Adaptive strategies of Yersinia pestis to persist during inter-epizootic and epizootic periods
Vet. Res., 40 2 (2009) 01
Published online: 2008-09-23
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):
Experimental evidence of early-phase transmission of Yersinia pestis by Synopsyllus fonquerniei and Xenopsylla brasiliensis
Ravo Rakotobe Harimanana, Florent Sebbane, Mireille Harimalala and Rui QiPLOS Neglected Tropical Diseases 20 (6) e0014463 (2026)
https://doi.org/10.1371/journal.pntd.0014463
Emergence, global dispersal, and local adaptations of Yersinia pestis , the agent of plague
Victoria Carcauzon, Anne Laudisoit, Philip Slavin, Steven M. Goodman, Florent Sebbane, Pablo Tortosa and Edward G. DudleyApplied and Environmental Microbiology 92 (4) (2026)
https://doi.org/10.1128/aem.01658-25
Attenuation of virulence in Yersinia pestis across three plague pandemics
Ravneet Kaur Sidhu, Guillem Mas Fiol, Pierre Lê-Bury, Christian E. Demeure, Emelyne Bougit, Rémi Beau, Charlotte Balière, Aurelia Kwasiborski, Valérie Caro, Jennifer Klunk, Daniel J. Salkeld, Ann Carmichael, Nükhet Varlık, Debi Poinar, David J. D. Earn, Benjamin M. Bolker, Jonathan Dushoff, G. Brian Golding, Nicolas Rascovan, Olivier Dussurget, Edward C. Holmes, Javier Pizarro-Cerdá and Hendrik N. PoinarScience 388 (6750) (2025)
https://doi.org/10.1126/science.adt3880
1117 (2025)
https://doi.org/10.1016/B978-0-323-82763-8.00112-6
(2025)
https://doi.org/10.1101/2025.09.26.678789
Interaction of Bacteria and Fleas, Focusing on the Plague Bacterium—A Review
Patric U. B. Vogel and Günter A. SchaubMicroorganisms 13 (11) 2619 (2025)
https://doi.org/10.3390/microorganisms13112619
(2025)
https://doi.org/10.21203/rs.3.rs-8201273/v1
Intraspecific diversity of Meriones persicus (Rodentia; Gerbillinae), the main plague reservoir in Iran, and its connection to enzootic plague in Iran
Ahmad MAHMOUDI, Ehsan MOSTAFAVI and Boris KRYŠTUFEKIntegrative Zoology 20 (2) 289 (2025)
https://doi.org/10.1111/1749-4877.12835
Flea infestation of rodent and their community structure in frequent and non-frequent plague outbreak areas in Mbulu district, northern Tanzania
Stella T. Kessy, RhodesH. Makundi, Apia W. Massawe and Alfan A. RijaInternational Journal for Parasitology: Parasites and Wildlife 23 100921 (2024)
https://doi.org/10.1016/j.ijppaw.2024.100921
Population dynamics of the Multimammate rat (Mastomys natalensis) and Makundi’s brush fur rat (Lophuromys makundii) and their implications in disease persistence in Mbulu District, Tanzania
Stella T. Kessy, Christopher Sabuni, Apia W. Massawe, Rhodes Makundi and Alfan A. RijaEuropean Journal of Wildlife Research 70 (2) (2024)
https://doi.org/10.1007/s10344-024-01773-8
Review of genotyping methods for Yersinia pestis in Madagascar
Lovasoa Nomena Randriantseheno, Voahangy Andrianaivoarimanana, Javier Pizarro-Cerdá, David M. Wagner, Minoarisoa Rajerison and Vladimir L. MotinPLOS Neglected Tropical Diseases 18 (6) e0012252 (2024)
https://doi.org/10.1371/journal.pntd.0012252
Flea Burden on Rodents and Its Associated Determinants in Plague‐Endemic Localities of Karatu District, Tanzania: A Cross‐Sectional Study
Joshua Reuben Jakoniko, Apia Massawe, Elisa Daniel Mwega and Stella Thadeus KessyPublic Health Challenges 3 (2) (2024)
https://doi.org/10.1002/puh2.201
Comparison of flea diversity in the burrows of Richardson's ground squirrels (Urocitellus richardsonii) in urban and rural sites in central Saskatchewan, Canada
Jessica T. Thoroughgood and Neil B. ChiltonJournal of Vector Ecology 49 (2) (2024)
https://doi.org/10.52707/1081-1710-49.2.R61
Emerging patterns in rodent-borne zoonotic diseases
Felicia Keesing and Richard S. OstfeldScience 385 (6715) 1305 (2024)
https://doi.org/10.1126/science.adq7993
Ubiquitous Existence of Cation-Proton Antiporter and its Structurefunction Interplay: A Clinical Prospect
Manish Dwivedi and Sowdhamini MahendiranCurrent Protein & Peptide Science 24 (1) 43 (2023)
https://doi.org/10.2174/1389203724666221114093235
Rodent abundance, diversity and community structure in a bubonic plague endemic area, northern Tanzania
Stella T. Kessy, Rhodes H. Makundi, Christopher Sabuni, Apia W. Massawe and Alfan A. RijaMammalia 87 (5) 488 (2023)
https://doi.org/10.1515/mammalia-2023-0012
Immunogenetics, sylvatic plague and its vectors: insights from the pathogen reservoir Mastomys natalensis in Tanzania
Lavinia Haikukutu, Japhet R. Lyaku, Charles M. Lyimo, Seth J. Eiseb, Rhodes H. Makundi, Ayodeji Olayemi, Kerstin Wilhelm, Nadine Müller-Klein, Dominik W. Schmid, Ramona Fleischer and Simone SommerImmunogenetics 75 (6) 517 (2023)
https://doi.org/10.1007/s00251-023-01323-7
Genomic epidemiological analysis of county-scale Yersinia pestis spread pattern over 50 years in a Southwest Chinese prefecture
Jingliang Qin, Liyuan Shi, Yarong Wu, et al.PLOS Neglected Tropical Diseases 17 (8) e0011527 (2023)
https://doi.org/10.1371/journal.pntd.0011527
Infectious Diseases along the Silk Roads
Günter A. Schaub and Patric U. B. VogelParasitology Research Monographs, Infectious Diseases along the Silk Roads 17 83 (2023)
https://doi.org/10.1007/978-3-031-35275-1_7
Genomic diversity of Yersinia pestis from Yunnan Province, China, implies a potential common ancestor as the source of two plague epidemics
Jingliang Qin, Yarong Wu, Liyuan Shi, Xiujuan Zuo, Xianglilan Zhang, Xiuwei Qian, Hang Fan, Yan Guo, Mengnan Cui, Haipeng Zhang, Fengyi Yang, Jinjiao Kong, Yajun Song, Ruifu Yang, Peng Wang and Yujun CuiCommunications Biology 6 (1) (2023)
https://doi.org/10.1038/s42003-023-05186-2
Combining deep sequencing and conventional molecular approaches reveals broad diversity and distribution of fleas and Bartonella in rodents and shrews from Arctic and Subarctic ecosystems
Kayla J. Buhler, Champika Fernando, Janet E. Hill, et al.Parasites & Vectors 15 (1) (2022)
https://doi.org/10.1186/s13071-022-05446-w
Exploring and Mitigating Plague for One Health Purposes
David A. Eads, Dean E. Biggins, Jeffrey Wimsatt, et al.Current Tropical Medicine Reports 9 (4) 169 (2022)
https://doi.org/10.1007/s40475-022-00265-6
A Role for Early-Phase Transmission in the Enzootic Maintenance of Plague
Cedar L. Mitchell, Ashley R. Schwarzer, Adélaïde Miarinjara, et al.PLOS Pathogens 18 (12) e1010996 (2022)
https://doi.org/10.1371/journal.ppat.1010996
Spatiotemporal Variations of Plague Risk in the Tibetan Plateau from 1954–2016
Xing Yuan, Linsheng Yang, Hairong Li and Li WangBiology 11 (2) 304 (2022)
https://doi.org/10.3390/biology11020304
139 (2021)
https://doi.org/10.1016/B978-0-323-85662-1.00011-2
(2021)
https://doi.org/10.1101/2021.02.21.21252152
Plague Prevention and Therapy: Perspectives on Current and Future Strategies
Raysa Rosario-Acevedo, Sergei S. Biryukov, Joel A. Bozue and Christopher K. CoteBiomedicines 9 (10) 1421 (2021)
https://doi.org/10.3390/biomedicines9101421
905 (2021)
https://doi.org/10.1016/B978-0-323-50934-3.00073-2
Effects of experimental flea removal and plague vaccine treatments on survival of northern Idaho ground squirrels and two coexisting sciurids
Amanda R. Goldberg, Courtney J. Conway and Dean E. BigginsGlobal Ecology and Conservation 26 e01489 (2021)
https://doi.org/10.1016/j.gecco.2021.e01489
Plague Transmission from Corpses and Carcasses
Sophie Jullien, Nipun Lakshitha de Silva and Paul GarnerEmerging Infectious Diseases 27 (8) 2033 (2021)
https://doi.org/10.3201/eid2708.200136
Ectoparasites of some wild rodents /shrews captured from Scrub typhus reported areas in Tamil Nadu, India
Paulraj Philip Samuel, Renu Govindarajan, Ranganathan Krishnamoorthi and Jaganathasamy NagarajInternational Journal of Acarology 47 (3) 218 (2021)
https://doi.org/10.1080/01647954.2021.1887932
No evidence for enzootic plague within black‐tailed prairie dog (Cynomys ludovicianus) populations
Rebecca E. COLMAN, R. Jory BRINKERHOFF, Joseph D. BUSCH, et al.Integrative Zoology 16 (6) 834 (2021)
https://doi.org/10.1111/1749-4877.12546
Infections of cats with blood mycoplasmas in various contexts
Dana Lobová, Jarmila Konvalinová, Iveta Bedáňová, Zita Filipejová and Dobromila MolinkováActa Veterinaria Brno 90 (2) 211 (2021)
https://doi.org/10.2754/avb202190020211
Plague reservoir species throughout the world
Ahmad MAHMOUDI, Boris KRYŠTUFEK, Alexander SLUDSKY, et al.Integrative Zoology 16 (6) 820 (2021)
https://doi.org/10.1111/1749-4877.12511
An Evaluation of the Flea Index as a Predictor of Plague Epizootics in the West Nile Region of Uganda
Paul S Mead, Kiersten J Kugeler, Titus Apangu, et al.Journal of Medical Entomology 57 (3) 893 (2020)
https://doi.org/10.1093/jme/tjz248
Drought-induced spatio-temporal synchrony of plague outbreak in Europe
Ricci P.H. Yue and Harry F. LeeScience of The Total Environment 698 134138 (2020)
https://doi.org/10.1016/j.scitotenv.2019.134138
Vector-Borne Pathogens in Ectoparasites Collected from High-Elevation Pika Populations
R. Jory Brinkerhoff, Hilary S. Rinsland, Shingo Sato, Soichi Maruyama and Chris RayEcoHealth 17 (3) 333 (2020)
https://doi.org/10.1007/s10393-020-01495-8
Putative Horizontally Acquired Genes, Highly Transcribed during Yersinia pestis Flea Infection, Are Induced by Hyperosmotic Stress and Function in Aromatic Amino Acid Metabolism
Luary C. Martínez-Chavarría, Janelle Sagawa, Jessica Irons, et al.Journal of Bacteriology 202 (11) (2020)
https://doi.org/10.1128/JB.00733-19
Prospects for the Synthesis of Ecological and Molecular-Genetic Approaches to the Problem of the Speciation of the Plague Microbe Yersinia pestis
V. V. SuntsovBiology Bulletin Reviews 10 (4) 324 (2020)
https://doi.org/10.1134/S2079086420040088
The Diverse Roles of the Global Transcriptional Regulator PhoP in the Lifecycle of Yersinia pestis
Hana S. Fukuto, Gloria I. Viboud and Viveka VadyvalooPathogens 9 (12) 1039 (2020)
https://doi.org/10.3390/pathogens9121039
(2019)
https://doi.org/10.1101/2019.12.16.877951
(2019)
https://doi.org/10.1101/563205
(2019)
https://doi.org/10.1101/699520
To kill a piroplasm: genetic technologies to advance drug discovery and target identification in Babesia
Caroline D. Keroack, Brendan Elsworth and Manoj T. DuraisinghInternational Journal for Parasitology 49 (2) 153 (2019)
https://doi.org/10.1016/j.ijpara.2018.09.005
(2019)
https://doi.org/10.1101/597013
Psychiatry of Pandemics
Damir HuremovićPsychiatry of Pandemics 7 (2019)
https://doi.org/10.1007/978-3-030-15346-5_2
(2018)
https://doi.org/10.64628/AAI.cm65vfu5q
Relationship of the Representatives of Eight Genera of Siphonaptera Order and Yersinia Pestis from Tuva Natural Plague Focus
L. P. Bazanova and A. Yu. NikitinEpidemiology and Vaccine Prevention 17 (3) 32 (2018)
https://doi.org/10.31631/2073-3046-2018-17-3-32-37
A Bead-Based Flow Cytometric Assay for Monitoring Yersinia pestis Exposure in Wildlife
Jeffrey C. Chandler, Laurie A. Baeten, Doreen L. Griffin, et al.Journal of Clinical Microbiology 56 (7) (2018)
https://doi.org/10.1128/JCM.00273-18
Simple multi-scale modeling of the transmission dynamics of the 1905 plague epidemic in Bombay
Bruce Pell, Tin Phan, Erica M. Rutter, Gerardo Chowell and Yang KuangMathematical Biosciences 301 83 (2018)
https://doi.org/10.1016/j.mbs.2018.04.003
Yersinia pestisSurvival and Replication in Potential Ameba Reservoir
David W. Markman, Michael F. Antolin, Richard A. Bowen, et al.Emerging Infectious Diseases 24 (2) 294 (2018)
https://doi.org/10.3201/eid2402.171065
Combating Multidrug-Resistant Pathogens with Host-Directed Nonantibiotic Therapeutics
Jourdan A. Andersson, Jian Sha, Michelle L. Kirtley, et al.Antimicrobial Agents and Chemotherapy 62 (1) (2018)
https://doi.org/10.1128/AAC.01943-17
Rat Fall Surveillance Coupled with Vector Control and Community Education as a Plague Prevention Strategy in the West Nile Region, Uganda
Karen A. Boegler, Linda A. Atiku, Russell E. Enscore, et al.The American Journal of Tropical Medicine and Hygiene 98 (1) 238 (2018)
https://doi.org/10.4269/ajtmh.17-0502
Plague: Bridging gaps towards better disease control
E. D’Ortenzio, N. Lemaître, C. Brouat, P. Loubet, F. Sebbane, M. Rajerison, L. Baril and Y. YazdanpanahMédecine et Maladies Infectieuses 48 (5) 307 (2018)
https://doi.org/10.1016/j.medmal.2018.04.393
The Deer Mouse (Peromyscus maniculatus) as an Enzootic Reservoir of Plague in California
Mary Danforth, James Tucker and Mark NovakEcoHealth 15 (3) 566 (2018)
https://doi.org/10.1007/s10393-018-1337-2
Exposure to Yersinia pestis increases resistance to plague in black rats and modulates transmission in Madagascar
Voahangy Andrianaivoarimanana, Minoarisoa Rajerison and Ronan JambouBMC Research Notes 11 (1) (2018)
https://doi.org/10.1186/s13104-018-3984-3
(2018)
https://doi.org/10.1101/401158
Arthropod Borne Diseases
Tereza Cristina Leal-Balbino, Maria Betânia Melo de Oliveira, Maria Paloma Silva de Barros, Marise Sobreira and Vladimir da Mota Silveira-FilhoArthropod Borne Diseases 155 (2017)
https://doi.org/10.1007/978-3-319-13884-8_11
Flea and Small Mammal Species Composition in Mixed-Grass Prairies: Implications for the Maintenance ofYersinia pestis
Lauren P. Maestas and Hugh B. BrittenVector-Borne and Zoonotic Diseases 17 (7) 467 (2017)
https://doi.org/10.1089/vbz.2016.2069
HmsC Controls Yersinia pestis Biofilm Formation in Response to Redox Environment
Gai-Xian Ren, Xiao-Peng Guo and Yi-Cheng SunFrontiers in Cellular and Infection Microbiology 7 (2017)
https://doi.org/10.3389/fcimb.2017.00355
The Effect of Seasonal Weather Variation on the Dynamics of the Plague Disease
Rigobert C. Ngeleja, Livingstone S. Luboobi and Yaw Nkansah-GyekyeInternational Journal of Mathematics and Mathematical Sciences 2017 1 (2017)
https://doi.org/10.1155/2017/5058085
Yersinia pestis Resists Predation by Acanthamoeba castellanii and Exhibits Prolonged Intracellular Survival
Javier A. Benavides-Montaño, Viveka Vadyvaloo and Janet L. SchottelApplied and Environmental Microbiology 83 (13) (2017)
https://doi.org/10.1128/AEM.00593-17
Evaluation of Yersinia pestis Transmission Pathways for Sylvatic Plague in Prairie Dog Populations in the Western U.S.
Katherine L. D. Richgels, Robin E. Russell, Gebbiena M. Bron and Tonie E. RockeEcoHealth 13 (2) 415 (2016)
https://doi.org/10.1007/s10393-016-1133-9
Plague cycles in two rodent species from China: dry years might provide context for epizootics in wet years
David A. Eads, Dean E. Biggins, Lei Xu and Qiyong LiuEcosphere 7 (10) (2016)
https://doi.org/10.1002/ecs2.1495
Rickettsia(Rickettsiales: Rickettsiaceae) Vector Biodiversity in High Altitude Atlantic Forest Fragments Within a Semiarid Climate: A New Endemic Area of Spotted-Fever in Brazil
Leonardo Moerbeck, Vinícius F. Vizzoni, Erik Machado-Ferreira, et al.Journal of Medical Entomology 53 (6) 1458 (2016)
https://doi.org/10.1093/jme/tjw121
Review: A review on classical and atypical scrapie in caprine: Prion protein gene polymorphisms and their role in the disease
L. Curcio, C. Sebastiani, P. Di Lorenzo, E. Lasagna and M. Biagettianimal 10 (10) 1585 (2016)
https://doi.org/10.1017/S1751731116000653
Cross-scale modeling of a vector-borne disease, from the individual to the metapopulation: The seasonal dynamics of sylvatic plague in Kazakhstan
Vincent Laperrière, Katharina Brugger and Franz RubelEcological Modelling 342 34 (2016)
https://doi.org/10.1016/j.ecolmodel.2016.09.023
Bartonellaspp. in Small Mammals, Benin
Aarón Martin-Alonso, Gualbert Houemenou, Estefanía Abreu-Yanes, et al.Vector-Borne and Zoonotic Diseases 16 (4) 229 (2016)
https://doi.org/10.1089/vbz.2015.1838
Detection of aYersinia pestisgene homologue in rodent samples
Timothy A. Giles, Alex D. Greenwood, Kyriakos Tsangaras, et al.PeerJ 4 e2216 (2016)
https://doi.org/10.7717/peerj.2216
Invertebrate Bacteriology
Aurelio CiancioInvertebrate Bacteriology 145 (2016)
https://doi.org/10.1007/978-94-024-0884-3_5
The Great Transition
Bruce M. S. CampbellThe Great Transition (2016)
https://doi.org/10.1017/CBO9781139031110
Yersinia pestis-Host Immune Cells Interactions at Early Events During Bubonic Plague Infection
Luary C. Martínez-ChavarríaCurrent Tropical Medicine Reports 3 (2) 51 (2016)
https://doi.org/10.1007/s40475-016-0071-5
Infection Prevalence, Bacterial Loads, and Transmission Efficiency inOropsylla montana(Siphonaptera: Ceratophyllidae) One Day After Exposure to Varying Concentrations ofYersinia pestisin Blood
Karen A. Boegler, Christine B. Graham, Tammi L. Johnson, John A. Montenieri and Rebecca J. EisenJournal of Medical Entomology 53 (3) 674 (2016)
https://doi.org/10.1093/jme/tjw004
Parasite spreading in spatial ecological multiplex networks
Massimo Stella, Cecilia S. Andreazzi, Sanja Selakovic, Alireza Goudarzi and Alberto AntonioniJournal of Complex Networks cnw028 (2016)
https://doi.org/10.1093/comnet/cnw028
Sympatric speciation of the plague microbe Yersinia pestis: Monohostal specialization in the host–parasite marmot–flea (Marmota sibirica–Oropsylla silantiewi) system
V. V. SuntsovBiology Bulletin 43 (2) 87 (2016)
https://doi.org/10.1134/S1062359016010155
CRP-Mediated Carbon Catabolite Regulation of Yersinia pestis Biofilm Formation Is Enhanced by the Carbon Storage Regulator Protein, CsrA
Stephan P. Willias, Sadhana Chauhan, Chien-Chi Lo, et al.PLOS ONE 10 (8) e0135481 (2015)
https://doi.org/10.1371/journal.pone.0135481
The Role of Early-Phase Transmission in the Spread ofYersinia pestis
Rebecca J. Eisen, David T. Dennis and Kenneth L. GageJournal of Medical Entomology 52 (6) 1183 (2015)
https://doi.org/10.1093/jme/tjv128
Arthropod-Spiroplasma relationship in the genomic era
L. M. Bolanos, L. E. Servin-Garciduenas and E. Martinez-RomeroFEMS Microbiology Ecology 91 (2) 1 (2015)
https://doi.org/10.1093/femsec/fiu008
Seasonal fluctuations of small mammal and flea communities in a Ugandan plague focus: evidence to implicate Arvicanthis niloticus and Crocidura spp. as key hosts in Yersinia pestis transmission
Sean M Moore, Andrew Monaghan, Jeff N Borchert, et al.Parasites & Vectors 8 (1) 11 (2015)
https://doi.org/10.1186/s13071-014-0616-1
Plague bacterium as a transformer species in prairie dogs and the grasslands of western North America
David A. Eads and Dean E. BigginsConservation Biology 29 (4) 1086 (2015)
https://doi.org/10.1111/cobi.12498
Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases
Paul S. MeadMandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases 2607 (2015)
https://doi.org/10.1016/B978-1-4557-4801-3.00231-9
Single-Nucleotide Polymorphisms Reveal Spatial Diversity Among Clones ofYersinia pestisDuring Plague Outbreaks in Colorado and the Western United States
Jennifer L. Lowell, Michael F. Antolin, Gary L. Andersen, et al.Vector-Borne and Zoonotic Diseases 15 (5) 291 (2015)
https://doi.org/10.1089/vbz.2014.1714
Increased Mycoplasma hyopneumoniae Disease Prevalence in Domestic Hybrids Among Free-Living Wild Boar
Daniel J. Goedbloed, Pim van Hooft, Walburga Lutz, et al.EcoHealth 12 (4) 571 (2015)
https://doi.org/10.1007/s10393-015-1062-z
Comparative Proteomic Studies of Yersinia pestis Strains Isolated from Natural Foci in the Republic of Georgia
Maia Nozadze, Ekaterine Zhgenti, Maia Meparishvili, et al.Frontiers in Public Health 3 (2015)
https://doi.org/10.3389/fpubh.2015.00239
Flea-Associated Bacterial Communities across an Environmental Transect in a Plague-Endemic Region of Uganda
Ryan Thomas Jones, Jeff Borchert, Rebecca Eisen, et al.PLOS ONE 10 (10) e0141057 (2015)
https://doi.org/10.1371/journal.pone.0141057
Yersinia murine toxin is not required for early-phase transmission of Yersinia pestis by Oropsylla montana (Siphonaptera: Ceratophyllidae) or Xenopsylla cheopis (Siphonaptera: Pulicidae)
Tammi L. Johnson, B. Joseph Hinnebusch, Karen A. Boegler, et al.Microbiology 160 (11) 2517 (2014)
https://doi.org/10.1099/mic.0.082123-0
Detection of Yersinia pestis in Environmental and Food Samples by Intact Cell Immunocapture and Liquid Chromatography–Tandem Mass Spectrometry
Jérôme Chenau, François Fenaille, Stéphanie Simon, et al.Analytical Chemistry 86 (12) 6144 (2014)
https://doi.org/10.1021/ac501371r
HmsC, a periplasmic protein, controls biofilm formation via repression of HmsD, a diguanylate cyclase in Yersinia pestis
Gai‐Xian Ren, Hai‐Qin Yan, Hui Zhu, Xiao‐Peng Guo and Yi‐Cheng SunEnvironmental Microbiology 16 (4) 1202 (2014)
https://doi.org/10.1111/1462-2920.12323
Yersinia pestis Requires the 2-Component Regulatory System OmpR-EnvZ to Resist Innate Immunity During the Early and Late Stages of Plague
A. Reboul, N. Lemaitre, M. Titecat, et al.Journal of Infectious Diseases 210 (9) 1367 (2014)
https://doi.org/10.1093/infdis/jiu274
Identification of Risk Factors for Plague in the West Nile Region of Uganda
Rebecca J. Eisen, Russell E. Enscore, Emily Zielinski-Gutierrez, et al.The American Journal of Tropical Medicine and Hygiene 90 (6) 1047 (2014)
https://doi.org/10.4269/ajtmh.14-0035
Development of antibodies after foot and mouth disease vaccination in pigs
Gil-Ho Ahn, Jin-Gyu Bae, Kwang Jung, et al.Korean Journal of Veterinary Service 36 (1) 15 (2013)
https://doi.org/10.7853/kjvs.2013.36.1.15
The in vivo extracellular life of facultative intracellular bacterial parasites: Role in pathogenesis
Manuel T. Silva and Nazaré T. Silva PestanaImmunobiology 218 (3) 325 (2013)
https://doi.org/10.1016/j.imbio.2012.05.011
Effects of Low-Temperature Flea Maintenance on the Transmission ofYersinia pestisbyOropsylla montana
Shanna K. Williams, Anna M. Schotthoefer, John A. Montenieri, et al.Vector-Borne and Zoonotic Diseases 13 (7) 468 (2013)
https://doi.org/10.1089/vbz.2012.1017
Vectors and vector-borne diseases of horses
A. C. Onmaz, R. G. Beutel, K. Schneeberg, et al.Veterinary Research Communications 37 (1) 65 (2013)
https://doi.org/10.1007/s11259-012-9537-7
Advances in Yersinia Research
Kenneth L. GageAdvances in Experimental Medicine and Biology, Advances in Yersinia Research 954 79 (2012)
https://doi.org/10.1007/978-1-4614-3561-7_11
Arthropods as Vectors of Emerging Diseases
Heinz MehlhornParasitology Research Monographs, Arthropods as Vectors of Emerging Diseases 3 301 (2012)
https://doi.org/10.1007/978-3-642-28842-5_13
Transmission of Flea-Borne Zoonotic Agents
Rebecca J. Eisen and Kenneth L. GageAnnual Review of Entomology 57 (1) 61 (2012)
https://doi.org/10.1146/annurev-ento-120710-100717
Climate Predictors of the Spatial Distribution of Human Plague Cases in the West Nile Region of Uganda
Katherine MacMillan, Rebecca J. Eisen, Andrew J. Monaghan, et al.The American Journal of Tropical Medicine and Hygiene 86 (3) 514 (2012)
https://doi.org/10.4269/ajtmh.2012.11-0569
Local persistence and extinction of plague in a metapopulation of great gerbil burrows, Kazakhstan
B.V. Schmid, M. Jesse, L.I. Wilschut, H. Viljugrein and J.A.P. HeesterbeekEpidemics 4 (4) 211 (2012)
https://doi.org/10.1016/j.epidem.2012.12.003
Flea Diversity as an Element for Persistence of Plague Bacteria in an East African Plague Focus
Rebecca J. Eisen, Jeff N. Borchert, Joseph T. Mpanga, et al.PLoS ONE 7 (4) e35598 (2012)
https://doi.org/10.1371/journal.pone.0035598