Characteristics and distribution of Listeria spp., including Listeria species newly described since 2009

Most species within Listeria sensu strictu are well documented to be widely distributed and commonly found in different environments. L. monocytogenes has been isolated throughout the world, including in North America (Chapin et al. 2014; Sauders et al. 2012; Stea et al. 2015), South America (Hofer et al. 2000; Montero et al. 2015; Ruiz-Bolivar et al. 2011; Vallim et al. 2015), Europe (Gnat et al. 2015; Linke et al. 2014), Asia (Huang et al. 2015; Sugiri et al. 2014; Tango et al. 2014), Africa (Ahmed et al. 2013; Hmaied et al. 2014; Ndahi et al. 2014), and Oceania (McAuley et al. 2014). Human listeriosis cases have been reported throughout the world, including Africa, Oceania, South America, North America, Europe, and Asia (Ariza-Miguel et al. 2015; Barbosa et al. 2015; Hmaied et al. 2014; Huang et al. 2015; Lomonaco et al. 2015; Najjar et al. 2015; Negi et al. 2015; Ramdani-Bouguessa and Rahal 2000; Scallan et al. 2015a; Scallan et al. 2015b). Similarly, animal listeriosis cases caused by L. monocytogenes have also been reported throughout the world, including Africa (Akpavie and Ikheloa 1992; Meredith and Schneider 1984; Schroeder and van Rensburg 1993), South America (Headley et al. 2013; Headley et al. 2014), North America (Wiedmann et al. 1997; Wiedmann et al. 1994; Wiedmann et al. 1999; Woo-Sam 1999), Asia (Gu et al. 2015; Malik et al. 2002), Oceania (Fairley and Colson 2013; Fairley et al. 2012), and Europe (Rocha et al. 2013; Vela et al. 2001; Wagner et al. 2005). Animal listeriosis cases due to L. ivanovii has been recorded in different continents, including Oceania (McAuley et al. 2014; Sergeant et al. 1991), North America (Alexander et al. 1992), Europe (Gill et al. 1997; Kimpe et al. 2004), South America (Hofer et al. 2000), and Asia (Chand and Sadana 1999). We were not able to identify any reports of animal listeriosis caused by L. ivanovii in Africa. While L. ivanovii has rarely been linked to human listeriosis, L. ivanovii isolation from humans with listeriosis symptoms has been reported in different continents, including Europe (Cummins et al. 1994; Guillet et al. 2010; Lessing et al. 1994) and Asia (Snapir et al. 2006). We were unable to identify any reports of human listeriosis caused by L. ivanovii in Africa, Oceania, South America, and North America.

L. innocua, L. seeligeri, and L. welshimeri have also been identified throughout the world in most studies that identified reasonable large sets of Listeria isolates that were not L. monocytogenes to the species level (Chapin et al. 2014; Fox et al. 2015; Hofer et al. 2000; Linke et al. 2014; Sauders et al. 2012; Stea et al. 2015). A number of these studies have often failed to isolate L. ivanovii from environmental samples (Chapin et al. 2014; Fox et al. 2015; Sauders et al. 2012). For example, Sauders et al. (2012) reported that 23.4 and 22.3 % of samples obtained from natural and urban environments in New York State (USA), respectively, were positive for Listeria; the 442 Listeria isolates characterized in this study represented L. seeligeri (234 isolates), L. monocytogenes (80 isolates), L. welshimeri (74 isolates), L. innocua (50 isolates), and L. marthii (4 isolates). In a study in Austria (Linke et al. 2014), 149 out of 467 soil samples (30 %) were positive for Listeria spp.; species identified included L. monocytogenes (6 % of all samples), L. seeligeri (15 % of samples), L. innocua (6 % of samples), L. ivanovii (3 % of samples), L. welshimeri (2 % of samples), and unidentified Listeria spp. (2 % of samples). L. seeligeri thus has been the most commonly isolated Listeria species in two largest studies on Listeria diversity in natural environments. In a study in Canada (Stea et al. 2015), Listeria spp. were isolated from 53.8 % of the 329 water samples with a detection rate of 72.1 % in rural watersheds compared to 35.4 % for urban watersheds. L. monocytogenes was found in 30.3 and 34.5 % of the positive rural and urban watershed samples, respectively, and L. ivanovii was found in 8.4 and 6.9 % of these samples. Other Listeria spp. were not individually identified in this study but grouped into two large groups. The L. innocua group, including L. innocua, L. seeligeri, L. marthii, and L. grayi, was isolated from 56.3 and 34.5 % of the positive rural and urban watershed samples, respectively. The L. welshimeri group, which included L. welshimeri and all other Listeria spp., was isolated from 37 and 43.1 % of the positive rural and urban watershed samples, respectively (Stea et al. 2015). Despite the less frequent isolation of L. ivanovii, this species has been isolated from farm environments (McAuley et al. 2014). While these data indicate that L. ivanovii is one of the least commonly isolated Listeria sensu strictu species, this could also be due to reduced recovery of this species in the enrichment media and isolation protocols that have typically been optimized for recovery of L. monocytogenes.

Conversely, the one Listeria sensu strictu species that may not be globally distributed is L. marthii. Thus far, this species has only been isolated from very specific natural areas in a small part of New York State (USA), Connecticut Hill and Finger Lakes National Forest, which are natural areas in close proximity to each other (Chapin et al. 2014; Sauders et al. 2012). In these same studies, L. marthii was not found in other natural areas and urban areas (Chapin et al. 2014; Sauders et al. 2012). A PubMed search as of November 11, 2015 also was not able to locate other studies that have reported identification of L. marthii. This could at least be partially due to the fact that L. marthii cannot be easily distinguished from the closely related L. innocua and thus could have been misclassified in other studies.

In general, there is no clear indication that different Listeria sensu strictu species are preferably found in certain environments, even though individual studies have identified statistical associations between different environments and isolation of specific Listeria species. For example, a study in the state of New York (USA) reported that L. seeligeri and L. welshimeri were significantly associated with natural environments (P < 0.0001), while L. innocua and L. monocytogenes were significantly associated with urban environments (P < 0.0001) (Sauders et al. 2012). A study carried out in Austria (Linke et al. 2014) found a significant association between the presence of Listeria spp. in soil samples and abiotic conditions such as moisture, pH, and soil type. The authors specifically found that Listeria spp. were more frequently isolated from soil samples with low moisture content, neutral pH, and soil types consisting of a mixture of sand and humus. The same authors also observed a seasonal effect on the prevalence of Listeria spp. in soil with the lowest isolation rates observed in July (winter).

Only the two species considered pathogenic, L. monocytogenes and L. ivanovii, as well as a few L. innocua strains (Johnson et al. 2004; McLauchlin and Rees 2009) show phosphatidylinositol-specific phospholipase C (PI-PLC) activity, while L. monocytogenes, L. ivanovii, and L. seeligeri as well as some L. innocua strains show hemolytic capabilities (Johnson et al. 2004; McLauchlin and Rees 2009). L. ivanovii can be differentiated from L. monocytogenes by its unique ability, among sensu strictu species, to ferment D-ribose (Bertsch et al. 2013; Bille et al. 1992; den Bakker et al. 2014; McLauchlin and Rees 2009; Weller et al. 2015). L. welshimeri can be identified by its ability to ferment D-tagatose, while L. seeligeri is the only sensu strictu species capable of fermenting D-xylose but not capable of fermenting D-ribose or D-tagatose (Bertsch et al. 2013; Bille et al. 1992; den Bakker et al. 2014; McLauchlin and Rees 2009; Weller et al. 2015). L. marthii is the only sensu strictu species incapable of fermenting sucrose, a characteristic that can be used to differentiate strains from this species from other sensu strictu species (den Bakker et al. 2014). While L. innocua is typically identified by its inability to cause hemolysis and ferment D-xylose combined by its ability to ferment glycerol (Bertsch et al. 2013; Bille et al. 1992; den Bakker et al. 2014; McLauchlin and Rees 2009; Weller et al. 2015), hemolytic L. innocua strains are difficult to differentiate from L. monocytogenes and L. seeligeri based on standard biochemical tests (Johnson et al. 2004).

Importantly, phenotypic characteristics do not always allow for unambiguous classification of Listeria isolates. Phenotypic data alone, sometimes in combination with genetic data, have led to description of a number of “atypical” Listeria isolates both before and after 1985. For example, hemolytic L. innocua strains (as discussed above) could be considered atypical Listeria. Similarly, a number of atypical (including non-hemolytic) L. monocytogenes have been described (Burall et al. 2014; Hof 1984; Moreno et al. 2014; Pine et al. 1987). While one could argue that these non-hemolytic L. monocytogenes strains that were described before the taxonomic description of L. marthii may indeed have been L. marthii, a number of these strains were confirmed to truly be atypical L. monocytogenes. For example, the initial ATCC strain (ATCC 15313) which was found to be non-hemolytic (Jones and Seeliger 1983) appears to clearly represent L. monocytogenes. More recently, another non-hemolytic strain was confirmed as belonging to the species L. monocytogenes after whole genome sequencing (Burall et al. 2014). Overall, one cannot exclude though that at least some of the atypical Listeria strains that have been described in the past may represent species that either were not described at the times or have not been identified at all. Future characterization of atypical Listeria isolates by whole genome sequencing and phylogenetic analysis would help to resolve some of these identification challenges and may yield additional species that have not yet been described.

Listeria sensu strictu genomes share many characteristics. The G+C content varies from 34.6 to 41.6 %; genome sizes vary from 2.8 to 3.2 Mb, and Listeria genomes are highly syntenic (i.e., the order of the genes are highly conserved across different species) (den Bakker et al. 2010b). The Listeria sensu strictu pan-genome has been estimated as approximately 6500 genes, 17 % of which are involved in nucleobase, nucleotide, nucleoside, and nucleic acid metabolism, 14 % of which are involved in cellular macromolecular metabolism, and 10 % of which are involved in protein metabolic process (den Bakker et al. 2010b). The high number of internalin genes is another characteristic of Listeria sensu strictu genomes. L. welshimeri seems to have the lowest number of internalin genes among sensu strictu species with nine of these genes found in the only strain analyzed (den Bakker et al. 2010b). On the other hand, five different L. monocytogenes genomes were shown to have between 18 and 28 internalin genes encoded in their genomes (den Bakker et al. 2010b). Three Listeria pathogenicity islands (LiPI) have been identified in the genomes of Listeria sensu strictu strains. These LiPIs are further discussed below. Moreover, a 53-kb island that includes genes involved in the metabolism of ethanolamine, cobalamin, and propanediol has been identified in all Listeria sensu strictu species (Chiara et al. 2015). This island includes 82 genes involved in the cobalamin (vitamin B12) biosynthetic process and utilization of both ethanolamine and propane-2-diol, two carbon sources whose utilization is necessary for L. monocytogenes and Salmonella to cause disease in vertebrate hosts (Conner et al. 1998; Joseph et al. 2006; Klumpp and Fuchs 2007; Mellin et al. 2014). Absence of this island in all Listeria sensu lato species in conjunction with its homology and conserved arrangement of the genes in comparison to sequences from other bacteria led to speculations that the entire island has been transferred to Listeria sensu strictu ancestor through horizontal gene transfer from a Salmonella-like bacterium (Buchrieser et al. 2003) or from gram-positive bacteria (Chiara et al. 2015).

L. monocytogenes is a facultative intracellular pathogen that causes a rare, yet severe, human illness; typical symptoms include septicemia, abortions, and encephalitis (McLauchlin and Rees 2009). In addition, a few instances have been reported where L. monocytogenes infection of humans has led to gastrointestinal illnesses without systemic infections (Aureli et al. 2000; Dalton et al. 1997; Frye et al. 2002). Human listeriosis is virtually always caused by foodborne exposure to L. monocytogenes (Scallan et al. 2011). In addition to human disease, L. monocytogenes also has been reported to cause invasive disease in >40 animal species. L. ivanovii is also considered a pathogen but has been predominantly linked to animal disease with some studies suggesting that L. ivanovii predominantly infects sheep (Chand and Sadana 1999; Sergeant et al. 1991), but occasional isolation of L. ivanovii from bovines (Alexander et al. 1992; Gill et al. 1997) and humans with symptoms consistent with listeriosis suggests that this organism may also be able to cause disease in other animals, including rarely in humans (Cummins et al. 1994; Guillet et al. 2010; Lessing et al. 1994; Ramage et al. 1999; Snapir et al. 2006). In most human cases, L. ivanovii was isolated from the patient’s blood, with no clear evidence of the transmission route. However, at least in one case, the septicemic condition was preceded by a gastrointestinal illness suggesting that the strain was orally acquired (Guillet et al. 2010).

L. innocua was initially considered non-pathogenic (hence its name) and non-hemolytic. Recent work has however identified a number of hemolytic L. innocua isolates. Presumably, these isolates would have been (mis-)classified as L. monocytogenes before the use of molecular methods that allow for identification and phylogenetic characterization (e.g., MLST methods), which clusters hemolytic L. innocua strains with non-hemolytic L. innocua. Interestingly, some hemolytic L. innocua (e.g., FSL J1-023) have been shown to invade (human) Caco-2 cells at same levels as L. monocytogenes (den Bakker et al. 2010b), while another study has characterized the hemolytic L. innocua strain PRL/NW 15B95 as avirulent in a mouse model (Johnson et al. 2004). L. innocua has also been isolated at least once from a fatal human case (Perrin et al. 2003), further supporting that at least some L. innocua may be able to cause human disease. No information whether this strain was hemolytic or not was provided, though. L. innocua strains carrying a L. monocytogenes lineage I-specific pathogenicity island, LiPI-3, have also been found and shown to be hemolytic when the gene llsA, encoded within LiPI-3, was expressed from a constitutive highly expressed Listeria promoter (Clayton et al. 2014). One of these strains was isolated from a human patient with meningitis in the UK (Clayton et al. 2014). Whole genome sequencing has confirmed that hemolytic L. innocua strains contain a complete Listeria pathogenicity island 1 (also referred as the prfA cluster); specifically, the hemolytic isolate FSL J1-023 was found to contain a Listeria pathogenicity island 1 (LiPI-1) that shows a high level of homology with the L. monocytogenes pathogenicity island 1 (den Bakker et al. 2010a). This and genomically similar hemolytic L. innocua strains thus will test positive by PCR-based and other molecular methods that detect L. monocytogenes based on the presence of hly or other genes located in the pathogenicity island 1. Interestingly, this same hemolytic L. innocua isolate (FSL J1-023) did not contain the complete inlAB operon, which encodes two internalins (InlA and InlB) that are critical virulence factors, but only contained inlA. Other atypical L. innocua strains encoding LiPI-1 and inlA have been found in Brazil (Moreno et al. 2014) and in Korean-imported clams (Johnson et al. 2004), suggesting that these atypical L. innocua strains are widespread. The specific implications that the presence of inlA and the absence of inlB have on virulence in humans and other animals remain to be determined. While InlA is essential for invasion of human intestinal epithelial cells, InlB appears to contribute to invasion of human hepatic and placental cells (Lecuit 2007). While the data available to date suggest that at least some L. innocua may have the potential to cause invasive human disease, further data are thus needed to determine whether all or some hemolytic L. innocua are a human health hazard and what their virulence is relative to L. monocytogenes.

While isolates of the species L. seeligeri also typically are hemolytic, this species is generally considered non-pathogenic. Interestingly, non-hemolytic L. seeligeri strains have been reported (Volokhov et al. 2006), and one study suggested that non-hemolytic L. seeligeri represent a recent loss of the Listeria pathogenicity island 1 (prfA cluster) (den Bakker et al. 2010a). Some possible cases of human disease caused by L. seeligeri have been described, including a human meningitis case (Rocourt et al. 1986). Genomic studies suggest that hemolytic L. seeligeri contain a variant of the Listeria pathogenicity island 1 (prfA cluster), which is characterized by the presence of additional genes not found in L. monocytogenes and a partial duplication of the gene plcB (Schmid et al. 2005), which seems to have been split into two independent ORFs in some strains (den Bakker et al. 2010b). To date, the inlAB operon has not been found among L. seeligeri strains. A functional study (Stelling et al. 2010) on selected L. seeligeri virulence genes indicates that (i) regulation of prfA expression differs between L. monocytogenes and L. seeligeri, although hly transcription is temperature dependent in both species, and (ii) PrfA and Hly functions are largely, but not fully, conserved between L. seeligeri and L. monocytogenes. While virulence gene homologs and their expression thus appear to have adapted to distinct but possibly related functions in L. monocytogenes and L. seeligeri (Stelling et al. 2010), it remains to be determined whether L. seeligeri is pathogenic in specific, yet to be determined, host species. Despite rare isolation from humans with illness symptoms, there is no evidence that L. seeligeri should be considered a pathogen or presents a human health risk comparable to L. monocytogenes.

On the other hand, all L. marthii and L. welshimeri isolates characterized to date have been non-hemolytic. None of the (few) L. marthii and L. welshimeri genomes sequenced so far contain the Listeria pathogenicity island 1 (prfA cluster), further supporting that members of these two species are non-pathogenic.

Like the Listeria sensu strictu species, all sensu lato species are catalase positive, non-spore-forming, non-capsulated, and rod-shaped. Listeria sensu lato species present several phenotypic characteristics that distinguish them from Listeria sensu strictu species (see Table 1 for details). While all sensu strictu species are Voges-Proskauer reaction positive and hence able to produce acetoin from fermentation of glucose through the butanediol pathway, among sensu lato species, only L. grayi and one out of two L. aquatica strains analyzed have this ability (den Bakker et al. 2014). Conversely, while none of the sensu strictu species are able to reduce nitrate to nitrite, all sensu lato species but L. floridensis can reduce nitrate (den Bakker et al. 2014; Weller et al. 2015). Motility is another characteristic that appears restricted to the Listeria sensu strictu species and L. grayi, although contradictory results were initially obtained for L. rocourtiae and L. weihenstephanensis. In initial studies, Leclercq et al. (2010) and Lang Halter et al. (2013) reported that isolates representing these species were motile, while subsequent studies (Bertsch et al. 2013; den Bakker et al. 2014) reported no motility for representatives of these species. Subsequent motility tests carried out by Weller et al. (2015) also found no motility with all sensu lato strains tested (with the exception of L. grayi strains) at temperatures ranging from 4 to 37 °C. These findings are consistent with genomic studies that reported absence of flagellar genes from all Listeria sensu lato strains (except L. grayi), thus suggesting that L. grayi is the only motile Listeria sensu lato species (Chiara et al. 2015; den Bakker et al. 2013; den Bakker et al. 2014).

In terms of acid production from different carbohydrate substrates, a high variability has been observed within and between sensu lato species. All sensu lato species were able to acidify D-xylose and D-glucose, but none were able to acidify glucose 1-phosphate nor inulin. Other molecules presented variable results depending on the species (Weller et al. 2015). Interestingly, the species L. fleischmannii, L. aquatica, and L. floridensis all seem to have lost the ability to grow in liquid media at 4 °C, a key characteristic shared among other members of the genus Listeria. These three species form a cluster within the genus Listeria and share the most common recent ancestor with Listeria sensu strictu species and L. grayi, which suggests that the inability to grow at low temperatures was lost in this group.

While molecular methods provide for most reliable species classification, some specific phenotypic characteristics can be used to differentiate each species within Listeria sensu lato. L. grayi can be distinguished from other sensu lato species by a positive result in the Voges-Proskauer test and by a positive result in a motility test (McLauchlin and Rees 2009; Weller et al. 2015). Moreover, L. grayi can be differentiated from Listeria sensu strictu species by its ability to ferment D-mannitol (McLauchlin and Rees 2009; Weller et al. 2015). L. fleischmannii is unable to grow well at low temperatures and can be differentiated from other sensu lato species by its ability to ferment D-arabitol, L-rhamnose, and D-ribose (Bertsch et al. 2013; den Bakker et al. 2013; Weller et al. 2015). In addition to being characterized by its inability to grow at temperatures below 7 °C, L. floridensis is the only sensu lato species unable to reduce nitrate (den Bakker et al. 2014; Weller et al. 2015). L. aquatica is the only Listeria species unable to ferment maltose and α-methyl D-glucoside and the only sensu lato species able to ferment D-tagatose (den Bakker et al. 2014; Weller et al. 2015). L. newyorkensis can be differentiated from other Listeria species by its inability to acidify D-arabitol, absence of α-mannosidase activity, and ability to acidify D-ribose, D-galactose, and L-arabinose (Weller et al. 2015). L. cornellensis can be distinguished from other sensu lato species by being unable to ferment L-rhamnose at 37 °C and presents a weak acidification of lactose (den Bakker et al. 2014; Weller et al. 2015). L. rocourtiae can be distinguished from other sensu lato species by its positive α-mannosidase activity combined with its inability to ferment L-arabinose and D-arabitol (Leclercq et al. 2010; Weller et al. 2015). L. weihenstephanensis can be differentiated from other sensu lato species by its ability to ferment D-arabitol, L-rhamnose, and D-mannitol (Lang Halter et al. 2013; Weller et al. 2015). L. grandensis may be differentiated from L. cornellensis by its stronger ability to ferment lactose (den Bakker et al. 2014; Weller et al. 2015). L. riparia can be distinguished from other sensu lato species by its positive α-mannosidase activity in combination with the ability to ferment L-rhamnose, D-galactose, and L-arabinose (den Bakker et al. 2014; Weller et al. 2015). L. booriae can be differentiated from other Listeria by its ability to ferment melibiose, L-arabinose, and D-arabitol (Weller et al. 2015). While a number of phenotypic characteristics can thus be used to differentiate Listeria sensu lato species, identification of Listeria sensu lato isolates using standard biochemical test kits may often not be straight forward as carbohydrate substrates that allow for species differentiation may not be included and as identification schemes and databases may not yet have been updated with information on the recently described Listeria species.

In terms of pathogenicity, none of the sensu lato species seem to be pathogenic as they all failed to produce positive results in both hemolytic tests and phosphoinositide phospholipase C activity tests (Bertsch et al. 2013; den Bakker et al. 2013; den Bakker et al. 2014; Lang Halter et al. 2013; Leclercq et al. 2010; Weller et al. 2015). Moreover, invasion assays using human carcinogenic cell lines (Caco-2) showed that L. fleischmannii is not able to internalize into human intestinal epithelial cells further supporting that this specific species is not pathogenic for humans (Bertsch et al. 2013).

The availability of genome sequence data for all Listeria sensu lato species not only presented unique opportunities to better characterize these species but also allowed for novel insights in the evolution of virulence related and other relevant phenotypes in the overall genus Listeria (Fig. 2). The G+C content of sensu lato genomes varies from 38.3 % (L. fleischmannii) to 45.2 (L. newyorkensis and L. booriae). As expected based on phenotypic data, genome analyses showed that none of the Listeria sensu lato species harbor the Listeria pathogenicity island 1, which includes the major virulence genes prfA, plcA, hly, mpl, actA, plcB, or the Listeria pathogenicity island 2, which includes inlA and inlB. With the exception of L. grayi, none of the other sensu lato species carry the motility genes that encode flagellar proteins, which explains why these species are not motile. Phylogenetic analyses suggest that the ancestor of Listeria sensu strictu and L. grayi acquired the whole flagellar biosynthetic genes through horizontal gene transfer from an ancestor of the Bacillus cereus complex (Chiara et al. 2015) (see Fig. 2). The only gene related to motility that is present in a sensu lato species (other than L. grayi) is mogR, which was identified only in L. fleischmannii. This gene encodes for the motility gene repressor MogR (den Bakker et al. 2013); its specific function in this species remains to be determined. Another interesting genomic feature was observed among the genome sequences for two L. grayi strains. Four genes, genomically clustered, were found among these strains and encode for proteins involved in the biosynthesis of riboflavin (Chiara et al. 2015). The origin of these genes is not clear. However, the absence of these genes from all other Listeria species suggests that the cluster was acquired via horizontal gene transfer by the ancestor of L. grayi from another bacterial species.

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Interestingly, Listeria sensu lato species genomes showed an underrepresentation of genes associated with internalin domains when compared to sensu strictu species (Chiara et al. 2015; den Bakker et al. 2010b). This suggests that expansion of internalin genes happened after the divergence between Listeria sensu strictu and Listeria sensu lato and further supports that Listeria sensu lato strains are unlikely to be pathogenic for mammalian species as internalins have been shown to typically be important for interactions between Listeria and mammalian hosts (Pizarro-Cerda et al. 2012). Interestingly, L. fleischmannii subsp. coloradonensis genome has also been found to harbor a gene encoding a putative mosquitocidal toxin MTX2 from Bacillus, which also resembles the Clostridium perfringens potent epsilon toxin ETX that causes rapid fatal enterotoxemia in animals (den Bakker et al. 2013); this raises the possibility that at least some sensu lato isolates may be able to cause disease in non-mammalian hosts such as insects.

In taxonomy, delineation of different species is governed by fairly well-defined criteria. While, traditionally, DNA-DNA hybridization values of <70 % were used to delineate different species (Wayne et al. 1987), more recently whole genome sequencing-based criteria (ANIb) have been used to define different species (Richter and Rossello-Mora 2009). In Listeria, this approach was used by den Bakker et al. (2014) and Weller et al. (2015) to classify newly identified Listeria strains into seven distinct species and to confirm classification into separate species for other species that had been proposed previously (Bertsch et al. 2013; Lang Halter et al. 2013; Leclercq et al. 2010).

While clear cutoffs exist for classification of isolates into a new species, cutoffs for defining new genera are much less well defined (Qin et al. 2014). It has been suggested that a 16S rRNA diversity higher than 5 % or an amino acid identity (AAI) lower than 70 % could be used to determine whether two species should belong to distinct genera (Konstantinidis and Tiedje 2007). Qin et al. (2014) have suggested that a percentage of conserved proteins (POCP) > 50 % should be used as a threshold to define whether two species should be classified into the same genus or not. Deloger et al. (2009) suggested the utilization of the DNA maximal unique matches (MUMs) shared by two genomes as a tool for classification of species and genus. However, there is no clear agreement on definitive thresholds that could be used to determine boundaries of bacterial genera. A clear convergence of phylogenetic and phenotypic data as well as whole genome sequencing-based similarity measures suggested though that the current genus Listeria may warrant reclassification into more than one genus. Listeria sensu strictu clearly represents a distinct and well-defined group of organisms that should be maintained as a single genus with the name Listeria. The species currently grouped in Listeria sensu lato on the other hand appear to warrant reclassification into three different genera (see Fig. 1); reclassification into more than one genus is not only required to avoid phylogenetically incongruent genera but also yields proposed genera with distinct and unique phenotypic characteristics (e.g., all species in the proposed genus Mesolisteria are not able to grow at 4 °C). Specifically, we propose that L. grayi could be classified into a distinct new genus named Murraya; this represents a revival of the previously proposed genus Murraya (Wemekamp-Kamphuis et al. 2002). ANIb values based on comparisons of genome sequences of Murraya strains and Listeria sensu stricto strains support that these taxa are highly divergent (ANIb <73 %). L. fleischmannii, L. aquatica, and L. floridensis could be classified into another genus named Mesolisteria (referring to the mesophillic nature of species within this genus). Finally, the species L. newyorkensis, L. cornellensis, L. rocourtiae, L. weihenstephanensis, L. grandensis, L. riparia, and L. booriae could be classified into the new genus named Paenilisteria (almost Listeria, referring to the phenotypic resemblance to the genus Listeria). Importantly, Listeria sensu lato species present some phenotypic features different from those that characterize the genus Listeria. For example, with the exception of L. grayi, all sensu lato species are non-motile, while all sensu strictu species are motile. All sensu lato species with the exception of L. floridensis are capable of reducing nitrate to nitrite, an ability not present among sensu strictu species. Moreover, three sensu lato species (L. fleischmannii, L. floridensis, and L. aquatica) are unable to grow at low temperatures, one of the major characteristics of the genus Listeria. Genomically, sensu lato species also lack features characteristic of the genus Listeria such as a high number of genes encoding for internalin-like proteins. Based on the data available to date, we thus would like to propose that the Listeria sensu lato species may warrant classification into separate genera according to their phylogenetic and phenotypic characteristics (Fig. 2), even though further genome sequence analyses (e.g., determination of AAI, POCP, and MUM values) may be helpful and needed for a final reclassification proposal.