EDP Sciences logo
Search
Menu
All issues Vet. Res., 39 5 (2008) 42 Article references

Articles citing this article

The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).

Cited article:

Research progress into the principles and methods underlying capsular typing of Glaesserella parasuis

Yaxin Zhu, Lijun Guan, Junfeng Zhang, Yun Xue and Zhanqin Zhao
Veterinary Research 55 (1) (2024)
https://doi.org/10.1186/s13567-024-01395-7

Evaluation of immunoregulation and immunoprotective efficacy of Glaesserella parasuis histidine kinase QseC

Xuefeng Yan, Congwei Gu, Wudian Xiao, Yuhong Zhou, Xinyi Xiang, Zehui Yu, Manli He, Qian Yang, Mingde Zhao and Lvqin He
Microbial Pathogenesis 192 106685 (2024)
https://doi.org/10.1016/j.micpath.2024.106685

Pili Subunit PilA Contributes to the Cytoadhesion of Glaesserella Parasuis to Host Cells and Provides Immunoprotection

Jiahui An, Jinshuang Cai, Baoge Zhang, Yufeng Li and Charles M. Dozois
Applied and Environmental Microbiology 89 (4) (2023)
https://doi.org/10.1128/aem.02002-22

Blood–Brain Barrier Integrity Damage in Bacterial Meningitis: The Underlying Link, Mechanisms, and Therapeutic Targets

Ruicheng Yang, Jundan Wang, Fen Wang, et al.
International Journal of Molecular Sciences 24 (3) 2852 (2023)
https://doi.org/10.3390/ijms24032852

Glaesserella parasuis QseBC two-component system senses epinephrine and regulates capD expression

Ju Sun, Siting Wen, Zhichao Wang, Wei Liu, Yan Lin, Jiayun Gu, Weiting Mao, Xiaojuan Xu, Qigai He, Xuwang Cai and Olaya Rendueles
Microbiology Spectrum 11 (6) (2023)
https://doi.org/10.1128/spectrum.01508-23

Sex-specific association between placental inflammatory cytokine mRNA expression and preschoolers’ behavioral development: The Ma’anshan birth cohort study

Jixing Zhou, Yuzhu Teng, Fu Zhang, et al.
Brain, Behavior, and Immunity 104 110 (2022)
https://doi.org/10.1016/j.bbi.2022.05.017

Deletion of two-component system QseBC weakened virulence of Glaesserella parasuis in a murine acute infection model and adhesion to host cells

Xuefeng Yan, Ke Dai, Congwei Gu, et al.
PeerJ 10 e13648 (2022)
https://doi.org/10.7717/peerj.13648

Glaesserella parasuis induces IL-17 production might through PKC-ERK/MAPK and IκB/NF-κB signaling pathways

Xinyi He, Xin Song, Hui Cao, Qun Zhou, Jiaqi Zhang, Hua Yue and Bin Zhang
Veterinary Microbiology 273 109521 (2022)
https://doi.org/10.1016/j.vetmic.2022.109521

Baicalin Protects Vascular Tight Junctions in Piglets During Glaesserella parasuis Infection

Yu Liu, Xiaoyi Li, Zhaoran Zhang, et al.
Frontiers in Veterinary Science 8 (2021)
https://doi.org/10.3389/fvets.2021.671936

Proteomic analysis of bEnd.3 cells infected with wild-type and stk-deficient strains of Streptococcus suis serotype 2 reveals protein and pathway regulation

Weiyi Li, Yifan Yin, Yu Meng, Hong Zhou, Zhe Ma, Huixing Lin and Hongjie Fan
Journal of Proteomics 230 103983 (2021)
https://doi.org/10.1016/j.jprot.2020.103983

Sialylated Lipooligosaccharide Contributes to Glaesserella parasuis Penetration of Porcine Respiratory Epithelial Barrier

Huan Wang, Wenbin Wei, Qi Cao, et al.
ACS Infectious Diseases 7 (3) 661 (2021)
https://doi.org/10.1021/acsinfecdis.0c00850

LncRNA-MEG3 Regulates the Inflammatory Responses and Apoptosis in Porcine Alveolar Macrophages Infected with Haemophilus parasuis Through Modulating the miR-210/TLR4 Axis

Rong H. Yin, Zhong B. Guo, Yuan Y. Zhou, et al.
Current Microbiology 78 (8) 3152 (2021)
https://doi.org/10.1007/s00284-021-02590-x

Sialidase of Glaesserella parasuis Augments Inflammatory Response via Desialylation and Abrogation of Negative Regulation of Siglec-5

Yuping Song, Qicong Pan, Jing Xiao, et al.
Infection and Immunity 89 (5) (2021)
https://doi.org/10.1128/IAI.00696-20

Association between the Phenotypes and Genotypes of Antimicrobial Resistance in Haemophilus parasuis Isolates from Swine in Quang Binh and Thua Thien Hue Provinces, Vietnam

Chao Nguyen Van, Lijun Zhang, Tam Vu Thi Thanh, et al.
Engineering 6 (1) 40 (2020)
https://doi.org/10.1016/j.eng.2019.10.014

Mycoplasma hyorhinis as a possible cause of fibrinopurulent meningitis in pigs? - a case series

Moritz Bünger, Rene Brunthaler, Christine Unterweger, et al.
Porcine Health Management 6 (1) (2020)
https://doi.org/10.1186/s40813-020-00178-8

Haemophilus parasuis VtaA2 is involved in adhesion to extracellular proteins

Mar Costa-Hurtado, Laura Garcia-Rodriguez, Sergi Lopez-Serrano and Virginia Aragon
Veterinary Research 50 (1) (2019)
https://doi.org/10.1186/s13567-019-0687-2

Optimized cultivation of porcine choroid plexus epithelial cells, a blood–cerebrospinal fluid barrier model, for studying granulocyte transmigration

Alexa N. Lauer, Martin März, Svenja Meyer, et al.
Laboratory Investigation 99 (8) 1245 (2019)
https://doi.org/10.1038/s41374-019-0250-9

TLR2, Siglec-3 and CD163 expressions on porcine peripheral blood monocytes are increased during sepsis caused by Haemophilus parasuis

Álvaro Álvarez-Estrada, Elías Fernando Rodríguez-Ferri, Sonia Martínez-Martínez, et al.
Comparative Immunology, Microbiology and Infectious Diseases 64 31 (2019)
https://doi.org/10.1016/j.cimid.2019.02.001

Characterization of serotypes and virulence genes of Haemophilus parasuis isolates from Central Vietnam

Chao Nguyen Van, Tam Vu Thi Thanh, Geng Zou, et al.
Veterinary Microbiology 230 117 (2019)
https://doi.org/10.1016/j.vetmic.2019.02.008

Baicalin Inhibits Haemophilus Parasuis-Induced High-Mobility Group Box 1 Release during Inflammation

Shulin Fu, Huashan Liu, Xiao Chen, Yinsheng Qiu, Chun Ye, Yu Liu, Zhongyuan Wu, Ling Guo, Yongqing Hou and Chien-An Andy Hu
International Journal of Molecular Sciences 19 (5) 1307 (2018)
https://doi.org/10.3390/ijms19051307

Haemophilus parasuis α-2,3-sialyltransferase-mediated lipooligosaccharide sialylation contributes to bacterial pathogenicity

Huan Wang, Lu Liu, Qi Cao, et al.
Virulence 9 (1) 1247 (2018)
https://doi.org/10.1080/21505594.2018.1502606

lgtF effects of Haemophilus parasuis LOS induced inflammation through regulation of NF-κB and MAPKs signaling pathways

Ze Zeng, Bin Zhang, Huan He, et al.
Microbial Pathogenesis 110 380 (2017)
https://doi.org/10.1016/j.micpath.2017.06.035

Molecular analysis of lungs from pigs immunized with a mutant transferrin binding protein B-based vaccine and challenged with Haemophilus parasuis

S. Martínez-Martínez, E.F. Rodríguez-Ferri, R. Frandoloso, et al.
Comparative Immunology, Microbiology and Infectious Diseases 48 69 (2016)
https://doi.org/10.1016/j.cimid.2016.08.005

Baicalin suppresses NLRP3 inflammasome and nuclear factor-kappa B (NF-κB) signaling during Haemophilus parasuis infection

Shulin Fu, Lei Xu, Sali Li, et al.
Veterinary Research 47 (1) (2016)
https://doi.org/10.1186/s13567-016-0359-4

Two Glycosyltransferase Genes of Haemophilus parasuis SC096 Implicated in Lipooligosaccharide Biosynthesis, Serum Resistance, Adherence, and Invasion

Qi Zhou, Saixiang Feng, Jianmin Zhang, et al.
Frontiers in Cellular and Infection Microbiology 6 (2016)
https://doi.org/10.3389/fcimb.2016.00100

Novel bla ROB-1 -Bearing Plasmid Conferring Resistance to β-Lactams in Haemophilus parasuis Isolates from Healthy Weaning Pigs

Javier Moleres, Alfonso Santos-López, Isidro Lázaro, et al.
Applied and Environmental Microbiology 81 (9) 3255 (2015)
https://doi.org/10.1128/AEM.03865-14

Haemophilus parasuis induces activation of NF-κB and MAP kinase signaling pathways mediated by toll-like receptors

Yushan Chen, Ting Liu, Paul Langford, et al.
Molecular Immunology 65 (2) 360 (2015)
https://doi.org/10.1016/j.molimm.2015.02.016

The outer membrane protein P2 (OmpP2) of Haemophilus parasuis induces proinflammatory cytokine mRNA expression in porcine alveolar macrophages

Suming Zhou, Xianhui He, Chenggang Xu, et al.
The Veterinary Journal 199 (3) 461 (2014)
https://doi.org/10.1016/j.tvjl.2013.12.010

Biofilm formation by virulent and non-virulent strains of Haemophilus parasuis

Bernardo Bello-Ortí, Vincent Deslandes, Yannick DN Tremblay, et al.
Veterinary Research 45 (1) (2014)
https://doi.org/10.1186/s13567-014-0104-9

Porcine Coronin 1A Contributes to Nuclear Factor-Kappa B (NF-κB) Inactivation during Haemophilus parasuis Infection

Chong Liu, Yang Wang, Hengling Zhang, et al.
PLoS ONE 9 (8) e103904 (2014)
https://doi.org/10.1371/journal.pone.0103904

Comparative proteomic analysis of the membrane proteins of two Haemophilus parasuis strains to identify proteins that may help in habitat adaptation and pathogenesis

Luhua Zhang, Yiping Wen, Ying Li, et al.
Proteome Science 12 (1) (2014)
https://doi.org/10.1186/1477-5956-12-38

The use of genome wide association methods to investigate pathogenicity, population structure and serovar in Haemophilus parasuis

Kate J Howell, Lucy A Weinert, Roy R Chaudhuri, et al.
BMC Genomics 15 (1) 1179 (2014)
https://doi.org/10.1186/1471-2164-15-1179

Deletion of the rfaE gene in Haemophilus parasuis SC096 strain attenuates serum resistance, adhesion and invasion

Bin Zhang, Yuandi Yu, Ze Zeng, Yupeng Ren and Hua Yue
Microbial Pathogenesis 74 33 (2014)
https://doi.org/10.1016/j.micpath.2014.07.006

Time course Haemophilus parasuis infection reveals pathological differences between virulent and non-virulent strains in the respiratory tract

Bernardo Bello-Orti, Mar Costa-Hurtado, Veronica Martinez-Moliner, Joaquim Segalés and Virginia Aragon
Veterinary Microbiology 170 (3-4) 430 (2014)
https://doi.org/10.1016/j.vetmic.2014.01.011

Immunogenicity and protective efficacy of recombinant Haemophilus parasuis SH0165 putative outer membrane proteins

Shulin Fu, Minmin Zhang, Juan Xu, et al.
Vaccine 31 (2) 347 (2013)
https://doi.org/10.1016/j.vaccine.2012.11.003

Involvement of lipooligosaccharide heptose residues of Haemophilus parasuis SC096 strain in serum resistance, adhesion and invasion

Chenggang Xu, Lingyun Zhang, Bin Zhang, et al.
The Veterinary Journal 195 (2) 200 (2013)
https://doi.org/10.1016/j.tvjl.2012.06.017

Haemophilus parasuisSubunit Vaccines Based on Native Proteins with Affinity to Porcine Transferrin Prevent the Expression of Proinflammatory Chemokines and Cytokines in Pigs

R. Frandoloso, S. Martínez-Martínez, E. F. Rodríguez-Ferri, et al.
Clinical and Developmental Immunology 2013 1 (2013)
https://doi.org/10.1155/2013/132432

Structure of the capsular polysaccharides and lipopolysaccharides from Haemophilus parasuis strains ER-6P (serovar 15) and Nagasaki (serovar 5)

Malcolm B. Perry, Leann L. MacLean, Marcelo Gottschalk, Virginia Aragon and Evgeny Vinogradov
Carbohydrate Research 378 91 (2013)
https://doi.org/10.1016/j.carres.2013.04.023

Differences in Haemophilus parasuis adherence to and invasion of AOC-45 porcine aorta endothelial cells

Rafael Frandoloso, Mateus Pivato, Sonia Martínez-Martínez, et al.
BMC Veterinary Research 9 (1) 207 (2013)
https://doi.org/10.1186/1746-6148-9-207

Haemophilus parasuis serovar 5 Nagasaki strain adheres and invades PK-15 cells

Rafael Frandoloso, Sonia Martínez-Martínez, César B. Gutiérrez-Martín and Elías F. Rodríguez-Ferri
Veterinary Microbiology 154 (3-4) 347 (2012)
https://doi.org/10.1016/j.vetmic.2011.07.022

New insights in cellular immune response in colostrum-deprived pigs after immunization with subunit and commercial vaccines against Glässer’s disease

R. Frandoloso, S. Martínez-Martínez, S. Yubero, E.F. Rodríguez-Ferri and C.B. Gutiérrez-Martín
Cellular Immunology 277 (1-2) 74 (2012)
https://doi.org/10.1016/j.cellimm.2012.05.010

Haemophilus parasuis infection activates the NF-κB pathway in PK-15 cells through IκB degradation

Yushan Chen, Hui Jin, Ping Chen, et al.
Veterinary Microbiology 160 (1-2) 259 (2012)
https://doi.org/10.1016/j.vetmic.2012.05.021

VtaA8 and VtaA9 from Haemophilus parasuis delay phagocytosis by alveolar macrophages

Mar Costa-Hurtado, Maria Ballester, Nuria Galofré-Milà, Ayub Darji and Virginia Aragon
Veterinary Research 43 (1) (2012)
https://doi.org/10.1186/1297-9716-43-57

Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells

Tufária Mussá, Carolina Rodríguez-Cariño, Alejandro Sánchez-Chardi, et al.
Veterinary Research 43 (1) (2012)
https://doi.org/10.1186/1297-9716-43-80

Correlation between clinico-pathological outcome and typing of Haemophilus parasuis field strains

Virginia Aragon, Marta Cerdà-Cuéllar, Lorenzo Fraile, et al.
Veterinary Microbiology 142 (3-4) 387 (2010)
https://doi.org/10.1016/j.vetmic.2009.10.025

Understanding Haemophilus parasuis infection in porcine spleen through a transcriptomics approach

Hongbo Chen, Changchun Li, Mingdi Fang, et al.
BMC Genomics 10 (1) (2009)
https://doi.org/10.1186/1471-2164-10-64

Studies on the interactions of Haemophilus parasuis with porcine epithelial tracheal cells: Limited role of LOS in apoptosis and pro-inflammatory cytokine release

Bénédicte Bouchet, Ghyslaine Vanier, Mario Jacques, Eliane Auger and Marcelo Gottschalk
Microbial Pathogenesis 46 (2) 108 (2009)
https://doi.org/10.1016/j.micpath.2008.10.008

Differences in phagocytosis susceptibility inHaemophilus parasuisstrains

Alexandre Olvera, Maria Ballester, Miquel Nofrarias, Marina Sibila and Virginia Aragon
Veterinary Research 40 (3) 24 (2009)
https://doi.org/10.1051/vetres/2009007