Moreover, the occurrence of fragmented 23S rRNA correlated with the presence of an IVS within the 23S rRNA genes. It was described that the presence of transcribed spacers is common in Tozasertib ic50 Campylobacter spp. (59%; n = 21 C. jejuni and n = 11 C. coli) [19]. All Campylobacter isolates containing transcribed spacers in their 23S rRNA gene sequences produced fragmented

23S rRNAs [19]. Most recently, among 104 strains of C. coli from turkeys, 69 strains harbored Bucladesine solubility dmso IVSs in all three 23S rRNA genes, whereas the other 35 strains lacked IVSs from at least one of the genes [20]. We have already reported the absence of IVSs shown in both the helix 25 (first quarter) and 45 (central) regions within 23S rRNA genes among a total of 65 isolates of C. lari [n = 38 urease-positive thermophilic Campylobacter (UPTC) [21] and n = 27 urease-negative (UN) C. lari] obtained from different sources and in several countries, by using PCR amplification, TA cloning and sequencing procedures [22]. In addition, the intact 23S rRNA was also identified in the C. lari isolates examined, resulting in no production of the fragmented 23S rRNA [22]. Thus, it would be important to clarify the molecular biological entities of the occurrence and the sequence structures of IVSs within the 23S rRNA genes in the

much more isolates of several other species Caspase Inhibitor VI mouse than C. lari of the genus Campylobacter including atypical species. However, studies on molecular characterization and comparative analysis of IVSs within the 23S rRNA genes and these 23S rRNA fragmentations in much more than 200 Campylobacter isolates of C. jejuni, C. coli, C. fetus, and some other atypical Campylobacter species, namely C. upsaliensis, C. hyointestinalis, C. sputorum biovar sputorum, biovar fecalis, biovar paraureolyticus, C. concisus and C. curvus have not yet been reported. Therefore, we aimed to clarify molecular characteristics of IVSs within the 23S rRNA gene sequences and 23S rRNA fragmentations in these campylobacters other than C. lari, which has already been demonstrated not to harbor any

IVSs [22]. In addition, the authors wished to comparatively analyze the IVSs among the Campylobacter organisms. SPTBN5 Results IVSs in the helix 25 region In the present study, two PCR primer pairs, f-/r-Cl23h25, designed to generate the helix 25 (first quarter) and, f-/r-Cl23h45, the helix 45 (central) regions within the 23S rRNA gene sequences with the 204 Campylobacter isolates were employed. When PCR was first carried out on the 204 isolates using the primer pair (f-/r-Cl23h25), amplicons were generated. Some of the examples are shown in Fig. 1. Following sequencing and analysis, only the four cases, C. sputorum biovar sputorum LMG7975 and biovar fecalis LMG8531, LMG8534 and LMG6728 isolates, were shown to carry IVSs in the helix 25 region among these isolates of more than 200. The sequence data in the helix 25 region from C. sputorum isolates are aligned in Fig. 2. As shown in Fig.