Evidence map›Paper›PMID 39449113›Full record

ArticleVirology journal2024

A first report of rotavirus B from Zambian pigs leading to the discovery of a novel VP4 genotype P[9].

Hayato Harima, Yongjin Qiu, Michihito Sasaki, Joseph Ndebe, Kapila Penjaninge, Edgar Simulundu, Masahiro Kajihara, Aiko Ohnuma, Keita Matsuno, Naganori Nao and 6 more

Abstract read
In one paragraph

Article in Virology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Hayato HarimaLaboratory of Veterinary Public Health, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Fuchu, 183-8509, Tokyo, Japan.
Yongjin QiuDivision of International Research Promotion, International Institute for Zoonosis Control, Hokkaido University, Sapporo, 001-0020, Japan.
Michihito SasakiDivision of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, 001-0020, Japan.
Joseph NdebeDivision of International Research Promotion, International Institute for Zoonosis Control, Hokkaido University, Sapporo, 001-0020, Japan.
Kapila PenjaningeDepartment of Disease Control, School of Veterinary Medicine, the University of Zambia, Lusaka, 10101, Zambia.
Edgar SimulunduDepartment of Disease Control, School of Veterinary Medicine, the University of Zambia, Lusaka, 10101, Zambia.
Masahiro KajiharaDivision of International Research Promotion, International Institute for Zoonosis Control, Hokkaido University, Sapporo, 001-0020, Japan.
Aiko OhnumaTechnical office, International Institute for Zoonosis Control, Hokkaido University, Sapporo, 001- 0020, Japan.
Keita MatsunoDivision of Risk Analysis and Management, International Institute for Zoonosis Control, Hokkaido University, Sapporo, 001-0020, Japan.
Naganori NaoDivision of International Research Promotion, International Institute for Zoonosis Control, Hokkaido University, Sapporo, 001-0020, Japan.
Yasuko OrbaDivision of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, 001-0020, Japan.
Ayato TakadaDepartment of Disease Control, School of Veterinary Medicine, the University of Zambia, Lusaka, 10101, Zambia.
Kanako IshiharaLaboratory of Veterinary Public Health, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Fuchu, 183-8509, Tokyo, Japan.
William W HallInstitute for Vaccine Research and Development, Hokkaido University, North 21 West 11, Kita-ku, Sapporo, 001-0021, Japan.
Bernard M Hang'ombeAfrica Center of Excellence for Infectious Diseases of Humans and Animals, the University of Zambia, Lusaka, 10101, Zambia.
Hirofumi SawaInstitute for Vaccine Research and Development, Hokkaido University, North 21 West 11, Kita-ku, Sapporo, 001-0021, Japan. h-sawa@ivred.hokudai.ac.jp.

Funding

AMED and the Japan International Cooperation Agency (JICA) within the framework of the Science and Technology Research Partnership for Sustainable Development (SATREPS) JP23jm0110019Japan Agency for Medical Research and Development JP243fa627005Japan Program for Infectious Diseases Research and Infrastructure from AMED JP23wm0125008
6 · The paper itself

Abstract

backgroundRotavirus B (RVB) causes diarrhea in humans and pigs. Although various RVB strains were identified in humans and various animals globally, little is known about the epidemiology RVB infection in Africa. In this study, we attempted to examine the prevalence of RVB infection in pig populations in Zambia.

methodsMetagenomic analyses were conducted on pig feces collected in Zambia to detect double stranded RNA viruses, including RVB. To clarify the prevalence of RVB infection in pig populations in Zambia, 147 fecal samples were screened for the RVB detection by RT-qPCR. Full genome sequence of a detected RVB was determined by Sanger sequencing and genetically analyzed.

resultsThe metagenomic analyses revealed that RVB sequence reads and contigs of RVB were detected from one fecal sample collected from pigs in Zambia. RT-qPCR screening detected RVB genomes in 36.7% (54/147) of fecal samples. Among 54 positive samples, 13 were positive in non-diarrheal samples (n = 48, 27.1%) and 41 in diarrheal samples (n = 99, 41.4%). Genetic analyses demonstrated that all the segments of ZP18-18, except for VP4, had high nucleotide sequence identities (80.6-92.6%) with all other known RVB strains detected in pigs. In contrast, the VP4 sequence of ZP18-18 was highly divergent from other RVB strains (< 64.6% identities) and formed a distinct lineage in the phylogenetic tree. Notably, the VP8 subunit of the VP4 showed remarkably low amino acid identities (33.3%) to those of known RVB strains, indicating that the VP8 subunit of ZP18-18 was unique among RVB strains. According to the whole genome classification for RVB, ZP18-18 was assigned to a genotype constellation, G18-P[9]-I12-R4-C4-M4-A8-N10-T5-E4-H7 with the newly established VP4 genotype P[9].

conclusionsThis current study updates the geographical distribution and the genetic diversity of RVB. Given the lack of information regarding RVB in Africa, further RVB surveillance is required to assess the potential risk to humans and animals.

Indexed as

Capsid ProteinsFecesGenome, ViralGenotypePhylogenyRotavirusRotavirus InfectionsSwine DiseasesAnimalsDiarrheaMetagenomicsPrevalenceRNA, ViralSequence Analysis, DNASwineZambiaCapsid ProteinsRNA, ViralVP4 protein, RotavirusFull genome sequencePigPrevalenceRotavirus BZambia

Identifiers

PMID39449113
PMCPMC11515359

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.