Abstract

The Mapputta group comprises antigenically related viruses indigenous to Australia and Papua New Guinea that are included in the family Bunyaviridae but not currently assigned to a specific genus. We determined and analyzed the genome sequences of five Australian viruses isolated from mosquitoes collected during routine arbovirus surveillance in Western Australia (K10441, SW27571, K13190, and K42904) and New South Wales (12005). Based on matching sequences of all three genome segments to prototype MRM3630 of Trubanaman virus (TRUV), NB6057 of Gan Gan virus (GGV), and MK7532 of Maprik virus (MPKV), isolates K13190 and SW27571 were identified as TRUV, 12005 as GGV, and K42904 as a Mapputta group virus from Western Australia linking GGV and MPKV. The results confirmed serum neutralization data that had linked SW27571 to TRUV. The fifth virus, K10441 from Willare, was most closely related to Batai orthobunyavirus, presumably representing an Australian variant of the virus. Phylogenetic analysis also confirmed the close relationship of our TRUV and GGV isolates to two other recently described Australian viruses, Murrumbidgee virus and Salt Ash virus, respectively. Our findings indicate that TRUV has a wide circulation throughout the Australian continent, demonstrating for the first time its presence in Western Australia. Similarly, the presence of a virus related to GGV, which had been linked to human disease and previously known only from the Australian southeast, was demonstrated in Western Australia. Finally, a Batai virus isolate was identified in Western Australia. The expanding availability of genomic sequence for novel Australian bunyavirus variants supports the identification of suitably conserved or diverse primer-binding target regions to establish group-wide as well as virus-specific nucleic acid tests in support of specific diagnostic and surveillance efforts throughout Australasia.

Highlights

  • In 1960, Mapputta virus (MAPV; isolate MRM186), the first of four Australasian bunyaviruslike viruses of the Mapputta serogroup was discovered in Anopheles (Cellia) meraukensis mosquitoes collected at Mitchell River Mission ( Kowanyama) in northern Queensland [1, 2]

  • The S-segment of K10441 coded for a NSs protein, whereas the other four isolates did not possess an analogous open reading frame (ORF)

  • In comparison to other orthobunyaviruses as well as among them, the S-segment sequences of SW27571, K13190, 12005 and K42904 showed significant variation in commonly conserved N motifs around invariant amino acids T91/R94 and G150/P162

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Summary

Introduction

In 1960, Mapputta virus (MAPV; isolate MRM186), the first of four Australasian bunyaviruslike viruses of the Mapputta serogroup was discovered in Anopheles (Cellia) meraukensis mosquitoes collected at Mitchell River Mission ( Kowanyama) in northern Queensland [1, 2]. Trubanaman virus (TRUV; isolate MRM3630) obtained from Anopheles (Cellia) annulipes mosquitoes collected in1965 at Kowanyama, and Maprik virus (MPKV; isolate MK7532) obtained in 1966 from Verrallina (Verallina) funerea mosquitoes collected at Maprik, New Guinea, were recognized ([3], https://wwwn.cdc.gov/Arbocat/Default.aspx). The fourth virus was Gan Gan virus (GGV; isolate NB6057), isolated first from Aedes (Ochlerotatus) vigilax mosquitoes collected at Nelson Bay, Port Stephens Peninsula, New South Wales in 1970 [4, 5]. Recent sequence analyses of MAPV MRM186 and MPKV MK7532 indicated a relationship of Mapputta group viruses to the genus Orthobunyavirus of the Bunyaviridae [10]. Genome sequence analysis of GGV NB6057 indicated that another previously reported virus, Salt Ash (SAHV; [11]), represents an isolate of GGV instead of a distinct virus [13, 14]

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