest.

Hantaviruses (family Bunyaviridae) are RNA viruses primarily carried by rodents and soricomorphs (shrews and moles), although 2 new species have recently been described in bats (2,3). Arenaviruses (family Arenaviridae) are primarily rodent-borne RNA viruses. Members of both genera can cause life-threatening diseases in humans: arena-viruses cause hemorrhagic fevers in the Americas and Africa, and hantaviruses cause hemorrhagic fever with renal syndrome in Asia and Europe and hantavirus cardiopulmonary syndrome in the Americas. In Africa, only Lassa and Lujo arenaviruses are known to be highly pathogenic to humans. In contrast, hantaviruses have not yet been found to cause life-threatening human diseases in Africa, but hantavirus-specific antibodies have been found in human serum samples from several countries in Africa (4,5). To investigate the role of synanthropic small mammals as potential reservoirs of emerging pathogens in Ethiopia, we sampled rodent and shrew species in areas near human habitations and screened them for hantavirus and arenavirus RNA.

The Study

Small mammals from domestic and peridomestic areas were trapped during August-December 2010 in 2 high-altitude localities, Golgolnaele (13[degrees]52'N, 39[degrees]43'E, elevation 2,700 m) and Mahbere Silassie (13[degrees]39'N, 39[degrees]08'E, elevation 2,600 m), and in 1 lower-altitude locality, Aroresha (12[degrees]25'N, 39[degrees]33'E, elevation 1,600 m), in the Tigray region of the Ethiopian Highlands. Kidney samples preserved in RNAlater reagent (QIAGEN, Hilden, Germany) and stored at -80[degrees]C were used for total RNA extraction by using the NucleoSpin RNA II Kit (Macherey-Nagel, Duren, Germany). Samples were pooled in pairs by locality and host species. RNA was reverse transcribed by using random hexamers as primers. Screening for arenaviruses was performed by using a pan-Old World arenavirus PCR targeting the large (L) gene (6). Screening for hantaviruses was performed by using a nested PCR assay targeting the hantavirus L gene (7).

A total of 201 small mammals from 6 species were screened for arenaviruses and hantaviruses (Table). Among them, 1 Ethiopian white-footed mouse (Stenocephalemys albipes) from Golgolnaele and 2 Awash multimammate mice (Mastomys awashensis) from Aroresha were positive for arenavirus RNA; 10 white-footed mice from the 2 highland localities (6 from Golgolnaele, 4 from Mahbere Silassie) were positive for hantavirus RNA. Amplicons were purified and sequenced, and nucleotide sequences were aligned on the basis of the amino acid alignment. Phylogenetic analyses were performed on the nucleotide sequences by using a maximum-likelihood (ML) approach (8).

After sequencing of the 3 arenavirus-positive samples, 3 distinct arenavirus sequences were obtained, and an ML tree was constructed for these 3 arenavirus sequences and the partial L gene (340 bp) of representatives of Old World arenaviruses (Figure 1). The 3 sequences cluster with Mobala virus (80% bootstrap support), an arenavirus discovered in Praomys sp. in the Central African Republic in 1983 (10). However, the 3 sequences from Ethiopia are not monophyletic; the 2 sequences from multimammate mice cluster together (94% bootstrap support), but the sequence from the white-footed mouse from Golgolnaele is basal to the clade (Mobala + M. awashensis virus sequences), with the Menekre virus, found in Hylomyscus sp. in Guinea (11), used as outgroup. The sequences from multimammate mice on average differ from those of Mobala virus and the sequence from the white-footed mouse by the same order of magnitude in terms of amino acids: 5.0 [+ or -] 2.1% and 5.9 [+ or -] 2.2%, respectively. The average amino acid difference between the sequence from the white-footed mouse and that from Mobala virus was 8.1 [+ or -] 2.6%. Therefore, these arenaviruses seem to be 2 strains of Mobala virus carried by 2 rodent species and found in 2 localities [much less than] 250 km apart from each other and with an altitude difference of 1,100 m.

After sequencing of the 10 hantavirus-positive samples, 4 distinct hantavirus sequences were obtained, 2 from Golgonaele and 2 from Mahbere Silassie. Figure 2 shows the ML tree for these 4 sequences and the partial L gene (347 bp) of representatives of hantaviruses. The tree is not well resolved, and shrew- and mole-associated hantaviruses do not cluster. Two rodent-associated clades are supported: the previously known Murinae-associated hantaviruses (69% bootstrap support) and the Cricetidae-associated hantaviruses (92% bootstrap support, with 1 exception, Rockport, Soricomorpha-associated hantavirus). Although all 4 sequences were found in S. albipes mice, a Murinae species endemic to Ethiopia, they do not group with the Murinae-associated hantaviruses or with hantaviruses found in other African small mammals, such as bats (2,3) or shrews (12,13). The 4 sequences form a unique, divergent clade with the 2 sequences from Mahbere Silassie basal to the sequences from Golgonaele, which cluster together. The average amino acid difference between the sequences from Ethiopia and those from Murinae-associated hantaviruses was 27.0 [+ or -] 4.0%. Because the new amino acid sequences are at least 21.0 [+ or -] 4.0% divergent from those of other hantaviruses, we conclude that S. albipes mice are carrying a novel hantavirus. We propose the name Tigray virus for this virus because it was found in the Tigray region of Ethiopia. Additional genetic characterization, in particular of the small and medium segments, will be conducted to further clarify the evolutionary relationship of this virus within the hantavirus genus.


Two rodent species living in close proximity to human settlements in Ethiopia are carriers of arenaviruses and hantaviruses. Recently, several new arenaviruses and hantaviruses have been described in small mammals in Africa, but no clear association with human diseases has been found (2,3,9,11-13). However, arenavirus and hantavirus infections are likely severely underreported because symptoms may resemble those of many other febrile infections (2). Investigating the presence of antibodies for Mobala virus and the proposed Tigray virus in humans in the Ethiopian Highlands is the next step in evaluating their pathogenicity. A recent study in Guinea showed that 2/68 patients with fever of unknown origin had antibodies for Sangassou hantavirus (5); a case of putative hantavirus disease (hemorrhagic fever with renal syndrome) was also reported in the Central African Republic (14). Hantavirus infections may thus be an unrecognized medical problem in Africa and deserve more attention.

In conclusion, our screening of 201 small mammals led to the identification of 2 novel strains of Mobala arenavirus and a novel hantavirus in 2 rodent species found in Ethiopia, M. awashensis and S. albipes. These rodents belong to the exclusively African Praomyini tribe (15), which hosts 5/11 arenaviruses (Lassa, Mopeia, Luna, Mobala, and Menekre viruses) and the only Murinae-associated hantavirus (Sangassou virus) described in Africa. Our results support a major role for Praomyini as hosts in the evolutionary history of arenaviruses and hantaviruses in Africa.

This work was supported by the Flemish Interuniversity Council, Belgium; the University of Antwerp; the Fund for Scientific Research-Flanders (FWO grant no.; the Czech Science Foundation (GACR grant P502/11/J070); and the German Research Foundation (DFG grant GU 883/2-1). During this study, Y.M. was a PhD fellow with the Mekelle University-Institutional University Cooperation project.

Dr Meheretu is a lecturer at Mekelle University and a postdoctorate researcher at the Academy of Sciences of the Czech Republic Institute of Vertebrate Biology. His research interests are rodent pests that cause agricultural damage and act as natural reservoirs of human pathogens in Ethiopia.

DOI: 10.3201/eid1812.120596

Author affiliations: Academy of Sciences of the Czech Republic Institute of Vertebrate Biology, Brno, Czech Republic (Y. Meheretu, D. Cizkova, J. Tesikova, J. Bryja, A. Bryjova, J. Gouy de Bellocq); Mekelle University, Mekelle, Ethiopia (Y. Meheretu, K. Welegerima, Z. Tomas, D. Kidane, K. Girmay); University of Antwerp, Antwerp, Belgium (Y. Meheretu, H. Leirs, J. Gouy de Bellocq); and Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany (J. Schmidt-Chanasit, S. Gunther)


(1.) Woolhouse M, Gaunt E. Ecological origins of novel human pathogens. Crit Rev Microbiol. 2007;33:231-42. http://dx.doi. org/10.1080/10408410701647560

(2.) Weiss S, Witkowski PT, Auste B, Nowak K, Weber N, Fahr J, et al. Hantavirus in bat, Sierra Leone. Emerg Infect Dis. 2012;18:159-61.

(3.) Sumibcay L, Kadjo B, Gu SH, Kang HJ, Lim B, Cook J, et al. Divergent lineage of a novel hantavirus in the banana pipistrelle (Neoromicia nanus) in Cote d'Ivoire. Virol J. 2012;9:34. http://dx.doi. org/10.1186/1743-422X-9-34

(4.) Gonzalez JP, McCormick JB, Baudon D, Gautun JP, Meunier DY, Dournon E, et al. Serological evidence for Hantaan-related virus in Africa. Lancet. 1984;324:1036-7.

(5.) Klempa B, Koivogui L, Sylla O, Koulemou K, Auste B, Kruger DH, et al. Serological evidence of human hantavirus infections in Guinea, West Africa. J Infect Dis. 2010;201:1031-4. http://dx.doi. org/10.1086/651169

(6.) Vieth S, Drosten C, Lenz O, Vincent M, Omilabu S, Hass M, et al. 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

(7.) Klempa B, Fichet-Calvet E, Lecompte E, Auste B, Aniskin V, Meisel H, et al. Hantavirus in African wood mouse, Guinea. Emerg Infect Dis. 2006;12:838-40.

(8.) Guindon S, Dufayard J-F, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol. 2010;59:307-21.

(9.) Gouy 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. 2010;16:692-5. http://dx.doi. org/10.3201/eid1604.091721

(10.) Gonzalez JP, McCormick JB, Saluzzo JF, Herve JP, Georges AJ, Johnson KM. An arenavirus isolated from wild-caught rodents (Praomys species) in the Central African Republic. Intervirology. 1983;19:105-12.

(11.) Coulibaly-N'Golo D, Allali B, Kouassi SK, Fichet-Calvet E, BeckerZiaja B, Rieger T, et al. Novel arenavirus sequences in Hylomyscus sp. and Mus (Nannomys) setulosus from Cote d'Ivoire: implications for evolution of arenaviruses in Africa. PLoS ONE. 2011;6:e20893.

(12.) Klempa B, Fichet-Calvet E, Lecompte E, Auste B, Aniskin V, Meisel H, et al. Novel hantavirus sequences in shrew, Guinea. Emerg Infect Dis. 2007;13:520-2.

(13.) Kang HJ, Kadjo B, Dubey S, Jacquet F, Yanagihara R. Molecular evolution of Azagny virus, a newfound hantavirus harbored by the West African pygmy shrew (Crocidura obscurior) in Cote d'Ivoire. Virol J. 2011;8:373.

(14.) Coulaud X, Chouaib E, Georges AJ, Rollin P, Gonzalez JP. First human case of haemorrhagic fever with renal syndrome in the Central African Republic. Trans R Soc Trop Med Hyg. 1987;81:686. http://

(15.) Lecompte E, Aplin K, Denys C, Catzeflis F, Chades M, Chevret P. Phylogeny and biogeography of African Murinae based on mitochondrial and nuclear gene sequences, with a new tribal classification of the subfamily. BMC Evol Biol. 2008;8:199 http://dx.doi. org/10.1186/1471-2148-8-199.

Yonas Meheretu, [1] Dagmar Cizkova, [1] Jana Tesikova, Kiros Welegerima, Zewdneh Tomas, Dawit Kidane, Kokob Girmay, Jonas Schmidt-Chanasit, Josef Bryja, Stephan Gunther, Anna Bryjova, Herwig Leirs, and Joelle Gouy de Bellocq

[1]These authors contributed equally to this article.

Address for correspondence: Joelle Gouy de Bellocq, Evolutionary Ecology Group, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp, Belgium; email:

Table. Small mammal species screened for arenaviruses
and hantaviruses, Ethiopian Highlands, August-December 2010 *

                               No. animals by locality and elevation

                               Aroresha,           Golgolnaele,
Species                        1,600 m             2,700 m

Ethiopian white-footed mouse           0                33
(Stenocephalemys albipes)
Awash multimammate mouse              16                1
(Mastomys awashensis)
Mus (Nannomys) sp. mice               11                20
Black rat (Rattus rattus)             37                2
African giant shrew                    6                2
(Crocidura olivieri)
Dembea grass rat                       8                13
(Arvicanthis dembeensis)
Total                                 78                71

                               No. animals by
                               locality and elevation

                               Mahbere Silassie,   Total no.
Species                        2,600 m             animals

Ethiopian white-footed mouse          23                56
(Stenocephalemys albipes)
Awash multimammate mouse               1                18
(Mastomys awashensis)
Mus (Nannomys) sp. mice                2                33
Black rat (Rattus rattus)              5                44
African giant shrew                   17                25
(Crocidura olivieri)
Dembea grass rat                       4                25
(Arvicanthis dembeensis)
Total                                 52               201

* Species identification was confirmed by sequencing the partial
mitochondrial cytochrome b gene (11). Representative sequences are
available in GenBank (accession nos. JQ956464-JQ956479). Voucher
specimens from representative rodents have been deposited at the
Evolutionary  Ecology group, University of Antwerp, and are
available from the authors on request.
COPYRIGHT 2012 U.S. National Center for Infectious Diseases
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2012 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:DISPATCHES
Author:Meheretu, Yonas; Cizkova, Dagmar; Tesikova, Jana; Welegerima, Kiros; Tomas, Zewdneh; Kidane, Dawit;
Publication:Emerging Infectious Diseases
Article Type:Report
Geographic Code:6ETHI
Date:Dec 1, 2012
Previous Article:Cygnet River virus, a novel orthomyxovirus from Ducks, Australia.
Next Article:West Nile Virus neurologic disease in humans, South Africa, September 2008-May 2009.

Terms of use | Privacy policy | Copyright © 2018 Farlex, Inc. | Feedback | For webmasters