key: cord-0715930-uox9pu2t
authors: Fawzy, Ahmad; Rau, Jörg; Riße, Karin; Schauerte, Nicole; Geiger, Christina; Blom, Jochen; Imirzalioglu, Can; Falgenhauer, Jane; Bach, Alexa; Herden, Christiane; Eisenberg, Tobias
title: Streptobacillus felis, a member of the oropharynx microbiota of the Felidae, isolated from a tropical rusty-spotted cat
date: 2020-08-09
journal: Antonie Van Leeuwenhoek
DOI: 10.1007/s10482-020-01454-x
sha: ef5ed79925e5ef75119e387b2de2680fea9b3e1f
doc_id: 715930
cord_uid: uox9pu2t

Streptobacillus felis is a fastidious microorganism and a novel member of the potentially zoonotic bacteria causing rat bite fever. Since its description, this is the second isolation of S. felis in a diseased member of the Felidae. Interestingly, the strain from this study was isolated from a zoo held, rusty-spotted cat (Prionailurus rubiginosus), with pneumonia, thereby indicating a possible broader host range in feline species. A recent preliminary sampling of domestic cats (Felis silvestris forma catus) revealed that this microorganism is common in the oropharynx, suggesting that S. felis is a member of their normal microbiota. Due to unawareness, fastidiousness, antibiotic sensitivity and lack of diagnostics the role of S. felis as a cat and human pathogen might be under-reported as with other Streptobacillus infections. More studies are necessary to elucidate the role of S. felis in domestic cats and other Felidae in order to better estimate its zoonotic potential. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10482-020-01454-x) contains supplementary material, which is available to authorized users.

Streptobacillus (S.) moniliformis (Leptotrichiaceae, Fusobacteriales) has been the longstanding unique species in this genus (Levaditi et al. 1925) . This bacterium represents the most important causative microorganism of rat bite fever (RBF) and its foodborne variant, Haverhill fever (Eisenberg et al. 2018) . RBF is typically characterized by a triad of fever, arthritis and a maculopapular, petechial or pustular rash, but severe causes of infection may include lifethreatening sequelae (Eisenberg 2017; Eisenberg et al. 2017a; Gaastra et al. 2009) . A number of studies have stated a risk for RBF even through contacts to various non-rodent animal species like dogs, cats, weasels and ferrets as well as livestock animals. However, the proper identification of these microorganisms was not carried out and such isolates have not been stored. Recently, [S.] hongkongensis (Woo et al. 2014 ), S. felis (Eisenberg et al. 2014 ), S. notomytis (Eisenberg et al. 2015b ), S. ratti ) and S. canis (Eisenberg et al. 2020b ) were described as novel species. Whereas S. notomytis and S. ratti are closely associated with black rats (Rattus rattus), [S.] hongkongensis has exclusively been isolated from humans (Lau et al. 2016; Woo et al. 2014) and was recently found to belong to a novel genus, Pseudostreptobacillus (Eisenberg et al. 2020a ). S. felis and S. canis were only once isolated from clinical disease in animals, i.e. from a cat with pneumonia and a dog with phlegmon, respectively (Eisenberg et al. 2015a (Eisenberg et al. , 2020b . However, with respect to zoonotic potential, S. notomytis has been found to also cause RBF in humans (Fukushima et al. 2017; Ogawa et al. 2018 ) and a similar case of RBF could recently be attributed to S. felis for the first time (Matt et al. 2020) . Interestingly, various Streptobacillus phylotypes consistent with 16S rRNA gene sequence based operational taxonomic units (OTU) have been described from humans and various animal species (Fig. 1) . We here report a second strain of S. felis, isolated from a tropical rusty-spotted cat (Prionailurus rubiginosus), one of the smallest members of Felidae, that succumbed to infection.

A breeding group of the endangered rusty-spotted cat (Prionailurus rubiginosus phillipsi), a subspecies native to humid zones of Sri Lanka, is managed for ex situ breeding purposes in a German zoo. The cats have been bred in the same zoo or within the European studbook program and are housed individually or in breeding pairs. From the breeding group no significant morbidities and mortalities have occured, but individual animals have suffered from intermittant signs of kitty flu like sneezing, epiphora, elevated respiratory rate, reduced appetite, corneal ulceration in the years before this study. In the actual case, a female displayed bilateral blepharitis, weakness, respiratory distress and anorexia. Intra vitam tests for feline parvovirus, coronavirus and protozoa revealed negative results. Due to disease progression, the animal was euthanized.

A gross pathology examination and histology were performed. For histopathological examination, specimens of multiple organs were fixed in buffered 4% formalin, processed by standard methods and embedded in paraffin. Microtome sections were stained with hematoxylin-eosin (HE).

The IHC examination of the formalin fixed paraffin embedded (FFPE) samples taken for histopathological examination was performed using a recently established and not yet published protocol. Briefly, this protocol utilizes a standard IHC procedure with the use of heat induced antigen demasking in target retrieval solution (Dako Cytomation Denmark AS, Glostrup, Denmark), followed by goat serum (Life Technologies Corporation, Paisley, UK) and avidin/ biotin blocking agent (Linaris Biologische Produkte GmbH, Dossenheim, Germany) in order to block nonspecific binding and reactions, respectively. The primary antibody used was an affinity purified polyclonal rabbit-anti-S. moniliformis antibody supplied by Davids Biotechnologie GmbH (Regensburg, Germany). A goat-anti-rabbit IgG biotinylated antibody (Vector Laboratories, Burlingame, USA) served as a secondary antibody and allowed the detection of the antigen-antibody complex using the Vectastain ABC-Elite Kit (Linaris). Diaminobenzidine (DAB; Sigma-Aldrich Chemie GmbH, Steinheim, Germany) was added, resulting in a brown-colored precipitate forming where antibody have bound. FFPE samples of the lung of a C57BL/6 mouse that was experimentally infected with S. moniliformis (Fornefett et al. 2017 ) underwent the same protocol and served as positive controls. For a negative control, FFPE samples of the rusty-spotted cat underwent the described protocol with only the primary antibody being replaced with negative control rabbit (1,000 bootstraps). GenBank accession numbers are given in parentheses. Numbers at branch nodes refer to bootstrap values; Fusobacterium nucleatum is used as outgroup. ''T'' indicating type strain; Bar, 0.02 nucleotide substitutions per site immunoglobulin fraction (Dako). Evaluation of the immune-histochemical examination was performed using a transmission light microscope.

Bacterial isolates were obtained and isolates were identified using standard microbiological examinations. Briefly, native tissue samples were processed for microbial culture by inoculating flame sterilized, freshly cut tissue surfaces onto culture media (Columbia agar with 5% sheep blood [SBA; Oxoid, Wesel, Germany] and Gassner agar [VWR, Darmstadt, Germany]). Agar plates were incubated for up to 48 h at 20°C using aerobic and microaerobic culture conditions. Phenotypic characterization of streptobacilli is known to yield only few weakly positive reactions (Eisenberg et al. 2015c) , however, standard microbiological procedures included tests for hemolysis on SBA, catalase activity with 3% H 2 O 2 on microscopic slides and for presence of cytochrome oxidase with the BBL DrySlide Ò oxidase system (Becton-Dickinson, Heidelberg, Germany). Urease, hydrogen sulfide, indole, motility and oxidative and fermentative glucose assimilation were tested on Christensen agar, SIM and OF medium in slant agar tubes, respectively (all Merck, Darmstadt, Germany). Microscopic examinations of fixed smears were performed using Gram's stain. For further identification attempts, the Omnilog GEN III plate identification system (Biolog, Hayward, USA) was utilized for the first time using the most sensitive protocols for fastidious bacteria (C1 and C2) with and without addition of 10% bovine serum according to manufacturer's recommendations.

Mass spectrometry procedure has been recently described in detail (Eisenberg et al. 2018 (Eisenberg et al. , 2020b . The commercial database used (DB 8,468; Bruk-erDaltonics) comprised 24 spectra each from 10 S. moniliformis strains. Reference spectra from wellcharacterized, quality-controlled strains of all other Streptobacillus/Pseudostreptobacillus species and most other members of the Leptotrichiaceae were added to the database from previous studies (Eisenberg et al. 2020b; Rau et al. 2016) . Identification was done with the commercial Bruker database, and with the extended database.

Molecular characterization of isolate LHL191014123 obtained from liver tissue PCR analysis Two earlier designed PCR assays for the detection of S. moniliformis were employed to detect characteristic amplicon sizes of approximately 269 and 1,190 bp also for the rusty-spotted cat strain LHL191014123 (primers S5: 5 0 -CAT ACT CGG AAT AAG ATG G-3 0 and AS2: 5 0 -GCT TAG CTC CTC TTT GTA C-3 0 ) ( Kimura et al. 2008 ) and [primers SbmF: 5 0 -GAG AGA GCT TTG CAT CCT-3 0 and SbmR: 5 0 -GTA ACT TCA GGT GCA ACT-3 0 ; Nicklas, cited in (Rohde et al. 2008) ]. It was recently found that these PCR assays are rather genus than species specific (Eisenberg et al. 2015c ). Therefore, we have recently designed primers (forward: 5 0 -AGT ATG GGA AAT AGT AGA TAA TAG-3 0 and reverse 5 0 -ACT GTA GAT TGT GAG TTC TT-3 0 ) that could specifically amplify a partial sequence of the gyrB gene (732 bp) of the S. felis genome (Matt et al. 2020 ). The PCR reaction components and cycling conditions were carried out as previously described in Fawzy et al. (2016) with minor modifications (annealing temperature was 53°C and elongation time was 90 s).

Whole genome sequencing (WGS) was carried out to get insight into a core genome based phylogeny and compare the rusty-spotted cat's strain with established type strain genomes from the same family. The genome sequence of strain LHL191014123 was generated by de-novo assembly with reads from Illumina technology. In brief, DNA was isolated from cells grown for 3 days at 37°C on TSA supplemented with 20% horse serum using a PureLink genomic DNA kit (Thermo Fisher). The library was prepared with a Nextera XT library preparation kit (Illumina) and sequenced on NextSeq 500 (mid output kit v2, 2 9 150 bp) instruments. The genome assembly was carried out by SPAdes (version 3.10.1), resulting in 163 contigs with 179 9 average coverage.

Phylogenetic and phylogenomic analyses For a first phylogenetic placement, a tree based on nearly full-length 16S rRNA gene sequences was constructed with Geneious vers. 8.1.9 (Kearse et al. 2012 ) using a Clustal W nucleotide alignment with standard settings and a Neighbor-Joining (NJ) tree (data not shown). Therefore, the 16S rRNA gene sequences of all type strains of the Leptotrichiaceae were obtained from GenBank and for strain LHL191014123 deduced from the full genome sequence (s. below). For a more detailed view into the phylogenetic relationship of strain LHL191014123 and all other Streptobacillus species the criteria of Woo et al. (2014) were considered. Phylogenetic analyses based on near full-lengths nucleotide sequences of the groEL, gyrB and recA genes were performed for all Streptobacillus species and the type species of all other genera of the Leptotrichiaceae. Respective nucleotide sequences were aligned using ClustalW implemented in Geneious vers. 8.1.9 (Kearse et al. 2012 ) and visualized as unweighted pair group method with arithmetic mean (UPGMA) phylogenetic trees (based on 1,000 replications [bootstrap analysis]). A representative tree for the gyrB gene is shown in Suppl. Fig. S1 . The average nucleotide identity (ANI) values and core genome phylogeny were calculated for strain LHL191014123 in comparison with type strain genomes of the family Leptotrichiaceae using the EDGAR 2.3 platform (Blom et al. 2016) . ANI values were computed as described by Goris et al. (2007) and as implemented in JSpecies (Richter and Rossello-Mora 2009) .

The rusty-spotted cat weighed approx. 1.9 kg, which constitutes a normal weight of this small wildcat. The female was born in 2010 and was 9-years old at the time of death. During post mortem examination a light creamy fur, possibly indicating signs of chronic cat flu, was found in the left cavum nasi, accompanied by a light hemorrhagic exudate.

A moderate follicular hyperplasia was noted in the spleen. Focal edema and emphysema were found in histological sections of lung tissue. Focally, fibrin, desquamated alveolar macrophages and neutrophil granulocytes with occasional phagocytized bacteria were detected in bronchioles and pulmonary alveoli. Single cysts were found in the kidneys.

The IHC examination using a method designed for the detection of S. moniliformis in tissue samples revealed negative results in all examined tissues of the rustyspotted cat. Positive and negative controls were successfully showing the expected results, reaffirming sufficient specificity for the detection of S. moniliformis.

Bacterial culture revealed growth of S. felis in all tissues, except intestine and intestinal lymph node. The semiquantitative number of streptobacilli as obtained by counting colonies on the directly inoculated agar surface was found to be low (\ 20) in spleen and kidney, moderate (20-50) in liver and lung and high ([ 50) in the nasal cavity.

Varied growths of other Gram-positive and Gramnegative microbiota were cultivated from other tissues and identified as Enterococcus faecalis, Vagococcus teuberi and Escherichia coli using MALDI-TOF MS. Selective verification procedures for purely microaerobic bacteria, Chlamydia spp., Mycoplasma spp. or Salmonella spp. and herpesviruses revealed negative results throughout (data not shown).

A coproscopy flotation technique was negative.

Phenotypic characterization of isolate LHL191014123 obtained from liver tissue

Due to the fastidious growth, physiological reaction patterns are generally very weak in members of the genus Streptobacillus [Eisenberg et al. 2015c ]. The physiological characterization of strain LHL191014123 with the Omnilog GEN III plate identification system did not reveal a superior resolution compared to other standard tests, although a panel of 94 different reactions was assessed. Even the most sensitive protocols for fastidious bacteria (C1 [24 h] and C2 [48 h incubation]) with and without addition of 10% bovine serum resulted in very weak reactions. Slightly positive reactions were found only for Laspartic acid, L-glutamic acid, D-glucuronic acid, glucuronamide, L-lactic acid, citric acid, a-ketobutyric acid, sodium butyrate and sodium bromate (data not shown).

show the m/z signals typical of Streptobacillus genus at 3,631.2 ± 3.6, 7,262.0 ± 7.3, and 7,392.0 ± 7.4 (data not shown, Eisenberg et al. 2018 ). Nevertheless, the strain LHL191014123 had score values lower than 1.5 with the used commercial Bruker database version and was, therefore, not identified. The application of the enlarged database, extended by reference entries for each of the known members of the genus Streptobacillus, including the type strain of S. felis 131000547 T , allowed the unequivocal assignment of strain LHL191014123 to S. felis (score values up to 2.719). Custom-made MSP of all Streptobacillus species were prepared from known type strains based on Bruker quality criteria and used in this study; respective MSP are available for exchange via the MALDI-user platform MALDI-UP (https://maldi-up. ua-bw.de) . A dendrogram depicting the topologic position of the reference spectrum of strain LHL191014123 from the rusty-spotted cat from this study to closely related strains of the other known streptobacilli and related taxa is shown in Fig. 2 .

Both earlier published PCR protocols for the detection of S. moniliformis are based on the Streptobacillus 16S rRNA gene. As expected, strain LHL191014123 from this study gave a positive amplification in these two PCR assays. The recently designed gyrB gene PCR was also positive for strain LHL191014123. (Zhou et al. 2011) ) and 96 tandem repeats (Benson 1999) . However, screening for CRISPR regions was negative in contrast to S. felis type strain (131000547 T ) that was found to possess a relatively large CRISPR region (2,078 bp) with 31 spacers (Grissa et al. 2007) . Five genomic islands with a size range 3,220 to 66,556 bp were also identified (Bertelli et al. 2017) . Four islands possess mainly hypothetical proteins and none seems to express pathogenic factors. However, one island (26,565 bp) seems to be associated with transport and metabolism of different substrates including carbohydrates and minerals. Interestingly, genome analysis with Pathogenfinder (Cosentino et al. 2013 ) suggested that S. felis (LHL191014123 as well as 131000547 T ) has a probability of 0.976 to be a human pathogen since it harbors seven pathogenic families, all of which originate from S. moniliformis, the classical pathogen of the RBF zoonosis. This web-tool predicts the pathogenicity of a submitted genome based on a model that compares its sequence data to a protein family database containing proteins known to be associated with pathogenic or non-pathogenic bacteria.

The 16S rRNA gene sequence of strain LHL191014123 was derived from WGS and represents a stretch of 1,514 unambiguous nucleotides. This sequence was blasted against the quality-controlled database EzBioCloud (Yoon et al. 2017) and highest similarities to the type strains of S. felis (99.93%), S. canis (98.68%), S. notomytis (98.26%), S. ratti (97.85%), S. moniliformis (97.64%) and P. hongkongensis (94.23%), followed by Oceanivirga salmonicida (91.10%) and 'Sneathia amnii' (90.58%) were found. In a 16S rRNA gene sequence phylogenetic tree (ML algorithm), strain LHL191014123 clustered most closely and in a separate branch together with the type strain of S. felis. The next closely related species was S. canis that grouped as a sister clade to S. felis with high bootstrap support (data not shown). Based on partial nucleotide sequences of the groEL, gyrB (Suppl. Fig. S1 ) and recA genes, this topologic position was also identical for the investigated housekeeping genes. A core genome phylogeny of strain LHL191014123 and 20 genomes of the family Leptotrichiaceae was calculated in EDGAR 2.3 based on MUSCLE alignment as previously described (Eisenberg et al. 2017b) . This resulted in one multiple alignment of 267 core genes per genome (5,607 genes in total), with 95,146 amino acid residues per genome (1,998,066 in total). The Neighbor-Joining algorithm (Fig. 3) as well as the approximately-Maximum Likelihood phylogeny (data not shown) both confirmed the taxonomic position of strain LHL191014123 as a member of Streptobacillus felis with S. canis being the closest relative, still with a larger phylogenetic distance. Species identity between the rusty-spotted cat's strain to S. felis was once more confirmed by mean average nucleotide identity (ANI) values of 99.32% (reciprocal 99.24), which is clearly above the [ 95-96% proposed boundary for identical species (Goris et al. 2007 ).

The GenBank/ENA/DDBJ accession numbers for the 16S rRNA, groEL, gyrB and recA gene sequences of strain LHL191014123 as well as for the complete genome sequence are MN764137, MN793979, MN793980, MN793981 and genome acc. no. (JABMKT000000000; BioSample SAMN14996772; BioProject PRJNA634464), respectively. Further accession numbers of gyrB sequences from mouth swabs from cats are MT498840-MT498846 and have been published in Matt et al. (2020) . Strain LHL191014123 has been deposited at the German Collection of Microorganisms and Cell Cultures (DSMZ), the Culture Collection of the University Gotenburg (CCUG), the Collection of Institute Pasteur (CIP) and the strain collection of the Hessian State Laboratory (LHL) under identifiers DSM110500, CCUG74119, CIP111794 and LHL191014123.

It is evident from the depicted molecular results and from MALDI-TOF MS analysis that LHL191014123 is an additional strain of S. felis. To our knowledge, this is the second available strain with proper species identification and an extended genetic and phenotypic knowledge base. Although we could recently show that approximately 50% of randomly selected, mostly healthy domestic cats harbor S. felis (Matt et al. 2020) , the isolation of these streptobacilli from cats is a rare exceptional case. A number of studies have indicated dogs and cats as possible vectors of S. moniliformis to humans, especially after mouthing wild rats (Gascard et al. 1967; Maynard et al. 1986; Mollaret 1969; Peel 1993; Wouters et al. 2008) . However, isolates have not been stored and phylotypes are not available for most of the mentioned studies. Therefore, these microorganisms cannot be verified as S. moniliformis. Conversely, 16S rRNA gene phylotypes from one former and additional studies in dogs suggested a much closer relationship of their Streptobacillus OTUs to S. canis than to S. moniliformis (Dewhirst et al. 2012; Xenoulis et al. 2008) (Fig. 1) . Relatively few dogs have suffered from streptobacillosis (Das 1986; Ditchfield et al. 1961) .

OTU sequences of cats that are most closely related to S. felis were previously lacking, but have recently been found in half of the investigated cats (Matt et al. 2020) and also closely related bacterial species (uncultured 'Leptotrichia', 'Leptotrichiaceae') have been detected at various body sites (Older et al. 2019; Sturgeon et al. 2014) . One study mentions two Streptobacillus isolates but without any further identification or disease association (Whyte et al. 2017 ).

The species S. felis has been described from cats as well as from a human patient with contact to cats, suggesting that this microorganism may be a member of the cats' microbiota with the potential to cause zoonotic infections (Eisenberg et al. 2015a; Matt et al. 2020) . The high occurrence (50% found in Matt et al. (2020) ) should be considered with respect to the potential role of S. felis both as a cat pathogen and a potentially zoonotic microorganism because cats represent the most popular pet animal species and streptobacillosis is considered a significantly underreported disease. However, possible reasons why streptobacilli have been infrequently diagnosed may include a lack of awareness of the disease among clinicians, an absence of pathognomic signs of disease in animals, a lack of reliable diagnostics, fastidious growth of the pathogen, susceptibility to most antibiotics used for empiric therapy, unnoticed animal contact and that this is a non-notifiable disease worldwide (Eisenberg 2017) .

S. felis has first been isolated from a cat with acute bronchopneumonia and a myocardium with multifocal haemorrhages on the endo-and epicardium (Eisenberg et al. 2014) . In this second report, again lungs were predominantly affected, but streptobacilli were isolated from all major organs pointing towards an agonal spread of these bacteria or an early septicemia. Likewise, the next closely related species, S. canis, has recently been found to also constitute a member of Fig. 3 Core genome phylogenetic tree depicting strain LHL191014123 within the family Leptotrichiaceae. Core genes of these genomes were computed in EDGAR 2.3 based on MUSCLE alignments and the Neighbor-Joining algorithm as implemented in the PHYLIP package. The core genome analysis was based on of 267 genes per genome in 17 type species genomes (5,607 in total) of the family Leptotrichiaceae. The core has 95,146 amino acid residues and 1,998,066 bp per genome in total. GenBank accession numbers are given in parentheses. ''Sneathia amnii'' and ''Leptotrichia massiliensis'' were included, however, these taxonomic names have been effectively published but not validly published under the rules of the International Code of Nomenclature of Bacteria. Fusobacterium nucleatum is used as outgroup. ''T'' indicating type strain; Bar, 0.01 amino acid substitutions per site canine oral microbiota (Matt et al. 2020 ) and has been isolated from a phlegmon on a dog's hindleg (Eisenberg et al. 2020b) . Hypothesizing that bite wounds are often caused by oral microbiota (Abrahamian and Goldstein 2011) , one can speculate that streptobacilli from cats might occasionally also be involved in wound infections.

Interestingly, a novel diagnostic immune-histology tool for the detection of S. moniliformis turned out to reveal negative results throughout. The method was found to successfully detect experimentally infected mice (data not shown). Because the lack of suitable diagnostics for the detection of streptobacillosis is often referred to as a diagnostic dilemma (Mahmoodi et al. 2016; Rumley et al. 1987) , the novel IHC assay represents a promising diagnostic tool to improve this situation and to identify S. moniliformis in situ. The lack of binding in the here presented case suggests deviant epitopes in S. felis.

This is the second isolation of S. felis in a diseased cat species. A preliminary sampling of cats revealed that this microorganism is frequently found in the oropharynx and that cats represent a reservoir for S. felis. However, this is further evidence that this species is cat specific but with a broader distribution in feline hosts than previously thought. Further studies are necessary to elucidate the role of S. felis in domestic and other cat species in order to better estimate its zoonotic potential.

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Acknowledgements Open Access funding provided by Projekt DEAL. We like to thank all cat owners for their participation in the prevalence assessment. For excellent technical assistance, we thank Mersiha Curic, Matrin Dyk, Katharina Engel, Jens Heinbächer, Ulrike Kling and Marie-Luise Sonneborn. The Hessian Ministry for the Environment, Climate Change, Agriculture and Consumer Protection (HMUKLV) supports the Hessian State Laboratory.

Authors' contributions AF and TE designed the microbiological study. NS and CG were responsible for animal care. TE isolated the S. felis strain. KR conducted gross pathology and histology; AB and CH were responsible for IHC. JR was in charge of the MALDI-TOF MS analysis. JF and CI performed the WGS, JB and AF were involved in data analyses. TE and AF interpreted the data and wrote the manuscript. All authors critically checked and contributed to the final version of the manuscript.Funding This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors. The Hessian Ministry for the Environment, Climate Change, Agriculture and Consumer Protection supports the Hessian State Laboratory.Availability of data and material All data have been made fully available to the public.

Conflicts of interest Not applicable.Ethics approval There are no ethical issues associated with this manuscript. Animal husbandry fulfilled ethical standard guidelines according to the code of ethics and animal welfare of the World Association of Zoos and Aquariums (WAZA; https:// www.waza.org/priorities/animal-welfare/). Sampling of the rusty-spotted cat followed veterinary euthanasia of the diseased animal.Consent to participate All authors gave their consent to participate in this study.Consent for publication All authors gave their consent to publish results from this study and to be listed as a co-author.Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.