Skip to main content

Monitoring of Neutrophil Recruitment to Mice Lungs During Pneumonic Plague

  • Protocol
  • First Online:
Book cover Pathogenic Yersinia

Part of the book series: Methods in Molecular Biology ((MIMB,volume 2010))

Abstract

Early sensing of bacterial infection and the immediate recruitment of neutrophils to the lung is a major and decisive stage of the innate immune response to pulmonary bacterial infections. This chapter details the preparation of lung tissue suspensions from mice infected intra-nasally (I.N.) with the plague bacterium Yersinia pestis to study in vivo neutrophil responses to the infection. The samples were used for the quantification of neutrophil levels and for the characterization of the pro-inflammatory response required for neutrophil recruitment to the lung. The specific requirements for performing the procedures under Biosafety Level 3 containment and the proper handling and sterilization of the samples are discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 89.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 119.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Craig A, Mai J, Cai S, Jeyaseelan S (2009) Neutrophil recruitment to the lungs during bacterial pneumonia. Infect Immun 77(2):568–575

    Article  CAS  Google Scholar 

  2. Strieter RM, Kunkel SL (1994) Acute lung injury: the role of cytokines in the elicitation of neutrophils. J Invest Med 42(4):640–651

    CAS  Google Scholar 

  3. Williams MR, Azcutia V, Newton G, Alcaide P, Luscinskas FW (2011) Emerging mechanisms of neutrophil recruitment across endothelium. Trends Immunol 32(10):461–469. https://doi.org/10.1016/j.it.2011.06.009

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Mocsai A (2013) Diverse novel functions of neutrophils in immunity, inflammation, and beyond. J Exp Med 210(7):1283–1299. https://doi.org/10.1084/jem.20122220

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Perry RD, Fetherston JD (1997) Yersinia pestis--etiologic agent of plague. Clin Microbiol Rev 10(1):35–66

    Article  CAS  Google Scholar 

  6. Inglesby TV, Dennis DT, Henderson DA, Bartlett JG, Ascher MS, Eitzen E et al (2000) Plague as a biological weapon: medical and public health management. Working Group on Civilian Biodefense. JAMA 283(17):2281–2290

    Article  CAS  Google Scholar 

  7. Kool JL (2005) Risk of person-to-person transmission of pneumonic plague. Clin Infect Dis 40(8):1166–1172

    Article  Google Scholar 

  8. Pechous RD, Sivaraman V, Stasulli NM (2016) GoldmanWE. Pneumonic plague: the darker side of Yersinia pestis. Trends Microbiol 24(3):190–197

    Article  CAS  Google Scholar 

  9. Agar SL, Sha J, Foltz SM, Erova TE, Walberg KG, Parham TE et al (2008) Characterization of a mouse model of plague after aerosolization of Yersinia pestis CO92. Microbiology 154(Pt 7):1939–1948

    Article  CAS  Google Scholar 

  10. Bubeck SS, Cantwell AM, Dube PH (2007) Delayed inflammatory response to primary pneumonic plague occurs in both outbred and inbred mice. Infect Immun 75(2):697–705

    Article  CAS  Google Scholar 

  11. Lathem WW, Crosby SD, Miller VL, Goldman WE (2005) Progression of primary pneumonic plague: a mouse model of infection, pathology, and bacterial transcriptional activity. Proc Natl Acad Sci U S A 102(49):17786–17791

    Article  CAS  Google Scholar 

  12. Price PA, Jin J, Goldman WE (2012) Pulmonary infection by Yersinia pestis rapidly establishes a permissive environment for microbial proliferation. Proc Natl Acad Sci U S A 109(8):3083–3088

    Article  CAS  Google Scholar 

  13. Vagima Y, Zauberman A, Levy Y, Gur D, Tidhar A, Aftalion M, Shafferman A, Mamroud E (2015) Circumventing Y. pestis virulence by early recruitment of neutrophils to the lungs during pneumonic plague. PLoS Pathog 11:e1004893

    Article  Google Scholar 

  14. Vagima Y et al (2012) Early sensing of Yersinia pestis airway infection by bone marrow cells. Front Cell Infect Microbiol 2:143

    Article  Google Scholar 

  15. Cornelis GR, Wolf-Watz H (1997) The Yersinia Yop virulon: a bacterial system for subverting eukaryotic cells. Mol Microbiol 23(5):861–867

    Article  CAS  Google Scholar 

  16. Viboud GI, Bliska JB (2005) Yersinia outer proteins: role in modulation of host cell signaling responses and pathogenesis. Annu Rev Microbiol 59:69–89

    Article  CAS  Google Scholar 

  17. Zauberman A, Cohen S, Mamroud E, Flashner Y, Tidhar A, Ber R et al (2006) Interaction of Yersinia pestis with macrophages: limitations in YopJ-dependent apoptosis. Infect Immun 74(6):3239–3250

    Article  CAS  Google Scholar 

  18. Spinner JL, Cundiff JA, Kobayashi SD (2008) Yersinia pestis type III secretion system-dependent inhibition of human polymorphonuclear leukocyte function. Infect Immun 76:3754–3760. https://doi.org/10.1128/IAI.00385-08

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Pechous RD et al (2013) Early host cell targets of Yersinia pestis during primary pneumonic plague. PLoS Pathog 9:e1003679

    Article  Google Scholar 

  20. Chung LK, Bliska JB (2016) Yersinia versus host immunity: how a pathogen evades or triggers a protective response. Curr Opin Microbiol 29:56–62

    Article  CAS  Google Scholar 

  21. Stasulli NM, Eichelberger KR, Price PA, Pechous RD, Montgomery SA, Parker JS, Goldman WE (2015) Spatially distinct neutrophil responses within the inflammatory lesions of pneumonic plague. MBio 6:e01530–e15

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yaron Vagima .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2019 Springer Science+Business Media, LLC, part of Springer Nature

About this protocol

Check for updates. Verify currency and authenticity via CrossMark

Cite this protocol

Vagima, Y., Levy, Y., Mamroud, E. (2019). Monitoring of Neutrophil Recruitment to Mice Lungs During Pneumonic Plague. In: Vadyvaloo, V., Lawrenz, M. (eds) Pathogenic Yersinia. Methods in Molecular Biology, vol 2010. Humana, New York, NY. https://doi.org/10.1007/978-1-4939-9541-7_10

Download citation

  • DOI: https://doi.org/10.1007/978-1-4939-9541-7_10

  • Published:

  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-4939-9540-0

  • Online ISBN: 978-1-4939-9541-7

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics