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We read with interest an article reporting the novel detection of tet(A) among thermophilic Campylobacter spp. poultry isolates in Iran [1] and the subsequent detection of tet(A) among a pool of Campylobacter spp. chicken isolates in Kenya [2]. It is a timely reminder of emerging antibiotic resistance associated with the mobilisation of genes from other bacterial genera. However, we believe that it remains to be determined whether tet(A) exists among thermophilic Campylobacter spp.

Tetracycline-containing therapeutics are the most commonly administered antimicrobial in poultry production and animal husbandry in Ireland, used for the treatment of enteric, respiratory and dermal infections [3, 4]. Tetracycline resistance in Campylobacter spp. is usually mediated by a ribosomal protection protein Tet(O), which confers resistance by preventing tetracycline ribosomal binding, thus abolishing the inhibitory effect of the antibiotic by preventing bacterial protein synthesis via association of aminoacyl tRNA with the bacterial ribosome [3, 5].

In our study, during the investigation of antibiotic resistance mechanisms among a sample of 350 Irish broiler Campylobacter spp. isolates, we were especially interested in tetracycline resistance genes, as resistance to tetracycline was most prevalent (34%) by phenotypic sensitivity testing (Unpublished 2019). Tetracycline-resistant isolates were preliminarily screened for the presence of tet(O), using the method described by Aminov et al. [6] and it was determined that 100% of tetracycline-resistant isolates harboured the tet(O) gene. However, accessory tetracycline-resistance mechanisms were considered as minimum inhibitory concentrations ranged from 4 to ≥ 64 mg/L. Moreover, the mobilisation of tetracycline-resistant determinants is associated with the presence of tet genes on plasmids [3]. Hence, the tet(A) gene, which codes for an efflux protein and has been reported to co-exist with tet(O) in Campylobacter, was considered as part of the investigation [1, 2]. However, we seek clarification about the results published in the referenced articles [1, 2], and the true prevalence of tet(A) among thermophilic Campylobacter spp.

We tested the tet(A) primers described by Abdi-Hachesoo et al. [1] (Table 1) but they failed to produce an amplicon using the positive control strain Escherichia coli K12 SK1592 containing the pBR322 plasmid (DSM 3879). In addition, a selection of tetracycline-resistant thermophilic Camplyobacter spp. isolates also failed to generate an amplicon. New tet(A)-targeting primers were thus designed on SnapGene2.3.2, based on homologous regions of the tet(A) gene from the pBR322 plasmid (GenBank J01749.1) and from the Pseudomonas putida strain Fars110 (GenBank JN937120.1) (Table 1)—the latter strain having been reported by Abdi-Hachesoo et al. [1] as a tet(A) positive control. A 407 bp product was successfully amplified using the new primers (Tet(A)-Camp-F and Tet(A)-Camp-R) with the E. coli K12 positive control strain but none of the tetracycline-resistant thermophilic Camplyobacter spp. isolates generated a product.

Table 1 Primer used for the detection of tet(O) and tet(A)
Full size table

With reference to the methods used in our study, DNA was extracted using PureLink™ Genomic DNA Mini Kit (Invitrogen, CA, USA). PCR mixtures (50 µL) contained 2.5U Amplitaq™ DNA polymerase (Applied Biosystems, CA, USA), 1× buffer I (Applied Biosystems, CA, USA), 2.5 mM magnesium chloride, 0.2 mM of each dNTP (Sigma Aldrich, MO, USA), 200 µM forward and reverse primer (Table 1) and 1 µL of genomic DNA (between 50 and 100 ng/µL starting concentration). The PCR cycling conditions were: 95 °C for 2 min, 35 cycles of 94 °C for 30 s, annealing temperatures as described in Table 1 for 30 s, 72 °C for 1 min and final extension at 72 °C for 5 min. Amplified tet(O) and tet(A) products were resolved by electrophoresis in a 2% and a 1.5% agarose gel, respectively. All primers used are listed in Table 1.

The failure of the tet(A) primers listed by Abdi-Hachesoo et al. [1] to produce an amplicon with the same E. coli (DSM 3879 positive control strain), under less stringent conditions, prompted further investigation within our study. In the Abdi-Hachesoo et al. [1] publication, the original tet(A) primer (Tet(A)-F and Tet(A)-R) reference is not listed in their bibliography, although these primers were previously reported by Maynard et al. [7] for the detection of tet(A) among Canadian swine E. coli isolates (Table 1) [1, 7].

We scanned the C. coli and C. jejuni tet(A) sequences, Shiraz3 and Shiraz4 (GenBank accession numbers JX891463.1 and JX891464.1, respectively) deposited in GenBank in the Abdi-Hachesoo et al. [1] publication against all Campylobacteraceae (taxid 72294) sequences using BLASTn. Multiple tet(O) sequences were returned with 100% identity, including C. jejuni 81-176 (GenBank NG_048260.1). Furthermore, our alignment studies using SnapGene2.3.2 demonstrated absolute homology between tet(O) (GenBank M18896.2) and Shiraz3 and 4 tet(A) sequences (GenBank JX891463.1 and JX891464.1, respectively). We propose that the true identity of the Shiraz 3 and 4 sequences are Campylobacter tet(O).

Furthermore, in 2016, a second study reporting a high prevalence of tet(A) among thermophilic Campylobacter spp. isolated from extensively reared Kenyan broilers was published by Nguyen and coworkers [2]. In that study, the tet(A) primers included the same primers as those used by Abdi-Hachesoo et al. [1] (but they produced an anomalous amplicon size) and a second set of in-house designed tet(A) primers (designated tet-A-1 and tet-A-2) [2]. However, the primers designed by Nguyen et al. [2] were based on the Shiraz 3 and 4 sequences (GenBank JX891463.1 and JX891464.1, respectively) [1], which we clarified above as tet(O). To confirm this, we performed an in silico PCR using SnapGene2.3.2 with the tet-A-1 and tet-A-2 primers [2] and Campylobacter tet(O) sequences (GenBank M18896.2 and NG_048260.1). A 486 bp product was predicted, which correlates to the amplicon length reported by Nguyen et al. [2]. We believe that this reported high prevalence of tet(A) among this subset (n = 53) of thermophilic Campylobacter isolates is erroneous. Our opinion also explains why clusters of tet(A) harbouring Campylobacter spp. isolates are not described in any database, to our knowledge.

In conclusion, further study would be required to determine whether the homology between tet(A) potentially present in Campylobacter and known tet(A) genes would be sufficient to allow amplification using the primers designed in our study. The investigation of alternative Campylobacter-associated tetracycline resistance mechanisms is certainly worthwhile, but the presence of tet(A) in Campylobacter spp. is an open question.