Small mammals from domestic and peridomestic areas were trapped during August–December 2010 in 2 high-altitude localities, Golgolnaele (13°52′N, 39°43′E, elevation 2,700 m) and Mahbere Silassie (13°39′N, 39°08′E, elevation 2,600 m), and in 1 lower-altitude locality, Aroresha (12°25′N, 39°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°C were used for total RNA extraction by using the NucleoSpin RNA II Kit (Macherey-Nagel, Düren, 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).

Figure 1

Figure 1. . Maximum-likelihood tree of Old World arenaviruses showing the position of 3 arenaviruses (boldface; GenBank accession nos. JQ956481–JQ956483) found in kidney samples of Awash multimammate mice (Mastomys awashensis) and Ethiopian white-footed...

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), 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 ± 2.1% and 5.9 ± 2.2%, respectively. The average amino acid difference between the sequence from the white-footed mouse and that from Mobala virus was 8.1 ± 2.6%. Therefore, these arenaviruses seem to be 2 strains of Mobala virus carried by 2 rodent species and found in 2 localities ≈250 km apart from each other and with an altitude difference of 1,100 m.

Figure 2

Figure 2. . Maximum-likelihood tree of hantaviruses showing the position of the 4 sequences of Tigray hantavirus (boldface; GenBank accession nos. JQ956484–JQ956487) found in kidney samples of Ethiopian white-footed mice (Stenocephalemys albipes). The...

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 ± 4.0%. Because the new amino acid sequences are at least 21.0 ± 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.