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Journal of Clinical Microbiology, April 2000, p. 1638-1640, Vol. 38, No. 4
Department of Medical Microbiology,
Malmö University Hospital, Lund University, S-205 02 Malmö,1 and Department of
Clinical Microbiology, Örebro Medical Centre Hospital, S-701 85 Örebro,2 Sweden
Received 12 October 1999/Accepted 27 January 2000
A cluster of a Neisseria meningitidis serogroup C
strain causing invasive disease was investigated. Five out of seven
cases were associated with a particular discotheque. The strains were indistinguishable, as revealed by pulsed-field gel electrophoresis and
sequencing of variable regions of the porA gene, but caused strikingly different clinical presentations during 5 months.
Neisseria meningitidis
causes both endemic and epidemic disease (8, 12, 13, 18).
Although the vast majority of the estimated 2,600 annual cases of
meningococcal disease in the United States are sporadic, the frequency
of serogroup C meningococcal clusters has increased in, for example,
military camps and universities (6-8). During recent years,
however, meningococcal serogroup C spread has also been associated with
discotheques, hence the designation "Disco Fever." A limited
outbreak that involved six individuals who attended a dance club in
Argentina was reported (4). A similar epidemic involving 10 young adults who visited a nightclub in Australia was described
(9).
Characterization of meningococcal strains isolated during outbreaks is
crucial in understanding an epidemic. Isolates may change their
phenotype by, for example, capsular switching, justifying approaches
other than serogroup typing when disease-causing strains are traced
(19). In addition to the standard pulsed-field gel electrophoresis (PFGE) (15, 19), multilocus enzyme
electrophoresis (13), ribosomal DNA restriction profiles
(21), and PCR analysis followed by restriction fragment
length polymorphism analysis of the porA gene have, among
other methods, been used for characterization of N. meningitidis serogroup C (5, 14).
Blood culturing was performed using aerobic flasks (BacT/Alert; Organon
Teknika, Durham, N.C.). Cerebrospinal fluid (CSF) was cultured on
Columbia blood agar (Difco, Detroit, Mich.) and chocolate agar, and
enrichment culturing was performed with brain heart infusion medium
including factors V and X (Difco). Serogrouping was carried out by
coagglutination (11), and all isolates were serotyped and
serosubtyped with monoclonal antibodies for outer-membrane protein
(1). PFGE was done using a contour-clamped homogeneous electric field 2 apparatus (Bio-Rad Laboratories, Richmond, Calif.). For porA gene sequencing, chromosomal DNAs were directly
isolated from bacterial suspensions using Dynabeads DNA DIRECT system I (Dynal, Oslo, Norway). The porA gene was amplified by PCR,
and variable region 1 (VR1), VR2, and VR3 were labeled with a BigDye Terminator Cycle Sequencing kit followed by sequencing with an ABI
PRISM 310 genetic analyzer (Perkin-Elmer, Foster City, Calif.). To
assign VR sequences to families (2), deduced amino acid sequences of the VRs were aligned with sequences available in the
N. meningitidis PorA VR database
(http://mlst.zoo.ox.ac.uk/porA-vr/), where the VR family
designation is based on the scheme of Suker et al. (17).
Three patients (Table 1; patients D, E,
and F) with N. meningitidis serogroup C disease were
admitted to a local hospital on three subsequent days. The first
patient (patient D) was a 25-year-old male who fell ill with fever,
petechiae, cutaneous bleedings, and hypotension. The patient developed
a fulminant septicemia and a fatal disseminated intravascular
coagulation within 5 h. The following day, a 21-year-old female
attended the hospital due to a swollen knee joint (Table 1; patient E).
Septic arthritis was suspected, and N. meningitidis group C
was isolated from the joint fluid. The third patient, a 21-year-old
male with an artificial eye (enucleation performed due to an uveal
tumor at the age of 3 years), suffered from conjunctivitis and
displayed symptoms of meningitis (Table 1; patient F). None of these
patients knew each other or listed close friends when answering the
question of social contacts. However, they had all visited the same
discotheque in Malmö on the same night (Fig.
1). The strains from all three patients
were phenotypically identical (C2aP1.nst). Genosubtyping showed the
same nucleotide sequences in VR1, VR2, and VR3 of the porA
gene, namely, those of genosubtypes 5a, 10d, and 36b (Table 1). Healthy
individuals who had had contact with patients D, E, and F were either
checked with pharyngeal swab cultures or directly prescribed
ciprofloxacin. One strain of N. meningitidis with full
identity with the invasive isolates was detected among the healthy
contacts (Table 1).
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Long-Term Persistence of a Discotheque-Associated
Invasive Neisseria meningitidis Group C Strain as Proven by
Pulsed-Field Gel Electrophoresis and porA Gene
Sequencing
ABSTRACT
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TABLE 1.
Summary of cases, contacts with healthy individuals, and
unrelated cases
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FIG. 1.
Chronology of occurrences of meningococcal disease and
discotheque attendance. Upper arrows indicate dates when patients fell
ill, and lower arrows indicate dates when patients C to F attended the
discotheque. The distance between the two residential districts is
shown.
All invasive N. meningitidis group C strains (n = 11) collected in the surveillance area (Skåne, Sweden; population, 1.1 million people) during 1992 were analyzed. Four strains isolated from patients A, B, C, and G displayed the same PFGE patterns and VRs in their porA genes as the strains associated with the discotheque (Table 1). Patient C was a 24-year-old male who also had visited the same discotheque 3 weeks before patients D, E, and F (Fig. 1). He was admitted with septicemia and menigitis complicated by convulsions and required respirator therapy for 6 days. Patient G, a 21-year-old male who had visited the discotheque in July, fell ill in early September. A few days before his admission to the hospital, he had gotten a splinter in his right ankle, accompanied by local tenderness and arthritis in his right knee joint. Surprisingly, meningococci with full identity with the cluster strain were isolated from his knee joint. Two additional patients carrying the cluster strain were detected in our study; patient A was a 9-year-old boy (Table 1) who initially presented with a sore throat, followed by a fulminant septicemia. Due to necrosis in a finger, amputation of the two distal phalanges had to be performed. Suspected cerebral damage resulting in a considerably delayed puberty was observed after 4 years. Patient B was a 2-year-old girl suffering from septicemia without any manifest sequelae. No epidemiological connection was found either between patients A, B, and C (except for living in the same city [Landskrona, Sweden; population, 37,000]) or between the different disco attendees. The genetic diversity within the group C meningococci in the surveillance area is illustrated by the characterization of the four unrelated cases during 1992 (Table 1).
A relationship between alcohol consumption, tobacco smoke exposure, male gender, and meningococcal disease is statistically proven (4, 7). These hallmarks are, however, less prominent during sporadic serogroup C meningococcal disease (13, 16). Except for environmental factors, it is presently obscure why patients are differently affected by the same strain. Various disease manifestations from fulminant septicemia to less severe disease, including primary arthritis (20) and conjunctivitis (3), were observed in our study (Table 1). The meningeal tropism and interactions with most human cell types by N. meningitidis (10) suggests that a patient's phenotype as well as acquired specific and nonspecific immunity plays a crucial role in the clinical outcome. In conclusion, we found that porA gene sequencing (genosubtyping) together with PFGE provided meaningful information during a meningococcal outbreak with the cluster strain lasting 5 months.
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FOOTNOTES |
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* Corresponding author. Mailing address: Dept. of Medical Microbiology, Malmö University Hospital, Lund University, S-205 02 Malmö, Sweden. Phone: 46 40 331340. Fax: 46 40 336234. E-mail: kristian.riesbeck{at}mikrobiol.mas.lu.se.
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Journal of Clinical Microbiology, April 2000, p. 1638-1640, Vol. 38, No. 4
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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