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Table 1.

Group C orthobunyavirus (GRCV) reference strains used in the study.

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Table 1 Expand

Table 2.

Primers used in RT-PCR and sequencing for group C orthobunyavirus (GRCV).

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Table 2 Expand

Fig 1.

Distribution of febrile patient samples in Peru.

Number of febrile surveillance samples (denominator) and number of group C isolates (numerator). The green circles represent the places where group C viruses were isolated and the size of the circle is proportional to the number of isolates.

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Fig 1 Expand

Fig 2.

Phylogenetic analysis of group C viruses based on partial nucleotide sequences of the S segment.

The phylogenetic tree was constructed using the neighbor-joining method. Bootstrap values were obtained based on 1000 replicates on the bases of partial coding sequence of N and NSs protein. The evolutionary distances were computed using the Kimura 2-parameter method. Members of the Simbu, California and Bunyamwera serogroups were used as outgroups to root the tree.

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Fig 2 Expand

Table 3.

Nucleotide and amino acid sequence identity values for a partial sequence of the S segment from some isolates and reference group C orthobunyaviruses.

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Table 3 Expand

Fig 3.

Phylogenetic analysis of group C viruses based on partial nucleotide sequences of the M segment.

The phylogenetic tree was constructed using the neighbor-joining method. Bootstrap values were obtained based on 1000 replicates using the partial coding sequence of the polyprotein. The evolutionary distances were computed using the Kimura 2-parameter method. Members of the Simbu, California and Bunyamwera serogroups were used as outgroups to root the tree.

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Fig 3 Expand

Table 4.

Nucleotide and amino acid sequence identity values for partial sequence of the M segment from some isolates and reference group C orthobunyaviruses.

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Table 4 Expand

Fig 4.

Phylogenetic analysis of group C viruses based on partial nucleotide sequences of the L segment.

The phylogenetic tree was constructed using the neighbor-joining method. Bootstrap values were obtained based on 1000 replicates on the bases of partial coding sequence of RdRp. The evolutionary distances were computed using the Kimura 2-parameter method. Members of the Simbu, California and Bunyamwera serogroups were used as outgroups to root the tree.

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Fig 4 Expand

Table 5.

Nucleotide and amino acid sequence identity values for a partial sequence of the L segment of some isolations and referential group C orthobunyavirus.

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Table 5 Expand

Table 6.

Microneutralization test of group C orthobunyavirus (GRCV) using hyperimmune mouse ascitic fluids (HMAFs) prepared with prototype strains.

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Table 6 Expand