key: cord-0840348-2oux1ghd
authors: Basmaci, Romain; Bidet, Philippe; Bonacorsi, Stéphane
title: Kingella kingae and Viral Infections
date: 2022-01-21
journal: Microorganisms
DOI: 10.3390/microorganisms10020230
sha: 181e34054843d07d9c912b46839d4f92c4ef0eec
doc_id: 840348
cord_uid: 2oux1ghd

Kingella kingae (K. kingae) is an oropharyngeal commensal agent of toddlers and the primary cause of osteoarticular infections in 6–23-month-old children. Knowing that the oropharynx of young children is the reservoir and the portal of entry of K. kingae, these results suggested that a viral infection may promote K. kingae infection. In this narrative review, we report the current knowledge of the concomitance between K. kingae and viral infections. This hypothesis was first suggested because some authors described that symptoms of viral infections were frequently concomitant with K. kingae infection. Second, specific viral syndromes, such as hand, foot and mouth disease or stomatitis, have been described in children experiencing a K. kingae infection. Moreover, some clusters of K. kingae infection occurring in daycare centers were preceded by viral outbreaks. Third, the major viruses identified in patients during K. kingae infection were human rhinovirus or coxsackievirus, which both belong to the Picornaviridae family and are known to facilitate bacterial infections. Finally, a temporal association was observed between human rhinovirus circulation and K. kingae infection. Although highly probable, the role of viral infection in the K. kingae pathophysiology remains unclear and is based on case description or temporal association. Molecular studies are needed.

Kingella kingae (K. kingae), a species of Gram-negative bacteria facultative β-hemolytic coccobacillus, is an oropharyngeal commensal agent of toddlers and the primary cause of osteoarticular infections (OAI) in children in several countries, especially in the 6-23-month age group [1] [2] [3] [4] [5] .

Several virulence factors and clones have been suggested to be involved in the pathophysiology of K. kingae invasive infections [6] [7] [8] [9] , but the role of viral infections has also been suggested. An accumulation of data sustain this hypothesis: (i) symptoms of viral infections are frequently concomitant with K. kingae infection [1] ; (ii) some respiratory viruses have been identified in children experiencing a K. kingae infection [10] ; (iii) some day-care center outbreaks of K. kingae infection followed outbreaks of viral infections [11] ; and (iv) a temporal association has been observed between human rhinovirus circulation in the population and the epidemiology of K. kingae infection [12] .

In this narrative review, we attempt to describe the current knowledge of the interaction between Kingella kingae and viral infections.

A narrative review based on the published literature was performed. A literature search with free terms related to viral infections, with no quotations (virus; "OR" viral infection; "OR" viral symptoms; "OR" enterovirus; "OR" coxsackievirus; "OR" rhinovirus; "OR" varicella; "OR" influenza; "OR" adenovirus; "OR" parainfluenzae; "OR" metapneumovirus; "OR" Ebstein Barr virus; "OR" cytomegalovirus; "OR" herpes simplex; "OR" parvovirus) combined with "AND" K. kingae was conducted using the PubMed database with the PubMed Advanced Search Builder until 9 November 2021. No language restriction was used. Potential articles were screened step-by-step starting with the title, then the abstract, and finally the full text when necessary.

However, this search strategy did not accurately identify those papers on K. kingae infections suggesting that the oropharynx was the portal of entry for these infections, and that viral symptoms were frequently concomitant with K. kingae infections. To complete the narrative review, these papers were identified from the references linked to the articles found with the search strategy or to recent published review papers on K. kingae [1, 3, 11] .

Overall, only 50 published articles were identified by the search strategy. Thirty-one articles were excluded because they were outside of the relevant topics, 3 were excluded because they specifically described K. kingae infection in adult HIV patients, which is very rare, and is not representative of the majority of K. kingae infections. Finally, 16 published articles were found to describe the association between K. kingae and viral infections. Five additional papers were included in the review.

Many authors have described the temporal relationship between viral symptoms and series of K. kingae sporadic infection. However, most of these studies do not specify the virus or the specific viral syndrome involved.

As early as 1985, Claesson et al. described that 12/33 (36%) patients with K. kingae infection had a history of recent or current upper respiratory tract infection [13] . In addition, two patients had an extremely poor dental status, and data were missing for the 19 remaining cases. Overall, the authors estimated that an obvious possibility of invasion through a damaged mucosal barrier in the oral or nasopharyngeal tract was observed in at least 42% of patients [13] .

Similarly, in 1993, Yagupsky et al. observed that 14/25 (56%) patients with K. kingae infection had a concomitant upper respiratory tract infection or stomatitis [14] . In addition to seasonal distribution of K. kingae infection, the putative role of respiratory virus to facilitate tissue invasion by bacteria was suggested, as previously described with Haemophilus infuenzae b [15] .

These data were confirmed in 2010, when Dubnov-Raz et al. published a large series of 322 K. kingae infections in Israel [16] . In 200 out of 322 (62.1%) episodes, patients had an acute illness reported in the week before or coincidental with the invasive K. kingae infection. These were upper respiratory tract infection, pharyngitis, acute otitis media, aphthous stomatitis, vomiting, or diarrhea [16] .

In a study assessing oropharyngeal viral carriage in children with a K. kingae osteoarticular infection in a 1-year period, Basmaci et al. observed that 10/17 (58.9%) patients presented at least one symptom of upper respiratory tract infection, and that among the seven patients with no symptoms, six carried a respiratory virus [10] .

In a small series of K. kingae tenosynovitis from three tertiary care centers in France, Switzerland and Israel published in 2018, authors observed that eight out of nine children had viral infection in the preceding month [17] .

Overall, more than 60% of reported patients in these studies presented viral symptoms before or concomitantly with a K. kingae infection (Table 1 ) [10, [13] [14] [15] [16] [17] . Similar results were observed under the specific conditions of K. kingae infection occurring in day-care centers. In a review published in 2016, which summarized the data of eight published outbreaks on 27 patients, authors found that previous or concomitant oral ulceration was detected in 10 out of 18 patients (55.6%), for whom the data were available [11] .

Knowing that the oropharynx of young children is the reservoir and the portal of entry of K. kingae, these results suggested that a viral infection may promote K. kingae infection [1, 18] .

To go further, some case reports or series describe the association of K. kingae with a specific viral syndrome or identify some viruses. However, to the best of our knowledge, only one article has performed a systematic screening of respiratory viruses in patients during K. kingae infection, using a FilmArray ® respiratory panel [10] . In this paper, the authors described that among 21 K. kingae osteoarticular infections in a 1-year period, 19 (90.5%) carried at least one respiratory virus in their oropharynx. The distribution was as follows: human rhinovirus, 12 (57.1%); coronavirus OC43, 4 (19.0%); parainfluenzae (1, 2, 3 or 4), 3 (14.3%); enterovirus, 2 (9.5%); and adenovirus, 2 (9.5%) [10] .

Other published articles have focused on one virus or specific viral syndrome. However, very few papers have focused on this topic, and fewer than 50 patients have been fully described. For the sake of clarity and consistency, we chose to describe the literature for each virus independently. The full description of identified viruses or viral syndromes is shown in Table 2 .

Three published articles describe the presence of human rhinovirus during K. kingae infection, and one assesses the temporal association between these two pathogens (see Section 3.3 below).

The largest series was described above, when HRV was identified in 12/21 children with K. kingae OAI between January and December 2013 in France [10] . In addition, the same authors published two atypical cases of K. kingae infection in children, with one case involving a soft tissue abscess and one case a femoral Brodie abscess; both patients had concomitant human rhinovirus infection [19] . In 1991, Carden et al. published a case of an 11-month-old girl with metastatic endophthalmitis due to K. kingae, and a rhinovirus was isolated from her nasopharynx [20] . 

Five papers describe the concomitance of K. kingae infection with hand, foot and mouth disease (HFMD) [21] [22] [23] [24] and one paper identifies enterovirus infection [10] . HFMD is a childhood disease caused by human enteroviruses that particularly affects toddlers in the age range of 6-23 months [33] . From April to October 2013, seven children ranging from 10 to 23 months old were diagnosed with K. kingae osteoarticular infections in Marseille, France, and with HFMD or stomatitis in the previous weeks. A coxsackievirus-A6 was identified in the stools of one child having HFMD [21] . The same authors described an outbreak of K. kingae infections in five toddlers attending the same classroom in a day-care center in Marseille [22] . These patients were probably the same as those in the former study. In this K. kingae outbreak, the authors observed that an outbreak of herpangina and HMFD, with an attack rate of clinical infections of 38.3% (8/21), began in the index classroom 2 weeks before the first K. kingae case was diagnosed. Moreover, upper respiratory tract infections and fever affected a large number of the index classmates during the same period [22] .

In 2007, an outbreak of K. kingae infection was observed in a daycare center in the USA [25] . An 11-month-old young girl presented with altered mental status and fever. She was diagnosed with K. kingae endocarditis and meningitis, and she had presented with HFMD 3 weeks earlier.

In 2017, an article described the case of a 14-month-old girl with an 11-day history of fever and a 1-day period of vomiting due to a K. kingae endocarditis [23] . She was attending a childcare center, where a severe outbreak of HFMD (five toddlers out of 15 attendees) had occurred a few weeks preceding the child's admission to hospital. The case reported experienced HFMD infection during the outbreak. Of these five children, a 14-month-old boy was also suspected of having K. kingae infection.

As previously mentioned, an enterovirus was identified in two patients of the series published by Basmaci et al. [10] .

Finally, a case was reported in a 31-year-old woman with K. kingae septicemia in the context of oral lesions from coxsackievirus infection, proven by serology [24] .

In a study published in 1998, 16 patients with K. kingae infection had erosions in the buccal, gingival and/or glossal surfaces [26] . Duration of the stomatitis before blood sampling was 2 to 6 days. In four children with gingivostomatitis, herpes simplex virus was isolated from oral lesions, and in an additional four patients, the clinical data suggested herpetic gingivostomatitis.

A recent paper reported the case of a previously healthy 18-month-old young girl with a diagnosis compatible with herpetic gingivostomatitis and K. kingae occult bacteremia [27] .

In 1997, Waghorn et al. reported a case of fatal K. kingae endocarditis following acute chickenpox with erythrobastopenia and thombocytopenia in a 9-month-old infant. He was first admitted 10 days after developing chickenpox, was discharged after 5 days with initial clinical improvement, but he was readmitted 5 days after discharge with sudden breathing difficulties and cardiorespiratory arrest. No viral test was performed to isolate VZV [28] .

In 1998, among patients with stomatitis, Amir et al. identified one K. kingae infection in a child concomitantly with a clinically diagnosed VZV infection [26] .

More recently, Kampouroglou et al. reported a subacute osteomyelitis by K. kingae in a 5-year-old boy after chickenpox infection [29] .

Other viral infections were more rarely identified concomitantly with K. kingae infection. As previously discussed, in the study published by Basmaci et al., different viruses were identified: coronavirus OC43 in 4 (19.0%) children; parainfluenzae (1, 2, 3 or 4) in 3 (14.3%) children; and adenovirus in 2 (9.5%) children [10] . Chosidow et al. reported the case of a 16-month-old boy with recurrent K. kingae septic arthritis with a concomitant viral infection with parainflenzae 3 virus [30] .

To the best of our knowledge, only one case was associated with Epstein-Barr virus (EBV) and one with influenza virus.

A healthy 2-year-old child presented febrile torticollis with painful 1-cm cervical lymph nodes [31] . Blood tests showed an acute EBV infection. A CT scan associated with MRI showed an inflammatory process at the C1-C2 vertebrae and K. kingae-specific PCR was positive on biopsy.

A 14-month-old-girl was admitted with influenza A infection. She was suspected of encephalomyelitis based on fever, prostration, hypertonia, hyperalgesia, urinary retention, and meningitis. She was treated with 5 methylprednisolone bolus. After the last bolus, a systolic cardiac murmur was heard and a K. kingae endocarditis was diagnosed, complicated with several cerebral and renal complications [32] .

Recently, a French study analyzed the seasonality of K. kingae OAI in two tertiary-care centers in Paris on a 7-year period, including 322 cases of K kingae osteoarticular infection and compared the seasonality with the data of respiratory virus detection from the Réseau National des Laboratoires network in coordination with the National Influenza Center of France [12] . The authors observed high activity for both K. kingae osteoarticular infection and HRV during the fall (98 (30.4%) and 2401 (39.1%) cases, respectively) and low activity during summer (59 (18.3%) and 681 (11.1%) cases, respectively). Weekly distributions of K. kingae osteoarticular infection and rhinovirus activity were significantly correlated (r = 0.30; p = 0.03), while no significant correlation was found between the weekly distribution of K. kingae osteoarticular infection and respiratory syncytial virus, influenza virus, and metapneumovirus [12] (Figure 1 ). 

The peak of incidence of many respiratory viral infections coincides with th K. kingae carriage and invasive infections [1] . Knowing that the reservoir of K. kin oropharynx of young children [1, 34] , and that K. kingae possesses some virulenc such as type IV pili (allowing adhesion to respiratory epithelium) [6, 35, 36] , and R (having a cytotoxic activity able to breach the respiratory epithelium) [7, 37, 38] , plausible that damage to the mucosal layer caused by a viral disease facilitates of K. kingae organisms in the bloodstream [1] .

In this review, we observed that the majority of available and published da fied human rhinovirus or enterovirus, especially coxsackievirus responsible o during K. kingae infection [10, 12, [19] [20] [21] [22] [23] [24] , whereas other viruses were less commo tified.

Of interest, rhinovirus and enterovirus are both members of the Picornaviri ily, which includes nine genera, six of which are pathogenic for humans: enterov novirus, hepatovirus, parechovirus, cardiovirus, and kobuvirus [39] .

Three different species of HRV were described: HRV-A, HRV-B, and HRVwas discovered more recently [39, 40] . It has previously been described that HRV infection may predispose to bac fections. Indeed, temporal correlation between HRV infection and Streptococc moniae has been described [41] . Moreover, HRV infection induces overexpression let-activating factor (PAF) receptor and activation of NF-kB increasing S. pneum herence to the airway epithelial cells [41] . It has also been described that HRV ma Staphylococcus aureus infections [42] . Finally, HRV is able to increase paracellular bility of airway epithelial cells after infection by disrupting airway epithelial barr tion [43] .

Apart from one study that observed a temporal association between HRV kingae infections and small series or case reports, no data are available from ce animal models to explain the interaction between HRV, respiratory epithelial cell 

The peak of incidence of many respiratory viral infections coincides with the age of K. kingae carriage and invasive infections [1] . Knowing that the reservoir of K. kingae is the oropharynx of young children [1, 34] , and that K. kingae possesses some virulence factors such as type IV pili (allowing adhesion to respiratory epithelium) [6, 35, 36] , and RTX toxin (having a cytotoxic activity able to breach the respiratory epithelium) [7, 37, 38] , it seems plausible that damage to the mucosal layer caused by a viral disease facilitates the entry of K. kingae organisms in the bloodstream [1] .

In this review, we observed that the majority of available and published data identified human rhinovirus or enterovirus, especially coxsackievirus responsible of HFMD during K. kingae infection [10, 12, [19] [20] [21] [22] [23] [24] , whereas other viruses were less commonly identified.

Of interest, rhinovirus and enterovirus are both members of the Picornaviridae family, which includes nine genera, six of which are pathogenic for humans: enterovirus, rhinovirus, hepatovirus, parechovirus, cardiovirus, and kobuvirus [39] .

Three different species of HRV were described: HRV-A, HRV-B, and HRV-C, which was discovered more recently [39, 40] . It has previously been described that HRV infection may predispose to bacterial infections. Indeed, temporal correlation between HRV infection and Streptococcus pneumoniae has been described [41] . Moreover, HRV infection induces overexpression of plateletactivating factor (PAF) receptor and activation of NF-kB increasing S. pneumoniae adherence to the airway epithelial cells [41] . It has also been described that HRV may induce Staphylococcus aureus infections [42] . Finally, HRV is able to increase paracellular permeability of airway epithelial cells after infection by disrupting airway epithelial barrier function [43] .

Apart from one study that observed a temporal association between HRV and K. kingae infections and small series or case reports, no data are available from cellular or animal models to explain the interaction between HRV, respiratory epithelial cells, and K. kingae, although further studies would be interesting to address this hypothesis. Moreover, whether an HRV species is more involved in the K. kingae pathogenesis remains to be determined.

Enterovirus is a large genus including different species (enterovirus, poliovirus, coxsackievirus) and more than 300 serotypes. Coxsackievirus are organized in two groups: 23 types of coxsakievirus A and six types of coksackievirus B. Coxsakievirus A is responsible for HFMD, whereas coxsakievirus B is often responsible for more severe disease, such as myocarditis.

The effect on coxsakieviruses B on adherence and invasion on Hep-2 epithelial cells was different depending on the bacteria, whereby adherence and invasion increased for Campylobacter and Salmonella Typhimurium, while they decreased for Escherichia coli and Shigella [44] [45] [46] . These scarce data cannot be extrapolated to different serotypes of enterovirus or coxsakievirus nor in respiratory epithelial cells and to the putative interaction with K. kingae. To date, only the clinical descriptions that we have reported in this review support the hypothesis of such interaction between both pathogens [10, [21] [22] [23] [24] [25] ; however, further studies are needed to better understand the potential interaction between some serotypes of enterovirus and K. kingae.

Finally, our narrative review has some limitations. Despite an increasing available literature on K. kingae infection over three decades, very few papers have focused on the concomitance between viral infections and K. kingae infections in terms of either epidemiology, microbiology, or molecular studies. A limited number of papers was analyzed in this review, which may not be representative of the majority of K. kingae infections and is not sufficient to draw strong conclusions.

Although we observed that more than 60% of reported patients presented viral symptoms before or concomitantly with a K. kingae infection, we cannot exclude that this number is overestimated, because this review focused on published papers describing virus and K. kingae coinfection.

Current knowledge suggests that respiratory viral infections play a probable major role in the pathophysiology of K. kingae in breaching the respiratory epithelium; however, this hypothesis is based on only a small number of cases or series and temporal association. Molecular studies on cellular cultures would be of great interest in better understanding such mechanisms.

Kingella kingae: Carriage, transmission, and disease

Evaluation of a real-time PCR assay for simultaneous detection of Kingella kingae and Staphylococcus aureus from synovial fluid in suspected septic arthritis

Kingella kingae-Associated Pediatric Osteoarticular Infections: An Overview of 566 Reported Cases

New Real-Time PCR-Based Method for Kingella kingae DNA Detection: Application to Samples Collected from 89 Children with Acute Arthritis

Kingella kingae osteoarticular infections in young children: Clinical features and contribution of a new specific real-time PCR assay to the diagnosis

Kingella kingae expresses type IV pili that mediate adherence to respiratory epithelial and synovial cells

Identification and characterization of an RTX toxin in the emerging pathogen Kingella kingae

Modulation of Kingella kingae adherence to human epithelial cells by type IV Pili, capsule, and a novel trimeric autotransporter

Genotyping of Invasive Kingella kingae Isolates Reveals Predominant Clones and Association with Specific Clinical Syndromes

High respiratory virus oropharyngeal carriage rate during Kingella kingae osteoarticular infections in children

Patterns of Kingella kingae Disease Outbreaks

Temporal Association Between Rhinovirus Activity and Kingella kingae Osteoarticular Infections

Kingella kingae Infections: A Review and a Presentation of Data from 10 Swedish cases. Scand

Clinical features and epidemiology of invasive Kingella kingae infections in southern Israel

Nasopharyngeal viral isolates in children with Haemophilus influenzae type B meningitis

Invasive pediatric Kingella kingae Infections: A nationwide collaborative study

Kingella kingae hand and wrist tenosynovitis in young children

Pharyngeal colonization by Kingella kingae in children with invasive disease

Two atypical cases of Kingella kingae invasive infection with concomitant Human Rhinovirus infection

Kingella kingae endophthalmitis in an infant

Foot and Mouth Disease and Kingella kingae Infections

An outbreak of Kingella kingae infections associated with hand, foot and mouth disease/herpangina virus outbreak in Marseille

An Outbreak of Kingella kingae Infections Complicating a Severe Hand, Foot, And Mouth Disease Outbreak

Kingella kingae septicemia in a patient with coxsackievirus infection

Kingella kingae endocarditis and a cluster investigation among daycare attendees

Invasive Kingella kingae infection associated with stomatitis in children

Occult bacteremia due to Kingella kingae associated with herpetic gingivostomatitis

Kingella kingae endocarditis following chickenpox in infancy

Subacute osteomyelitis by Kingella kingae in a 5-year-old boy after chickenpox infection

Recurrent Acute Septic Arthritis Caused by Kingella kingae in a 16-Month-Old Boy

Rare cause of cervical osteoarthritis

Kingella kingae Sequence Type 25 Causing Endocarditis with Multiple and Severe Cerebral Complications

An epidemiological study

Prevalence of Kingella kingae oropharyngeal carriage and predominance of type a and type b polysaccharide capsules among French young children

Expression of Kingella kingae type IV pili is regulated by sigma54, PilS, and PilR

Examination of type IV pilus expression and pilus-associated phenotypes in Kingella kingae clinical isolates

RTX Toxin Plays a Key Role in Kingella kingae Virulence in an Infant Rat Model

Cytotoxic effects of Kingella kingae outer membrane vesicles on human cells

Ratification vote on taxonomic proposals to the International Committee on Taxonomy of Viruses

Temporal association between rhinovirus circulation in the community and invasive pneumococcal disease in children

Rhinoviruses promote internalisation of Staphylococcus aureus into non-fully permissive cultured pneumocytes

Rhinovirus disrupts the barrier function of polarized airway epithelial cells

Coxsackie B1 virus-induced changes in cell membrane-associated functions are not responsible for altered sensitivity to bacterial invasiveness

Effect of enteroviruses on adherence to and invasion of HEp-2 cells by Campylobacter isolates

Invasiveness of Salmonella typhimurium in HEp-2 cell cultures preinfected with Coxsackie B 1 virus