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Journal of Clinical Microbiology, 07 1997, 1835-1841, Vol 35, No. 7
B Kaltenbock, N Schmeer and R Schneider
A nested PCR for genus-specific amplification of the Chlamydia omp1 locus
was established. This PCR detected single template molecules in 200-microl
specimen aliquots. Amplified chlamydial omp1 alleles were typed by
heminested species PCRs and allele PCRs. We applied this method to 407
specimens from several host animals with various clinical conditions, and
we detected prevalences of chlamydiae from 6 to 50%. Amplicons from peacock
enteritis and equine infertility specimens were not typeable according to
present omp1 allelic criteria for the chlamydial species. DNA sequencing
revealed novel omp1 alleles which were 29.9 and 47.6% divergent in the
deduced peptide sequences from the most closely related chlamydiae.
Phylogenetic reconstruction indicated segregation of these alleles from the
current four chlamydial species (90 and 97% bootstrap support), thus
strongly suggesting the existence of additional chlamydial species. Allele
typing of amplicons from swine with intestinal, urogenital, and respiratory
infections demonstrated several unique omp1 allelic variants of Chlamydia
trachomatis. These novel alleles had deduced peptide sequences which were
11.6 to 19% divergent from porcine C. trachomatis S45. Mutations were
clustered in the C-terminal region of variable segment IV of the omp1 locus
encoding subspecies and serovar determinants of the chlamydial major outer
membrane protein, thus implying that there are numerous serovars of porcine
C. trachomatis. These results demonstrate the need for routine application
of sensitive genus-specific detection of chlamydiae in animal specimens and
suggest a more prominent role than anticipated for chlamydiae in animal
diseases.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Evidence for numerous omp1 alleles of porcine Chlamydia trachomatis and novel chlamydial species obtained by PCR
II. Medizinische Universitatsklinik fur Klauentiere, Veterinarmedizinische Universitat Wien, Vienna, Austria. kaltebe@vetmed.auburn.edu
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