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1.
J Infect Dis ; 191(1): 33-9, 2005 Jan 01.
Article in English | MEDLINE | ID: mdl-15593000

ABSTRACT

In 2000, a large international outbreak of meningococcal disease caused by Neisseria meningitidis serogroup W-135 was identified among pilgrims returning from the Hajj in Saudi Arabia. To assess ongoing risk, we evaluated N. meningitidis carriage among US travelers to the 2001 Hajj. Of 25 N. meningitidis isolates obtained, 15 (60%) were nongroupable and 8 (32%) were serogroup W-135 when tested by standard slide-agglutination techniques. Two additional nongroupable isolates were characterized as serogroup W-135 when tested by polymerase chain reaction. Nine of 10 serogroup W-135 isolates were indistinguishable from the Hajj-2000 clone. None of the departing, but 9 (1.3%) of the returning, pilgrims carried serogroup W-135 (P=.01); all carriers reported previous vaccination. Carriage of N. meningitidis serogroup W-135 increased significantly in pilgrims returning from the Hajj. Although the risk of disease to pilgrims appears to be low, the risk of spread to others of this pathogenic strain remains a concern.


Subject(s)
Carrier State/epidemiology , Meningococcal Infections/epidemiology , Neisseria meningitidis, Serogroup W-135/isolation & purification , Travel , Adult , Aged , Carrier State/microbiology , Female , Humans , Islam , Male , Meningococcal Infections/microbiology , Middle Aged , Neisseria meningitidis, Serogroup W-135/classification , Pharynx/microbiology , Polymerase Chain Reaction , Saudi Arabia , Serotyping , United States
2.
J Clin Microbiol ; 41(1): 393-6, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12517878

ABSTRACT

To resolve discrepancies in slide agglutination serotyping (SAST) results from state health departments and the Centers for Disease Control and Prevention (CDC), we characterized 141 of 751 invasive Haemophilus influenzae isolates that were identified in the United States from January 1998 to December 1999 through an active, laboratory-based, surveillance program coordinated by the CDC. We found discrepancies between the results of SAST performed at state health departments and those of PCR capsule typing performed at the CDC for 56 (40%) of the isolates characterized: 54 isolates that were identified as a particular serotype by SAST were shown to be unencapsulated by PCR, and two isolates that were reported as serotypes b and f were found to be serotypes f and e, respectively, by PCR. The laboratory error most likely to affect the perceived efficacy of the conjugate H. influenzae type b (Hib) vaccine was the misidentification of isolates as serotype b: of 40 isolates identified as serotype b by SAST, 27 (68%) did not contain the correlating capsule type genes. The frequency of errors fell substantially when standardized reagents and routine quality control of SAST were used during a study involving three laboratories. An overall 94% agreement between SAST and PCR results showed that slide agglutination could be a valid and reliable method for serotyping H. influenzae if the test was performed correctly, in accordance with standardized and recommended procedures. An ongoing prospective analysis of all H. influenzae surveillance isolates associated with invasive disease in children less than 5 years old will provide more accurate national figures for the burden of invasive disease caused by Hib and other H. influenzae serotypes.


Subject(s)
Haemophilus influenzae/isolation & purification , Polymerase Chain Reaction/methods , Serotyping/methods , Agglutination , DNA, Bacterial/analysis , Haemophilus influenzae/classification , Haemophilus influenzae/genetics , Humans , Statistics as Topic
3.
J Infect Dis ; 185(11): 1596-605, 2002 Jun 01.
Article in English | MEDLINE | ID: mdl-12023765

ABSTRACT

In 2000, >400 cases of disease caused by Neisseria meningitidis serogroup W135 (MenW135), the largest MenW135 outbreak reported to date, occurred worldwide among Hajj pilgrims and their contacts. To elucidate the origin of the outbreak strains and to investigate their relatedness to major clonal groups, genotypic and phenotypic subtyping was performed on 26 MenW135 outbreak-associated isolates and 50 MenW135 isolates collected worldwide from 1970 through 2000. All outbreak-associated isolates were members of a single clone of the hypervirulent electrophoretic type (ET)-37 complex, designated the "(W)ET-37 clone"; 19 additional MenW135 strains were also members of this clone, and the remaining 31 MenW135 strains were clearly distinct. The 2000 MenW135 outbreak was not caused by emergence of a new MenW135 strain but rather by expansion of the (W)ET-37 clone that has been in circulation at least since 1970; the strains most closely related to those causing the 2000 outbreak have been isolated in Algeria, Mali, and The Gambia in the 1990s.


Subject(s)
Disease Outbreaks , Meningococcal Infections/epidemiology , Neisseria meningitidis/classification , Neisseria meningitidis/genetics , Bacterial Typing Techniques , DNA, Bacterial/analysis , DNA, Bacterial/genetics , Electrophoresis/methods , Genotype , Global Health , Humans , Islam , Meningococcal Infections/microbiology , Neisseria meningitidis/physiology , Phenotype , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA/methods , Travel , Virulence/genetics
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