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Journal of Clinical Microbiology, November 2000, p. 3984-3990, Vol. 38, No. 11
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Molecular Epidemiological Analysis of Cryptosporidium
spp. in the United Kingdom: Results of Genotyping
Cryptosporidium spp. in 1,705 Fecal Samples from Humans
and 105 Fecal Samples from Livestock Animals
J.
McLauchlin,1,*
C.
Amar,1
S.
Pedraza-Díaz,1 and
G. L.
Nichols2
Food Safety Microbiology Laboratory, Division
of Gastrointestinal Infections, PHLS Central Public Health Laboratory,
London NW9 5HT,1 and Environmental
Surveillance Unit, PHLS Communicable Disease Surveillance Centre,
London NW9 5EQ,2 United Kingdom
Received 16 May 2000/Returned for modification 10 July
2000/Accepted 5 September 2000
Cryptosporidium present in 1,705 fecal samples from
humans and 105 from livestock animals were analyzed by PCR-restriction fragment length polymorphism of the Cryptosporidium oocyst
wall protein. Overall, genotype 1 (human exclusive type) was detected in 37.8% of the samples from humans, genotype 2 (broad host range) was
detected in 61.5%, a third genotype designated genotype 3 (Cryptosporidium meleagridis) was detected in 0.3%, and
both genotypes 1 and 2 were recovered from 0.4%. All samples from
livestock yielded genotype 2. Among 469 patients infected during eight
drinking water-related outbreaks, five outbreaks were predominantly due to genotype 1, and three were due to genotype 2. Fifty-four samples were collected from patients involved with five swimming
pool-associated outbreaks: two outbreaks were due to genotype 1, one
was due to genotype 2, and the remaining two involved both genotypes 1 and 2. Among 26 family outbreaks and 1 children's nursery outbreak (2 to 3 members per group), the same genotype was recovered from the
different members of each outbreak: 13 were due to genotype 1, and 14 were due to genotype 2. In eighteen patients reporting contact with
animals and/or farms, genotype 1 was recovered from one patient and
genotype 2 was recovered from the remaining 17. Among the sporadic
cases, there were distinct geographical and temporal variations in the
distribution of the genotypes. The spring peak in cases was due to
genotype 2. Genotype 1 was significantly more common in patients
infected during the late-summer-autumn peak and in those with a
history of foreign travel.
*
Corresponding author. Mailing address: Food Safety
Microbiology Laboratory, Division of Gastrointestinal Infections, PHLS Central Public Health Laboratory, 61 Colindale Ave., London NW9 5HT,
United Kingdom. Phone: 020 8200 4400, ext. 3505. Fax: 020 8200 8264. E-mail: jmclauchlin{at}phls.nhs.uk.
Journal of Clinical Microbiology, November 2000, p. 3984-3990, Vol. 38, No. 11
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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