Author Correction: Septicemia due to Streptococcus dysgalactiae subspecies dysgalactiae in vampire bats (Desmodus rotundus)

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Results
Clinical signs. From the 20 Desmodus rotundus that were kept in captive, 18 of them became ill and presented various signs, such as anorexia (1/18), neurologic symptoms (paralysis) (8/18), pneumonia (1/18), and sudden death (8/18), within 13 weeks, on average, of captivity and observation. At post-mortem necropsy, encephalitis and congestion of different organs were observed (Fig. 1). The brain congestion in accordance with the neurologic symptoms presented suggested the possibility of rabies, and also because some cases of rabies in cattle had been reported in the area of capture. All animals were negative for rabies in real-time PCR (data not shown). In attempt to elucidate the causative agent, bacterial isolation was performed from different tissues (lung, liver, intestine, brain) of five bats.
Characteristics of the isolates. Gram-positive, catalase-negative, coccus-shaped organisms were isolated from all clinical samples of different organs suggesting bacteremia. Grey beta-hemolytic colonies were isolated on blood agar after 24 h of incubation at 37 °C. All isolates were characterized as Lancefield group C (Table 1).

MALDI-TOF MS identification.
The Streptococcus dysgalactiae species were identified by MALDI-TOF MS for all isolates. Considering this result, 16 S rRNA sequencing and phylogenetic analysis were proceeded for subspecies identification.  SE-AFLP analysis. SE-AFLP genotyping of the 12 studied isolates resulted in three profiles (A1-A3) with high genetic similarity (>80%) (Fig. 3). The gel with SE-AFLP profiles of SDSD can be found as Supplementary  Fig. S1. The A1 cluster comprised eight isolates originated from three animals from different cities, while the A2 profile comprised three strains isolated from two animals of the same city. The 13L isolate presented a distinct fingerprint pattern from the other studied strains, even though it originated from the same animal of the 13Li and 13I isolates (A1 cluster).

Discussion
Streptococci are predominant members of the commensal microbiota of the mucous membranes of the human oral cavity and to a lesser extent of the nasopharynx 2 . Although some streptococcal commensals have no significant record of disease transgressions, others streptococci have a lot of virulence factors, acting as pathogens capable of spread and of initiating infection in immunocompromised individuals 2,9,17 . The disease-associated streptococcal species may also occur in the asymptomatic host in which they are maintained in a sub-disease threshold load 2 . Changes in the pathogen population or to the host environment, such as decrease of competitors, acquisition of virulence factors, immunosuppression, and dietary changes, can affect the host-pathogen relationship and initiate the disease process 2,18 . This could explain the observed outbreak, considering that the stress provoked by the environmental changes and animals diet could originate a momentary immunosuppression and favor the pathogen development. As the feeding blood was not contaminated, the S. dysgalactiae was probably introduced by a healthy bat harboring the pathogen, previously to the capture, that started to manifest the disease and excrete the bacteria due to the stressful changes. The horizontal transmission is sustained by the SE-AFLP genotyping that demonstrates high genetic similarity within the studied isolates and also the A1 cluster comprised isolates from three different cities that died in different days.
The symptoms described in the observed bats are common to streptococcal infection and especially to S. dysgalactiae. Also, in captive bats pneumonia has already been related to α-hemolytic Streptococcus infection 15 . As observed here, sudden death and organ congestion related to SDSD β-hemolytic Lancefield group C infection were also evidenced in puppies 6 . Streptococcus dysgalactiae is reported as a cause of bacteremia, meningoencephalitis, and mastitis in sheep 2 , and articular abscess in pigs 5 . S. dysgalactiae of group C occasionally causes lower limb cellulitis, meningitis, and bacteremia in humans [19][20][21] . β-hemolytic S. dysgalactiae of groups C and G can cause severe and recurring invasive infections 21 .
Among the mammalian class, bats are the most important reservoir of zoonotic pathogens and are estimated that they possibly may harbor several "missing zoonoses" that still were not detected 22 . For this reason, the order of Chiropteran is incriminated as of highest value for surveillance, especially in South and Central America and parts of Asia 22 . Furthermore, several pathogens that may affect humans such as Bartonella spp 23,24 ., Polyomaviridae 25 , influenza A virus 26 , among several others 22 , and the isolation of pathogenic SDSD shows the probability of transmission of another pathogen by bats to animals and humans. The interface of bats and humans can occur in a variety of ways like incidental contact, degradation of the environment by humans, controlled contact for research proposes and predation 27 . The widespread distribution of vampire bats on the American continent, ranging from Mexico to southern South America 22,28,29 , encompasses around fourteen countries 29 and shows that millions of people and animals are vulnerable to bats attacks in rural areas and also in places where the degradation of the environment alters the proximity between human and animals, and those scenarios are very common in the geographic areas where the vampire bat is found.
The S. dysgalactiae species identification was obtained through MALDI-TOF MS and subspecies dysgalactiae was only identified by 16 S rRNA sequencing and phylogenetic analysis. Even though MALDI-TOF MS has comparable discriminatory power to molecular techniques for bacterial species differentiation 30 and presented high-confidence for β-hemolytic streptococci species identification 31 , this technique still does not enable proper S. dysgalactiae subspecies differentiation. For subspecies identification, the phenotypic characterization still causes confusion, as corroborated by our results since Lancefield group C β-hemolytic colonies could be allocated in both subspecies. Considering that the misclassification of β-hemolytic SDSD into subspecies equisimilis has been previously reported 4,6 and was only solved by 16S rRNA analysis, the molecular techniques still are more appropriate for this differentiation level of S. dysgalactiae. Interestingly, Jensen & Kilian 4 observed that all β-hemolytic SDSD originated from invasive infections, which also corroborates our results.
We present the first report of SDSD infection in vampire bats (Desmodus rotundus) causing septicemia and encephalitis. Even though the clinical relevance of SDSD for animal health further increases, its zoonotic potential remains unknown. Therefore, due to the importance of S. dysgalactiae subspecies, they should be properly identified by veterinary diagnostic laboratories. Also, the presence of SDSD in bats corroborates with the theory that bats harbor a lot of pathogens, which raises the question about the possible involvement of this species in the dissemination of this and others pathogens.

Methods
Animals. The study was designed for the study of serological evaluation of anti-rabies antibodies in bats as an epidemiological tool for the control of the disease in hematophagous chiropterans. Twenty Desmodus rotundus were kept in captive (authorization number 51231-1, issued by the Ministry of the Environment of Brazil) for research proposes. The bats were captured from natural caverns in three nearby cities from São Paulo state (Anhembi, Botucatu, and Bofete) ( Table 1) and were considered as asymptomatic. The bats were housed and handled following the ethical principles adopted by Bioethics Commission of the Faculty of Veterinary Medicine and Animal Production of São Paulo State University (protocol number 85/2015) and all experimental protocols were approved by the same institution. Animals were fed with defibrinated blood that was collected in slaughterhouses, supplemented with cobalamin. The bats were observed for 137 days and within 85 days of the quarantine period, on average, 18 of them became ill presenting various signs (Table 1).
Bacterial isolation and Lancefield group determination. Samples from different tissues (lung, liver, intestine, brain) of five bats were used in an attempt for bacterial isolation. The samples were inoculated on blood agar plates (CM0055, Oxoid, Hampshire, England) supplemented with 5% defibrinated sheep blood and incubated aerobically for 24 h at 37 °C. For isolated colonies, the Lancefield group was determined through commercial latex agglutination kit (Avipath Strep ® , Omega Diagnostics, Scotland, United Kingdom) following manufacturer's instructions. Samples of the blood used in the bats feeding were also inoculated on blood agar plates; however, no isolation was obtained.

MALDI-TOF mass spectrometry identification. The obtained isolates were initially identified as
Streptococcus dysgalactiae by matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry. MALDI-TOF MS sample preparation, data processing, and analysis were done as previously described by Hijazin et al. 30 . Mass spectra were acquired by Microflex ™ mass spectrometer (Bruker Daltonik), with a mass range of 2-20 kDa, using flexControl ™ 3.0 software (Bruker Daltonik). Spectra were loaded into MALDI BioTyper ™ 3.0 (Bruker Daltonik), using default settings, and compared with the manufacturer's library. Standard Bruker interpretative criteria were applied; scores ≥ 2.0 were accepted for species assignment and scores ≥1.7 but ≤2.0 for identification at the genus level.
16S rRNA sequencing and phylogenetic analysis. The subspecies identification was achieved through 16 S rRNA sequencing (1-1.3 kb) and phylogenetic analysis. DNA extraction was performed according to Boom et al. 32 protocol with previous enzymatic treatment with lysozyme (100 mg) and proteinase K (20 mg) (US Biological, Swampscott, MA, USA) at 37 °C for 60 min. The 16 S rRNA gene amplification was performed using Twomey et al. 33 primers. The Illustra GFXTM PCR DNA and Gel Band Purification kit (GE Healthcare) was used for amplicon purification and sequencing was performed by the Human Genome Research Center (Universidade de São Paulo, Brazil). The phylogenetic analysis was performed with Mega 5.10 software using the maximum-likelihood method, and 1000 bootstrap replicates were used for branch support statistical inference. All DNA sequences from this study were deposited in GenBank under accession numbers MF113276 -MF113287.
SE-AFLP genotyping. The obtained isolates were further genotyped by single enzyme amplified fragments length polymorphism (SE-AFLP) following McLauchlin et al. 34 protocol. DNA fragments were detected by electrophoresis at 24 V for 26 h in 2% agarose gel stained with BlueGreen ® (LGC Biotecnologia, São Paulo, Brazil). Fingerprint patterns were analyzed by comprehensive pairwise comparisons using Dice coefficient. A dendrogram was generated by Bionumerics 7.6 (Applied Maths, Saint-Martens-Latem, Belgium) and a 90% genetic similarity cut-off value was applied for cluster analysis 35 .