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During infection, Listeria monocytogenes is capable of crossing the blood-brain barrier to colonize the brain. In this protocol, we demonstrate how to assess bacterial colonization of organs following infection of mice. A procedure to perform whole organ perfusion for specific determination of bacterial numbers in the brain parenchyma is provided.
Listeria monocytogenes is an intracellular bacterial pathogen that is frequently associated with food-borne infection. The ability of L. monocytogenes to cross the blood-brain barrier (BBB) is concerning as it can lead to life-threatening meningitis and encephalitis. The BBB protects the brain microenvironment from various toxic metabolites and microbial pathogens found in the blood following infection, and therefore supports brain homeostasis. The mechanisms by which L. monocytogenes present in the bloodstream cross the BBB to cause brain infections are not fully understood and there is also a lack of a robust model system to study brain infections by L. monocytogenes. Here, we present a simple mouse infection model to determine whether bacteria have crossed the BBB and to quantitate the burden of bacteria that have colonized the brain in vivo. In this method, animals were infected intravenously with L. monocytogenes and were humanely euthanized by exposure to CO2 followed by cervical dislocation. Cardiac perfusion of the animals was performed prior to harvesting infected organs. Blood was collected before perfusion and the number of bacteria per organ or mL of blood was determined by plating dilutions of the blood or organ homogenates on agar plates and counting the number of colonies formed. This method can be used to study novel receptor-ligand interactions that enhance infection of the brain by L. monocytogenes and can be easily adapted for the study of multiple bacterial pathogens.
The Gram-positive bacterium Listeria monocytogenes is a facultative intracellular pathogen and one of the most deadly food-borne pathogens worldwide. Ingestion of L. monocytogenes contaminated food can lead to listeriosis in humans, a severe invasive disease targeting mostly pregnant women, newborns, the elderly, and immunocompromised individuals1. L. monocytogenes is among the leading causes of death by a food-borne pathogen in the U.S. and case fatality rates from listeriosis are as high as 20–30%, the highest for all food-borne pathogens2. No vaccine currently exists for L. monocyt....
All animals are to be maintained and handled with maximum care to minimize discomfort during the course of the procedure. The procedure is to be conducted in compliance with the Institutional Animal Care and Use Committee and all federal, state and local laws. Also note that the laboratory experiments are to be conducted in accordance with Biosafety Level 2 guidelines.
1. Growth of L. monocytogenes for Mouse Infection Studies
The brain is highly vascularized and L. monocytogenes is known to infect cell types present in the blood3,13. The described protocol is used to demonstrate the ability of L. monocytogenes to cross the blood-brain barrier (BBB) leading to infection of the brain in mice. To determine if bacteria have crossed the BBB in vivo, perfusion of blood in the mouse is performed prior to determining bacterial burden.......
L. monocytogenes is able to cause life-threatening meningoencephalitis in humans. Prior studies have demonstrated the ability of bacteria to cross the blood-brain-barrier (BBB) and to colonize the brain. Three routes of brain invasion have been proposed during infection: direct penetration of the BBB by bacteria, stealth transport by bacteria contained inside of mononuclear cells3, and axonal migration by L. monocytogenes strains that cause rhombencephalitis15
This work was supported by U.S. Public Health Service grant AI103806 from the National Institutes of Health.
....Name | Company | Catalog Number | Comments |
Brain Heart Infusion media | Becton Dickinson | 237200 | |
Streptomycin sulfate | Amresco | 0382-50G | |
Petri dishes | VWR | 25384-342 | |
Glycerol | VWR | 97062-832 | |
IKA T18 ULTRA-TURRAX Basic Homogenizer | IKA | 3352109 | Model: T18BS1 |
Spectrophotometer | Beckman Coulter | DU 800 series | |
BALB/c mice | Jackson Laboratory | Model #000651 | |
1 mL syringes | Becton Dickinson | 309659 | |
26-gauge needles | Becton Dickinson | 305115 | |
21-gauge butterfly needles | Becton Dickinson | 367281 | |
Ethylenediaminetetraacetic acid | Sigma-Aldrich | 60004 | |
15 mL conical tubes | VWR | 21008-918 | |
Round-bottom test tubes | VWR | 60819-546 | |
Phosphate-buffered saline | Corning | 46-013-CM | |
Stainless steel spatula | VWR | 82027-520 | |
Stainless steel scissors (6.5 in) | VWR | 82027-592 | |
Stainless steel scissors (4.5 in) | VWR | 82027-578 | |
Stainless steel blunt forceps (4.5 in) | VWR | 82027-440 | |
Stainless steel fine tip forceps (6 in) | VWR | 82027-406 |
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