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Microbiology 150 (2004), 1191-1195; DOI  10.1099/mic.0.26897-0
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Microbiology 150 (2004), 1191-1195; DOI  10.1099/mic.0.26897-0
© 2004 Society for General Microbiology

Intron-containing {beta}-tubulin transcripts in Cryptosporidium parvum cultured in vitro

Xiaomin Cai1, Cheryl A. Lancto3, Mitchell S. Abrahamsen3 and Guan Zhu1,2

1 Department of Veterinary Pathobiology, College of Veterinary Pathobiology, Texas A&M University, 4467 TAMU, College Station, TX 77843-4467, USA
2 Faculty of Genetics Program, Texas A&M University, 4467 TAMU, College Station, TX 77843-4467, USA
3 Department of Veterinary Pathobiology, University of Minnesota, St Paul, MN 55108, USA

Correspondence
Guan Zhu
gzhu{at}cvm.tamu.edu

The genome of Cryptosporidium parvum contains a relatively small number of introns, which includes the {beta}-tubulin gene with only a single intron. Recently, it was observed that the intron was not removed from some of the {beta}-tubulin transcripts in the late life cycle stages cultured in vitro. Although normally spliced {beta}-tubulin mRNA was detected in all parasite intracellular stages by RT-PCR (e.g. HCT-8 or Caco-2 cells infected with C. parvum for 12–72 h), at 48–72 h post-infection unprocessed {beta}-tubulin transcripts containing intact introns started to appear in parasite mRNA within infected host cells. The intron-containing transcripts could be detected by fluorescence in situ hybridization (FISH) using an intron-specific probe. The intron-containing {beta}-tubulin transcripts appeared unique to the in vitro-cultured C. parvum, since they were not detected in parasite-infected calves at 72 h. As yet, it is unclear whether the late life cycle stages of C. parvum are partially deficient in intron-splicing or the intron-splicing processes have merely slowed, both of which would allow the detection of intron-containing transcripts. Another possible explanation is that the decay in transcript processing might simply be due to the onset of parasite death. Nonetheless, the appearance of intron-containing transcripts coincides with the arrest of C. parvum development in vitro. This unusual observation prompts speculation that the abnormal intron-splicing of {beta}-tubulin transcripts may be one of the factors preventing complete development of this parasite in vitro. Furthermore, the presence of both processed and unprocessed introns in {beta}-tubulin transcripts in vitro may provide a venue for studying overall mechanisms for intron-splicing in this parasite.


Abbreviations: FAM, carboxyfluorescein; FISH, fluorescence in situ hybridization; TAMRA, carboxytetramethylrhodamine




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