Coexistence of two novel resistance plasmids, bla_KPC-2-carrying p14057A and tetA(A) -carrying p14057B, in Pseudomonas aeruginosa

KEYWORDS:

• KPC-2
• multidrug resistance
• plasmid
• Pseudomonas aeruginosa
• tetA

Klebsiella pneumoniae carbapenamases (KPCs) are class A β-lactamases that efficiently hydrolyze almost all β-lactams including carbapenems, with exception of cephamycins. The bla_KPC genes were initially discovered in K. pneumoniae in 1996 and have been frequently detected all over the world in particular among the species belonging to the family Enterobacteriaceae.¹ KPC-producing Pseudomonas aeruginosa isolates were initially found in 2006 from Colombia and increasingly being reported in South America, North America, the Caribbean islands, and China,^2,3 indicating a potential worldwide spread of KPC-producing P. aeruginosa. The bla_KPC genes from P. aeruginosa are located on chromosome or plasmids.⁴ Up to now, five fully sequenced bla_KPC-carrying plasmids from P. aeruginosa are available in public databases: two IncP-6 plasmids pCOL-1 (accession number KC609323) and p10265-KPC (accession number KU578314) from Colombia⁵ and China,⁶ respectively, two IncU plasmids pPA-2 (accession number KC609322) and pD5170990 (accession number KX169264) from Colombia⁵ and Brazil, respectively, and pBH6 (accession number CM003767; it could not be assigned into any of known incompatibility groups) from Brazil.⁷ Each of pCOL-1, p10265-KPC, pPA-2, and pBH6 contains the sole resistance gene bla_KPC-2, while pD5170990 carries bla_KPC-2, strAB (aminoglycoside resistance), cmx (chloramphicol resistance), qacED1 (quaternary ammonium compound resistance), and sul1 (sulphonamide resistance).

The tet loci responsible for inducible tetracycline resistance commonly contain a tetA gene encoding the transmembrane tetracycline efflux protein, and a tetR gene encoding the tetracycline repressor.⁸ At least 38 different classes (A, B, etc) of tet efflux have been identified, giving the designations tetA(A)-tetR(A), tetA(B)-tetR(B), etc.⁸ In P. aeruginosa, the class A tetracycline resistance module tetA(A)-tetR(A) has been detected in only IncP-1α plasmids, including RP1/RP4/R18/R68/RK2 (identical to each other; accession number L27758) from United Kingdom,⁹ pBS228 (accession number AM261760) from Russia,¹⁰ and R1033 (accession number HM804085) from Spain;¹¹ among them RP1/RP4/R18/R68/RK2 and pBS228 were fully sequenced. This study dealt with detailed genomic characterization of two novel plasmids p14057A and p14057B found in a single clinical P. aeruginosa isolate.

On January 1st 2016, a middle-aged male with acute epigastric pain, which occurred upon nocturnal excessive drinking, was hospitalized in a local hospital in Nanjing City, China, and diagnosed to have acute pancreatitis. The symptoms of severe respiratory/renal failure and obnubilation progressed although the patient received the rehydration, acid suppression, and anti-inflammatory therapies. The patient was transferred to Jinling Hospital on January 3rd and received a series of symptomatic treatments, especially including continuous (until January 27th) and subsequent intermittent (until February 7th) mechanical ventilation, and repeated abdominal cavity drainage (until February 18th), and his symptoms associated with pancreatitis gradually improved. The patient started to suffer again from fever and respiratory difficulty since January 13th and was diagnosed to have ventilator-associated pneumonia. P. aeruginosa 14057 was isolated from the sputum specimens after repeated sampling and cultivation from January 13th to 15th. Bacterial species was confirmed by 16S rRNA gene sequencing¹² and PCR detection of P. aeruginosa-specific oafA gene.¹³ According to antimicrobial susceptibility test results (see below), the patient received intravenous administration with amikacin plus ceftriaxone, and his symptoms associated with pneumonia progressively disappeared.

The major plasmid-borne carbapenemase genes were screened for by PCR,¹⁴ followed by amplicon sequencing on ABI 3730 Sequencer (LifeTechnologies, CA, USA). Out of all the carbapenemase genes tested, only bla_KPC-2 was detected in the 14057 isolate.

Plasmid DNA was isolated from the 14057 isolate using a Qiagen large construct kit, followed by sequencing from a mate-pair library with average insert size of 5,000 bp, using a MiSeq sequencer (Illumina, CA, USA). Sequence assembly and annotation were performed as described previously.¹⁵ The contigs were assembled using Newbler 2.6.¹⁶ Open reading frames and pseudogenes were predicted using RAST 2.0¹⁷ combined with BLASTP/BLASTN¹⁸ searches against the UniProtKB/Swiss-Prot database¹⁹ and the RefSeq database.²⁰ Annotation of resistance genes, mobile elements, and other features was carried out using online databases including CARD,²¹ ResFinder,²² BacMet,²³ ISfinder,²⁴ INTEGRALL,²⁵ and the Tn Number Registry.²⁶ Multiple and pairwise sequence comparisons were performed using MUSCLE 3.8.31²⁷ and BLASTN, respectively. Gene organization diagrams were drawn in Inkscape 0.48.1.

It was revealed that the 14057 isolate harbored two circularly closed DNA sequences, designated p14057A and p14057B, which were 51,663 bp and 35,306 bp in length with mean G+C contents of 59.2% and 56.8% and contained 65 and 43 predicted ORFs, respectively (Fig. 1). The modular structure of each of p14057A and p14057B was discriminated as the backbone regions with insertion of a single accessory module, namely the bla_KPC-2 region and the tetA(A) region, respectively (Fig. 1). The accessory modules were defined as acquired DNA regions associated with and bordered by mobile elements.

Figure 1. Schematic map of p14057A and p14057B. Genes are denoted by arrows, and the backbone and accessory module regions are highlighted in black and color, respectively. The innermost circle presents GC-skew [(G-C)/(G+C)], with a window size of 500 bp and a step size of 20 bp. The next-to-innermost circle presents GC content. Shown also are backbone and accessory modules.

The backbones of p14057A and p14057B, 40.6 kb and 29.7kb in length, respectively, showed very low levels of similarity (≤11% query coverage) to DNA sequences available in public sequence databases. Located in the p14057A backbone were repA and its iterons responsible for plasmid replication initiation, parAB for plasmid partition, higBA encoding the toxin-antitoxin system for post-segregational killing, and a 27-kb conjugal transfer region that harbored tivB genes encoding a type IV secretion system.²⁸ The p14057B backbone contained genes involved in plasmid replication initiation (repA and its iterons) and maintenance (parAB, higBA, xerC, xamIM, and umuCD), but lacked those for conjugal transfer. xerC encoded a site-specific recombinase helping to resolve DNA dimers into monomers after termination of replication.²⁹ xamIM encoded a restriction-modification system involved in post-segregational killing.³⁰ umuCD encoded the SOS stress-inducible DNA polymerase for DNA lesion bypass.³¹ The deduced RepA proteins of p14057A and p14057B had the highest matches (>97% amino acid similarity) to two different P. aeruginosa RepA proteins (accession numbers ERX63685 and WP_059309776.1), respectively. All the above replication proteins could not be assigned into any of known incompatibility groups.

The bla_KPC-2 region (Fig. 2) of p14057A was organized in order of a 3.5-kb partial region of the Tn1403 backbone, a 6.5-kb ΔTn6296 region, and an IS6100 element. Tn1403 was a multi-drug resistant transposon with insertion of In28 within the resolution (res) site and that of Tn5393c within orfB.³² Insertion of foreign MDR regions at the sites within res and other regions generated Tn1403 derivatives such as Tn6060, Tn6061, Tn6162 and Tn6249 in P. aeruginosa.³³ The ΔTn3:ISKpn27 to ΔrepB region represented a core bla_KPC platform, and its insertion into the mcp gene of the cryptic transposon Tn1722 carried in Tn1721,³⁴ leaving mcp to be truncated, generated the prototype Tn6296 as observed in pKP048.³⁵ Various Tn6296 derivatives with different deletions, insertions and rearrangements had been found in KPC-encoding plasmids from China.^6,36 In p14057A, ΔTn6296 manifested as a partial fragment of Tn6296 and consisted of res and the core bla_KPC platform with further truncation of Tn3 (likely resulted from its connection with downstream IS6100), while the partial Tn1403 backbone region was composed of the 38-bp inverted repeat left (IRL) and the core transposition module tnpA (transposase)-tnpR (resolvase) lacking res. Both Tn1403 and Tn6296 belonged to the Tn21 subgroup of the Tn3 family, and their terminal inverted repeats and core transposition modules shared significant nucleotide sequence homology, which might facilitate homologous recombination between Tn1403- and Tn6296-like elements, generating the bla_KPC-2 region of p14057A.

Figure 2. The accessory regions of p14057A and p14057B and comparison to related genetic contents. Genes are denoted by arrows. Genes, mobile elements and other features are colored based on function classification. Shading denotes regions of homology (>95% nucleotide identity). Numbers in brackets indicate the nucleotide positions within the corresponding plasmids. The accession numbers of Tn1721, Tn3, Tn6296, and Tn1403 for reference are X61367, HM749966, FJ628167, and AF313472, respectively.

The tetA(A) region (Fig. 2) of p14057B was organized sequentially as an 150-bp remnant of ISPst3, a 5.5-kb ΔTn1721 region, orf453, orf1158, orf642, a 201-bp remnant of ISEcp1, and an 1.4-kb remnant of a novel Tn3-family transposon core transposition module. Tn1721 was also a member of the Tn21 subgroup of Tn3 family, and had an unusual structure that included three 38-bp IR elements and a partial duplication of the tnpA gene.³⁴ Tn1722 was a independently transposable transposon with an IRL-tnpAR-res-mcp-IRR structure and located at the 3'-region of Tn1721, while the other end of Tn1721 included the pecM-tetA(A)-tetR(A) region, which represented a core genetic platform of class A tetracycline resistance genes.³⁴ The ΔTn1721 region was a 3'-terminal resistance fragment of Tn1721,³⁴ and carried the class A tetracycline resistance module tetA(A)-tetR(A). This is the first report of detecting tetA(A) and tetR(A) in P. aeruginosa from China.

Plasmids were transferred in attempt from the 14057 isolate into Escherichia coli TOP10 or DH10B and EC600 (highly resistant to rifampicin) through electroporation and conjugal transfer, respectively.¹⁵ For selection of electroporant or transconjugant containing tetA(A) or bla_KPC, 10 μg/ml tigecycline, 2 μg/ml imipenem, and 1000 μg/ml rifampicin were used in accordance with specific circumstances. Neither p14057A nor p14057B could be transferred into EC600 through conjugal transfer. p14057A was transferred into TOP10 through electroporation, yielding the bla_KPC-2-carrying electroporant TOP10(p14057A), but p14057B could not be transferred into DH10B. Activity of Ambler class A/B/D carbapenemases in bacterial cell extracts was determined by a modified CarbaNP test.¹⁵ Both 14057 and TOP10(p14057A) had the activity of class A carbapenemase, which was attributable to production KPC-2 enzyme (data not shown). Bacterial antimicrobial susceptibility was tested by the broth dilution method, and interpreted as per CLSI guidelines.³⁷ The 14057 isolate was resistant to ampicillin, ceftazidime, imipenem, aztreonam, azithromycin, minocycline, ciprofloxacin, trimethoprim, and sulfamethoxazole, but susceptible to amikacin, tigecycline, and colistin; TOP10(p14057A) was resistant to ampicillin, ceftazidime, imipenem, and aztreonam, but susceptible to all the other drugs tested (Table 1).

Table 1. Antimicrobial drug susceptibility profiles.

	MIC (mg/L)/antimicrobial susceptibility
Antibiotics	14057	TOP10 (p14057A)	TOP10
Ampicillin	>1024/R@	512/R	<4/S
Ceftazidime	512/R	16/R	<4/S
Imipenem	32/R	8/R	<1/S
Aztreonam	>512/R	32/R	<4/S
Azithromycin	32/R@	<4/S	<4/S
Minocycline	128/R@	4/S	4/S
Ciprofloxacin	8/R	<1/S	<1/S
Trimethoprim	4/R@	<0.25/S	<0.25/S
Sulfamethoxazole	76/R	4.75/S	4.75/S
Amikacin	<8/S	<8/S	<8/S
Tigecycline	<1/S	<1/S	<1/S
Colistin	<1/S	<1#	<1#

Note.

S = sensitive; R = resistant; R@ = intrinsically resistant; # = clinical breakpoints non-available

p14057A appears to be potentially self-transmissible due to the fact that is harbors a potentially complete set of conjugative transfer genes. p14057B seems unlikely to be self-transmissible because it contains none of putative mobilization or conjugal transfer regions. Each of these two plasmids carries a single accessory module, namely the bla_KPC-2 region and the tetA(A) region, respectively, and these two resistance genes serve as the sole resistance determinant of the corresponding plasmid. The core genetic environments of bla_KPC-2 and tetA(A)-tetR(A) have been well characterized previously, but they are connected with additional transposon- and insertion sequence-like elements to generate the novel bla_KPC-2 and tetA(A) regions inserted in p14057A and p14057B, respectively, which might be resulted from complex recombination events. These two accessory resistance regions cannot be identified as native transposition units because they lack paired terminal inverted repeats at both ends. Co-existence of two different resistance plasmids has been reported in the clinical P. aeruginosa isolates from India,^38,39 but none of these plasmids were sequenced. This work presented the first two fully sequenced resistance plasmids coexisting in P. aeruginosa, which is a significant cause of nosocomial infection. Data presented here provides a deeper insight into how P. aeruginosa becomes drug-resistant by diversified mechanisms, and illustrates the way that genomic sequence analysis allows assessment of the genetic basis of plasmid-mediated resistance profile and appears to eventually promote establishment of successful antimicrobial treatment.

Nucleotide sequence accession numbers: The p14057A and p14057B sequences were submitted to GenBank under accession numbers KY296095 and KY296096, respectively.

Disclosure of potential conflicts of interest

No potential conflicts of interest were disclosed.

Funding

This work was supported by the Special Key Project of Biosafety Technologies (2017YFC1200800) for the National Major Research & Development Program of China.