A pathogenic and recombinant infectious bronchitis virus variant (CK/CH/GX/202109) with multiorgan tropism

Abstract Despite vaccine use, novel strains and variants of infectious bronchitis virus (IBV) have emerged continuously, leading to economic losses to the poultry industry worldwide. This study aimed to characterize the IBV isolate CK/CH/GX/202109 from three yellow broilers in Guangxi, China. Recomb...

Full description

Bibliographic Details
Main Authors: Chenyan Wang, Bo Hou
Format: Article
Language:English
Published: BMC 2023-07-01
Series:Veterinary Research
Subjects:
Online Access:https://doi.org/10.1186/s13567-023-01182-w
_version_ 1797784497608982528
author Chenyan Wang
Bo Hou
author_facet Chenyan Wang
Bo Hou
author_sort Chenyan Wang
collection DOAJ
description Abstract Despite vaccine use, novel strains and variants of infectious bronchitis virus (IBV) have emerged continuously, leading to economic losses to the poultry industry worldwide. This study aimed to characterize the IBV isolate CK/CH/GX/202109 from three yellow broilers in Guangxi, China. Recombination was shown to have occurred in regions of the 1ab gene. Compared to the whole genome of ck/CH/LGX/130530, which is genotypically related to tl/CH/LDT3-03, the 202109 strain had 21 mutations. The pathological assessment showed that this variant caused 30% and 40% mortality in 1-day-old chicks infected with oral and ocular inoculum, respectively. Nephritis, enlarged proventriculus, inflammation of the gizzard, and atrophy of the bursa of Fabricius were also observed at both 7 and 14 days post-infection (dpi). Viral loads in the trachea, proventriculus, gizzard, kidney, bursa, and cloacal swabs were higher at 7 dpi than at 14 dpi. Clinicopathological and immunohistochemical analyses revealed that this virus exhibited multiple organ tropisms capable of infecting the trachea, proventriculus, gizzard, kidney, bursa, ileum, jejunum, and rectum. Almost none of the 1-day-old infected chicks seroconverted until 14 dpi. While the virus was found in the ileum, jejunum, and rectum in the 28-day-old ocular group, the majority of 28-day-old infected chickens seroconverted at 10 dpi. These study findings demonstrate that recombination events and mutations during the evolution of IBV may greatly alter tissue tropism and emphasize the need for the continued surveillance of novel strains and variants in order to control this infection.
first_indexed 2024-03-13T00:40:45Z
format Article
id doaj.art-8535ceef66a54c278f0c950c5c17ad1c
institution Directory Open Access Journal
issn 1297-9716
language English
last_indexed 2024-03-13T00:40:45Z
publishDate 2023-07-01
publisher BMC
record_format Article
series Veterinary Research
spelling doaj.art-8535ceef66a54c278f0c950c5c17ad1c2023-07-09T11:21:35ZengBMCVeterinary Research1297-97162023-07-0154111410.1186/s13567-023-01182-wA pathogenic and recombinant infectious bronchitis virus variant (CK/CH/GX/202109) with multiorgan tropismChenyan Wang0Bo Hou1Institute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agricultural Sciences/Fujian Animal Disease Control Technology Development CenterInstitute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agricultural Sciences/Fujian Animal Disease Control Technology Development CenterAbstract Despite vaccine use, novel strains and variants of infectious bronchitis virus (IBV) have emerged continuously, leading to economic losses to the poultry industry worldwide. This study aimed to characterize the IBV isolate CK/CH/GX/202109 from three yellow broilers in Guangxi, China. Recombination was shown to have occurred in regions of the 1ab gene. Compared to the whole genome of ck/CH/LGX/130530, which is genotypically related to tl/CH/LDT3-03, the 202109 strain had 21 mutations. The pathological assessment showed that this variant caused 30% and 40% mortality in 1-day-old chicks infected with oral and ocular inoculum, respectively. Nephritis, enlarged proventriculus, inflammation of the gizzard, and atrophy of the bursa of Fabricius were also observed at both 7 and 14 days post-infection (dpi). Viral loads in the trachea, proventriculus, gizzard, kidney, bursa, and cloacal swabs were higher at 7 dpi than at 14 dpi. Clinicopathological and immunohistochemical analyses revealed that this virus exhibited multiple organ tropisms capable of infecting the trachea, proventriculus, gizzard, kidney, bursa, ileum, jejunum, and rectum. Almost none of the 1-day-old infected chicks seroconverted until 14 dpi. While the virus was found in the ileum, jejunum, and rectum in the 28-day-old ocular group, the majority of 28-day-old infected chickens seroconverted at 10 dpi. These study findings demonstrate that recombination events and mutations during the evolution of IBV may greatly alter tissue tropism and emphasize the need for the continued surveillance of novel strains and variants in order to control this infection.https://doi.org/10.1186/s13567-023-01182-wInfectious bronchitis virusproventriculusrecombinationtissue tropism
spellingShingle Chenyan Wang
Bo Hou
A pathogenic and recombinant infectious bronchitis virus variant (CK/CH/GX/202109) with multiorgan tropism
Veterinary Research
Infectious bronchitis virus
proventriculus
recombination
tissue tropism
title A pathogenic and recombinant infectious bronchitis virus variant (CK/CH/GX/202109) with multiorgan tropism
title_full A pathogenic and recombinant infectious bronchitis virus variant (CK/CH/GX/202109) with multiorgan tropism
title_fullStr A pathogenic and recombinant infectious bronchitis virus variant (CK/CH/GX/202109) with multiorgan tropism
title_full_unstemmed A pathogenic and recombinant infectious bronchitis virus variant (CK/CH/GX/202109) with multiorgan tropism
title_short A pathogenic and recombinant infectious bronchitis virus variant (CK/CH/GX/202109) with multiorgan tropism
title_sort pathogenic and recombinant infectious bronchitis virus variant ck ch gx 202109 with multiorgan tropism
topic Infectious bronchitis virus
proventriculus
recombination
tissue tropism
url https://doi.org/10.1186/s13567-023-01182-w
work_keys_str_mv AT chenyanwang apathogenicandrecombinantinfectiousbronchitisvirusvariantckchgx202109withmultiorgantropism
AT bohou apathogenicandrecombinantinfectiousbronchitisvirusvariantckchgx202109withmultiorgantropism
AT chenyanwang pathogenicandrecombinantinfectiousbronchitisvirusvariantckchgx202109withmultiorgantropism
AT bohou pathogenicandrecombinantinfectiousbronchitisvirusvariantckchgx202109withmultiorgantropism