Morbillivirus and coronavirus survey in stranded cetaceans, Brazil

Abstract

Since 2010, Guiana dolphin morbillivirus (GDMV; family Paramyxoviridae, genus Morbillivirus, species Morbillivirus ceti, syn. Cetacean morbillivirus) is recognized as the cause of death of multiple cetacean species along the Brazilian coast, including an unusual mortality event in Rio de Janeiro state. Coronaviruses of the genus Gammacoronavirus (family Coronaviridae) have been previously detected in cetaceans in the northern hemisphere. After the emergence of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), responsible for the COVID-19 pandemic and with the potential to affect several mammal species, there is an increased concern about the risk of infection in aquatic mammals. The goal of this study was to molecularly screen the presence of morbillivirus and coronavirus infections in cetaceans stranded in several regions of the Brazilian coast in order to determine their occurrence rates, pathogenicity, and range of potentially susceptible cetacean species. We molecularly tested tissue samples of 118 cetaceans, belonging to 20 species, found stranded in Brazil, between 2015 and 2022. Overall, 2.5% (3/118) of the analyzed cetaceans were positive for GDMV infection: a Guiana dolphin (Sotalia guianensis), an Atlantic spotted dolphin (Stenella frontalis), and a humpback whale (Megaptera novaeangliae). None of the animals were positive for coronavirus. Our findings indicate that the morbillivirus sequence type identified in Indo-Pacific bottlenose dolphins (Tursiops aduncus) of Australia and our GDMV sequences from Brazil belong to the same strain. The systematic monitoring of cetacean morbilliviruses is recommended to properly estimate the occurrence rate, pathogenicity and evolution of these viruses, which may help anticipate novel epizooties and reduce their impact on endangered cetacean populations.

Introduction

The Brazilian coast is one of the largest in the world, sustaining a rich biodiversity, with descriptions of over 45 cetacean species; nine mysticetes (i.e., baleen whales) and 36 odontocetes (e.g., dolphins and porpoises) [1]. Due to their ecologic and physiologic adaptations to a fully aquatic life, cetaceans are considered environmental sentinels of the marine environment [2]. Therefore, the study of emerging and reemerging infectious diseases in these animals is crucial to evaluate the health of their ecosystems, subjected to several threats over the last decades [3,4].

Morbillivirus ceti (syn. Cetacean morbillivirus [CeMV], genus Morbillivirus, family Paramyxoviridae) is an enveloped negative-sense single-stranded RNA virus considered an important cause of morbidity and mortality in cetaceans and pinnipeds worldwide [5]. Seven strains of CeMV are recognized to date: Dolphin morbillivirus (DMV) [6], Porpoise morbillivirus (PMV) [7], Pilot whale morbillivirus (PWMV) [8,9], Beaked whale morbillivirus (BWMV) [10], Guiana dolphin morbillivirus (GDMV) [11], one strain found in Indo-Pacific bottlenose dolphins (Tursiops aduncus) [12], and the Fraser dolphin morbillivirus [13]. In Brazil, two morbillivirus strains have been reported in cetaceans: GDMV and PWMV [14–20]. GDMV was detected in multiple cetacean species [14–18], including in an unusual mortality event (UME) that killed at least 270 Guiana dolphins (Sotalia guianensis) in Rio de Janeiro state, between November 2017 and March 2018 [19]. PWMV infections were reported in short-finned pilot whales (Globicephala macrorhynchus) of Brazil in 2020 [20], indicating that other strains also circulate in Brazilian waters. Despite these reports, the current knowledge regarding morbillivirus infection occurrence rate, pathogenesis, and epidemiology in Brazil is still scarce.

Coronaviruses, subfamily Letovirinae, family Coronaviridae, order Orthocoronavirus, are enveloped positive-sense single-stranded RNA viruses divided into four genera: Alpha-, Beta-, Gamma-, and Deltacoronavirus. Coronavirus infection can affect several systems (e.g., respiratory, gastrointestinal, nervous) in a broad range of mammal and bird species [21–23]. Coronaviruses are considered important emerging infectious agents due to their potential to switch hosts and also due to their zoonotic potential, as seen in the severe acute respiratory syndrome (SARS) and the COVID-19 pandemic [22,24]. In cetaceans, there is limited information regarding coronavirus infection, with few reports of gammacoronavirus infection in captive and free-ranging odontocetes [25–27]. Clinical signs and histopathologic examination of cetaceans infected with gammacoronaviruses portrayed gastrointestinal problems (e.g., diarrhea) in Atlantic bottlenose dolphins (Tursiops truncatus) [26], and pulmonary lesions, and hepatic failure due to hepatic necrosis in beluga whales (Delphinapterus leucas) [25].

A broad investigation of morbillivirus and coronaviruses infection in wild marine mammals is essential to shed light into the pathogenicity and epidemiological aspects of these infections, and to understand these viruses dynamics and potential impacts in cetacean populations [5,28]. Additionally, following the 2017–2018 GDMV-associated UME reported in Brazil [19], there is an increasing concern about the impact of infectious diseases on cetacean conservation, particularly on threatened species. Therefore, applying a One Health approach to the study of infectious agents in marine mammals of Brazil is an essential conservation measure. The objective of this study was to survey morbillivirus and coronavirus in a large panel of cetacean species occurring in different regions of Brazil. We also evaluated other important epidemiological aspects: the occurrence rate of these infections, viral detection in novel susceptible species, the circulating viral strains, and their pathogenicity.

Materials and methods

Samples

The selection criteria used herein aimed on a broad diversity of cetacean species and stranding locations. Thus, we selected individuals of resident species (Guiana dolphin, Lahille’s dolphin [Tursiops truncatus gephyreus] and Franciscana [Pontoporia blainvillei]) from different coastal regions, including animals with signs of infectious processes, animals that died due to anthropogenic interactions, and also individuals of non-resident species that occur less frequently in the studied region.

Overall, we selected 118 cetaceans, comprising 20 species, that stranded between November 2015 and January 2022, in the northeastern (25/118), southeastern (64/118) and southern (29/118) regions of Brazil. These individuals were either found dead or stranded alive and died under treatment; or died shortly after admission into rehabilitation centers. Animals were selected according to their decomposition condition status (DCS) (from fresh to moderate autolysis) [29] and unusual records of the species. Cases in advanced autolysis were included if they were found in an underrepresented region or belonged to an undersampled species (e.g., humpback whale Megaptera novaeangliae, in the Abrolhos Archipelago, northeastern Brazil). All individuals that were mummified or only presented the skeleton were excluded. Age class (i.e., fetus, calf, juvenile and adult) was stablished based on total body length [30], and characteristics such as the presence of vibrissae, and sexual maturity were confirmed by histopathology analyzes. All 118 animals were tested for paramyxovirus infection (618 analyzed tissue samples), while 93 cetaceans were tested for coronavirus (345 analyzed tissue samples). The epidemiological and biological data of the tested individuals are summarized in S1 Table.

Pathological analyses

Samples for histological (10% neutral buffered formalin) and molecular analyses (frozen at -20 °C and stored at -80 °C until processing) were collected during standardized necropsies (29). RT-PCR-positive cases were also evaluated by histology (hematoxylin and eosin).

Molecular analyzes

The following frozen samples from each animal were selected for the molecular screening of coronavirus and morbillivirus: cerebrum, cerebellum, brainstem, spinal cord, kidney, liver, lung, mesenteric lymph node, prescapular lymph node, pulmonary lymph node, small intestine, spleen, feces. Total RNA extraction was performed with TRIzol-LS (Life Technologies Corporation, CA, USA), and reverse transcription reaction was performed using random primers and M-MLV Reverse Transcriptase (Life Technologies Corporation).

For paramyxovirus and coronavirus screening, two consensus nested broad-range RT-PCRs were performed to amplify a 530 base pair (bp) fragment of the RNA dependent RNA polymerase (RdRp) gene of Paramyxoviridae—including Morbillivirus and other paramyxovirus genera (RdRp-PAR-nPCR) [31], and a 432 bp fragment of coronavirus RdRp (RdRp-COV-nPCR [32]. Paramyxovirus-positive samples were further tested using a RT-PCR directed to the phosphoprotein (P) gene of the genus Morbillivirus (P-MV-nPCR), yielding a 420 bp fragment, in order to confirm morbillivirus infection and strain typing [7]. In RT-PCR-positive animals, all the available tissues were tested by RdRp-PAR-nPCR and RdRp-COV-nPCR, and subsequently tested by P-MV-nPCR, if applicable.

Amplicons of the expected size obtained with the P-MV-nPCR were purified using PureLink^™ Quick Gel Extraction Kit (Life Technologies Corporation). Both strands were directly sequenced by Sanger using the ABI PRISM BigDye^® Terminator v3.1 kit (Ready Reaction Cycle Sequencing, Applied Biosystems, Foster City, USA), and assembled using the Codon Code aligner v.4.2.1 software (Codon Code Corp. Dedham, USA). The obtained consensus sequences of partial P genes were queried for similarity using the Basic Local Alignment Search Tool (BLAST). Subsequently, the alignments with other CeMV P gene sequences available were conducted using Mega 7 [33]. The deduced CeMV amino acid P sequences obtained in this study, along with the selected CeMV P sequences in GenBank/EMBL/DDBJ database were used for inferring molecular phylogeny, totalizing 32 sequences. Phocine distemper virus was selected as outgroup. Phylogenetic analyzes were conducted in MEGA7 software. In addition, a fragment of 164 nucleotides of the P gene of 107 CeMV sequences was used to evaluate the PMV, DMV, BWMV, GDMV and PWMV intra and inter strain diversity, based on pairwise identity distance (Table 1). That 164 bp fragment of the P gene was chosen to increase the representation of a large number of CeMV strains, once it is available for most of the sequences in GenBank. For the GDMV strain, the intra-group variability was also verified using a longer fragment (206–389 nucleotides in length and 70–130 amino acids in length), available for this variant in GenBank. The nucleotide and amino acid substitutions are shown in Table 1. The alignments, evolutionary and diversity analyzes were conducted in MEGA7 software. The sequences obtained in this study were compared with those found in Indo-Pacific bottlenose dolphins of western Australia, based on p-distance.

[Figure omitted. See PDF.]

Permits

The field studies and sample collections were performed in full compliance with specific federal permits issued by the Brazil Ministry of Environment (MMA) and the Chico Mendes Institute for Biodiversity Conservation (ICMBio), under the Biodiversity Information and Authorization System (SISBIO 69115–4) and National System of Genetic Resource Management and Associated Traditional Knowledge (SISGEN ADA22DD), all in accordance with the Ethic Committee on Animal Use of the School of Veterinary Medicine and Animal Sciences (University of São Paulo)–CEUA/FMVZ (certificate number 6819150419). Consent to participate: not applicable.

Results

Samples

Herein, we analyzed 57 males, 58 females, and three cetaceans of undetermined sex (due to their advanced decomposition status, e.g., predation), identified as adults (n = 58), juveniles (n = 41), calves (n = 17), and two fetuses (S1 Table).

Molecular findings

Three out of 118 individuals (2.5%) were positive for CeMV: (i) an Atlantic spotted dolphin (Stenella frontalis, case 1) stranded in Florianópolis, Santa Carina state (southern region), which tested positive in brain, tongue and kidney; (ii) a Guiana dolphin (case 2) stranded in São Mateus, Espírito Santo state (southeastern region), positive in prescapular lymph node; and (iii) a humpback whale (case 3) stranded in São Francisco do Sul, Santa Catarina state (southern region), which tested positive in brain and lungs (Fig 1). According to cetacean species, one out of five Atlantic spotted dolphins (1/5), 3.6% in Guiana dolphins (1/28) and 6.3% in humpback whales (1/16) were morbillivirus-RT-PCR-positive. None of the individuals tested positive to coronavirus.

[Figure omitted. See PDF.]

ES = Espírito Santo state, SC = Santa Catarina state.

The retrieved P gene nucleotide sequences (377 bp length) of the three cases were identical amongst them, except for a synonymous substitution (A/G) in position 97 of the sequenced fragment obtained from the humpback whale (case 3, Table 1). All samples were assigned as GDMV strain. The sequences obtained herein are highly similar to those from previous GDMV cases reported in Brazil, including those from the 2017–2018 UME (GenBank accession no. MG845551 and MG845552, Table 1). The substitutions observed in nucleotide and amino acid sequences of the P gene among all the GDMV reported in Brazil in relation to the sequence type MQ904P (MG845551) are shown in Table 1. The GDMV P gene sequences obtained in this study in the humpback whale, the Guiana dolphin and the Atlantic spotted dolphin were submitted to GenBank/DDBJ/ENA database under accession numbers PP475487, PP475488, and PP475489, respectively.

The phylogenetic tree based on the 118 amino acid fragment of the P gene of 32 cetacean morbillivirus sequences clearly classified our sequences within the Guiana dolphin morbillivirus strain, and also grouped them (99% bootstrap value) with a sequence retrieved from an Indo-Pacific bottlenose dolphin of the Swan river, Australia. The other cetacean morbillivirus sequences analyzed in the phylogram were also accurately classified (Fig 2).

[Figure omitted. See PDF.]

A phocine distemper virus phosphoprotein sequence was selected as outgroup. The bootstrap consensus tree inferred from 1000 replicates. Bootstrap values lower than 70 were omitted. GDMV: Guiana dolphin morbillivirus.

The divergence analysis of the gene fragment (pairwise identity distance analysis) showed significant divergence between each group of viral strains (Table 2), corroborating with the phylogram. Nevertheless, low divergence was observed in the intra-group of CeMV variants using this molecular marker (Table 2). Considering the detected GDMV sequence types, the variability observed using the 181 bp fragment of the P gene was lower than the one observed when a longer fragment was analyzed (206–377 bp; Table 2). Based on P-distance, the morbillivirus P sequence of Indo-Pacific bottlenose dolphins of western Australia and the GDMV sequences of the same length (all three obtained in this study and two from Guiana dolphins MG845551 and MG845552) present high similarity (nucleotide identities ranging from 99.4 to 99.7% and amino acid similarities from 98.3% to 99.2%).

[Figure omitted. See PDF.]

Pathological findings in GDMV-positive animals

Case 1, the Atlantic spotted dolphin, presented good body condition. The main gross findings were generalized congestion, moderate diffuse pulmonary distention and congestion, presence of mild to moderate multifocal necrosis areas in occipital cortex (Table 3, Fig 3A), and a mild focal ulcerative lesion in the dorsal aspect of the tongue (Fig 3B). Additionally, postmortem linear cuts were observed in the caudal fin and abdominal region, with organ exposure, suggesting anthropic interaction. Case 2, the Guiana dolphin, was in advanced autolysis, which hampered its examination. Finally, Case 3, the humpback whale, stranded alive at the end of the reproductive season (in Brazil, from July to November), and died soon after. Upon external examination, the animal was in poor body condition, with diffuse moderate whale lice (Cyamus boopis) infestation (Fig 3C), mild presence of barnacles, and mild multifocal coockiecutter shark (Isistius sp.) bites in different scar stages. This individual also presented moderate diffuse petechiae and congestion of cerebrum and cerebellum, with perivascular cuffs of mononuclear infiltrate (Fig 3D), diffuse pleural thickness and pulmonary congestion, moderate diffuse hepatic congestion, and a focal nodule in the mucosal layer of the bladder. The histopathological findings are described in Table 3.

[Figure omitted. See PDF.]

(A) Atlantic spotted dolphin (Stenella frontalis). Brain. Congestion, focal lesion in occipital cortex surrounded by an area of malacia (white arrow); (B) Atlantic spotted dolphin. Mild focal ulcerative lesion in the right edge of the tongue (arrow); (C) Humpback whale (Megaptera novaeangliae) stranded in poor body condition with moderate diffuse whale lice; (D) Humpback whale. Cerebrum presenting perivascular cuffs and mononuclear infiltrate; (E) Humpback whale. Note the lymphoid depletion and the disorganization of the splenic parenchyma. (F) Humpback whale. Observe the periportal lymphoplasmacytic-histiocytic hepatitis, mild hepatic congestion and mild amount of brown intracytoplasmic pigment.

[Figure omitted. See PDF.]

Discussion

The evaluation of a large diversity of cetacean species conducted in the present study allowed the identification of the first GDMV infection potentially associated with tissue lesions in humpback whales (case 3), and the first morbillivirus infection in Atlantic spotted dolphins (case 1) presenting compatible pathological findings, expanding the host range of species susceptible to GDMV. Previous GDMV infections were reported in exhaled breath of humpback whales and in tissue samples of Guiana dolphins, a killer whale (Orcinus orca), and southern right whales (Eubalaena australis) [14–18]. Further serological surveys are required in order to understand the exposure of cetaceans against GDMV in Brazil.

The GDMV detection rate in the present study was 2.5% (3/118). Studies conducted worldwide reported variable values of CeMV infection rates (ranging from 1.8% to 31.9%) in areas that suffered UMEs [34–36]; however, such discrepancies between occurrence rates are expected. Both GDMV and DMV strains are able to infect several cetacean species, but circulate in different regions (e.g. GDMV in Southeastern Atlantic and likely in the Indian Ocean, based on the analysis of the sequence from Australia, and DMV in the Northern Atlantic and Mediterranean Sea) and may have distinct pathogenic features and host susceptibility. Characteristics of the cetacean populations used in each study may also contribute to these discrepancies, such as the diversity of cetacean species sampled (some species seem to be highly susceptible to CeMV infections, such as striped dolphins), and the eligibility criteria used for sampling (e.g., carcass decomposition stage, animals with/without viral related lesions). In addition, the distinct diagnostic methods and protocols used in these studies should also be considered. In Brazil, a high morbillivirus occurrence rate (27.5%, 40/325) was reported in Guiana dolphins of Paraná state, southern Brazil, between February 2016 and November 2018 [16]. Nevertheless, the diagnosis was based solely on tissue antigen detection through immunohistochemistry, and none of the positive cases were confirmed by RT-PCR, which limits direct comparisons with the results obtained herein. The GDMV-positive animals detected in this study were collected in northeastern, southeastern and southern Brazil, indicating this virus’ circulation along the Brazilian coast [11,14,15,17].

The Atlantic spotted dolphin (case 1) had an ulcerative lingual lesion similar to those described in morbillivirus-infected cetaceans [37]. Additionally, this individual had an extensive area of parasitic malacia in the central nervous system, which along with the morbillivirus infection, may have contributed to its stranding. The impact of this strain over the Atlantic spotted dolphin population is still unknown. Of note, the Atlantic spotted dolphin population of the Santos Basin is one of the largest cetacean populations in the area, with 26,909 estimated individuals (personal communication with the Cetacean Monitoring Program-Santos Basin, Brazil).

BWMV was the first detected CeMV strain in humpback whales, reported in a stranded animal in the USA, in 1998 [10]. Another CeMV strain—GDMV, was detected in the exhaled breath of apparently healthy adult humpback whales (2/48 groups of whales), sampled in 2011 and 2012, in a study conducted in the Abrolhos Bank, northeastern Brazil [17], and recently, in tissue samples of two juvenile males of that species stranded in southern Brazil, in 2022 [18]. Herein, the GDMV-positive humpback whale (case 3) presented lesions suggestive of morbillivirus infection, such as bronchopneumonia and non-suppurative encephalitis, consistent with an acute GDMV infection. The animal stranded in poor body condition and presented high whale lice infestation, which indicates impaired locomotion. Our whale stranded in 2020, two years after the Rio de Janeiro UME [19], and almost 10 years after the GDMV detection in exhaled humpback whale breath [17]. Thus, our findings, alongside those reported by de Amorim et al. (2024), suggest that GDMV circulates in the humpback whale population of Brazil (Breeding stock A), which sustains high site fidelity to breeding areas of the southwestern Atlantic.

GDMV infection with associated lesions was reported in Guiana dolphins in two previous studies in Brazil [11,19]. Herein, we tested 28 Guiana dolphins from Ceará, Espírito Santo, São Paulo, and Santa Catarina states, and found one positive individual (case 2) that stranded in November 2018, in São Mateus, Espírito Santo (northeastern region). Of note, this animal was found dead in the same location as the first GDMV case reported in Brazil [11]—a Guiana dolphin that stranded in 2010, suggesting that GDMV is recurrently circulating in Guiana dolphins. The studied animal died in the same year of the Rio de Janeiro UME, but over 350 km away.

The GDMV found in Brazil clustered with a high support with a morbillivirus detected in an Indo-Pacific bottlenose dolphin in western Australia, which was previously considered a different strain [12] and was not present in public databases, but published by Jacob et al. [10]. When compared with the closest GDMV phosphoprotein sequences of the same size, the sequence from Australia presented only a single amino acid substitution with the closest GDMV sequences, the same difference that we observed between different GDMV phosphoprotein sequences. Therefore, the GDMV and the Australian sequence are likely comprised within the same viral strain. Our findings suggest that GDMV circulates in the southern Atlantic and the Indian Ocean, although the analyzes of other genes is recommended to confirm this possibility.

Despite the reports of some systemic infections in the Mediterranean sea, most DMV infections outside outbreak periods were associated with the chronic encephalitic form, especially in striped dolphin populations [5,28,34,36,38–42]. There is no available information regarding the extent of the GDMV strain association with restricted central nervous system (CNS) infections. In our study, all the positive cases presented systemic infections; however, only 64 of the 118 studied individuals had samples of CNS available for molecular testing, which may have underestimated the number of obtained positives if they presented chronic encephalitic forms [43]. According to immunohistochemical analysis, the GDMV found in the Guiana dolphins of the Brazilian outbreak showed lower neurotropism and less severe pathological findings than those observed in dolphins with DMV infections [44]. The impact of chronic encephalic infections on virus transmission and endemicity has been discussed, but is still unknown [43].

Several large-scale outbreaks have been reported in the Mediterranean Sea, with two main types of DMV identified according to the geographical origin—the Mediterranean and northeastern (NE) Atlantic, with the latter gradually replacing the former, possibly due to the overlapping of migrating cetacean species coming from the Atlantic [36]. The introduction of the new NE-Atlantic DMV lineage in the Mediterranean Sea into an immune naïve cetacean population seems to explain, at least in part, the frequent epizooties in the region [34,36,42,45]. In Brazil, there is no high divergence among the detected GDMV sequence types (based only on partial P gene sequences), which should be one of the explanations for the infrequent outbreaks in the region. Nevertheless, one should consider that the low variability observed in Brazilian sequence types may also reflect the reduced number of samples available for analysis. It is a matter of debate if the GDMV strain is endemic in resident cetacean populations (e.g., Guiana dolphins) or if it has been sporadically introduced into Brazilian waters by other cetacean species that migrate to the region, especially because we have no serological data regarding anti-morbillivirus antibodies in cetaceans of this country. Nevertheless, the low number of outbreaks occurring in the region suggests some degree of immunity, characteristic of endemic infections. There are several locations considered relevant in terms of cetacean conservation in the Brazilian coast, including breeding grounds for humpback whales like the Abrolhos Bank [46]. Of note, other locations, particularly coastal waters, sustain important host resident cetacean populations: Lahille’s bottlenose dolphin (Tursiops truncatus gephyreus) [47], Guiana dolphin [48], and franciscana—the latter classified as the most endangered cetacean in the southwestern Atlantic Ocean [49]. This study evaluated 25 franciscanas, 28 Guiana dolphins and one Lahille’s bottlenose dolphin; however, only one Guiana dolphin was GMDV-positive. To this date, there are no reports of morbillivirus infections in franciscana or in Lahille’s bottlenose dolphin.

Although some studies suggested high susceptibility of certain cetacean species to SARS-CoV-2 based on the sequence similarity between theirs and humans’ ACE-2 receptor [50,51], neither SARS-CoV-2 nor any other coronavirus were detected in this study. The three reports of gammacoronaviruses in cetaceans were from captive and free-ranging animals [25–27]. We should also emphasize that in a previous report, coronavirus viral nucleic acids were detected in feces, liver and heart samples [26–28], and herein, mesenteric lymph node (n = 39)/intestinal content (n = 4) were available for analysis in a reduced number of animals, which could explain the observed negative results.

Our findings emphasize the importance of implementing long-term systematic CeMV surveillance in Brazil to determine the occurrence rate of infection and to monitor viral evolution, in order to anticipate epizootic events and their impacts on the conservation of threatened cetacean populations. Further CeMV whole genome sequencing studies are required, particularly regarding poorly characterized strains as GDMV. Regarding coronaviruses, despite the negative results, the evaluation of fecal samples, especially of animals with diarrhea or undergoing rehabilitation should be considered in beach monitoring approaches conducted in Brazil.

Supporting information

S1 Table. Epidemiological and biological data (common name, species, age class, sex and region of stranding) of the cetaceans stranded on the Brazilian coast, and tested for morbillivirus and coronavirus.

https://doi.org/10.1371/journal.pone.0316050.s001

(XLSX)

Acknowledgments

We thank Aquasis, R3 Animal, Instituto Baleia Jubarte, Argonauta, Instituto Biopesca, Ipec, Instituto Mamíferos Aquáticos, UDESC and Universidade da Região de Joinville (UNIVILLE) for the logistic and technical support, and Leonardo Wedekin for the maps used in this research. We also thank the Santos Basin Beach Monitoring Project (Projeto de Monitoramento de Praias da Bacia de Santos—PMP-BS) and Potiguar Basin Beach Monitoring Project (Projeto de Monitoramento de Praias da Bacia Potiguar–PMP-BP), conducted by Petrobrás, licensed by the Brazilian Institute of the Environment and Renewable Natural Resources (IBAMA) of the Brazilian Ministry of Environment, under ABIO Nº 640/2015. We thank the Coordination for the Improvement of Higher Education Personnel (CAPES), National Council for Technological and Scientific Development (CNPq), São Paulo Research Foundation (FAPESP), and Consejo Superior de Investigaciones Científicas (CSIC) for their support. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We acknowledge support of the publication fee by the CSIC Open Access Publication Support Initiative through its Unit of Scientific Information Resources for Research (URICI).

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Citation: Costa-Silva S, Sacristán C, Duarte-Benvenuto A, Ewbank AC, Soares RM, Carvalho VL, et al. (2025) Morbillivirus and coronavirus survey in stranded cetaceans, Brazil. PLoS ONE 20(3): e0316050. https://doi.org/10.1371/journal.pone.0316050

About the Authors:

Samira Costa-Silva

Roles: Conceptualization, Data curation, Formal analysis, Funding acquisition, Writing – original draft, Writing – review & editing

E-mail: [email protected] (CS); [email protected] (SC-S)

Affiliation: Faculdade de Medicina Veterinária e Zootecnia – Universidade de São Paulo, São Paulo, Brazil

Carlos Sacristán

Roles: Conceptualization, Data curation, Formal analysis, Funding acquisition, Methodology, Writing – original draft, Writing – review & editing

E-mail: [email protected] (CS); [email protected] (SC-S)

Affiliation: Centro de Investigación en Sanidad Animal (CISA-INIA), CSIC, Valdeolmos, Madrid, Spain

Arícia Duarte-Benvenuto

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Faculdade de Medicina Veterinária e Zootecnia – Universidade de São Paulo, São Paulo, Brazil

Ana Carolina Ewbank

Roles: Writing – original draft, Writing – review & editing

Affiliation: Centro de Investigación en Sanidad Animal (CISA-INIA), CSIC, Valdeolmos, Madrid, Spain

ORICD: https://orcid.org/0000-0002-5617-9287

Rodrigo M. Soares

Roles: Conceptualization, Data curation, Formal analysis, Writing – original draft, Writing – review & editing

Affiliation: Faculdade de Medicina Veterinária e Zootecnia – Universidade de São Paulo, São Paulo, Brazil

Vitor L. Carvalho

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Associação de Pesquisa e Preservação de Ecossistemas Aquáticos - AQUASIS, Caucaia, Ceará, Brazil

Pedro V. Castilho

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Universidade do Estado de Santa Catarina-UDESC, Laguna, Snata Catarina, Brazil

Marta J. Cremer

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Laboratório de Ecologia e Conservação de Tetrápodes Marinhos e Costeiros - TetraMar, Universidade da Região de Joinville, São Francisco do Sul, Santa Catarina, Brazil

Jenyffer V. Vieira

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Laboratório de Ecologia e Conservação de Tetrápodes Marinhos e Costeiros - TetraMar, Universidade da Região de Joinville, São Francisco do Sul, Santa Catarina, Brazil

ORICD: https://orcid.org/0000-0001-7785-5670

Giulia G. Lemos

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Laboratório de Ecologia e Conservação de Tetrápodes Marinhos e Costeiros - TetraMar, Universidade da Região de Joinville, São Francisco do Sul, Santa Catarina, Brazil

Jéssica R. Moreira

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Laboratório de Processamento Histológico – LAPHIS, Universidade da Região de Joinville, São Francisco do Sul, Santa Catarina, Brazil

Gladys D. Rogge Renner

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Laboratório de Processamento Histológico – LAPHIS, Universidade da Região de Joinville, São Francisco do Sul, Santa Catarina, Brazil

Cristiane K. M. Kolesnikovas

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Associação R3 Animal, Florianópolis, Santa Catarina, Brazil

Natalia S. Peres

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Faculdade de Medicina Veterinária e Zootecnia – Universidade de São Paulo, São Paulo, Brazil

Thalita Faita

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Faculdade de Medicina Veterinária e Zootecnia – Universidade de São Paulo, São Paulo, Brazil

Larissa Pavaneli

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto Mamíferos Aquáticos - IMA, Salvador, Bahia, Brazil

Joana Ikeda

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto Mamíferos Aquáticos - IMA, Salvador, Bahia, Brazil

Adriana C. Colosio

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto Baleia Jubarte – IBJ, Caravelas, Bahia, Brazil

Milton C. C. Marcondes

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto Baleia Jubarte – IBJ, Caravelas, Bahia, Brazil

Angélica M. Sánchez-Sarmiento

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto Argonauta para a Conservação Costeira e Marinha, Ubatuba, São Paulo, Brazil

Carla B. Barbosa

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto Argonauta para a Conservação Costeira e Marinha, Ubatuba, São Paulo, Brazil

ORICD: https://orcid.org/0000-0002-5044-0974

Raquel B. Ferioli

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto Argonauta para a Conservação Costeira e Marinha, Ubatuba, São Paulo, Brazil

ORICD: https://orcid.org/0000-0001-9212-7778

Vanessa L. Ribeiro

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto Biopesca, Praia Grande, Santa Catarina, Brazil

Carolina P. Bertozzi

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto de Biociências, Universidade Estadual Paulista (UNESP), São Vicente, São Paulo, Brazil

Caroline F. Pessi

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto de Pesquisas de Cananéia, Cananéia, São Paulo, Brazil

Henrique Chupill

Roles: Data curation, Formal analysis, Writing – review & editing

Affiliation: Instituto de Pesquisas de Cananéia, Cananéia, São Paulo, Brazil

José L. Catão-Dias

Roles: Conceptualization, Funding acquisition, Writing – original draft, Writing – review & editing

Affiliation: Faculdade de Medicina Veterinária e Zootecnia – Universidade de São Paulo, São Paulo, Brazil

Lara B. Keid

Roles: Conceptualization, Data curation, Formal analysis, Funding acquisition, Writing – original draft, Writing – review & editing

Affiliation: Faculdade de Engenharia de Alimento e Zootecnia – Universidade de São Paulo, Pirassununga, São Paulo, Brazil

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28. Mira F, Rubio-Guerri C, Purpari G, Puleio R, Caracappa G, Gucciardi F, et al. Circulation of a novel strain of dolphin morbillivirus (DMV) in stranded cetaceans in the Mediterranean Sea. Sci Rep. 2019;9(1):1–9.

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