Aerosol exposure enhanced infection of low pathogenic avian influenza viruses in chickens.

To assess the impact of different routes of inoculation on experimental infection of avian influenza (AI) viruses in chickens, this study compared virus replication and cytokine gene expression in respiratory and gastrointestinal organ tissues of chickens, which were inoculated with four low pathogenic subtypes, H6N1, H10N7, H10N8, and H13N6 AI viruses via the aerosol, intranasal, and oral routes respectively. Aerosol inoculation with the H6N1, H10N7, and H10N8 viruses significantly increased viral titres and upregulated the interferon (IFN)-γ, interleukin (IL)-6, and IL-1β genes in the trachea and lung tissues compared to intranasal or oral inoculation. Furthermore, one or two out of six chickens died following exposure to aerosolized H6N1 or H10N8 virus respectively.

H9N2 avian influenza virus retained low pathogenicity after serial passage in chickens.

The H9N2 strains of avian influenza viruses (AIVs) circulate worldwide in poultry and cause sporadic infection in humans. To better understand the evolution of these viruses while circulating in poultry, an H9N2 chicken isolate was passaged 19 times in chickens aerosol inoculation. Whole-genome sequencing showed that the viruses from the initial stock and those after the 8th and 19th passages (P0, P8, and P19) all had the same monobasic cleavage site in the hemagglutinin (HA), typical for viruses of low pathogenicity.

Replication of an H9N2 Avian Influenza Virus and Cytokine Gene Expression in Chickens Exposed by Aerosol or Intranasal Routes.

This study related the replication of an H9N2 avian influenza virus in chickens to the induction of host acute immune response after aerosol or intranasal inoculation with the virus. On 1, 2, 4, and 7 days postinoculation (dpi), oropharyngeal swabs and tissue specimens of trachea, lungs, spleen, and cecal tonsils were collected for quantification of viral RNA. Expression of cytokine genes in lungs, spleen, and cecal tonsils was quantified by reverse transcriptase-PCR.

Aerosol transmission of an avian influenza H9N2 virus with a tropism for the respiratory tract of chickens.

A low pathogenic avian influenza virus (LPAI H9N2) was administered to 3-wk-old chickens by aerosol exposure, intranasal inoculation, and by oral inoculation. Tests for virus were by in ovo assay and by real-time reverse-transcriptase PCR. The aerosol dosage was determined by aerosolizing virus into a chamber when it was empty and when it contained chickens.

[Expression of mRNAs for GHR, IGF-IR, FSHR and LHR in granulosa and theca layers of ovarian follicles of Shaoxing ducks].

Expression of genes encoding growth hormone receptor (GHR), type I insulin-like growth factor receptor (IGF-IR), follicle-stimulating hormone receptor (FSHR) and luteinizing hormone receptor (LHR) was measured in granulosa and theca layers of the largest (F1), third largest (F3), fifth largest (F5) preovulatory follicles and large white follicles (LWF) in the ovary of Shaoxing ducks, with relative quantitative reverse transcription-polymerase chain reaction (RT-PCR) using beta-actin as an internal standard. The results showed that GHR mRNA was more abundant in theca layer than in granulosa layer in all the follicles investigated, in theca layer, the LWF follicle expressed highest the level of GHR mRNA, while no differences in granulosa layer were observed among follicles at different stages of development. In contrast, the expression of IGF-IR mRNA in theca layer was evidently lower than that in granulosa layer, but no significant changes were found among different stages of follicles in either layers, except that LWF trended to express higher IGF-IR mRNA in the theca layer compared to other preovulatory follicles.