The RND efflux pump AcrAB has been documented to be associated with tigecycline resistance in different strains. One study conducted transposon-mutagenesis of tigecycline resistant clinical Enterobacter cloacae isolates to obtain susceptible mutants (Keeney et al., 2007). The results indicated that mutants had transposon insertions in the acrA or acrB genes, whereas the complementation of the acrAB cloning plasmid restored their resistance phenotypes. Further RNA blotting demonstrated that the acrAB transcription was elevated in all strains exhibiting reduced tigecycline susceptibility. The overexpression of acrAB was observed to be associated with an increase in the expression of the transcriptional regulatory gene ramA, suggesting that tigecycline resistance in E. cloacae is a consequence of RamA-mediated overexpression of the AcrAB efflux pump. Liu et al. also demonstrated that the overexpression of regulatory genes ramA and soxS was associated with heterogeneous resistance to tigecycline (Liu et al., 2019). It was observed that the AcrAB and OqxAB efflux pumps were notably overexpressed in carbapenem-resistant tigecycline heterogeneous resistant E. cloacae, in which the increased expression of their regulatory genes ramA and/or soxS was presumed to be a key factor in the heterogeneous resistance of tigecycline.

In Escherichia coli, it has been reported that the transcriptional activator MarA is associated with the overexpression of the AcrAB efflux pump (Keeney et al., 2008). The transcriptional analysis of homozygous clinical isolates isolated from the same patient revealed that the expressions of marA, acrA, acrB, and tolC were significantly increased in strains with higher tigecycline minimum inhibitory concentrations (MICs). Transposon mutagenesis was also employed to generate tigecycline susceptible mutants, with the analysis revealing that the majority of which were marA or AcrB inactivated. Further sequence analysis showed a single nucleotide insertion (354_355insC) in the open reading frame of the marR gene in E. coli with higher tigecycline MICs, suggesting that the overexpression of MarA and AcrAB caused by the loss of MarR function due to the frame-shift mutation might, in turn, reduce the susceptibility to tigecycline. Furthermore, the AcrEF efflux pump in E. coli has been documented to be associated with decreased tigecycline sensitivity (Hirata et al., 2004). A series of research has identified that the loss-of-function mutation in the protease Lon in Klebsiella pneumoniae, E. coli, and Salmonella typhimurium can also cause tigecycline resistance (Nicoloff and Andersson, 2013; Fang et al., 2016; Linkevicius et al., 2016). Lon is involved in the degradation of MarA, and its inactivation leads to the overexpression of MarA and increases the expression of the AcrAB efflux pump, which in turn may result in resistance.

The overexpression of AcrAB and AcrEF in Salmonella enterica also results in tigecycline resistance (Horiyama et al., 2011). Horiyama et al. investigated the tigecycline MICs of S. enterica strains that overexpress or delete efflux pump and regulatory genes. The deletion of acrAB was found to increase the susceptibility to tigecycline, while the complementation of both acrAB and acrEF would restore the MIC in the deletion strains. Both the overexpression of ramA and the deletion of the negative regulatory gene ramR decreased the susceptibility but remained unchanged in the acrAB-deletion strains, suggesting that AcrAB and AcrEF confer resistance to tigecycline in S. enterica with the regulation of RamA and RamR. Moreover, the overexpression of the AcrAB efflux pump, which is the result of frame-shift and deletion mutations in ramR and amino acid substitution mutations in ramA, is the primary cause of tigecycline resistance in E. aerogenes (Veleba et al., 2013). Decreased tigecycline susceptibility caused by ramR mutations has also been observed in E. hormaechei (Gravey et al., 2020). Gravey et al. found an E. hormaechei isolate developed tigecycline resistance in a hospitalized patient after treatment without any relevant resistance genes acquisition except for a 16 bp deletion in ramR, which resulted in the overexpression of RamA, AcrAB, and TolC, as well as the downregulated expression of pore protein OmpF. This indicated that partial deletion of the ramR can lead to the overexpression of RamA, which in turn causes the increased efflux of AcrAB-TolC and decreased antibiotic permeability through OmpF, collectively contributing to tigecycline resistance.

AcrAB overexpression associated with tigecycline resistance in K. pneumoniae is frequently accompanied by the increased transcription of ramA and the inactivation mutations of ramR, and overexpression of the global regulators rarA and marA (Bratu et al., 2009; Hentschke et al., 2010b; Veleba et al., 2012a; Roy et al., 2013; Sheng et al., 2014; Villa et al., 2014; Zhong et al., 2014; Wang et al., 2015; Fang et al., 2016). Sequence analysis revealed that approximately 83% of tigecycline non-susceptible K. pneumoniae carried mutations in ramR and/or local repressor acrR, including missense or nonsense mutations, insertions, and deletions in ramR, as well as amino acid substitutions and frame-shift mutations in acrR. The results of real-time quantitative PCR (RT-qPCR) demonstrated increased expression of the acrB in all resistant strains, indicating that the combination of RamR and AcrR mutations might be involved in the reduced susceptibility to tigecycline (Moghimi et al., 2021). Mutations in the acrR gene may also be related to tigecycline non-susceptibility. Through the antimicrobial susceptibility tests in the presence of the efflux pump inhibitor, Zhang et al. isolated an efflux pump-related tigecycline non-susceptible K. pneumoniae strain only with a frame-shift mutation in acrR caused by a 2 bp deletion, suggesting that the acrR gene mutation might be associated with reduced tigecycline susceptibility (Zhang et al., 2021c). Furthermore, mutations in the negative regulatory genes ramR and soxR were also found to be relevant with tigecycline heterogeneous resistance in K. pneumoniae (Zhang et al., 2021a). A heterogeneous resistance subpopulation was identified in tigecycline-sensitive K. pneumoniae by the disk diffusion method, in which mutations in ramR and soxR were found. The mutations would induce the expression of ramA and soxS, which in turn would cause the overexpression of AcrAB-TolC, thereby resulting in tigecycline heterogeneous resistance and resistance.

OqxAB is also a class of RND efflux pumps that have been involved with tigecycline resistance. Previous study has investigated the expression of efflux pumps and regulatory genes in tigecycline-resistant K. pneumoniae by RT-qPCR (Zhong et al., 2014). The results presented that the susceptible strains exhibited higher expression levels for both oqxB and the regulatory gene rarA in OqxAB. For isolates with MICs up to 8 mg/L, the AcrAB-TolC efflux pump plays the most important role in tigecycline resistance, in contrast, both the AcrAB-TolC and OqxAB efflux pumps are required for isolates with MICs ≥ 16 mg/L. The overexpression of rarA in K. pneumoniae has been reported to upregulate the neighboring OqxAB efflux pump, resulting in tigecycline resistance (Veleba and Schneiders, 2012b). The knockout of another regulator ramA showed a slight increase in tigecycline susceptibility, further resistance screening revealed that the transcription of oqxAB, acrAB, rarA, and marA were significantly elevated in the resistant strains (Veleba and Schneiders, 2012b). This indicated that regulators RarA and MarA provide an alternative pathway for tigecycline resistance in K. pneumoniae. Chen et al. also found OqxAB efflux pump was associated with tigecycline heterogeneous resistance in S. enterica (Chen et al., 2017). The addition of the efflux pump inhibitor restored the susceptibility of tigecycline and reduced its accumulation in the cells, suggesting that the heterogeneous resistance was due to the overexpression of the AcrAB-TolC and OqxAB efflux pumps (Chen et al., 2017).

It has been reported that the overexpression of three RND efflux pumps, AdeABC, AdeFGH, and AdeIJK, is associated with tigecycline resistance in Acinetobacter baumannii (Coyne et al., 2011). AdeABC plays a significant role in the efflux of tigecycline, while the two-component system AdeSR, which contains a sensor kinase protein AdeS and a regulatory protein AdeR, regulates the transcription of the efflux pump. In contrast, AdeFGH is regulated by the LysR-type transcriptional regulator AdeL, and AdeIJK is regulated by the TetR transcriptional regulator AdeN. Many previous studies have found that the tigecycline resistance caused by elevated levels of efflux pump transcription may be related to amino acid substitutions or insertions of insertion sequences (ISs) in regulatory genes (mutation sites are shown in Table 2 ) (Coyne et al., 2010; Rumbo et al., 2013; Yoon et al., 2013; Yoon et al., 2015; Sun et al., 2016; Hua et al., 2021; Lucaßen et al., 2021a; Lucaßen et al., 2021b; Salehi et al., 2021). The most common insertion sites for ISAba1 are positions 371, 379, 422, and 430 of adeS and positions 52, 200, and 402 of adeR. Nevertheless, the tigecycline resistance resulting from the ISAba1 insertion at adeS is prone to instability during successive passages in the absence of tigecycline, which belongs to heterogeneous resistance, and can be reversed to a susceptible strain by additional insertion of ISAba1 into adeR (Jo and Ko, 2021).

The most prevalent and widely distributed mechanism identified is the inactivation of the AdeIJK repressor gene adeN, which may have been caused by premature stop codon resulting from ISs insertion or nucleotide deletion. In contrast, mutation or inactivation of the AdeABC regulatory system adeRS occurs less frequently but is often associated with higher tigecycline MICs (Lucaßen et al., 2021a). Lucaßen et al. have evaluated the effect of frequently reported amino acid substitutions on adeB expression, efflux activity, and tigecycline susceptibility through the construction of related knockout and complementary strains (Lucaßen et al., 2021b). The complementation of D26N mutant AdeR and T156M mutant AdeS into the adeRS knockout strain led to higher tigecycline MICs as well as a significant increase in adeB expression and antibiotic efflux. Conversely, the complementation with D21V mutant AdeR did not affect the susceptibility or efflux pump expression, indicating that amino acid substitutions D26N (AdeR) and T156M (AdeS) disrupted their regulatory functions and impacted the efflux. Another two-component regulatory system baeRS has also been shown to affect the tigecycline susceptibility in A. baumannii through the upregulation of adeAB (Lin et al., 2014). In addition to the aforementioned transcriptional regulators, the expression of adeABC can be overexpressed under low iron environments, indicating the potential for additional regulation of the efflux pump by iron (Modarresi et al., 2015).

The global regulator SoxR has been reported to increase tigecycline susceptibility by affecting the expression of efflux pumps (Li et al., 2017). Li et al. compared the molecular characterization between MDR and tigecycline susceptible A. baumannii strains and found that the frequency of the G39S mutation in SoxR was higher in MDR strains. Further overexpression of soxR revealed a minor decrease in tigecycline MIC and a reduction in the expression of the efflux pump genes adeJ and adeG, the small multidrug resistance family gene abeS, and the multidrug and toxic compound extrusion gene abeM, suggesting that SoxR might act as a negative regulator of efflux pump and contribute to tigecycline resistance in A. baumannii.

Moreover, the overexpression of the Ade efflux pump has been documented in A. nosocomialis and A. pittii. One study investigated the contribution of the RND efflux pump to tigecycline resistance in A. nosocomialis, focusing on the expression of the RND efflux pump and the adeR mutation (Yang et al., 2019). The RT-qPCR results revealed that tigecycline non-susceptible isolates exhibited a significantly increase transcription of adeB compared to susceptible ones, indicating that AdeABC was the major efflux pump related with tigecycline non-susceptible in A. nosocomialis. Further comparative sequence analysis identified five amino acid substitutions in AdeR and AdeS, including S16N and H56L in AdeS, D299N, T137N, and A220E in AdeR. The significant increases in the transcription of adeB and adeJ correlated with tigecycline resistance were also observed in tigecycline resistant A. pittii (Ding et al., 2022).

There are three intrinsic RND efflux pumps, namely SdeAB, SdeCDE, and SdeXY, in Serratia marcescens, whose efflux has been confirmed to be an important mechanism for tigecycline resistance (Hornsey et al., 2010). Hornsey et al. conducted the mutation screening by successive passaging under tigecycline pressure, resulting in the isolation of a mutant with a 256-fold increase in tigecycline MIC. The RT-qPCR analysis revealed that all three RND efflux pumps were overexpressed in the mutant, while the transcription of sdeXY was significantly higher than others. Further investigation of the constructed mutant indicated that the tigecycline MIC was significantly decreased when sdeY and the putative outer membrane component gene hasF were inactivated, suggesting that the overexpressed SdeXY-HasF pump was the possible reason for the tigecycline resistance in S. marcescens.

The overexpression of RND efflux pump SmeDEF is a predominant contributing factor for tigecycline resistance in Stenotrophomonas maltophilia (Blanco et al., 2019). During the experimental evolution, the tigecycline-evolved populations attained resistance through different mutational trajectories, with all initial mutations occurring in the SmeDEF repressor smeT, which might result in the overexpression of the efflux pump. An RND efflux pump, AxyEF-OprN, which mediates tigecycline efflux has also been identified in Achromobacter xylosoxidans (Nielsen et al., 2019). Following targeted AxyEF by transcriptome analysis, the study knocked down axyE and found a decrease in tigecycline MIC, demonstrating that AxyEF-OprN might efflux tigecycline and interfere with tigecycline resistance.

Previous studies have indicated that RND efflux pump gene clusters on plasmids may contribute to tigecycline resistance. Lv et al. identified a novel RND efflux pump gene cluster, tnfxB1-tMexCD1-toprJ1, on plasmids from pan-resistant K. pneumoniae (Lv et al., 2020b). The overexpression of the cluster resulted in the elimination of the in vitro and in vivo accumulation of tigecycline in bacteria, suggesting that TMexCD1-TOprJ1 could mediate tigecycline efflux and generate resistance that might lead to tigecycline treatment failure. Plasmids with TMexCD1-TOprJ1 have been discovered in Asia, Europe, and North America, indicating a risk of global spread of tigecycline resistance. Furthermore, a plasmid co-localizing tmexCD1-toprJ1 and the colistin resistance gene mcr has been reported in K. pneumoniae, which also carried an IncX3 plasmid with bla _NDM (Sun et al., 2020). The emergence of the mobile tigecycline and colistin resistance poses a substantial threat to public health, underscoring the urgent need for further global surveillance.

A novel plasmid-mediated RND efflux pump gene cluster, tnfxB2-tmexCD2-toprJ2, which exhibits high similarity to tnfxB1-tMexCD1-toprJ1, has been identified on the chromosome and plasmid of Raoultella ornithinolytica (Wang et al., 2021b). The overexpression of tmexCD2-toprJ2 demonstrated an 8-fold increase in tigecycline MIC, while the genetic environment analysis revealed its translocated potential between the plasmids and chromosomes. This cluster has been reported in various Klebsiella spp., and novel related isoforms tmexC1D1.2-toprJ1 and tmexC2D2.2-toprJ2 have also been identified in P. aeruginosa and Klebsiella spp, indicating that this plasmid-mediated tigecycline resistance mechanism has already spread among isolates and improved detection is necessary to prevent the resistance crisis (Wang et al., 2021d; Sun et al., 2022).

In addition to tmexCD1/2-toprJ1/2 and tmexCD3-toprJ3, which has been found in Proteus spp. and P. aeruginosa (Wang et al., 2021a), a fourth tmexCD-toprJ-like gene cluster, tmexCD4-toprJ4, has been identified in plasmids from K. quasipneumoniae and Enterobacter roggenkampii that mediates tigecycline resistance (Gao et al., 2022). The overexpression of tmexCD4-toprJ4 resulted in increased tigecycline efflux and MICs. Gao et al. further found that tmexCD4-toprJ4 could act synergistically with its upstream tet(A) to reduce the susceptibility. A recent epidemiological study of the clinical prevalence, genomic, and phenotypic characterization of tmexCD-toprJ has shown that among 7,517 clinical isolates collected in China, 48 isolates carried tmexCD-toprJ (0.64%), all of which were MDR and possessed other resistance genes simultaneously (Dong et al., 2022b). The presence of mobile elements in the genetic environment suggests that it may be capable of propagating among different species, prompting the necessity for monitoring and control of the further spread.

The major facilitator superfamily (MFS) efflux pumps represent another class of efflux pumps involved in tigecycline resistance. It has been demonstrated that the RND-type efflux pumps AdeABC and AdeIJK can synergize with the MFS efflux pump TetA to induce tigecycline resistance in A. baumannii (Foong et al., 2020). Foong et al. overexpressed tet(A) in the RND efflux pump knockout strains and detected decreased tigecycline MICs in tigecycline susceptible adeAB and adeIJ knockout strains, suggesting that the TetA pump played an important role in tigecycline efflux with AdeABC and AdeIJK acting in a synergistic and/or additive manner.

Mutations in the tet(A) gene have been associated with reduced tigecycline susceptibility in carbapenem-resistant K. pneumoniae (CRKP) (Chiu et al., 2017; Xu et al., 2021b; Peng et al., 2022b). Sixteen CRKP strains were found to have individual (81%) or combination (63%) mutations in ramR and tet(A) (Chiu et al., 2017). Through the complementation into the tet(A)/ramR-deficient strains, they discovered a notable elevation in tigecycline MICs in tet(A) frame-shift mutants complementary strains, meanwhile, a synergistic effect of resistance was observed in strain without ramR but a mutated tet(A) compared to the wild-type strain overexpressing the mutated tet(A). This implied that mutations in ramR and tet(A) might be the primary mechanism of tigecycline resistance and act synergistically. Another study performed whole genome sequencing of 63 CRKP isolates and chose isolates with tet(A) to conduct tigecycline resistance screening under selective pressure (Xu et al., 2021b). They identified that 71.4% of the tigecycline non-susceptible strains were found to have tet(A) mutations and exhibit high-level tigecycline resistance. These amino acid substitutions were confirmed in E. coli as the overexpression strains showed a 2-8-folds increase in tigecycline MICs.

The tigecycline resistance caused by tet(A) and ramR mutations is also present in S. enterica. Hentschke et al. discovered a tet(A) mutant that was located on a plasmid with Tn1721 in tigecycline resistance S. enterica and increased tigecycline MIC when transferred to E. coli (Hentschke et al., 2010a). The isolate also possessed a frame-shift mutation in ramR and the overexpression of the mutants did not affect tigecycline susceptibility compared to the increase when overexpressed wild-type ramR. It indicated that the resistance might related to the enhanced efflux of AcrAB through the up-regulation of RamA resulting from ramR mutation. Together with tet(A) mutation, these two mechanisms mediating low-level resistance may act synergistically, leading to high-level tigecycline resistance. The same synergetic effect has been identified in tigecycline non-susceptible S. enterica with tet(A) frame-shift mutation (Akiyama et al., 2013). This confirmed that tet(A) could decrease sensitivity to tigecycline at a low level, with ramR inactivation acting as an additional resistance mechanism that might confer high-level resistance.

Another MFS efflux pump, Tet(Y), has also been reported to be associated with tigecycline resistance in A. baumannii (Wang et al., 2021c). Whole-genome sequencing identified an isolate without any known tigecycline resistance genes and mutations but carried a novel MFS efflux pump-encoding gene, tet(Y) on its plasmid. The overexpression of tet(Y) and tet(Y) plasmid could increase the tigecycline MICs, indicating that tet(Y) is related to tigecycline susceptibility reduction. The adjacent Tn5393 in its genetic background suggested that resistance caused by the novel plasmid carrying tet(Y) might be transmitted between isolates.

Tet(L), an MFS efflux pump often reported in Gram-positive bacteria, has been discovered in Gram-negative bacteria recently. Sun et al. identified tet(L) in tigecycline-susceptible Moraxella catarrhalis, implying that it does not affect tigecycline resistance in M. catarrhalis (Sun et al., 2021). A variant of tet(L) was identified in the chromosomes of Campylobacter spp. with a prevalence rate of approximately 17%, of which the overexpression revealed a 4-fold increase in MIC (Yao et al., 2020). Genetic environment analysis revealed that the tet(L) variant was located in a genomic island with IS1216E and other resistance genes inserted into the conserved gene potB, suggesting that the variant might not only mediate resistance but also spread through horizontal gene transfer.

Except for the aforementioned common efflux pump families, novel efflux pumps associated with tigecycline resistance continue to be identified. An efflux pump, KpgABC, was identified in K. pneumoniae, which was associated with tigecycline nonsusceptibility (Nielsen et al., 2014). Following an increase in tigecycline MIC from 1 mg/L to 4 mg/L in clinical strains collected before and during patient tigecycline treatment, and no increase in the expression of known efflux pump-associated genes as revealed by RT-qPCR studies, whole-genome sequencing was performed to identify putative novel resistance genes. An IS5 insertion in the upstream of a putative efflux pump, which was named KpgABC, was identified. A 4-fold increase in MIC after overexpression of kpgABC verified its role in the reduction of tigecycline sensitivity.

An amino acid substitution mutation, V57L, in the ribosomal small subunit constitutive protein S10 encoding gene rpsJ has been identified in tigecycline resistant K. pneumoniae, which has been previously reported to relate to tetracycline resistance in Neisseria gonorrhoeae (Villa et al., 2014). This mutation is located at the tip of a conserved flexible loop consisting of amino acids 53-60 in the S10 ribosomal protein and this region is near the tigecycline target site and is associated with the ribosome binding to tigecycline. The article postulated that the mutation in rpsJ affected tigecycline susceptibility by altering the ribosome structure near the tigecycline-binding site or interfering with the coordination of Mg²⁺ ions, which resulted in reduced tigecycline binding to the 16S rRNA therefore reduced the tigecycline susceptibility. Mutations in rpsJ at V57 locus were identified in all resistant isolates through tigecycline resistance screening of E. coli, K. pneumoniae, and A. baumannii, as well as in another report about tigecycline resistant K. pneumoniae from clinical source and laboratory evolution (Beabout et al., 2015; Fang et al., 2016). Other rpsJ mutations, predominantly V57L amino acid substitutions, have been documented in S. maltophilia, K. pneumoniae, E. coli, and A. baumannii with the mutations reducing tigecycline susceptibility by affecting the structure of ribosomal protein S10 (Villa et al., 2014; Hammerstrom et al., 2015; Li et al., 2016a; He et al., 2018; Blanco et al., 2019; Xu et al., 2020; Zhang et al., 2021a). The overexpression of corresponding mutations in E. coli revealed that the majority of amino acid substitutions (V57L, V57D, and V57I) resulted in a modest elevation in tigecycline MICs, while the most pronounced increase was observed in V57L overexpression (Izghirean et al., 2021). However, none of these mutations were as significant as other resistance determinants, such as efflux pumps, on tigecycline susceptibility, suggesting that rpsJ mutation in conjunction with other resistance mutations or determinants is necessary to mediate high-level tigecycline resistance.

A report about a tigecycline resistant A. baumannii has found an amino acid substitution mutation in rrf, the gene encoding the ribosomal recycling factor RRF, with a slight reduction in tigecycline MIC after the complementation of wild-type rrf into the isolate possessed mutated rrf (Hua et al., 2021). Subsequent transcriptome analysis demonstrated that the expression levels of various genes associated with ribosome regulation, energy production, biosynthesis, and transportation increased. The western blotting and polysome profiling revealed that rrf mutants displayed a reduction in RRF expression and an accumulation of 70S ribosomes, suggesting that the mutation in rrf affected the presumed function of RRF in dissociating and recycling tigecycline-bound ribosomes, and at the same time decreased tigecycline’s binding affinity to the ribosomal A-site, leading to a decrease in tigecycline susceptibility. Hammerstrom et al. have discovered other rrf amino acid substitutions, deletion mutations, and upstream mutations in tigecycline resistant A. baumannii obtained through evolution under antibiotic stress (Hammerstrom et al., 2015). rrf mutation has also been identified in a tigecycline resistant S. maltophilia obtained under tigecycline pressure, suggesting that it might play a role in adaptation to tigecycline (Blanco et al., 2019).

In addition to the two ribosome-associated protein mutations previously discussed, mutations in the 30S ribosomal protein S21 encoding gene rpsU and in the ribosomal protein S1 encoding gene rpsA have been reported as potential contributors to tigecycline resistance in S. maltophilia (Hammerstrom et al., 2015).

It has been reported that tigecycline can maintain the binding to 16S rRNA in the presence of the ribosomal protection protein Tet(M) due to the C9-glycyl substituent hinders access of Tet(M) binding to the ribosome, which fails the ribosomal protection (Arenz et al., 2015). This ribosomal protection protein is frequently identified in tigecycline resistant Gram-positive bacteria, whereas among Gram-negative bacteria, it has only been reported to be associated with low tigecycline susceptibility in N. gonorrhoeae (Zhou et al., 2022). The tet(M) gene was carried by the plasmid of N. gonorrhoeae and the correlation analysis revealed that the carriage was significantly correlated with low tigecycline susceptibility (Zhou et al., 2022). Linkevicius et al. have found that tet(M) mutations may result in reduced tigecycline susceptibility (Linkevicius et al., 2015). They overexpressed tet(M) in E. coli and constructed mutant libraries for resistance screening that discovered 13 mutations that could cause increased MICs, in which L505 deletion mutation and the Q620R/S310P mutation combined with S508A significantly elevated tigecycline MICs. Furthermore, the Q620R/S310P combined with S508A caused the most significant MIC elevation. These mutations may contribute to tigecycline susceptibility reduction by affecting the structure and function of Tet(M).

A study about tigecycline resistance A. baumannii screening under antibiotic stress has found a frame-shift in S-adenosylmethionine (SAM)-dependent methyltransferase encoding gene trm due to the deletion mutation, which caused the truncation of the protein and reduced the susceptibility (Chen et al., 2014). The complementation of wild-type trm resulted in the restoration of susceptibility to minocycline, doxycycline, and tigecycline, indicating that the trm mutation might cause the isolate to become resistant to tetracyclines. Methyltransferases serve to safeguard the host genome from foreign DNA and play a vital role in epigenetic regulation and antibiotic resistance. They postulated that trm mutations may facilitate the emergence of tigecycline resistance by interfering with the ribosomal protein methylation. Many other tigecycline resistance-associated amino acid substitutions and deletion mutations in the trm gene have been documented in A. baumannii (Trebosc et al., 2016; Ghalavand et al., 2022).

The rpoB gene, which encodes the β subunit of DNA-dependent RNA polymerase, is evolutionarily conserved. Hua et al. have found a G136D amino acid substitution in rpoB from a tigecycline resistant A. baumannii (Hua et al., 2021). The Raman spectroscopy demonstrated that the overexpression of the mutation rpoB markedly enhanced the isolate’s tolerance to tigecycline, although it only induced a minimal reduction in tigecycline susceptibility. Further transcriptome analysis revealed that multiple transcriptional regulatory genes potentially implicated in stress response and drug resistance exhibited either increased or decreased expression, with a decreased expression of trm and a gene encoding an AcrR/TetR regulatory protein, indicating that the mutant rpoB might be involved in the regulation of trm expression and the transcriptional regulatory genes, thereby conferring resistance to tigecycline.

During the tigecycline resistance screening under antibiotic stress, a resistant A. baumannii isolate was generated, wherein a frame-shift mutation was identified in glycerol-3-phosphate acyltransferase encoding gene plsC, resulting in truncation of the protein (Li et al., 2015). The complementation of the wild-type plsC gene recovered the tigecycline MIC reduction, suggesting that plsC was related to decreased tigecycline susceptibility. The alterations in membrane potential were quantified and it implied that the mutant exhibited the highest membrane potential, while it decreased after the wild-type gene complementation, indicating that the mutation might influence the membrane permeability. They speculated that the plsC mutation mediated the tigecycline resistance primarily by affecting the phospholipid synthesis, altering the membrane, and, consequently, increasing the tigecycline permeability.

A mutation in the C13 family peptidase encoding gene abrp has been identified in tigecycline resistant A. baumannii, and the truncation of the protein might be associated with tigecycline resistance (Li et al., 2016b). They demonstrated that the abrp knockout resulted in reduced susceptibility to tigecycline and increased cell membrane permeability in the isolate, whereas complementation with wild-type abrp restored both susceptibility and cell membrane permeability. These findings implied that abrp deletion might affect the membrane permeability and consequently impact the tigecycline susceptibility.

He et al. conducted tigecycline resistance screening in the acrAB knockout and wild-type E. coli isolates and obtained resistant mutants (He et al., 2016). Sequencing analysis revealed that a 2-amino acid deletion in phospholipid translocation-related gene mlaA of the ATP-binding cassette transporter (ABC) transport system was presented in both the knockout and wild-type isolates. This mutation truncated and inactivated the MlaA protein. The tigecycline MICs of mlaA-absent strains remained unchanged, while the complementation strains demonstrated an 8-fold increase in tigecycline MIC. It led to the hypothesis that the mutation in mlaA might enhance phospholipid transfer from the outer to the inner membrane, thereby strengthening the outer membrane barrier and contributing to the resistance. Furthermore, the article identified mutations in marR and rpsJ after the mlaA mutation, suggesting that multiple resistance mechanisms can accumulate during the development of tigecycline resistance.

In another study of tigecycline resistance induced through antibiotic pressure in A. baumannii, mutations in UDP-N-acetylglucosamine dehydrogenase encoding gene gna and ABC-transporter encoding gene msbA have been identified in the obtained resistant strains and postulated to be associated with tigecycline resistance (Hammerstrom et al., 2015). gna is situated within the K motif, which encodes extracellular polysaccharide biosynthetic enzymes. This enzyme plays a role in the assembly of capsule or lipooligosaccharide (LOS). It is hypothesized that a frame-shift mutation in gna may inactivate the protein and cause structural changes in the capsular polysaccharide or LOS, affecting the rate of diffusion of tigecycline into the cell. MsbA functions as a transporter protein that facilitates the transfer of lipid A from the medial leaflet to the periplasmic side of the inner membrane. As the majority of the observed mutations are concentrated in their substrate-recognition and transmembrane regions, they postulate that mutations may enhance the specificity of the pump, thereby inducing the tigecycline efflux.

An ISAba16 insertion mutation in gnaA was also identified in high-level resistant A. baumannii (Xu et al., 2019). Even though they did not validate the function of the gene, the absence of any other tigecycline resistance-associated genes or mutations in the isolate may also corroborate the hypothesis that the gnaA mutation was correlated with resistance. In a separate study, mutations in tviB, the resistance-related gene encoding the UDP-N-acetylglucosamine dehydrogenase, were identified in A. baumannii (Lucaßen et al., 2021a). This study revealed a high degree of TviB amino acid sequence diversity in both resistant and susceptible isolates, in which a seven amino acid insertion variant might be relevant to tigecycline resistance. The presence of sequence diversity suggests that we need to be cautious in interpreting mutations in tviB and that further characterization is required.

The screening of tigecycline resistance in S. maltophilia also discovered mutations in genes encoding enzymes related to lipopolysaccharide (LPS) biosynthesis and phosphatidic acid biosynthesis, which may relate to tigecycline resistance (Blanco et al., 2019). The mutated genes included the phosphoethanolamine transferase encoding gene, lipid A biosynthesis lauroyl acyltransferase encoding gene htrB, the UDP-glucose dehydrogenase encoding gene ugd, and the diacylglycerol kinase encoding gene dgkA. They hypothesized that the mutations led to impacts on phospholipid and LPS synthesis, modifications of the bacterial outer membrane, preventing the uptake of tigecycline, and therefore increased the resistance to tigecycline.

Inactivation of the TolC-like outer membrane protein AbuO has also been reported in correlation to tigecycline resistance in A. baumannii (Srinivasan et al., 2015). Srinivasan et al. demonstrated a notable reduction in tigecycline MIC in abuO knockout strains, and the RT-qPCR analysis indicated that the expression of efflux pump genes like acrD, and regulatory genes like baeR was elevated. MerR-type transcriptional regulator SoxR binding to abuO promoter revealed that abuO in A. baumannii was regulated by SoxR.