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Journal of Clinical Microbiology, February 2001, p. 823-823, Vol. 39, No. 2
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.2.823.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
LETTERS TO THE EDITOR
First Report of Neisseria meningitidis
Intermediately Resistant to Penicillin in Croatia
 |
LETTER |
Neisseria meningitidis is one of the leading causes of
bacterial meningitis and sepsis in Croatia. Meningococcal strains with decreased susceptibility to penicillin (MIC > 0.12 mg/ml) have been reported worldwide since 1985 (1, 3-7). Here we
report the first identification of an isolate intermediately resistant to penicillin in Croatia.
An 8-month-old male child presented to the Emergency Department at
University Hospital for Infectious Diseases, Zagreb, Croatia, with a
2-day history of fever (>39°C). The child was somnolent, with
characteristic meningeal signs and petechia on its scrotum and entire
extremities. The white blood cell count was 5,800/mm3, with
51 segmented neutrophils and 32 lymphocytes. The cerebrospinal fluid
(CSF) contained 92,416 cells/mm3, the protein concentration
was 2,040 mg/liter, and the glucose concentration was 0.3 mmol/liter.
Gram-negative diplococci were visible on a Gram-stained smear, and
latex agglutination performed on the CSF was positive for N. meningitidis serogroup B (Slidex meningite-Kit 5; bioMerieux,
Marcy-l'Étoile, France). Ceftriaxone therapy was instituted,
and household contacts were treated with rifampin.
Cultures of both blood and CSF grew N. meningitidis
serogroup B. A penicillin MIC of 0.094 mg/ml was determined with the
Etest (AB Biodisk, Solna, Sweden) on Mueller-Hinton agar containing 5%
sheep blood, incubated in CO2. The MIC of 0.12 mg/ml was
determined at the Centers for Disease Control and Prevention according
to the recommendations of the National Committee for Clinical
Laboratory Standards, by using the broth microdilution method with
Mueller-Hinton broth containing 5% lysed horse blood (2).
Consequently, treatment with ceftriaxone was continued. Molecular
subtyping by multilocus enzyme electrophoresis indicated that the
electrophoretic type (ET) identified in the isolate, 1155, was
frequently found in other N. meningitidis serogroup B
isolates from Croatia, but interestingly this ET was not a member of
the well-described ET-5 complex.
The child's condition was defined as severe. He was febrile and
somnolent during the first 9 days of hospitalization. A computed tomography scan of the child's head showed subdural effusion in the
frontal, temporal, and parietal regions, and therefore cortisone was
added to the therapy protocol. CSF and blood collected on days 2, 6, and 9 following the administration of antibacterial therapy were all
negative by latex agglutination and culture. The patient was discharged
on day 27 in good condition.
This is the first report of identification of N. meningitidis intermediately resistant to penicillin in Croatia.
Surveillance for antimicrobial resistance of meningococci is needed for
early detection of isolates, such as that described in this report, that might affect recommendations for treatment.
 |
FOOTNOTES |
*
Phone: (404) 639-1730.
Fax: (404) 639-3172.
E-mail: txp1{at}cdc.gov.
 |
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A. Boras
D. Bozinovic
University Hospital for Infectious Diseases Zagreb, Croatia
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| | | | |
F. C. Tenover
Hospital Infections Program National Center for Infectious Diseases Centers for Disease Control and Prevention Atlanta, Georgia
|
| | | | |
T. Popovic*
Division of Bacterial and Mycotic Diseases National Center for Infectious Diseases Centers for Disease Control and Prevention Atlanta, Georgia
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Journal of Clinical Microbiology, February 2001, p. 823-823, Vol. 39, No. 2
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.2.823.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
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du Plessis, M., von Gottberg, A., Cohen, C., de Gouveia, L., Klugman, K. P., for the Group for Enteric Respiratory and Meningea,
(2008). Neisseria meningitidis Intermediately Resistant to Penicillin and Causing Invasive Disease in South Africa in 2001 to 2005. J. Clin. Microbiol.
46: 3208-3214
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