<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bai Y</submitter><funding>Guangdong Provincial Key R&amp;amp;amp;D Program</funding><funding>Heyuan Branch, Guangdong Laboratory for Lingnan Modern Agriculture Project</funding><funding>China Agriculture Research System of MOF and MARA</funding><funding>Guangdong Provincial Key R&amp;D Program</funding><funding>Guangdong Basic and Applied Basic Research Foundation</funding><funding>Science and Technology Program of Guangdong province, China</funding><funding>Provincial Science and Technology Special Fund Project for Zhongshan City(major special project + Task list management mode)</funding><funding>Special Project of National Modern Agricultural Industrial Technology System</funding><funding>construction project of modern agricultural science and technology innovation alliance in Guangdong province</funding><funding>Provincial Science and Technology Special Fund Project for Zhongshan City (major special project + task list management mode)</funding><funding>Natural Science Foundation of Guangzhou</funding><pagination>122</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10975772</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(3)</volume><pubmed_abstract>Among broilers, the main pathogen that leads to swollen head syndrome (SHS) is the subgroup C avian metapneumovirus (aMPV-C). The aMPV-C infection can lead to an upsurge in the rate of soft-shell eggs, resulting in reduced egg production and seriously affecting the economy of the livestock industry. Therefore, a rapid method for aMPV-C detection needs to be invented. According to the N gene of aMPV-C, we designed the specific probe and primer and created a reverse transcription recombinase-aided amplification assay (RT-RAA) for the detection of aMPV-C. aMPV-C could be detected quickly and specifically by this method at 41 °C for 30 min. The sensitivity assay inferred that the minimum detection threshold of RT-RAA was 3.38 × 10&lt;sup>1&lt;/sup> copies/μL. A specificity assay showed that the RT-RAA method did not cross-react with other subgroups (aMPV-A, aMPV-B, aMPV-D) or other viruses (H9N2, NDV, IBV, IBDV). Forty samples of known clinical background were tested by RT-RAA and RT-qPCR. The two approaches had a 100% correlation rate. In conclusion, this research successfully created an RT-RAA assay for aMPV-C.</pubmed_abstract><journal>Veterinary sciences</journal><pubmed_title>Establishment and Application Prospect of Reverse Transcriptase Recombinase-Aided Amplification Assay for Subgroup C Avian Metapneumovirus.</pubmed_title><pmcid>PMC10975772</pmcid><funding_grant_id>2023A1515010584</funding_grant_id><funding_grant_id>2021sdr003</funding_grant_id><funding_grant_id>2020KJ128</funding_grant_id><funding_grant_id>2020B020222001, 2019B020218004</funding_grant_id><funding_grant_id>2023A04J1461</funding_grant_id><funding_grant_id>2020B1212060060</funding_grant_id><funding_grant_id>2020B020222001</funding_grant_id><funding_grant_id>2021A1515010817</funding_grant_id><funding_grant_id>2023A1515010584, 2021A1515010817</funding_grant_id><funding_grant_id>DT20220003</funding_grant_id><funding_grant_id>2021KJ128</funding_grant_id><funding_grant_id>2019B020218004</funding_grant_id><funding_grant_id>2021KJ128, 2020KJ128</funding_grant_id><funding_grant_id>CARS-41</funding_grant_id><funding_grant_id>CARS-42-13</funding_grant_id><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Dong M</pubmed_authors><pubmed_authors>Bai Y</pubmed_authors><pubmed_authors>Xie Q</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Dai Z</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Establishment and Application Prospect of Reverse Transcriptase Recombinase-Aided Amplification Assay for Subgroup C Avian Metapneumovirus.</name><description>Among broilers, the main pathogen that leads to swollen head syndrome (SHS) is the subgroup C avian metapneumovirus (aMPV-C). The aMPV-C infection can lead to an upsurge in the rate of soft-shell eggs, resulting in reduced egg production and seriously affecting the economy of the livestock industry. Therefore, a rapid method for aMPV-C detection needs to be invented. According to the N gene of aMPV-C, we designed the specific probe and primer and created a reverse transcription recombinase-aided amplification assay (RT-RAA) for the detection of aMPV-C. aMPV-C could be detected quickly and specifically by this method at 41 °C for 30 min. The sensitivity assay inferred that the minimum detection threshold of RT-RAA was 3.38 × 10&lt;sup>1&lt;/sup> copies/μL. A specificity assay showed that the RT-RAA method did not cross-react with other subgroups (aMPV-A, aMPV-B, aMPV-D) or other viruses (H9N2, NDV, IBV, IBDV). Forty samples of known clinical background were tested by RT-RAA and RT-qPCR. The two approaches had a 100% correlation rate. In conclusion, this research successfully created an RT-RAA assay for aMPV-C.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-04-08T15:10:48.867Z</modification><creation>2025-04-05T23:16:18.352Z</creation></dates><accession>S-EPMC10975772</accession><cross_references><pubmed>38535856</pubmed><doi>10.3390/vetsci11030122</doi></cross_references></HashMap>