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Method Article

Studying Effects of Cigarette Smoke on Pseudomonas Infection in Lung Epithelial Cells

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DOI:

10.3791/61163

May 11th, 2020

In This Article

Summary

Described here is a protocol to study how cigarette smoke extract affects bacterial colonization in lung epithelial cells.

Abstract

Cigarette smoking is the major etiological cause for lung emphysema and chronic obstructive pulmonary disease (COPD). Cigarette smoking also promotes susceptibility to bacterial infections in the respiratory system. However, the effects of cigarette smoking on bacterial infections in human lung epithelial cells have yet to be thoroughly studied. Described here is a detailed protocol for the preparation of cigarette smoking extracts (CSE), treatment of human lung epithelial cells with CSE, and bacterial infection and infection determination. CSE was prepared with a conventional method. Lung epithelial cells were treated with 4% CSE for 3 h. CSE-treated cells were, then, infected with Pseudomonas at a multiplicity of infection (MOI) of 10. Bacterial loads of the cells were determined by three different methods. The results showed that CSE increased Pseudomonas load in lung epithelial cells. This protocol, therefore, provides a simple and reproducible approach to study the effect of cigarette smoke on bacterial infections in lung epithelial cells.

Introduction

Cigarette smoking affects the public health of millions of people worldwide. Many deleterious diseases, including lung cancer and chronic obstructive pulmonary disease (COPD), are reported to be related to cigarette smoking1,2. Cigarette smoking increases susceptibility to acute microbial infections in the respiratory system3,4,5. Furthermore, mounting evidence proves that cigarette smoking enhances the pathogenesis of many chronic disorders6,7,

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Protocol

1. 100% CSE preparation

  1. Draw 10 mL of serum-free cell culture media (DMEM/F12 for BEAS-2B cells; airway epithelial cell basal medium for HSAEC cells) into a 60 mL syringe.
  2. Reversely attach an appropriately trimmed 1 mL pipette tip to the nozzle of the syringe as an adapter to hold the cigarette (3R4F).
  3. Remove the filter of the cigarette. Attach a cigarette to the tip adaptor and combust the cigarette.
  4. Draw 40 mL of smoke-containing air into 10 mL of serum-free media. Mix the smoke with the medium by vigorously shaking (30 s per draw).
  5. Repeat step 1.4 about 11x in ~7 min until the cigarette is completely burned out.

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Results

A diagram is used to illustrate the protocol in Figure 1. Lung epithelial BEAS-2B cells were treated with CSE and challenged with Pseudomonas. Pseudomonas in the culture medium were killed by the added gentamycin and the cells were subjected to the drop plate assay, RT-qPCR detection of Pseudomonas ribosome 16S RNA, and flow cytometry. Compared with control, CSE treatment substantially increased bacterial infection in drop plate methods (Figure.......

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Discussion

Bacterial invasion into lung epithelial cells is a crucial step in the pathogenesis of bacterial infections. The process of bacterial invasion into the cells can be broken down into the following three steps: First, the bacteria contact and adhere to the surface of the epithelial cell using their flagella. Second, the bacteria either undergo internalization or penetrate the cellular membrane. Finally, the bacteria replicate and colonize the cells if they successfully escape cellular defense mechanisms25.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

This work was supported in part by a National Institutes of Health R01 grants HL125435 and HL142997 (to CZ).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
50mL syringeBD Biosciences
airway epithelial cell basal mediumATCCPCS-300-030
Bacteria shakerThermoFisher Scientific
bronchial epithelial cell growth kitATCCPCS-300-040
Cell CounterBio-Rad
CFX96 Real-Time PCR SystemBio-Rad
High-Capacity RNA-to-DNA KITThermoFisher Scientific4387406
HITES mediumATCCATCC 30-2004
human BEAS-2B cellsATCCATCC CRL-9609
human primary small airway epithelial cellsATCCATCC PCS-300-030
LSRII flow cytometerBD Biosciences
Nikkon confocal microscopeNikkon
OD readerUSA Scientific
PCR primersITD
Pseudomonas aeruginosaATCCATCC 47085PAO1-LAC
Pseudomonas fluorescens MigulaATCCATCC 27853P.aeruginosa GFP
Research-grade cigarettes (3R4F)University of KentuckyTP-7-VA
RNeasy Mini KitQiagen74106
Transprent PET Transwell InsertCorning Costar
Tryptic Soy BrothBD Biosciences

References

  1. Vogelmeier, C. F., et al. Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Lung Disease 2017 Report. GOLD Executive Summary. American Journal of Respiratory and Critical Care Medicine. 195 (5), 557-582 (2017).
  2. Malhotra, J., Malvezzi, M., Negri, E., La Vecchia, C., Boffetta, P.

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Tags

Cigarette Smoke ExtractBacterial Load DeterminationFlow CytometryqRT PCR AnalysisDrop Plate MethodCell Culture PreparationGentamycin TreatmentRNA Extraction