Differences in phagocytosis susceptibility in Haemophilus parasuis strains
Vet. Res., 40 3 (2009) 24
Published online: 2009-02-26
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:
This article has been cited by the following article(s):
Pathotyping and molecular serotyping of clinical isolates of Glaesserella parasuis in Taiwan
Wei-Hao Lin, Chia-Hung Yen, Cheng-Yao Yang, Chuen-Fu Lin, Yung-Fu Chang, Chao-Nan Lin and Ming-Tang ChiouBrazilian Journal of Microbiology (2025)
https://doi.org/10.1007/s42770-025-01620-1
TbpB-based oral mucosal vaccine provides heterologous protection against Glässer’s disease caused by different serovars of Spanish field isolates of Glaesserella parasuis
Alba González-Fernández, Oscar Mencía-Ares, María José García-Iglesias, Máximo Petrocchi-Rilo, Rubén Miguélez-Pérez, Alberto Perelló-Jiménez, Elena Herencia-Lagunar, Vanessa Acebes-Fernández, César B. Gutiérrez-Martín and Sonia Martínez-MartínezPorcine Health Management 10 (1) (2024)
https://doi.org/10.1186/s40813-024-00404-7
Genomic insight into the diversity of Glaesserella parasuis isolates from 19 countries
Xiaowei Gong, Qingpo Cui, Wanjiang Zhang, Yuqian Shi, Peng Zhang, Chaoyang Zhang, Gongzheng Hu, Orhan Sahin, Lu Wang, Zhangqi Shen, Mengjiao Fu and Raffaele ZarrillimSphere 9 (9) (2024)
https://doi.org/10.1128/msphere.00231-24
Enhanced Systemic and Mucosal Immune Responses to Haemophilus parasuis by Intranasal Administration of Lactic-Co-Glycolic Acid Microspheres
Tianyu Lei, Tingting Dai, Liyun Zhuang, Yiting Liu, Xiaohua Li, Cuiqin Huang and Xintian ZhengVaccines 12 (10) 1103 (2024)
https://doi.org/10.3390/vaccines12101103
HbpA from Glaesserella parasuis induces an inflammatory response in 3D4/21 cells by activating the MAPK and NF-κB signalling pathways and protects mice against G. parasuis when used as an immunogen
Zhen Yang, Yiwen Zhang, Qin Zhao, Senyan Du, Xiaobo Huang, Rui Wu, Qigui Yan, Xinfeng Han, Yiping Wen and San-Jie CaoVeterinary Research 55 (1) (2024)
https://doi.org/10.1186/s13567-024-01344-4
(2024)
https://doi.org/10.1101/2024.05.15.594294
Chemoenzymatic Synthesis of Phosphosaccharides from Haemophilus parasuis Strains ER-6P (Serovar 15) and Nagasaki (Serovar 5)
Xinhao Zhu, Wenlong Yao, Na Sun, Mei Chen, Hui Xia, Chang-Cheng Liu, Yugen Zhu and Hongzhi CaoOrganic Letters 26 (44) 9580 (2024)
https://doi.org/10.1021/acs.orglett.4c03665
(2024)
https://doi.org/10.1101/2024.10.23.619785
Assessment of the Macrophage Scavenger Receptor CD163 in Mediating Glaesserella parasuis Infection of Host Cells
Xiangwei Deng, Shuilian Li, Ying Zhu, et al.Veterinary Sciences 10 (3) 235 (2023)
https://doi.org/10.3390/vetsci10030235
Upregulation of TLR4-Dependent ATP Production Is Critical for Glaesserella parasuis LPS-Mediated Inflammation
Fei Liu, Yidan Gao, Jian Jiao, et al.Cells 12 (5) 751 (2023)
https://doi.org/10.3390/cells12050751
Interaction between Porcine Alveolar Macrophage-Tang Cells and Streptococcus suis Strains of Different Virulence: Phagocytosis and Apoptosis
Siqi Li, Chunsheng Wang, Yan-Dong Tang, Lei Qin, Tianfeng Chen, Shanghui Wang, Yuanzhe Bai, Xuehui Cai and Shujie WangMicroorganisms 11 (1) 160 (2023)
https://doi.org/10.3390/microorganisms11010160
Immune responses following neonatal vaccination with conserved F4 fragment of VtaA proteins from virulent Glaesserella parasuis adjuvanted with CAF®01 or CDA
Sergi López-Serrano, Yasser S. Mahmmod, Dennis Christensen, et al.Vaccine: X 14 100330 (2023)
https://doi.org/10.1016/j.jvacx.2023.100330
TbpBY167A-based vaccine is safe in pregnant sows and induces high titers of maternal derived antibodies that reduce Glaesserella parasuis colonization in piglets
Diego Dellagostin, Rafaela Luiza Klein, Igor Giacobbo, João Antônio Guizzo, Cláudia Cerutti Dazzi, Simone Ramos Prigol, César Bernardo Gutiérrez Martín, Luiz Carlos Kreutz, Anthony Bernard Schryvers and Rafael FrandolosoVeterinary Microbiology 276 109630 (2023)
https://doi.org/10.1016/j.vetmic.2022.109630
Screening of linear B-cell epitopes and its proinflammatory activities of Haemophilus parasuis outer membrane protein P2
Jingbo Wu, Wenjin Nan, Guoliang Peng, et al.Frontiers in Cellular and Infection Microbiology 13 (2023)
https://doi.org/10.3389/fcimb.2023.1192651
Upregulation of occludin by cytolethal distending toxin facilitates Glaesserella parasuis adhesion to respiratory tract cells
Zhen Yang, Yiwen Zhang, Senyan Du, Qin Zhao, Xiaobo Huang, Rui Wu, Qigui Yan, Xinfeng Han, Sanjie Cao, Yung-Fu Chang, Yiping Wen and Guy H. PalmerInfection and Immunity 91 (12) (2023)
https://doi.org/10.1128/iai.00351-23
Glaesserella parasuis autotransporters EspP1 and EspP2 are novel IgA-specific proteases
Zhichao Wang, Jiayun Gu, Kunxue Xiao, et al.Frontiers in Microbiology 13 (2022)
https://doi.org/10.3389/fmicb.2022.1041774
Expression Analysis of Outer Membrane Protein HPS_06257 in Different Strains of Glaesserella parasuis and Its Potential Role in Protective Immune Response against HPS_06257-Expressing Strains via Antibody-Dependent Phagocytosis
Xiaojun Chen, Hanye Shi, Xingyu Cheng, Xiaoxu Wang, Zongjie Li, Donghua Shao, Ke Liu, Jianchao Wei, Beibei Li, Jian Wang, Bin Zhou, Zhiyong Ma and Yafeng QiuVeterinary Sciences 9 (7) 342 (2022)
https://doi.org/10.3390/vetsci9070342
Effect of Vaccination against Glässer’s Disease in a Farm Suffering from Polyserositis in Weaned Pigs
Jasmine Hattab, Giuseppe Marruchella, Abigail Rose Trachtman, Luigino Gabrielli, Nicola Bernabò, Francesco Mosca and Pietro Giorgio TiscarVeterinary Sciences 9 (12) 691 (2022)
https://doi.org/10.3390/vetsci9120691
TurboID Screening of the OmpP2 Protein Reveals Host Proteins Involved in Recognition and Phagocytosis of Glaesserella parasuis by iPAM Cells
Changsheng Jiang, Ningning Ma, Hua Cao, et al.Microbiology Spectrum 10 (5) (2022)
https://doi.org/10.1128/spectrum.02307-22
Potential of Oral Nanoparticles Containing Cytokines as Intestinal Mucosal Immunostimulants in Pigs: A Pilot Study
Adrià López-Cano, Alex Bach, Sergi López-Serrano, Virginia Aragon, Marta Blanch, Jose J. Pastor, Gemma Tedó, Sofia Morais, Elena Garcia-Fruitós and Anna ArísAnimals 12 (9) 1075 (2022)
https://doi.org/10.3390/ani12091075
Temporal Patterns of Phenotypic Antimicrobial Resistance and Coinfecting Pathogens in Glaesserella parasuis Strains Isolated from Diseased Swine in Germany from 2006 to 2021
Isabeau Wiencek, Maria Hartmann, Jörg Merkel, Sara Trittmacher, Lothar Kreienbrock and Isabel Hennig-PaukaPathogens 11 (7) 721 (2022)
https://doi.org/10.3390/pathogens11070721
Studying the Interaction of Neutrophils and Glaesserella Parasuis Indicates a Serotype Independent Benefit from Degradation of NETs
Marta C. Bonilla, Simon Lassnig, Andrea Obando Corella, Rabea Imker, Peter Valentin-Weigand, Maren von Köckritz-Blickwede, Anne-Marie Luther, Isabel Hennig-Pauka and Nicole de BuhrPathogens 11 (8) 880 (2022)
https://doi.org/10.3390/pathogens11080880
Severe Inflammation Caused by Coinfection of PCV2 and Glaesserella parasuis Is Associated with Pyroptosis via Noncanonical Inflammasome Pathway
Jiahui An, Chao Zhang, Jinshuang Cai, Yufeng Li and Shiek AhmedCellular Microbiology 2022 1 (2022)
https://doi.org/10.1155/2022/7227099
(2022)
https://doi.org/10.1079/cabicompendium.81413
In Vitro Analysis of TGF-β Signaling Modulation of Porcine Alveolar Macrophages in Porcine Circovirus Type 2b Infection
Shunli Yang, Muhammad Umar Zafar Khan, Baohong Liu, Muhammad Humza, Shuanghui Yin and Jianping CaiVeterinary Sciences 9 (3) 101 (2022)
https://doi.org/10.3390/vetsci9030101
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
Deletion of the crp gene affects the virulence and the activation of the NF-κB and MAPK signaling pathways in PK-15 and iPAM cells derived from G. parasuis serovar 5
Changsheng Jiang, Jingping Ren, Xiaoqian Zhang, et al.Veterinary Microbiology 261 109198 (2021)
https://doi.org/10.1016/j.vetmic.2021.109198
Sow Vaccination with a Protein Fragment against Virulent Glaesserella (Haemophilus) parasuis Modulates Immunity Traits in Their Offspring
Sergi López-Serrano, Carlos Neila-Ibáñez, Mar Costa-Hurtado, Yasser Mahmmod, Jorge Martínez-Martínez, Iván José Galindo-Cardiel, Ayub Darji, Fernando Rodríguez, Marina Sibila and Virginia AragonVaccines 9 (5) 534 (2021)
https://doi.org/10.3390/vaccines9050534
Proteome Analysis of Outer Membrane Vesicles From a Highly Virulent Strain of Haemophilus parasuis
Kunli Zhang, Pinpin Chu, Shuai Song, et al.Frontiers in Veterinary Science 8 (2021)
https://doi.org/10.3389/fvets.2021.756764
The Role of Antibodies Against the Crude Capsular Extract in the Immune Response of Porcine Alveolar Macrophages to In Vitro Infection of Various Serovars of Glaesserella (Haemophilus) parasuis
Katarína Matiašková, Lenka Kavanová, Pavel Kulich, et al.Frontiers in Immunology 12 (2021)
https://doi.org/10.3389/fimmu.2021.635097
Glaesserella parasuis induces inflammatory response in 3D4/21 cells through activation of NLRP3 inflammasome signaling pathway via ROS
Xinran Luo, Xiaojing Chang, Hong Zhou, Huixing Lin and Hongjie FanVeterinary Microbiology 256 109057 (2021)
https://doi.org/10.1016/j.vetmic.2021.109057
Glässer’s disease in swine from Northeastern Brazil
Hisadora A.S.C. Bom, Givaldo B. Silva Filho, Elayne G. Silva, et al.Pesquisa Veterinária Brasileira 40 (9) 662 (2020)
https://doi.org/10.1590/1678-5150-pvb-6642
Serotyping and pathotyping of Glaesserella parasuis isolated 2012–2019 in Germany comparing different PCR-based methods
Lukas Schuwerk, Doris Hoeltig, Karl-Heinz Waldmann, et al.Veterinary Research 51 (1) (2020)
https://doi.org/10.1186/s13567-020-00862-1
Update on Glässer’s disease: How to control the disease under restrictive use of antimicrobials
Mar Costa-Hurtado, Emili Barba-Vidal, Jaime Maldonado and Virginia AragonVeterinary Microbiology 242 108595 (2020)
https://doi.org/10.1016/j.vetmic.2020.108595
Heterogeneity of Moraxella isolates found in the nasal cavities of piglets
Sergi López-Serrano, Nuria Galofré-Milà, Mar Costa-Hurtado, Ana M. Pérez-de-Rozas and Virginia AragonBMC Veterinary Research 16 (1) (2020)
https://doi.org/10.1186/s12917-020-2250-9
Generation and Evaluation of a Glaesserella (Haemophilus) parasuis Capsular Mutant
Kirsten C. Eberle, Samantha J. Hau, Shi-Lu Luan, et al.Infection and Immunity 88 (5) (2020)
https://doi.org/10.1128/IAI.00879-19
Haemophilus parasuis VtaA2 is involved in adhesion to extracellular proteins
Mar Costa-Hurtado, Laura Garcia-Rodriguez, Sergi Lopez-Serrano and Virginia AragonVeterinary Research 50 (1) (2019)
https://doi.org/10.1186/s13567-019-0687-2
Porcine Circovirus Type 2 Induces Single Immunoglobulin Interleukin-1 Related Receptor (SIGIRR) Downregulation to Promote Interleukin-1β Upregulation in Porcine Alveolar Macrophage
Shunli Yang, Baohong Liu, Shuanghui Yin, Youjun Shang, Xinming Zhang, Muhammad Umar Zafar Khan, Xiangtao Liu and Jianping CaiViruses 11 (11) 1021 (2019)
https://doi.org/10.3390/v11111021
Diseases of Swine
Virginia Aragon, Joaquim Segalés and A.W. (Dan) TuckerDiseases of Swine 844 (2019)
https://doi.org/10.1002/9781119350927.ch54
Porcine Alveolar Macrophages’ Nitric Oxide Synthase-Mediated Generation of Nitric Oxide Exerts Important Defensive Effects against Glaesserella parasuis Infection
Qi Cao, Huan Wang, Wenbin Wei, Yujin Lv, Zhao Wen, Xiaojuan Xu, Xuwang Cai, Huanchun Chen and Xiangru WangPathogens 8 (4) 234 (2019)
https://doi.org/10.3390/pathogens8040234
Haemophilus parasuis infection in 3D4/21 cells induces autophagy through the AMPK pathway
Yijuan Shen, Nini Zhou, Jiahui An, et al.Cellular Microbiology 21 (8) (2019)
https://doi.org/10.1111/cmi.13031
Characterisation of Bergeyella spp. isolated from the nasal cavities of piglets
M. Lorenzo de Arriba, S. Lopez-Serrano, N. Galofre-Mila and V. AragonThe Veterinary Journal 234 1 (2018)
https://doi.org/10.1016/j.tvjl.2018.01.004
Molecular serotyping ofHaemophilus parasuisisolated from diseased pigs and the relationship between serovars and pathological patterns in Taiwan
Wei-Hao Lin, Hsing-Chun Shih, Chuen-Fu Lin, et al.PeerJ 6 e6017 (2018)
https://doi.org/10.7717/peerj.6017
Limited Interactions between Streptococcus Suis and Haemophilus Parasuis in In Vitro Co-Infection Studies
Annabelle Mathieu-Denoncourt, Corinne Letendre, Jean-Philippe Auger, Mariela Segura, Virginia Aragon, Sonia Lacouture and Marcelo GottschalkPathogens 7 (1) 7 (2018)
https://doi.org/10.3390/pathogens7010007
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
Omp16-based vaccine encapsulated by alginate-chitosan microspheres provides significant protection against Haemophilus parasuis in mice
Xintian Zheng, Xiaoyan Yang, Xiaohua Li, et al.Vaccine 35 (10) 1417 (2017)
https://doi.org/10.1016/j.vaccine.2017.01.067
A robust PCR for the differentiation of potential virulent strains of Haemophilus parasuis
N. Galofré-Milà, F. Correa-Fiz, S. Lacouture, et al.BMC Veterinary Research 13 (1) (2017)
https://doi.org/10.1186/s12917-017-1041-4
Polychlorinated dibenzo‐p‐dioxins and dibenzofurans levels in piglet liver with various diseases
Jeoung Hwa Shin, Won Hyun Ji, Chanhee Chae, Shela Gorinstein and Yun Gyong AhnInternational Journal of Experimental Pathology 98 (4) 214 (2017)
https://doi.org/10.1111/iep.12238
New insights about functional and cross-reactive properties of antibodies generated against recombinant TbpBs of Haemophilus parasuis
Bibiana Martins Barasuol, João Antônio Guizzo, Jamie Elisabeth Fegan, et al.Scientific Reports 7 (1) (2017)
https://doi.org/10.1038/s41598-017-10627-0
iTRAQ-based quantitative proteomic analysis reveals multiple effects of Emodin to Haemophilus parasuis
Li Li, Ye Tian, Jiankang Yu, et al.Journal of Proteomics 166 39 (2017)
https://doi.org/10.1016/j.jprot.2017.06.020
Effect ofkpsMon the virulence of porcine extraintestinal pathogenicEscherichia coli
Bingbing Zong, Wugang Liu, Yanyan Zhang, et al.FEMS Microbiology Letters 363 (21) fnw232 (2016)
https://doi.org/10.1093/femsle/fnw232
Autophagy Is Associated with Pathogenesis of Haemophilus parasuis
Yaning Zhang, Yufeng Li, Wentao Yuan, Yuting Xia and Yijuan ShenFrontiers in Microbiology 7 (2016)
https://doi.org/10.3389/fmicb.2016.01423
Characterization and Vaccine Potential of Outer Membrane Vesicles Produced by Haemophilus parasuis
William D. McCaig, Crystal L. Loving, Holly R. Hughes, Susan L. Brockmeier and Alain CharbitPLOS ONE 11 (3) e0149132 (2016)
https://doi.org/10.1371/journal.pone.0149132
Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection
Bernardo Bello-Ortí, Kate J. Howell, Alexander W. Tucker, Duncan J. Maskell and Virginia AragonVeterinary Research 46 (1) (2015)
https://doi.org/10.1186/s13567-015-0225-9
Haemophilus parasuis: infection, immunity and enrofloxacin
Nubia Macedo, Albert Rovira and Montserrat TorremorellVeterinary Research 46 (1) (2015)
https://doi.org/10.1186/s13567-015-0263-3
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 AragonVeterinary Microbiology 170 (3-4) 430 (2014)
https://doi.org/10.1016/j.vetmic.2014.01.011
The two-component system NisK/NisR contributes to the virulence of Streptococcus suis serotype 2
Juan Xu, Shulin Fu, Manli Liu, et al.Microbiological Research 169 (7-8) 541 (2014)
https://doi.org/10.1016/j.micres.2013.11.002
Virulence and Draft Genome Sequence Overview of Multiple Strains of the Swine Pathogen Haemophilus parasuis
Susan L. Brockmeier, Karen B. Register, Joanna S. Kuehn, et al.PLoS ONE 9 (8) e103787 (2014)
https://doi.org/10.1371/journal.pone.0103787
Update on the pathogenesis of Haemophilus parasuis infection and virulence factors
Bin Zhang, Cheng Tang, Ming Liao and Hua YueVeterinary Microbiology 168 (1) 1 (2014)
https://doi.org/10.1016/j.vetmic.2013.07.027
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
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
Genetic diversity of Haemophilus parasuis from sick and healthy pigs
Patrick Boerlin, Zvonimir Poljak, Jackie Gallant, et al.Veterinary Microbiology 167 (3-4) 459 (2013)
https://doi.org/10.1016/j.vetmic.2013.07.028
Serum cross-reaction among virulence-associated trimeric autotransporters (VtaA) of Haemophilus parasuis
Alex Olvera, Verónica Martínez-Moliner, Sonia Pina-Pedrero, et al.Veterinary Microbiology 164 (3-4) 387 (2013)
https://doi.org/10.1016/j.vetmic.2013.02.022
Virulence, Transmission, and Heterologous Protection of Four Isolates of Haemophilus parasuis
Susan L. Brockmeier, Crystal L. Loving, Michael A. Mullins, et al.Clinical and Vaccine Immunology 20 (9) 1466 (2013)
https://doi.org/10.1128/CVI.00168-13
Changes in Macrophage Phenotype after Infection of Pigs with Haemophilus parasuis Strains with Different Levels of Virulence
Mar Costa-Hurtado, Alexandre Olvera, Verónica Martinez-Moliner, et al.Infection and Immunity 81 (7) 2327 (2013)
https://doi.org/10.1128/IAI.00056-13
Dilution effect in bovine tuberculosis: risk factors for regional disease occurrence in Africa
Z. Y. X. Huang, W. F. de Boer, F. van Langevelde, et al.Proceedings of the Royal Society B: Biological Sciences 280 (1765) 20130624 (2013)
https://doi.org/10.1098/rspb.2013.0624
Advances in the quest for virulence factors of Haemophilus parasuis
Mar Costa-Hurtado and Virginia AragonThe Veterinary Journal 198 (3) 571 (2013)
https://doi.org/10.1016/j.tvjl.2013.08.027
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 VinogradovCarbohydrate Research 378 91 (2013)
https://doi.org/10.1016/j.carres.2013.04.023
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
A complementary diagnosis of naturally occurring tuberculosis in water buffaloes (Bubalus bubalis) in Rio de Janeiro using a MPB70-ELISA, Brazil
Carlos F. O. Zarden, Carla D. Marassi, Walter Oelemann and Walter LilienbaumTropical Animal Health and Production (2012)
https://doi.org/10.1007/s11250-012-0347-2
Distribution of genes involved in sialic acid utilization in strains of Haemophilus parasuis
Verónica Martínez-Moliner, Pedro Soler-Llorens, Javier Moleres, Junkal Garmendia and Virginia AragonMicrobiology 158 (8) 2117 (2012)
https://doi.org/10.1099/mic.0.056994-0
Transcription analysis on response of porcine alveolar macrophages to Haemophilus parasuis
Yang Wang, Chong Liu, Ying Fang, et al.BMC Genomics 13 (1) (2012)
https://doi.org/10.1186/1471-2164-13-68
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
VtaA8 and VtaA9 from Haemophilus parasuis delay phagocytosis by alveolar macrophages
Mar Costa-Hurtado, Maria Ballester, Nuria Galofré-Milà, Ayub Darji and Virginia AragonVeterinary Research 43 (1) (2012)
https://doi.org/10.1186/1297-9716-43-57
Outer membrane protein P2 of the Haemophilus parasuis SC096 strain contributes to adherence to porcine alveolar macrophages cells
Bin Zhang, Changgang Xu and Ming LiaoVeterinary Microbiology 158 (1-2) 226 (2012)
https://doi.org/10.1016/j.vetmic.2012.01.023
Identification of potentially virulent strains of Haemophilus parasuis using a multiplex PCR for virulence-associated autotransporters (vtaA)
Alex Olvera, Sonia Pina, Núbia Macedo, et al.The Veterinary Journal 191 (2) 213 (2012)
https://doi.org/10.1016/j.tvjl.2010.12.014
Immunogenicity and protection against Haemophilus parasuis infection after vaccination with recombinant virulence associated trimeric autotransporters (VtaA)
Alex Olvera, Sonia Pina, Marta Pérez-Simó, et al.Vaccine 29 (15) 2797 (2011)
https://doi.org/10.1016/j.vaccine.2011.01.105
Invasion of endothelial cells by systemic and nasal strains of Haemophilus parasuis
Virginia Aragon, Bénédicte Bouchet and Marcelo GottschalkThe Veterinary Journal 186 (2) 264 (2010)
https://doi.org/10.1016/j.tvjl.2009.08.013
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