2023
DOI: 10.3390/jcm12041559
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High-Throughput Sequencing of Oral Microbiota in Candida Carriage Sjögren’s Syndrome Patients: A Pilot Cross-Sectional Study

Abstract: Background: This study sought to characterize the saliva microbiota of Candida carriage Sjögren’s syndrome (SS) patients compared to oral candidiasis and healthy patients by high-throughput sequencing. Methods: Fifteen patients were included, with five Candida carriage SS patients (decayed, missing, and filled teeth (DMFT) score 22), five oral candidiasis patients (DMFT score 17), and five caries active healthy patients (DMFT score 14). Bacterial 16S rRNA was extracted from rinsed whole saliva. PCR amplificati… Show more

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Cited by 8 publications
(5 citation statements)
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“…One of the possible reasons why caries experience is higher in dry mouth participants than in controls may be changes in the microbiota due to dry mouth conditions. A 2023 study suggested that such changes are specific for patients with Sjögren’s syndrome, while another study mentioned that dysbiosis is seen in all dry mouth patients despite the etiology of their conditions [ 30 , 31 ].…”
Section: Discussionmentioning
confidence: 99%
“…One of the possible reasons why caries experience is higher in dry mouth participants than in controls may be changes in the microbiota due to dry mouth conditions. A 2023 study suggested that such changes are specific for patients with Sjögren’s syndrome, while another study mentioned that dysbiosis is seen in all dry mouth patients despite the etiology of their conditions [ 30 , 31 ].…”
Section: Discussionmentioning
confidence: 99%
“…The high concentrations of the latter species, in turn, could explain the high incidence of caries in pSS (Siddiqui et al, 2016;Singh et al, 2021). In contrast, a recent study found that dental caries and Candida carriage were independent of SS (Xing et al, 2023).…”
Section: Salivary Microbiomementioning
confidence: 97%
“…The 20 µL PCR amplification system consisted of 4 µL of 5×FastPfu buffer, 2 µL of dNTPs (2.5 mM), 0.8 µL of forward primer (5 µM), 0.8 µL of reverse primer (5 µM), 0.4 µL of FastPfu polymerase, 0.2 µL of BSA, 10 ng of template DNA, and deionized water. PCR amplification was carried out on an ABI GeneAmp ® 9700 (Applied Biosystems, Waltham, MA, USA) with the following conditions: initial denaturation at 95 • C for 3 min, 35 cycles of 95 • C for 30 s, 55 • C for 30 s, 72 • C for 45 s, and a final extension at 72 • C for 10 min [23]. The amplified products were purified using the AxyPrep DNA Gel Extraction Kit (AXYGEN Biosciences, Union City, CA, USA) [24] and then sequenced using the Illumina MiSeq platform by Major Bio (Shanghai, China).…”
Section: Pcr Amplification and Sequencingmentioning
confidence: 99%