key: cord-0072106-dndu13bm
authors: Conrads, Georg; Klomp, Tim; Deng, Dongmei; Wenzler, Johannes-Simon; Braun, Andreas; Abdelbary, Mohamed M. H.
title: The Antimicrobial Susceptibility of Porphyromonas gingivalis: Genetic Repertoire, Global Phenotype, and Review of the Literature
date: 2021-11-24
journal: Antibiotics (Basel)
DOI: 10.3390/antibiotics10121438
sha: 662e2fb18bb82534082cf499188b4549e7022d3b
doc_id: 72106
cord_uid: dndu13bm

The in vitro antimicrobial susceptibility of 29 strains of the major periodontal pathogen Porphyromonas gingivalis and three P. gulae (as an ancestor) to nine antibiotics (amoxicillin, amoxicillin/clavulanate, clindamycin, metronidazole, moxifloxacin, doxycycline, azithromycin, imipenem, and cefoxitin) was evaluated by E-testing of minimal inhibitory concentration (MIC) according to international standards. The results were compared with 16 international studies reporting MICs from 1993 until recently. In addition, 77 currently available P. gingivalis genomes were screened for antimicrobial resistance genes. E-testing revealed a 100% sensitivity of P. gingivalis and P. gulae to all antibiotics. This was independent of the isolation year (1970 until 2021) or region, including rural areas in Indonesia and Africa. Regarding studies worldwide (675 strains), several method varieties regarding medium, McFarland inoculation standards (0.5–2) and incubation time (48–168 h) were used for MIC-testing. Overall, no resistances have been reported for amoxicillin + clavulanate, cefoxitin, and imipenem. Few strains showed intermediate susceptibility or resistance to amoxicillin and metronidazole, with the latter needing both confirmation and attention. The only antibiotics which might fail in the treatment of P. gingivalis-associated mixed anaerobic infections are clindamycin, macrolides, and tetracyclines, corresponding to the resistance genes erm(B), erm(F), and tet(Q) detected in our study here, as well as fluoroquinolones. Periodical antibiotic susceptibility testing is necessary to determine the efficacy of antimicrobial agents and to optimize antibiotic stewardship.

Porphyromonas gingivalis is a non-motile, Gram-negative, rod-shaped/filamentous (pleomorphic), anaerobic bacterium forming black-pigmented colonies after 3-4 days of incubation on supplemented (vitamin K, hemin) blood agar plates. It is an opportunistic pathogenic bacterium, commonly found in the human body and especially in the oral cavity, where it is associated with periodontal diseases. Together with Tannerella forsythia and Treponema denticola, it forms the red complex of etiologically important bacteria and is regarded as THE key periodontal pathogen [1, 2] . The detection rate of P. gingivalis increases with age [3] . In the periodontal sulcus P. gingivalis induces an inflammatory response upregulating the nutrient-rich flow of sulcus fluid causing bacterial overgrowth/proliferation and subsequently dysbiosis. Simultaneously, it impairs the bactericidal innate host defenses by blocking Toll-Like-Receptor 4 (TLR4) recognition, assuring its survival [4] . In addition to periodontitis, it has been frequently found in oral specimens from necrotizing ulcerative gingivitis, infected root canals, peri-implant lesions, and acute apical abscesses [5, 6] . Besides the oral cavity, it has been detected at various body sites, such as intra-abdominally [7] , vaginal samples in cases of vaginosis [8] , amniotic fluid [9] , synovial specimens of rheumatoid arthritis and psoriatic arthritis [10] , and together with some other periodontal organisms, in occluded arteries of the lower extremities of Buerger's disease patients [11] . Recently investigated links between P. gingivalis and age-related macular degeneration [12] , adverse pregnancy outcomes [13] , Alzheimer's disease [14, 15] , atherosclerotic disease [16] , and cancer [17] need confirmation.

From the clinical perspective and following appropriate antibiotic stewardship, systemic antibiotics should only be used in well-selected patients and cases. In periodontology, their application should be restricted to specific conditions of severe progressive periodontitis defined by international recommendations [18, 19] . Metronidazole, amoxicillin (plus/minus metronidazole or clavulanate), and clindamycin, as well as (less common) certain fluoroquinolones (mainly ciprofloxacin), tetracyclines (including doxycycline) and macrolides (erythromycin or azithromycin), are the antibiotics used and always in conjunction with mechanical debridement. If the debridement is neglected, antibiotics might not reach the bacteria in biofilm with the consequence of much higher minimal inhibitory concentration (MIC) [20] . Importantly, only for non-oral, severe mixed anaerobic infections, cefoxitin and imipenem are established treatment options and therefore included here.

The present study aimed to test the in vitro susceptibility of clinical P. gingivalis strains, isolated from periodontal pockets in adult patients with advanced forms of periodontitis in Germany and worldwide, to all antibiotics mentioned above and by standardized methods. We selected strains according to the following criteria: of local importance (Germany) or to fill gaps of regions under-represented in MIC testing so far (namely Indonesia, Kenya, Canada). We also included three P. gulae strains (isolated from Squirrel monkeys, Saimiri squirrius) as the probable ancestor of P. gingivalis [21] and known for their ability to acquire nitroimidazole resistance [22] . In addition to phenotypic testing, we retrieved the sequence reads of 77 publicly available P. gingivalis genomes and searched for resistance genes. By discussing our results with respect to 16 international studies addressing MIC data from 1993 until recently, we intended to meta-analyze the global antimicrobial susceptibility of P. gingivalis over time, as a snapshot from its origin until 2021.

The MIC of our strain collection of 29 P. gingivalis and three P. gulae isolates to nine antibiotics are presented in Table 1 . Next, we calculated the MIC range, MIC50 (median MIC value at which ≥50% of the isolates in a test population are inhibited) and MIC90 (90% of strains susceptible), and results are presented in Table 2 . Our MIC range, MIC50, and MIC90 were all in line with other studies conducted worldwide. No single strain of our collection reached resistance according to the breakpoints, so far defined by CLSI/EUCAST. In a few cases (strains AC07 from Germany and 083-02 from Indonesia), individual colonies showed a reduced susceptibility and were re-tested, but reached only a slightly higher, non-resistance-indicative MIC. The length of incubation needed for a clear MIC reading differed between strains (48 h, as recommended, up to 72 h). We did not find any pattern of resistance development among our limited number of strains. Almost the same MICs were measured for P. gulae (proclaimed ancestor of P. gingivalis), for strains from rural regions, or for recently isolated strains of Western countries (e.g., Germany, Canada) with access to antibiotics. Comparing five pairs of isolates from the same Java-Indonesian patients in 1994 and 2002 (young population with a high prevalence of periodontal diseases [23] ), no tendency for rising resistance was observed. In general, P. gingivalis showed very different phenotypes in terms of time to pigmentation, encapsulation (apparent by slimy colonies), or colony size, partially explaining the difficulties in obtaining MIC readings.

After carrying out an extensive search for global data on the in vitro antimicrobial susceptibility of P. gingivalis (Figure 1 ), here, we review the results in comparison of region and time (Table 3) . Interestingly, even though the methods for susceptibility testing underwent standardization processes, variations performed by several groups and in several regions can be recognized (Table 4 , including references). Some of these variations might be due to the availability of certain agar media or E-testing strips. In addition, different lengths of incubation before MIC reading were reported which might be related to both, different agar/broth media used and cultivability (e.g., oxygen sensitivity) of strains included. Comparing MICs over all antibiotics tested, the smallest ranges of MICs (four dilution steps) were reported for cefoxitin (≤0.125-1 mg/L) and imipenem (≤0.016-0.12 mg/L), but both antibiotics were only tested in three and five studies, including ours, respectively, and always found to be effective. The only other antibiotic demonstrating 100% effectiveness against P. gingivalis was amoxicillin/clavulanate (MIC range <0.016-0.75 mg/L, with a breakpoint for resistance of ≥8 mg/L). For all other antibiotics tested, very few resistant strains were recognized worldwide as the principal reason for the range-extension. Table 3 . Comparison of 16 studies (1993-2019) determining the MIC range, MIC50, and MIC90 (in mg/L) of the key periodontopathogen Porphyromonas gingivalis for 9 antibiotics (including three classes) applying different methods (see Table 2 ). Legend: Etest-epsilometer agar testing, BD-broth dilution, AD-agar dilution, MD-microdilution; BBA-Brucella blood agar, GAB-Gifu anaerobic broth, WC-Wilkins-Chalgren agar, BA-blood agar (non-selective), Ox-Oxoid, BB-Brucella broth.

The presence/absence of resistance genes was detected by various approaches that are described in the Materials and Methods section. In addition, we used two different databases, ARG-ANNOT [46] and CARD 2020 [47] , that include 2223 and 2631 sequences of antimicrobial genes, respectively. Our analysis using the CARD database revealed that all 77 investigated assembled genomes carried the pgpB gene producing lipid A 4 -phosphatase, which is responsible for polymyxin B (a cationic polypeptide antibiotic) resistance and, as dependent on complex formation with similar peptides called LPS binding protein (LBP), for evading TLR4-sensing and killing of P. gingivalis [48, 49] . Because of the nephro-and neurotoxicity, polymyxin B is only topically used (eye-, ear-, and woundinfections) and has no application in periodontology. Interestingly, only the two genomes ERX1066730 and ERX2022748 harbored any other genes encoding for antimicrobial resistance. These two genomes represented strains from Germany and the Netherlands (Supplementary Table S1 ), respectively. The Dutch ERX2022748 genome carried only the erm(F) gene. In contrast, the German ERX1066730 genome carried the following four resistance genes: erm(B) and erm(F) conferring resistance to macrolide, lincosamide, and streptogramin B (MLSB); the cat(A1) gene for the chloramphenicol-resistance (not of interest as no application in anaerobic infections); and the tet(Q) gene encoding for a ribosomal protection protein conferring resistance to tetracycline. These results were confirmed by an alternative pipeline and database. Resistance to fluoroquinolones in Gram-negative bacteria mostly occurs by two mechanisms: first, through mutations in the target enzyme DNA gyrase and topoisomerase IV and second, by reducing intracellular fluoroquinolones through efflux pumps. However, we did not detect any fluoroquinolone-resistance determinants among the 77 genomes investigated here. Resistance to metronidazole in Gram-negative anaerobes is known to be associated with nitroimidazole-resistance genes (nimA-J isoforms). These genes (located chromosomally or on plasmids) encode a 5-nitroimidazole reductase that converts nitro-imidazole to amino-imidazole, thus preventing the generation of bactericidal nitroso-residues [50] . Of note, we did not detect any nim isoforms here.

P. gingivalis MIC range, MIC50, and MIC90 data measured in our very limited number of strains were all within the range found by other studies conducted worldwide. We did not observe any trend of increased antibiotic resistance comparing data from P. gulae (a possible ancestor of P. gingivalis as isolated from monkeys [21] ), isolates from rural regions in Kenya or Indonesia, or isolates from the 1970s to recent ones. However, if integrating more strains and respecting outliers, the global situation has been different since the end of the 20th and the beginning of the 21st century. In Germany (1999), but especially in Colombia (2010, 2020 [pre-proof]), amoxicillin-resistant strains were isolated with MICs above the breakpoint of ≥8 mg/L [33, 41, 51, 52] . In Colombia, resistance against clindamycin (breakpoints between ≥4 [EUCAST] and ≥8 mg/L [CLSI], 23.5% resistant strains according to authors) and metronidazole (breakpoints between ≥4 [EUCAST) and ≥32 mg/L [CLSI], 21.6% resistant strains in 2010, rising to 24.6% in 2020 [pre-proof] according to authors) were also reported with an MIC90 as high as ≥16 mg/mL for both antibiotics. Resistance to metronidazole of a single (1 out of 10 tested) P. gingivalis strain was reported from Pakistan in 2020 also [53] . Although nim-associated metronidazole resistance is not highly numerous globally, there are reports with a prevalence between <1% (Prevotella) and 4% (Bacteroides) from quite a few regions such as Pakistan, North India, and Kuwait, but also the USA and Europe [50, 54] . As a matter of concern, a few metronidazole-resistant P. gulae strains with MICs > 512 µg/mL were already isolated from dogs [22] . Developing of resistance in pets is plausible as they are frequently treated for parasites, and the imidazole-derivative fenbendazole is a popular choice [55] . After in vitro metronidazole challenge with sub-inhibitory concentrations, an adaptation of P. gingivalis was also demonstrated [56] . On the other hand, resistance to metronidazole in humans, even after selection pressure by treatment [57] , seems to be unlikely, which might be due to a fitness cost associated with the acquisition of nim genes. Of note, nim genes were never found here according to the limited literature addressing this topic [58] , our genome analysis results, and the best of our knowledge.

Again from Columbia but from a different group, an intermediate susceptibility to tetracycline (reaching the CLSI-breakpoint of 8 mg/L) was reported applying M.I.C.Evaluator strips [45] . As two independent Colombian groups were reporting increased resistance by applying good standard testing procedures, these results seem to be plausible and a matter of concern, as germs of all kinds easily cross borders, very apparent with the current SARS-CoV-2 pandemic. Further reports of tetracycline-resistant strains came from Germany [33] , and the identification of tet(Q) genes underlines this risk (in our study and [59] ).

Finally, macrolides, even if not very much used for treating periodontitis or anaerobic infections, are interesting as used for prophylaxis of infective endocarditis perioperatively, including periodontal open flap operations. Here, breakpoints for anaerobes are only defined for erythromycin and by CLSI (≥2 mg/L), but MICs as high as 8 mg/L for erythromycin (found in Italy 2007, [39] ) or between 16 mg/L (found in Brazil 2006, [38] ) and 24 mg/L (found in Colombia recently as MIC90, [52] pre-proof status) for azithromycin may indicate intermediate susceptibility or resistance. To avoid over-interpreting the clinical impact of very few resistant strains, it might be more constructive to use MIC50 and MIC90 data provided for all studies, including ours, in Table 3 . The average P. gingivalis-MIC50 over all studies and about 700 strains (by exclusion of the Colombia strains which explains differences to Table 3 ) are promising and were the following (in mg/L): amoxicillin <0.016-<0.25, AMC < 0.016-<0.125, clindamycin < 0.016-≤0.125, metronidazole <0.016, fluoroquinolones 0.06-0.5, tetracyclines 0.015-0.75, macrolides < 0.016-0.25, imipenem 0.015-≤0.125, and cefoxitin 0.06-≤0.125. The same is true for MIC90 data (again by exclusion of the top resistant Colombia strains): amoxicillin <0.016-0.064, AMC < 0.016-0.125, clindamycin < 0.016-≤0.125, metronidazole < 0.016-0.75, fluoroquinolones 0.032-2, tetracyclines 0.023-16, macrolides <0.016-2, imipenem ≤ 0.125-0.06, and cefoxitin ≤ 0.125-0.5). Taken together, the only antibiotics which seem to have lost activity since the very late 20th century are tetracyclines, macrolides (both in accordance with the resistance genes found in 77 genomes investigated in depth here) as well as fluoroquinolones, the latter inactivated by mutation of target enzyme or by efflux pump-based extrusion.

Because of a reason given below, some important studies were not included in our analysis in the first instance. However, the results of these six studies will be discussed below for further comparison. Jepsen et al. tested antibiotic susceptibility of 5323 P. gingivalis isolates from 2008-2015 by agar diffusion only [60] . The average non-susceptibility in 2008-2011 versus 2012-2015 for doxycycline, azithromycin, and ciprofloxacin was: 0% versus 0.04%, 0.64% versus 1.56%, and 4.55% versus 11.51%, respectively. Furthermore, the authors found a significant increase in clindamycin non-susceptibility of P. gingivalis (0.46% versus 1.72%, in this particular case confirmed by E-testing), which is not seen worldwide and might be due to its widespread use in German dental practices (29.3% of all antibiotic prescriptions) [61] . All 5323 strains tested were metronidazole-and amoxicillin/clavulanatesusceptible, and 99.62% were amoxicillin-susceptible. Recently, Kulik et al. investigated susceptibility patterns of 56 P. gingivalis strains among Swiss periodontitis patients from different decades [62] . Because of the applied MICRONAUT-S anaerobe MIC plates method, with microdilution only for confirmation of elevated MICs, this study was not included in the first instance but is important for the discussion. In summary, their strains yielded low MIC50 (0.0625-0.5 mg/L) and MIC90 (0.125-2 mg/L) values for all the antimicrobials tested with two isolates needing attention: one was ermF-positive and had MIC values higher than 8 mg/L, 2 mg/L, and 0.25 mg/L for clindamycin, azithromycin, and moxifloxacin, respectively. The second isolate had a high MIC value of 4 mg/L for moxifloxacin. Sequence analysis of the quinolone resistance-determining region (QRDR) of the gyrA gene confirmed a gene mutation, namely Ser-83 ≥ Phe substitution. Dahlen et al. revealed antibiotic susceptibility against seven antibiotics among 67 consecutive fresh isolates of P. gingivalis in a Swedish population, with data given only in figures but not as tables [63] . The strains showed an overall susceptibility to all tested antibiotics except for kanamycin. However, reduced sensitivity was detected in one strain for penicillin G (MIC 1 mg/L), in four strains for ampicillin (MIC > 0.5 mg/L), and in nine strains for clindamycin (MIC > 0.1 mg/L). In a Japanese study in 2007, 48 P. gingivalis/P. endodontalis strains were examined but results not sorted by species [64] . However, all of the 13 antibiotics tested were highly active against both species with only one strain found resistant to amoxicillin. The overall susceptibility of strains (27, with 25 of them P. gingivalis) in Japan was recently confirmed, but with 4.9% moxifloxacin and 22.8% clindamycin resistance as exceptions and high MIC90 values (64-128 mg/L) for macrolides [65] .

Striking for many studies is the delay between the isolation of strains and publication of susceptibility data, which can be more than 5 years. Assuming that the antibiotic resistance would increase by the same rate as measured by Jepsen et al. [60] , presently (2021) the number of non-susceptible strains for doxycycline, azithromycin, and ciprofloxacin could have reached 0.1%, 2.5%, and 19%, respectively. However, this is highly speculative, as the counteracting antibiotic stewardship might break this tendency.

Of final note, during this study, we came across susceptibility data of other Porphyromonas species also, and it must be concluded that P. asaccharolytica, P. levii, and P. uenonis were less susceptible to antibiotics [35, 66] . For instance, two P. asaccharolytica and two P. levii strains from California were resistant to clindamycin (>32 mg/L). There were seven isolates (most likely non-P. gingivalis) with levofloxacin MICs of 4 mg/L and three with MICs of 8 mg/L [35] . Metronidazole resistance of non-oral Porphyromonas sp. with MIC < 256 mg/L was reported from Greece [67] .

The strains tested in our laboratory and their origin are summarized in Table 1 together with MIC values. Most historical strains are from the ACTA collection, and co-author D. Deng provided them with agreement of her institution. By means of a Google Scholar search, we could identify the most plausible country and year of strain isolation. The MICs of 29 P. gingivalis and 3 P. gulae isolates to nine antibiotics, including amoxicillin, amoxicillin/clavulanate, clindamycin, metronidazole, moxifloxacin (fluoroquinolone), doxy-cycline (tetracycline), and azithromycin (macrolide), as well as imipenem and cefoxitin (the latter two for severe infections only) were determined by E test method (AB Biodisk, Solna, Sweden). Bacterial strains were grown on Brucella blood agar plates (Becton Dickinson GmbH, Heidelberg, Germany), supplemented with 5% sheep blood, hemin (5 mg/L), and vitamin K1 (10 mg/L), for up to 5 days. The test strains (a few fresh colonies) were suspended in sterile phosphate-buffered saline equivalent to a 1.0 McFarland standard and streaked confluently over the surface blood agar plates with the aid of a sterile swab. Plates were incubated anaerobically for 2 to 5 days. Inhibition zones were measured at 48 h according to the recommendations of the manufacturer and the Clinical and Laboratory Standards Institute (CLSI), but for slow-growing strains, a longer incubation time was necessary before reading was possible. Percentages of resistant isolates were calculated using breakpoints advised by the CLSI (document M100-ED31:2021 Performance Standards for Antimicrobial Susceptibility Testing, 31st Edition with breakpoints publicly made available in Table 2J 

In addition to phenotypic testing, we retrieved the sequence reads of 77 publicly available P. gingivalis genomes that are listed in Supplementary Table S1 using Bactopia pipeline version 1.6.5 [68] . Within the Bactopia workflow, the quality check on the sequence reads was assigned, and reads below the quality requirements were filtered out. The remaining high-quality sequence reads were assembled using the Shovill pipeline version 1.1.0 (https://github.com/tseemann/shovill, accessed on 10 October 2021) and the default setting for the SKESA assembler version 2.4.0 [69] . Bactopia searches for antimicrobial resistance genes directly using the ARIBA pipeline version 2.14.6 [70] and the comprehensive antibiotic resistance database (CARD 2020) [47] as the default settings for predicting antibiotic resistance. In addition, we doubled checked for the presence or absence of acquired resistance genes by applying the ABRicate pipeline (version 0.8.132, https://github.com/tseemann/abricate, accessed on 10 October 2021) on the assembled genomes using default settings, and here, both the ARG-ANNOT (version V6, https://ifr48. timone.univ-mrs.fr/blast/arg-annot_v6.html, accessed on 10 October 2021) [46] and CARD 2020 (version 3.1.4, https://card.mcmaster.ca/, accessed on 10 October 2021) [47] public databases were used as references for detecting a wide variety of point mutations and reference sequences known to be associated with antimicrobial resistance. A list of all updated versions of the ARG-ANNOT database can be found under the following link: https: //www.mediterranee-infection.com/acces-ressources/base-de-donnees/arg-annot-2/ (accessed on 10 October 2021).

Fortunately, antimicrobial resistance of P. gingivalis is not yet emerging but an increase of MIC data of tetracyclines, macrolides, lincosamide, and fluoroquinolones, has been recognized since the end of the 20th century. Only very few relevant genes, such as erm(B) or erm(F) conferring MLSB-resistance and tet(Q) encoding resistance to tetracyclines, were detected in the 77 publicly available genomes. Of note, neither phenotypic metronidazole resistance (with very few exceptions needing confirmation) nor corresponding nim genes were reported for P. gingivalis. However, a resistance-transfer from related Bacteroides, Prevotella, or other Porphyromonas species (including pet isolates) could emerge, as these are increasing in many regions worldwide. Thus, adjunctive antimicrobial usage in the treatment of periodontitis must be restricted and antibiotic stewardship and resistance gene screening extended.

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The authors wish to thank the many colleagues at ACTA and worldwide for providing strains and/or samples. We thank Beate Melzer-Krick for her excellent technical assistance.

The authors declare no conflict of interest.