Streptococcus suis is a Gram-positive, facultative anaerobic bacterium belonging to the family Streptococcaceae, characterized by its spherical or ovoid morphology and tendency to occur in pairs or short chains, exhibiting α-hemolysis on blood agar.[1] Primarily a commensal in the upper respiratory tract (tonsils and nasal cavities), genital tract, and alimentary tract of pigs, it is also sporadically found in other animals such as horses, dogs, and cats.[1] As a major pathogen in the swine industry, it causes significant economic losses worldwide through diseases like meningitis, septicemia, arthritis, pneumonia, and endocarditis in post-weaned piglets, often acting as an opportunistic invader under stressful conditions.[2] Recognized as an emerging zoonotic agent since the 1960s, it poses a public health threat, with over 1,600 human cases reported across more than 30 countries as of 2013, predominantly in Southeast Asia and Europe.[2]In humans, S. suis infections typically result from occupational exposure, such as among pig farmers, butchers, and slaughterhouse workers, or through consumption of undercooked pork products, leading to severe manifestations including meningitis (the most common), septicemia, arthritis, endocarditis, and a distinctive streptococcal toxic shock-like syndrome (STSLS) characterized by high fever, rash, and multi-organ failure.[1]Hearing loss occurs in up to 60-70% of meningitis survivors, underscoring the bacterium's neuroinvasive potential.[2]Transmission occurs via direct contact with infected pigs or contaminated pork, with no evidence of sustained human-to-human spread, though outbreaks highlight its epidemic potential in high-risk settings.[1]Virulence is mediated by factors such as the polysaccharide capsule, suilysin (a pore-forming toxin), and mechanisms that induce immunosuppression, including apoptosis in immune cells and evasion of phagocytosis.[3]The species is classified into 29 serotypes based on capsular polysaccharide antigens, with serotype 2 (SS2) being the most prevalent and virulent, accounting for approximately 75% of humaninfections and widespread in porcine disease.[2][4] Other notable serotypes include 1, 9, 14, and 16, which cause sporadic cases, while emerging sequence types (e.g., ST7 in Asia) have been linked to severe outbreaks, such as the 2005 event in China affecting 215 people with a 18% fatality rate.[1] Recent research emphasizes its global distribution, including new cases in South America, antimicrobial resistance trends, emerging serotypes like 5, and impacts on immune organs like the thymus and spleen, contributing to ongoing challenges in prevention and control.[3][5][6]
Taxonomy and Characteristics
Classification and Nomenclature
Streptococcus suis was first described in 1966 by S.D. Elliott as a streptococcal agent causing various diseases in pigs, including arthritis, and initially classified within Lancefield group R based on serological reactions. These strains, along with groups S and RS identified earlier by de Moor in 1963 from pig septicemia, were recognized as distinct but related to group D streptococci, with capsular polysaccharides serving as key antigenic determinants.[7]In 1983, Perch et al. expanded the serological classification by identifying six additional serotypes (3 through 8) based on capsular polysaccharide antigens, building on the initial types 1, 2, and 1/2 derived from groups S, R, and RS, respectively.[8] Subsequent work led to the recognition of 35 serotypes in total by the mid-1990s, with serotype 2 emerging as the most frequently associated with pathogenic infections in pigs. However, subsequent taxonomic reappraisals have reclassified six serotypes (20, 22, 26, 32, 33, and 34) to other species, such as Streptococcus orisratti and Streptococcus parasuis, resulting in 29 recognized serotypes for S. suis as of 2024.[7][5] The species name Streptococcus suis was formally validated in 1987 by Kilpper-Bälz and Schleifer as a new species (sp. nov., nom. rev.), reflecting its distinct taxonomic status.[9]Currently, S. suis is classified in the genusStreptococcus, family Streptococcaceae, order Lactobacillales, class Bacilli, and phylum Firmicutes.[10] Identification often relies on 16S rRNA gene sequencing, which confirms its phylogenetic position within the streptococci and distinguishes it from closely related species.[11] The etymology of the specific epithet "suis" derives from the Latin genitive "suis," meaning "of a pig," denoting the primary host from which the bacterium was isolated.[12]
Morphology and Physiology
Streptococcus suis is a Gram-positive, facultatively anaerobiccoccus that measures less than 2 µm in diameter and typically appears in pairs or short chains under microscopic examination. In stained preparations, cells often exhibit a characteristic peanut-shaped or lancet-like morphology when occurring as diplococci. The bacterium is non-motile and catalase-negative, distinguishing it from related species.[13][14][15]Virulent strains, such as those of serotype 2, are encapsulated with a polysaccharide capsule that contributes to their structural integrity and evasion of host defenses. The cell wall composition includes peptidoglycan layered with teichoic acids and lipoteichoic acids, which anchor to the membrane and influence cell shape and division. These components are critical for maintaining the bacterium's coccoid form and interactions with the environment.[2][16][17]Under optimal growth conditions, S. suis thrives at 37°C on enriched media such as blood agar, where it forms small (approximately 1 mm), translucent colonies after 24 hours of incubation. These colonies typically display alpha-hemolysis, producing a greenish zone around them due to partial red blood celllysis; some strains may show beta-hemolysis. Growth is enhanced in atmospheres containing 5-10% CO₂, reflecting its microaerophilic preferences, and the bacterium requires nutritionally rich media for robust proliferation.[14][15][18]Biochemically, S. suis is negative for the Voges-Proskauer test, indicating no acetoin production from glucose fermentation. It hydrolyzes esculin and ferments carbohydrates such as lactose, sucrose, glucose, maltose, and trehalose, producing acid but no gas. These reactions, combined with its inability to grow in 6.5% NaCl or hydrolyze hippurate, aid in its differentiation from other streptococci.[19][14][20]
Pathogenesis and Virulence
Virulence Factors
Streptococcus suis possesses a thick capsular polysaccharide (CPS) layer that plays a crucial role in its virulence by conferring antiphagocytic properties and enabling immune evasion. The CPS, particularly in serotype 2, inhibits phagocytosis by host immune cells and reduces complement activation, thereby promoting bacterial survival in the bloodstream. This structure also limits adherence to and invasion of epithelial cells while enhancing persistence within the host. [21]Key surface proteins contribute significantly to the pathogen's ability to interact with host tissues and evade defenses. The muramidase-released protein (MRP), a fibrinogen-binding adhesin, enhances bacterial survival in blood by reducing killing by polymorphonuclear leukocytes and increasing blood-brain barrier permeability through disruption of adherens junctions. The extracellular factor (EF), often co-expressed with MRP, similarly binds host proteins and correlates with high virulence in serotype 2 isolates, aiding in immune modulation. Suilysin, a cholesterol-dependent cytolysin, forms pores in target cell membranes, leading to celllysis, enhanced bacterial invasion, and induction of pro-inflammatory responses such as TNF-α release and inflammasome activation. [21][1][22]Adhesins facilitate initial attachment of S. suis to host cells and extracellular matrix components. Fibronectin-binding proteins, such as enolase and the surface-anchored Ssa (S. suis surface adhesin), bind fibronectin and laminin, promoting adhesion to endothelial and epithelial cells while inducing apoptosis and increasing vascular permeability. Sortase-dependent pili structures further enable colonization by mediating tight binding to host tissues, particularly in the nasopharynx and during systemic spread. [21][23][24]Biofilm formation allows S. suis to persist in host environments, resisting clearance by immune responses and antibiotics. This process involves regulatory genes like otc, which promote adhesion and extracellular matrix production, enabling chronic infections in porcine tissues. Iron acquisition systems, including ABC transporters, are essential for nutrient scavenging in iron-limited host niches, supporting growth and virulence during infection; these transporters facilitate uptake of iron-bound siderophores and contribute to fitness in vivo. [25][26]Recent genomic analyses have identified 124 putative virulence factors in S. suis, of which 26 are considered potentially zoonotic, highlighting the bacterium's diverse pathogenic arsenal.[27]Genetic elements such as pathogenicity islands and plasmids enhance S. suis virulence and adaptability. The 89K pathogenicity island, prevalent in epidemic strains like sequence type 7, encodes factors including the NisK/R two-component system and hemolysin Hhly3, which boost zoonotic potential and systemic infection. Plasmids often carry antibiotic resistance genes, such as optrA for linezolid resistance, promoting survival in treated hosts and contributing to the emergence of multidrug-resistant strains. [28][29][30]
Mechanisms of Infection
Streptococcus suis initiates infection in pigs by colonizing the upper respiratory tract, particularly the tonsils and nasal cavities, where it adheres to the mucosal epithelium through surface adhesins such as fibronectin-binding proteins and other pili-like structures.[1][31] This adherence facilitates competition with the resident microflora and resistance to local mucosal defenses, allowing the bacterium to establish a persistent presence in the nasopharynx without immediate clearance.[31] From this site, S. suis breaches the epithelial barrier, often exploiting minor injuries or co-infections, to invade the underlying tissues and enter the bloodstream, resulting in bacteremia.[1]The polysaccharide capsule of S. suis plays a central role in systemic dissemination by evading host innate immunity, specifically by inhibiting complement deposition and phagocytosis by macrophages and neutrophils.[32][33] Encapsulated strains resist uptake by downregulating host signaling pathways, including PI-3K/Akt/PKCα, and activating phosphatases like SHP-1 to dephosphorylate phagocytic receptors, thereby resulting in markedly reduced bacterial internalization compared to non-encapsulated mutants, with encapsulated strains showing near-complete resistance to uptake in macrophage assays.[32] Once in the circulation, S. suis demonstrates tissue tropism; in meningitis cases, it traverses the blood-brain barrier via interactions with brain microvascular endothelial cells, where fimbria-like components such as SssP1 bind sialylated vimentin to promote adhesion and paracellular or transcellular crossing, increasing cerebrospinal fluid bacterial loads.[34] Similarly, the bacterium targets synovial tissues in joints, leading to arthritis, potentially through capsule-mediated adhesion to extracellular matrix components, though detailed molecular mechanisms for this tropism require further elucidation.[1][35]Infection progression is exacerbated by the induction of hyperinflammation, where virulence factors like suilysin, a cholesterol-dependent cytolysin, pore-form the membranes of host cells, triggering potassium efflux and NLRP3 inflammasome activation that drives a cytokine storm with elevated IL-1β, IL-18, TNF-α, and IL-6 levels, ultimately contributing to septic shock and multi-organ failure.[36][37] Host-pathogen interactions are mediated by pattern recognition receptors, notably Toll-like receptor 2 (TLR2), which detects bacterial lipoproteins and peptidoglycan to initiate NF-κB signaling and pro-inflammatory cytokine production, while S. suis counters this through capsule-dependent immunomodulation that suppresses TLR2-driven IL-12 and TNF-α while enhancing anti-inflammatory IL-10, thereby dampening effective immune clearance.[33][38]
Epidemiology
Prevalence and Distribution
Streptococcus suis is endemic in pig populations worldwide, particularly in regions with intensive swine production, where it serves as a commensal in the upper respiratory tract of healthy carriers. Carrier rates in the tonsils and nasopharynx of clinically healthy pigs can approach 100%, with nearly all pig farms globally harboring the bacterium, though virulent strains are less common.[2][15] Among healthy pigs, the overall isolation rate for S. suisserotype 2, the most prevalent serotype, is approximately 10%, while in diseased pigs it rises to about 16%.[39]Prevalence is highest in intensive farming areas of Asia, Europe, and North America. In Asia, particularly China and Vietnam, isolation rates often exceed 50% in pig populations from large-scale operations, with smallholder farms showing carrier rates greater than 40%.[40] In Europe, such as in Spain and the Netherlands, serotype 9 predominates alongside serotype 2 in clinical isolates, while North America reports high incidences of serotypes 1/2 and 2. Globally, serotype 2 accounts for 15-45% of isolates from diseased pigs depending on the region, representing the dominant serotype overall, though serotype 9 comprises up to 20-60% in parts of Europe.[2] Recent 2020s studies highlight emerging serotypes, including 5 and 9, with serotype 5 showing increased zoonotic potential and genomic diversity in isolates from pigs and humans in Asia and beyond.[6][41]Weaning piglets aged 4-10 weeks are most susceptible to infection due to stress and immature immunity, leading to higher disease incidence in this group. For humans, occupational exposure in slaughterhouses and pork processing facilities poses significant risk, with workers exhibiting elevated seropositivity rates compared to the general population, ranging from approximately 5% to over 20% in exposed cohorts depending on the study and region.[42][43] A 2023 study in smallholder farms in the Philippines reported that 15.8% of surveyed farms and 7.6% of sampled pigs tested positive, linked to local trade and farming practices.[44] As of 2025, human cases continue to be reported primarily in Asia and Europe, with emerging serotypes like 5 associated with zoonotic infections.[6]
Transmission
Streptococcus suis primarily transmits among pigs through direct contact involving respiratory secretions, nasal discharges, and saliva, particularly in overcrowded pens where nose-to-nose interactions facilitate horizontal spread.[45] Aerosols enable short-distance airborne transmission, mimicking natural exposure in farm settings.[46] Vertical transmission from sows to piglets via the birth canal occurs but is uncommon, with piglets often acquiring the bacterium postnatally through environmental colonization of the upper respiratory tract, including tonsils and nasal cavities.[47]Indirect transmission within pig populations happens via contaminated environments, including fomites such as feed troughs, water sources, and bedding, which harbor the bacterium from infected nasal or fecal secretions.[1] Introduction of subclinically infected pigs into naive herds exacerbates outbreaks, as carrier animals serve as reservoirs without overt disease.[45] Factors like weaning stress, transportation, and concurrent viral infections (e.g., porcine reproductive and respiratory syndrome virus) heighten shedding and susceptibility, promoting wider dissemination in intensive farming systems.[47] No evidence supports transmission via insect vectors.[48]Zoonotic transmission to humans occurs predominantly through direct contact with infected pig blood, tissues, or carcasses during slaughter or processing, entering via cutaneous wounds or abrasions on the hands and arms— a risk amplified for butchers and abattoir workers.[49] In regions like Southeast Asia, rare foodborne cases arise from consuming raw or undercooked pork products contaminated with the bacterium.[1] Person-to-person spread has not been documented.[45] While pig-to-human transmission predominates, occasional interspecies jumps to other mammals, such as dogs, cats, and horses, have been reported, though these are infrequent and less studied.[45] High carrier rates in global pig populations, often exceeding 20-30% in tonsils, underscore the potential for ongoing zoonotic risk in pork-handling industries.[48]
Disease in Pigs
Clinical Manifestations
Streptococcus suis infection in pigs manifests primarily as an acute bacterial disease affecting young animals, with clinical presentations ranging from systemic septicemia to localized or chronic conditions. The pathogen causes significant morbidity in swine herds, particularly post-weaning, leading to economic losses through reduced growth and mortality. Common signs include fever, depression, and loss of appetite, progressing to more severe neurological or locomotor impairments depending on the infection site.[50][1]Acute septicemia is the most severe form, often occurring suddenly in suckling piglets aged 1-2 weeks, who are highly susceptible due to immature immunity. Infected piglets exhibit high fever, anorexia, and cyanosis—evident as bluish discoloration of the ears and skin—followed by rapid collapse and death without prior warning signs. This peracute presentation reflects widespread bacterial dissemination, with mortality rates reaching up to 20% in untreated outbreaks.[1][51][50]Localized infections commonly involve the joints or central nervous system, particularly in weaner pigs aged 3-12 weeks. Polyarthritis presents as swollen, hot joints causing lameness and reluctance to move, often affecting multiple limbs and leading to chronic debility if untreated. Meningitis, a hallmark neurological form, develops with initial fever and depression, advancing to loss of balance, head tilt, paddling motions, convulsions, and occasionally blindness or deafness; these signs typically emerge 1-3 weeks post-weaning.[50][2][51]Chronic manifestations are less frequent but significant in older or recovering pigs, including endocarditis with heart murmurs and valvular damage, and pneumonia characterized by respiratory distress, coughing, and dyspnea. These forms often arise secondary to initial bacteremia, contributing to persistent carriers in herds. Overall, while suckling piglets face high risks of systemic disease, weaners are more prone to respiratory and joint involvement, with herd-level mortality typically below 5% under prompt antibiotic intervention but escalating in unmanaged cases.[2][50][1]
Veterinary Diagnosis
Veterinary diagnosis of Streptococcus suisinfection in pigs typically begins with necropsy examination of affected animals, particularly post-weaned piglets showing signs of sudden death, neurological distress, or lameness. Characteristic gross lesions include purulent or fibrinopurulent meningitis with cloudy exudates over the brain and meninges, fibrinous polyserositis affecting the pericardium, pleura, and peritoneum, and joint effusions leading to swollen, edematous synovial spaces in multiple limbs. These findings are highly suggestive of S. suis involvement but require confirmation through further testing, as similar lesions can occur in other bacterial septicemias.[15][52]Bacterial culture remains a cornerstone for isolating S. suis from clinical samples. Tissues such as brain, synovial fluid from affected joints, and tonsillar swabs are collected during necropsy or from live pigs and plated on selective media, including Columbia blood agar supplemented with 5% sheep blood, which supports the growth of alpha-hemolytic colonies typical of S. suis after 24-48 hours at 37°C in 5% CO₂. Identification is achieved through biochemical tests or matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS), confirming the organism as gram-positive cocci arranged in chains. However, culture sensitivity can be reduced in animals treated with antimicrobials, and S. suis may be present as a commensal in carrier pigs.[15][53]Molecular methods, such as polymerase chain reaction (PCR) assays, provide rapid and specific confirmation, particularly for serotype identification. Multiplex PCR targeting the capsular polysaccharide (cps) genes allows differentiation of the 29 recognized S. suis serotypes, with assays commonly detecting clinically relevant types like 2, 1/2, 9, and 14 directly from tissue samples without prior culture.[5] A recN gene-based PCR further distinguishes "true" pathogenic S. suis from non-pathogenic streptococci. These techniques are especially useful in outbreak investigations to identify virulent strains in brain or joint samples.[15][54]Serological testing via enzyme-linked immunosorbent assay (ELISA) is employed for herd-level screening to detect antibodies against S. suis antigens, such as capsular type 2 polysaccharides or recombinant proteins like GMD. Indirect ELISAs on serum samples from sows or piglets help assess exposureprevalence and immunity status, with positive titers indicating prior infection or vaccination; however, cross-reactivity with other streptococci limits specificity. This approach is valuable for monitoring subclinical carriers in endemically infected herds.[55][56]Histopathological examination of affected tissues supports diagnosis by revealing suppurative inflammation, such as neutrophilic infiltrates in meninges or synovium, often with gram-positive cocci visible on special stains. These findings link bacterial presence to lesions, though culture or PCR is needed to speciate S. suis.[15]Differential diagnosis involves ruling out similar pathogens causing polyserositis, meningitis, or arthritis in pigs, including Glaesserella parasuis, Mycoplasma hyorhinis, other streptococci (e.g., S. dysgalactiae), Actinobacillus suis, and Erysipelothrix rhusiopathiae. Serotyping, antimicrobial susceptibility patterns, and lesion distribution aid distinction, as A. suis often produces more hemorrhagic pneumonia while G. parasuis targets younger piglets with fibrinous exudates.[15]
Zoonotic Infections
Human Disease Symptoms
Streptococcus suis infections in humans most commonly present as meningitis, which accounts for approximately 68% of reported cases and is characterized by acute onset of severe headache, high fever, and neck stiffness in over 67% of patients.[57]Hearing loss, often sensorineural and affecting high frequencies, develops in 39–66% of meningitis cases, sometimes accompanied by vestibular dysfunction leading to dizziness.[57][1][58]Septicemia occurs in about 25% of cases and typically features high fever, chills, and petechial or purpuric skin lesions, potentially progressing to septic shock and multi-organ failure.[57][1][59] Less frequent complications include arthritis (7–13%) and endocarditis (12–26%).[57][59]The incubation period following exposure to infected pigs or contaminated pork products generally ranges from 1 to 10 days, with a mean of about 4 days.[57][60] Among survivors, permanent sequelae such as deafness affect 30–50%, contributing to long-term morbidity.[57][58] Infections predominantly impact at-risk occupational groups like butchers and farmers, with the highest incidence in Southeast Asia, including Vietnam, Thailand, and China.[57][1]The overall case fatality rate for human Streptococcus suis infections is 10–20%, rising significantly in the absence of timely antibiotic intervention.[57][1]
Notable Outbreaks
The first reported human case of Streptococcus suis infection occurred in 1968 in Denmark, involving a pig slaughterhouse worker who developed meningitis following occupational exposure to infected pigs.[61]The largest documented outbreak took place in Sichuan Province, China, during the summer of 2005, with 215 confirmed human cases and 38 deaths, primarily among pig farmers and butchers; the causative agent was S. suis serotype 2 of sequence type 7 (ST7), a highly virulent strain that emerged locally.[62] This epidemic coincided with ongoing circulation of avian influenza (H5N1) in China, leading to initial misdiagnoses of some cases as influenza due to overlapping flu-like symptoms such as high fever and toxic shock-like syndrome.[63]In the 2010s, sporadic clusters of human S. suis infections were reported in Vietnam and Thailand, with over 100 cases annually in Vietnam—where the pathogen is the leading cause of adult bacterial meningitis—and dozens in Thailand, often linked to consumption of raw or undercooked pork products like blood sausage or fermented meat.[48][64][65]From 2023 to 2025, serotype 5 strains of S. suis have emerged as a growing zoonotic concern in Europe, with isolated human cases of invasive infections such as septic arthritis reported amid calls for enhanced surveillance due to underdiagnosis.[66][6] In the Philippines, a 2023 study identified farm-linked S. suis circulation on smallhold swine farms, with 15.8% of surveyed sites positive for the bacterium in asymptomatic pigs, heightening zoonotic risk through direct contact and underscoring multiple prior human infections traced to occupational exposure.[44]In South America, 47 human S. suis infections were documented from 1995 to 2024 across Argentina (highest number), Brazil, Chile, French Guiana, and Uruguay, indicating underreporting and emergence in the region as of 2024.[5]Globally, S. suis human infections remain underreported in low-resource regions due to limited diagnostic capabilities and misattribution to other meningitides, with significant surveillance gaps highlighted by the World Health Organization in outbreak responses.[67][68]
Detection and Identification
Laboratory Methods
Clinical samples for isolating Streptococcus suis typically include cerebrospinal fluid (CSF), blood, and tissues such as brain, lung, or joint fluid from affected individuals or animals.[69] These specimens are collected aseptically to minimize contamination, with blood drawn into culture bottles and CSF via lumbar puncture.[70] For transport, tissues and swabs are placed in non-nutritive media like Stuart's transport medium to preserve viability without promoting overgrowth, and samples should reach the laboratory within 24 hours at 4°C.[52]Isolation begins with Gram staining of direct smears from fluid samples, revealing Gram-positive cocci arranged in chains, characteristic of streptococci.[71] Cultures are inoculated onto enriched media such as 5% sheep blood agar or Columbia agar with 5% defibrinated blood, incubated at 37°C in 5% CO₂ for 24-48 hours, where S. suis typically forms small, alpha-hemolytic colonies.[72] Selective agars, including those supplemented with crystal violet (5 μg/mL), nalidixic acid (15 μg/mL), and gentamicin (5 μg/mL) on tryptic soy base, enhance recovery by inhibiting competing flora while allowing S. suis growth.[73] Preliminary differentiation from Streptococcus pneumoniae involves optochin sensitivity testing; S. suis is resistant, showing no inhibition zone around a 6 mm optochin disk on blood agar.[74]Species confirmation employs biochemical test strips like the API 20 Strep system (bioMérieux), which assesses 20 reactions including fermentation of sugars (e.g., positive for sorbitol, negative for ribose) and enzymatic activities (e.g., positive Voges-Proskauer, negative hippurate hydrolysis), yielding a numerical profile matching S. suis with over 90% accuracy.[75] This panel distinguishes S. suis from other alpha-hemolytic streptococci in routine diagnostics.[76]Initial antimicrobial susceptibility profiling uses the disk diffusion method on Mueller-Hinton agar with 5% sheep blood, following Clinical and Laboratory Standards Institute (CLSI) guidelines for streptococci, to assess resistance to agents like penicillin, tetracycline, and erythromycin.[77] Zones of inhibition are measured after 24 hours at 35°C in 5% CO₂, providing rapid categorization as susceptible, intermediate, or resistant.[78]Due to its zoonotic potential causing severe infections like meningitis, laboratory work with S. suis requires Biosafety Level 2 (BSL-2) containment, including biosafety cabinets, personal protective equipment, and decontamination protocols to prevent aerosol exposure and accidental release.[79]
Serotyping and Genotyping
Streptococcus suis strains are classified into 29 serotypes based on the structural and antigenic differences in their capsular polysaccharides (CPS), which are encoded by specific gene clusters known as cps loci (originally described as 35 serotypes, but some have been reclassified to other species).[80] Traditional serotyping employs slide agglutination with specific antisera, but this method can be limited by cross-reactivity and the availability of antisera for all serotypes.[81] Molecular approaches, such as multiplex PCR targeting serotype-specific genes within the cps loci (e.g., the polymerasegenewzy), provide greater specificity and enable the identification of up to 29 confirmed serotypes, with serotypes 2, 9, and 14 recognized as highly virulent due to their association with severe infections in pigs and zoonotic transmission to humans.[82][83][84]Multilocus sequence typing (MLST) offers a robust genotyping method for S. suis by sequencing internal fragments of seven housekeeping genes—aroA, cpn60, dpr, gki, mutS, recA, and thrA—to define allelic profiles and assign sequence types (STs).[85] This scheme has identified over 3,000 STs as of 2025, with ST1 belonging to clonal complex 1 (CC1) and predominantly linked to human-adapted strains causing invasive disease, particularly in Europe and North America.[86][27][87] ST7, part of CC1, has been associated with severe outbreaks in Asia, underscoring MLST's utility in tracking epidemic potential and phylogenetic relationships.[88]Whole-genome sequencing (WGS) has revolutionized S. suisgenotyping by allowing comprehensive analysis of genomic features, including pathogenicity islands that harbor virulence factors like the suilysin gene cluster and mobile elements carrying antimicrobial resistance genes such as tet(M) and erm(B).[89][90]Pangenome studies, comparing hundreds of strains, reveal a core genome of approximately 1,500–1,800 genes conserved across serotypes, with an accessory genome exceeding 2,000 genes that drive diversity in virulence and adaptation.[91][92] WGS facilitates outbreak source attribution by integrating single-nucleotide polymorphism (SNP) data with resistance profiling.[93]Pulsed-field gel electrophoresis (PFGE) remains a valuable tool for outbreak tracing in S. suis, particularly for serotype 2, where restriction enzyme digestion (e.g., with SmaI) generates DNA fragment patterns that differentiate epidemic clones with high reproducibility.[94] Multiple-locus variable-number tandem-repeat analysis (MLVA), targeting variable tandem repeats in nine loci, offers superior discriminatory power over PFGE for subtyping ST7 strains during investigations, enabling rapid linkage of cases in swine and human outbreaks.[95][96]Emerging genotyping tools leverage CRISPR-Cas systems for rapid, field-deployable S. suis serotyping; for instance, CRISPR-Cas12a combined with recombinase polymerase amplification (RPA) achieves sensitive detection (10–100 copies/reaction) and specific identification of serotype 2, with adaptations extending to other serotypes like 7 and 9 for point-of-care diagnostics as of 2024–2025.[97][98] These methods enhance traditional approaches by reducing turnaround time from days to hours while maintaining 100% specificity across tested serotypes.[99]
Treatment and Prevention
Antimicrobial Therapy
The primary treatment for Streptococcus suis infections in humans, particularly meningitis, involves high-dose intravenous penicillin G or ceftriaxone as first-line antibiotics, with ceftriaxone often preferred empirically due to its excellent cerebrospinal fluid penetration.[100][101] In veterinary settings for swine infections such as septicemia or arthritis, ampicillin is commonly used as a first-line beta-lactam agent, often administered parenterally for systemic absorption.[15][102]Antimicrobial resistance in S. suis is a growing concern, with increasing minimum inhibitory concentrations (MICs) to penicillin observed in human isolates and high resistance rates to tetracyclines (up to 75%) and macrolides in farm environments.[103][104] Recent 2025 studies have identified emerging multidrug-resistant sequence types (STs), particularly ST1 and novel variants, complicating treatment in both porcine and zoonotic cases.[105]For severe complications like endocarditis, combination therapy with a beta-lactam (e.g., penicillin or ceftriaxone) plus gentamicin is recommended to enhance bactericidal activity, typically for a duration of 2-4 weeks depending on clinical response.[106] High-dose intravenous administration is essential for central nervous system infections to achieve adequate drug levels in the cerebrospinal fluid.[101]Susceptibility testing, including MIC determination via broth microdilution according to CLSI guidelines, is critical for guiding therapy, especially in regions with high resistance prevalence.[106][107]
Vaccines and Control Measures
Veterinary vaccines against Streptococcus suis primarily include autogenous bacterins and limited commercial products, aimed at reducing disease incidence in pig herds. Autogenous bacterins, custom-made from isolates prevalent on a specific farm, are frequently used to control outbreaks and are administered to sows to confer colostral immunity to piglets or directly to piglets for active immunization.[108][109] A commercial vaccine, Porcilis Strepsuis, targets serotype 2 and can be given to sows 6-8 weeks before farrowing (with boosters) to provide passive protection to offspring via colostrum, or to piglets from 2 weeks of age for active immunity, reducing mortality and clinical signs associated with infection.[110] Field studies on autogenous vaccines have reported overall efficacy ranging from 21% to 50% in nursery pigs, depending on herd conditions and vaccination coverage, though protection is often serotype-specific and variable.[111]No human vaccine against S. suis is currently available, as the pathogen primarily affects swine and human infections are sporadic zoonoses linked to occupational exposure.[47] For high-risk workers, such as those in pork processing, post-exposure prophylaxis with antibiotics like penicillin may be considered following significant contact with infected material, though evidence is limited and relies on prompt initiation to prevent invasive disease.[49]Non-vaccine control measures on farms emphasize biosecurity and management practices to limit S. suistransmission. Key strategies include improving ventilation to reduce environmental stress, lowering stocking densities to minimize overcrowding, implementing all-in-all-out production systems to break infection cycles, and culling infected herds when outbreaks occur.[112][113]Herd surveillance involves routine monitoring using tonsil swabs from piglets to detect carrier status and guide interventions, enabling early identification of virulent strains.[114][115]Challenges in S. suis control stem from the pathogen's serotype variability, with over 35 serotypes identified, limiting the broad-spectrum protection offered by current vaccines that often target only dominant types like serotype 2.[116] Recent 2025 research highlights progress in subunit vaccines targeting suilysin, a conserved toxin, showing promise for cross-serotype immunity through recombinant protein formulations administered to sows.[117][118]