Publications by authors named "Ying-wei Zhao"

Article Synopsis
  • The study aimed to find a new nucleic acid amplification test target for accurately detecting Mycobacterium tuberculosis complex (MTC).
  • Using ISSR genotyping technology, researchers obtained a specific 588 bp fragment from the MTC genome and designed primer pairs to test various mycobacterial strains.
  • Results showed that the new test could effectively distinguish MTC strains from non-tuberculous mycobacteria, with high accuracy in identifying MTC using the developed primer pairs.
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Objective: To establish inter-simple sequences repeat (ISSR) molecular makers based on (CAGCG)n repeat sequence in mycobacteria.

Methods: The distribution of pentanucleotide repeat sequence (CAGCG)n in mycobacterial genomes was analyzed by MICdb 2.0 software in the microsatellite database.

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Objective: To explore the association of spermatogenic arrest with the expression of estrogen receptor alpha (ERalpha) in human testes.

Methods: We examined the testicular biopsy specimens of 120 infertile men by HE staining, detected the expression of ERalpha in the specimens of those with spermatogenic arrest by the two-step immunohistochemical method, and compared the results with those of 10 healthy men.

Results: Of the 120 specimens from the infertile men, 31 (25.

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Objective: To compare the transcription difference of the mannitol PTS genes between epidemic and non-epidemic strains of Vibrio cholerae El Tor in mannitol ferment tests.

Methods: Growth curves of 10 epidemic strains (slow-ferment) and 10 non-epidemic strains (rapid-ferment) of Vibrio cholerae were detected in the process of fermentation test, and the transcriptional level of mannitol PTS operon of these strains were determined with quantitative reverse-transcriptional PCR.

Results: After 4 hours of test, the non-epidemic strains became positive and the average growth density of the non-epidemic strains was higher than that of the epidemic strains; however, some were still lower than the epidemic strains.

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The fermentation rates of mannitol in toxigenic and non-toxigenic El Tor strains of Vibrio cholerae are obviously different, which is a valuable indicator in the rapid identification of toxigenic strain. To determine the regulating role of mtlR in transcription of mannitol PTS operon in V. cholerae, and whether it plays a role in the ferment difference of the toxigenic and non-toxigenic strains, the mtlR deletion mutants from the mannitol rapid-ferment strain (non-toxigenic strain) and slow-ferment strain (toxigenic strain) were constructed.

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DNA sequence and the genome of phage VP3 (a typing phage of V. cholera) were analyzed. A random library of VP3 DNA was constructed by shot-gun library method.

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