Molecular Epidemiology of Infant Botulism in California and Elsewhere, 1976-2010

被引:26
作者
Dabritz, Haydee A. [1 ]
Hill, Karen K. [2 ]
Barash, Jason R. [1 ]
Ticknor, Lawrence O. [3 ]
Helma, Charles H. [2 ]
Dover, Nir [1 ]
Payne, Jessica R. [1 ]
Arnon, Stephen S. [1 ]
机构
[1] Calif Dept Publ Hlth, Infant Botulism Treatment & Prevent Program, Div Communicable Dis Control, Ctr Infect Dis, Richmond, CA 94804 USA
[2] Los Alamos Natl Lab, Biosci Div, Los Alamos, NM 87545 USA
[3] Los Alamos Natl Lab, Comp Computat & Stat Sci Div, Los Alamos, NM 87545 USA
关键词
botulinum toxin; clinical spectrum; Clostridium baratii; Clostridium botulinum; Clostridium butyricum; honey; infant botulism; molecular epidemiology; sudden infant death; FRAGMENT LENGTH POLYMORPHISM; TANDEM-REPEAT ANALYSIS; CLOSTRIDIUM-BOTULINUM; GENETIC-CHARACTERIZATION; NEUROTOXIN GENES; DEATH-SYNDROME; A STRAINS; TOXIN; DIFFERENTIATION; OUTBREAK;
D O I
10.1093/infdis/jiu331
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Infant botulism (IB), first identified in California in 1976, results from Clostridium botulinum spores that germinate, multiply, and produce botulinum neurotoxin (BoNT) in the immature intestine. From 1976 to 2010 we created an archive of 1090 BoNT-producing isolates consisting of 1012 IB patient ( 10 outpatient, 985 hospitalized, 17 sudden death), 25 food, 18 dust/soils, and 35 other strains. Methods. The mouse neutralization assay determined isolate toxin type (56% BoNT/A, 32% BoNT/B). Amplified fragment-length polymorphism (AFLP) analysis of the isolates was combined with epidemiologic information. Results. The AFLP dendrogram, the largest to date, contained 154 clades; 52% of isolates clustered in just 2 clades, 1 BoNT/A (n = 418) and 1 BoNT/B (n = 145). These clades constituted an endemic C. botulinum population that produced the entire clinical spectrum of IB. Isolates from the patient's home environment (dust/soil, honey) usually located to the same AFLP clade as the patient's isolate, thereby identifying the likely source of infective spores. C. botulinum A(B) strains were identified in California for the first time. Conclusions. Combining molecular methods and epidemiological data created an effective tool that yielded novel insights into the genetic diversity of C. botulinum and the clinical spectrum, occurrence, and distribution of IB in California.
引用
收藏
页码:1711 / 1722
页数:12
相关论文
共 50 条
[21]   ATYPICAL TOXIN VARIANT OF CLOSTRIDIUM-BOTULINUM TYPE-B ASSOCIATED WITH INFANT BOTULISM [J].
HATHEWAY, CL ;
MCCROSKEY, LM ;
LOMBARD, GL ;
DOWELL, VR .
JOURNAL OF CLINICAL MICROBIOLOGY, 1981, 14 (06) :607-611
[22]  
Henderson I, 1996, FEMS MICROBIOL LETT, V140, P151, DOI 10.1016/0378-1097(96)00172-3
[23]   Genetic diversity among botulinum neurotoxin-producing clostridial strains [J].
Hill, K. K. ;
Smith, T. J. ;
Helma, C. H. ;
Ticknor, L. O. ;
Foley, B. T. ;
Svensson, R. T. ;
Brown, J. L. ;
Johnson, E. A. ;
Smith, L. A. ;
Okinaka, R. T. ;
Jackson, P. J. ;
Marks, J. D. .
JOURNAL OF BACTERIOLOGY, 2007, 189 (03) :818-832
[24]   Genetic Diversity Within Clostridium botulinum Serotypes, Botulinum Neurotoxin Gene Clusters and Toxin Subtypes [J].
Hill, Karen K. ;
Smith, Theresa J. .
BOTULINUM NEUROTOXINS, 2013, 364 :1-20
[25]   Genetic characterization of Clostridium botulinum type A containing silent type B neurotoxin gene sequences [J].
Hutson, RA ;
Zhou, YT ;
Collins, MD ;
Johnson, EA ;
Hatheway, CL ;
Sugiyama, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) :10786-10792
[26]  
Hyytiä E, 1999, APPL ENVIRON MICROB, V65, P2057
[27]   Analysis of neurotoxin cluster genes in Clostridium botulinum strains producing botulinum neurotoxin serotype A subtypes [J].
Jacobson, Mark J. ;
Lin, Guangyun ;
Raphael, Brian ;
Andreadis, Joanne ;
Johnson, Eric A. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (09) :2778-2786
[28]   Characterization of Clostridium botulinum strains associated with an infant botulism case in the United Kingdom [J].
Johnson, EA ;
Tepp, WH ;
Bradshaw, M ;
Gilbert, RJ ;
Cook, PE ;
McIntosh, EDG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (06) :2602-2607
[29]  
KAUTTER DA, 1982, J FOOD PROTECT, V45, P1028, DOI 10.4315/0362-028X-45.11.1028
[30]   Efficient DNA fingerprinting of Clostridium botulinum types A, B, E, and F by amplified fragment length polymorphism analysis [J].
Keto-Timonen, R ;
Nevas, M ;
Korkeala, H .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (03) :1148-1154