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Applied and Environmental Microbiology, February 2000, p. 643-650, Vol. 66, No. 2
National Institute of Bioscience and
Human-Technology, Agency of Industrial Science and Technology,
Tsukuba, 305-8566,1 and Bio-Oriented
Technology Research Advancement Institution, Omiya,
331-8537,2 Japan
Received 26 July 1999/Accepted 16 November 1999
We characterized the intracellular symbiotic microbiota of the
bamboo pseudococcid Antonina crawii by performing a
molecular phylogenetic analysis in combination with in situ
hybridization. Almost the entire length of the bacterial 16S rRNA gene
was amplified and cloned from A. crawii whole DNA.
Restriction fragment length polymorphism analysis revealed that the
clones obtained included three distinct types of sequences. Nucleotide
sequences of the three types were determined and subjected to a
molecular phylogenetic analysis. The first sequence was a member of the
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Copyright © 2000, American Society for Microbiology. All rights reserved.
Endosymbiotic Microbiota of the Bamboo Pseudococcid
Antonina crawii (Insecta, Homoptera)
subdivision of the division Proteobacteria
(
-Proteobacteria) to which no sequences in the database
were closely related, although the sequences of endosymbionts of other
homopterans, such as psyllids and aphids, were distantly related. The
second sequence was a
-Proteobacteria sequence and
formed a monophyletic group with the sequences of endosymbionts from
other pseudococcids. The third sequence exhibited a high level of
similarity to sequences of Spiroplasma spp. from ladybird
beetles and a tick. Localization of the endosymbionts was determined by
using tissue sections of A. crawii and in situ hybridization with specific oligonucleotide probes. The
- and
-Proteobacteria symbionts were packed in the cytoplasm
of the same mycetocytes (or bacteriocytes) and formed a large mycetome (or bacteriome) in the abdomen. The spiroplasma symbionts were also
present intracellularly in various tissues at a low density. We
observed that the anterior poles of developing eggs in the ovaries were
infected by the
- and
-Proteobacteria symbionts in a
systematic way, which ensured vertical transmission. Five representative pseudococcids were examined by performing diagnostic PCR
experiments with specific primers; the
-Proteobacteria
symbiont was detected in all five pseudococcids, the
-Proteobacteria symbiont was found in three, and the
spiroplasma symbiont was detected only in A. crawii.
*
Corresponding author. Mailing address: National
Institute of Bioscience and Human-Technology, Agency of Industrial
Science and Technology, Tsukuba, 305-8566, Japan. Phone:
81-298-54-6087. Fax: 81-298-54-6080. E-mail:
fukatsu{at}nibh.go.jp.
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