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Listeria monocytogenes
There are several species in the genus Listeria. Of these, L monocytogenes is
important as a cause of a wide spectrum of disease in animals and humans. L
monocytogenes is capable of growing and surviving over a wide range of
environmental conditions. It can survive at refrigerator temperatures (4°C), under
conditions of low pH and high salt conditions. Therefore, it is able to overcome
food preservation and safety barriers, making it an important foodborne pathogen.
Recent data from the Centers for Disease Control and Prevention indicate that
foodborne listeriosis is declining. However, one of the largest and most deadly
outbreaks of listeriosis in the United States (147 cases across 28 states and 33
deaths) occurred in 2011 and was traced to contaminated cantaloupe from a
packaging plant in Colorado. This outbreak emphasizes the ubiquitous nature of
this organism and its ability to easily contaminate a variety of foods during any
stage of the food handling process.
Morphology and Identification
L monocytogenes is a short, gram-positive, non–spore-forming rod. It is
catalase positive and has a tumbling end-over-end motility at 22–28°C but not at
37°C; the motility test rapidly differentiates Listeria from diphtheroids that are
members of the normal microbiota of the skin.
Culture and Growth Characteristics
Listeria grows well on media such as 5% sheep blood agar on which it exhibits
the characteristic small zone of hemolysis around and under colonies. The
organism is a facultative anaerobe and is catalase positive, esculin hydrolysis
positive, and motile. Listeria produces acid but not gas from utilization of a variety
of carbohydrates. The motility at room temperature and hemolysin production are
primary findings that help differentiate Listeria from coryneform bacteria.
Microbiology
Medical bacteriology
Dr. Zainab D. Degaim

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Antigenic Classification
Serologic classification is done only in reference laboratories and is primarily
used for epidemiologic studies. There are 13 known serovars based on O (somatic)
and H (flagellar) antigens. Serotypes 1/2a, 1/2b, and 4b make up more than 95%
of the isolates from humans. Serotype 4b causes most of the foodborne outbreaks.
Less labor intensive, genomic based methods have been developed but serotyping
remains the gold standard.
Pathogenesis and Immunity
L monocytogenes enters the body through the gastrointestinal tract after
ingestion of contaminated foods such as cheese, fruit, or vegetables. The organism
has several adhesin proteins (Ami, Fbp A, and flagellin proteins) that facilitate
bacterial binding to the host cells and that contribute to virulence. It has cell wall
surface proteins called internalins A and B that interact with E-cadherin, a receptor
on epithelial cells, promoting phagocytosis into the epithelial cells. After
phagocytosis, the bacterium is enclosed in a phagolysosome, where the low pH
activates the bacterium to produce listeriolysin O.
This enzyme, along with two phospholipases, lyses the membrane of the
phagolysosome and allows the listeriae to escape into the cytoplasm of the
epithelial cell. The organisms proliferate, and ActA, another listerial surface
protein, induces host cell actin polymerization, which propels them to the cell
membrane. Pushing against the host cell membrane, they cause formation of
elongated protrusions called filopods.
These filopods are ingested by adjacent epithelial cells, macrophages, and
hepatocytes, the listeriae are released, and the cycle begins again. L
monocytogenes can move from cell to cell without being exposed to antibodies,
complement, or polymorphonuclear cells. Shigella flexneri and rickettsiae also
usurp the host cells’ actin and contractile system to spread their infections.
Iron is an important virulence factor. Listeriae produce siderophores and are able
to obtain iron from transferrin.

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Immunity to L monocytogenes is primarily cell mediated, as demonstrated by the
intracellular location of infection and by the marked association of infection with
conditions of impaired cell-mediated immunity such as pregnancy, advanced age,
AIDS, lymphoma, and organ transplantation. Immunity can be transferred by
sensitized lymphocytes but not by antibodies.
Clinical Findings
There are two forms of perinatal human listeriosis. Early onset syndrome
(granulomatosis infantiseptica) is the result of infection in utero and is a
disseminated form of the disease characterized by neonatal sepsis, pustular
lesions, and granulomas containing L monocytogenes in multiple organs. Death
may occur before or after delivery. The late-onset syndrome causes the
development of meningitis between birth and the third week of life; it is often
caused by serotype 4b and has a significant mortality rate.
Healthy persons exposed to L monocytogenes in food may not become ill or may
develop a mild, self-limiting febrile gastroenteritis lasting 1–3 days. This develops
after an incubation period of 6–48 hours. Symptoms include fever, chills,
headache, myalgias, abdominal pain, and diarrhea. Immunocompromised
individuals can develop Listeria meningoencephalitis, bacteremia, and (rarely)
focal infections. Listeria is one of the more common causes of meningitis in this
group of patients. Clinical presentation of Listeria meningitis varies from insidious
to fulminate and is nonspecific. Most clinical laboratories do not routinely culture
for Listeria from routine stool samples. The diagnosis of systemic listeriosis rests
on isolation of the organism in cultures of blood and spinal fluid.
Spontaneous infection occurs in many domestic and wild animals. In ruminants
(eg, sheep), Listeria may cause meningoencephalitis with or without bacteremia.
In smaller animals (eg, rabbits, chickens), there is septicemia with focal abscesses
in the liver and heart muscle and marked monocytosis.

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Many antimicrobial drugs inhibit Listeria species in vitro. Clinical cures have
been obtained with ampicillin, erythromycin, or intravenous trimethoprim–
sulfamethoxazole.
Cephalosporins and fluoroquinolones are not active against L monocytogenes.
Ampicillin plus gentamicin is often recommended for therapy, but gentamicin
does not enter host cells and may not help treat the Listeria infection.
Trimethoprim–sulfamethoxazole is the drug of choice for central nervous
system infections in patients who are allergic to penicillin.
Gram stain of the gram-positive bacillus Listeria monocytogenes in a blood culture, blood cells are
present in the background. Listeria organisms isolated from clinical specimens frequently show variation
in length and often in shape as well. Typically, they are 0.4–0.5 μm in diameter and 0.5–2 μm long.
(Courtesy of H. Tran.)