Hongjian Zhang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Hongjian Zhang has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Chunhui Feng
College of Agriculture and Animal Husbandry, Qinghai University, Xining 810016, China
1 shared publication - Fei Yang
College of Agriculture and Animal Husbandry, Qinghai University, Xining 810016, China
1 shared publication - Jing Zhao
College of Agriculture and Animal Husbandry, Qinghai University, Xining 810016, China
1 shared publication - Jinlin Ma
Hainbei Tibetan Autonomous Prefecture Animal Disease Prevention and Control Center, Haibei 810299, China
1 shared publication - Wei Zhang
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China
1 shared publication - Wenliang Li
Institute of Veterinary Medicine, Key Laboratory for Veterinary Bio-Product Engineering, Ministry of Agriculture and Rural Affairs, Jiangsu Academy of Agricultural Sciences, Nanjing, China
1 shared publication
Latest Publications
- Open Access
- 20 July 2026
- Published by MDPI AG in Microorganisms
- Vol. 14 (7) , 1582
Mechanism of Pasteurella multocida Lysis by Virulent Phage vB_PmuP_Pa7: Insights from a Strand-Specific Transcriptome Analysis
Virulent phage vB_PmuP_Pa7 is a promising candidate for controlling Pasteurella multocida infection, yet the molecular basis of its lytic process remains poorly understood. Here, we performed strand-specific RNA sequencing on P. multocida S34 infected with Pa7 at 0, 20, 30, and 120 min to characterize phage–host transcriptional dynamics. A total of 234, 433, and 558 differentially expressed genes (DEGs) were detected at 20, 30, and 120 min, respectively, indicating progressive host reprogramming during infection. PCA, expression distribution analysis, and sample correlation analysis confirmed clear stage-specific transcriptional shifts. GO and KEGG enrichment analyses indicated that Pa7 infection was associated with changes in translation, ribosome function, ABC transporters, amino sugar and nucleotide sugar metabolism, bacterial chemotaxis, and the TCA cycle. Four representative differentially expressed genes involved in transport, carbohydrate metabolism, and translation-related functions were selected for RT-qPCR analysis. The RT-qPCR results showed partial, gene- and time-point-dependent agreement with the RNA-seq-derived expression patterns. Together, these findings provide a time-resolved transcriptional profile of Pa7 infection and identify host pathways potentially associated with the infection process and bacterial cell lysis. However, the direct functional contributions of these genes and pathways remain to be experimentally determined.
- 20 July 2026
- Published by MDPI AG in Microorganisms
- Vol. 14 (7) , 1582
Open AccessMechanism of Pasteurella multocida Lysis by Virulent Phage vB_PmuP_Pa7: Insights from a Strand-Specific Transcriptome Analysis
Virulent phage vB_PmuP_Pa7 is a promising candidate for controlling Pasteurella multocida infection, yet the molecular basis of its lytic process remains poorly understood. Here, we performed strand-specific RNA sequencing on P. multocida S34 infected with Pa7 at 0, 20, 30, and 120 min to characterize phage–host transcriptional dynamics. A total of 234, 433, and 558 differentially expressed genes (DEGs) were detected at 20, 30, and 120 min, respectively, indicating progressive host reprogramming during infection. PCA, expression distribution analysis, and sample correlation analysis confirmed clear stage-specific transcriptional shifts. GO and KEGG enrichment analyses indicated that Pa7 infection was associated with changes in translation, ribosome function, ABC transporters, amino sugar and nucleotide sugar metabolism, bacterial chemotaxis, and the TCA cycle. Four representative differentially expressed genes involved in transport, carbohydrate metabolism, and translation-related functions were selected for RT-qPCR analysis. The RT-qPCR results showed partial, gene- and time-point-dependent agreement with the RNA-seq-derived expression patterns. Together, these findings provide a time-resolved transcriptional profile of Pa7 infection and identify host pathways potentially associated with the infection process and bacterial cell lysis. However, the direct functional contributions of these genes and pathways remain to be experimentally determined.