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Necrotizing placentitis in a cow caused by Bacillus cereus

Placentite necrotizante em uma vaca por Bacillus cereus

ABSTRACT:

This report described a case of necrotizing placentitis caused by Bacillus cereus in a cow associated with abortion and maternal lethality. The etiological diagnosis of placentitis by B. cereus was based on histopathology of placenta, cytology and bacterial isolation from intrauterine aminiotic fluid in retained placenta and further characterization of the pathogen by the MALDI-TOF. Although, B. cereus abortions are sporadic, the bacterium has the ability to release necrotizing toxins that can lead to placentitis, fetal death and abortion.

Key words:
Bacillus sp.; placenta; infectious abortion; cattle

RESUMO:

Este relato descreve a placentite necrotizante causada por Bacillus cereus em uma vaca associada a aborto e mortalidade materna. O diagnóstico etiológico de placentite por B. cereus foi baseado na histopatologia da placenta, citologia e isolamento bacteriano partir do líquido aminiótico em placenta retida e identificação do patógeno pela técnica de MALDI-TOF. Embora abortos por B. cereus sejam esporádicos, a bactéria tem a capacidade de liberar toxinas necrotizantes que podem levar a placentite e aborto.

Palavras-chave:
Bacillus sp.; placenta; aborto infeccioso; bovino

Bacillus cereus is a Gram-positive aerobic or anaerobic facultative spore-forming rod bacterium. It is mobile and found in water, soil, plants and various sediments in the environment (BOTTONE, 2010BOTTONE, E. J. Bacillus cereus, a volatile human pathogen. Clinical Microbiology Reviews, v.23, n.2, p.382-398, 2010. Available from: <Available from: https://cmr.asm.org/content/cmr/23/2/382.full.pdf >. Accessed: May, 25, 2020. doi: 10.1128/CMR.00073-09.
https://cmr.asm.org/content/cmr/23/2/382...
). In cattle, B. cereus and B. licheniformis are two species considered opportunistic that are associated with mastitis (SCHIEFER et al., 1976SCHIEFER, B. et al. Pathology of Bacillus cereus mastitis in dairy cows. The Canadian Veterinary Journal, v.17, n.9, p.239-243, 1976. Available from: <Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1697321/pdf/canvetj00394-0029.pdf >. Accessed: May, 25, 2020.
https://www.ncbi.nlm.nih.gov/pmc/article...
; PARKINSON et al., 1999PARKINSON, T. J. et al. A case of bovine mastitis caused by Bacillus cereus. New Zealand Veterinary Journal, v.47, n.4, p.151-152, 1999. Available from: <Available from: https://www.tandfonline.com/doi/abs/10.1080/00480169.1999.36134 >. Accessed: May, 25, 2020. doi: 10.1080/00480169.1999.36134.
https://www.tandfonline.com/doi/abs/10.1...
; MAVANGIRA et al., 2013MAVANGIRA, V. et al. Gangrenous mastitis caused by Bacillus species in six goats. Journal of the American Veterinary Medical Association, v.242, n.6, p.836-843, 2013. Available from: <Available from: https://avmajournals.avma.org/doi/abs/10.2460/javma.242.6.836 >. Accessed: May, 25, 2020. doi: 10.2460/javma.242.6.836.
https://avmajournals.avma.org/doi/abs/10...
) and abortion (SCHU & WEINSTOCK, 1985SCHUH, J.; WEINSTOCK, D. Bovine abortion caused by Bacillus cereus. Journal of the American Veterinary Medical Association, v.187, n.10, p.1047-1048, 1985.; ANDERSON et al., 1990ANDERSON, M. L. et al. A survey of causes of bovine abortion occurring in the San Joaquin Valley, California. Journal of Veterinary Diagnostic Investigation, v.2, n.4, p.283-287, 1990. Available from: <Available from: https://journals.sagepub.com/doi/10.1177/104063879000200405 >. Accessed: May, 25, 2020. doi: 10.1177/104063879000200405.
https://journals.sagepub.com/doi/10.1177...
; KIRKBRIDE, 1993KIRKBRIDE, C. A. Bacterial agents detected in a lo-year study of bovine abortions and stillbirths. Journal of Veterinary Diagnostic Investigation, v.5, n.1, p.64-68, 1993. Available from: <Available from: https://journals.sagepub.com/doi/pdf/10.1177/104063879300500114 >. Accessed: May, 25, 2020. doi: 10.1177/104063879300500114.
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; AGERHOLM et al., 1997AGERHOLM, J. S. et al. Diagnostic studies of abortion in Danish dairy herds. Journal of Veterinary Medicine Series A, v.44, n.1-10, p.551-558, 1997. Available from: <Available from: https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1439-0442.1997.tb01141.x >. Accessed: May, 25, 2020. doi: 10.1111/j.1439-0442.1997.tb01141.x.
https://onlinelibrary.wiley.com/doi/abs/...
). Reports of bovine abortion caused by Bacillus spp. have been described in Europe (AGERHOLM et al., 1997AGERHOLM, J. S. et al. Diagnostic studies of abortion in Danish dairy herds. Journal of Veterinary Medicine Series A, v.44, n.1-10, p.551-558, 1997. Available from: <Available from: https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1439-0442.1997.tb01141.x >. Accessed: May, 25, 2020. doi: 10.1111/j.1439-0442.1997.tb01141.x.
https://onlinelibrary.wiley.com/doi/abs/...
; ODDSDOTTIR et al., 2004ODDSDOTTIR, C. et al. Preliminary diagnostic survey on causes of prenatal mortality in Icelandic cattle. Acta Veterinaria Scandinavica (print Edition), v.45, n.3-4, p.225-228, 2004. Available from: <Available from: https://actavetscand.biomedcentral.com/articles/10.1007/BF03449136 >. Accessed: May, 25, 2020. doi: 10.1007/BF03449136.
https://actavetscand.biomedcentral.com/a...
; DI BLASIO et al., 2019DI BLASIO, A. et al. Isolation of Arcobacter species and other neglected opportunistic agents from aborted bovine and caprine fetuses. BMC Veterinary Research, v.15, n.1, p.257, 2019. Available from: <Available from: https://bmcvetres.biomedcentral.com/articles/10.1186/s12917-019-2009-3 >. Accessed: May, 25, 2020. doi: 10.1186/s12917-019-2009-3.
https://bmcvetres.biomedcentral.com/arti...
; WOLF-JÄCKEL et al., 2020WOLF-JÄCKEL, G. A. et al. Diagnostic studies of abortion in Danish cattle 2015-2017. Acta Veterinaria Scandinavica, v.62, n.1, p.1, 2020. Available from: <Available from: https://actavetscand.biomedcentral.com/articles/10.1186/s13028-019-0499-4 >. Accessed: May, 25, 2020. doi: 10.1186/s13028-019-0499-4.
https://actavetscand.biomedcentral.com/a...
), North America (ANDERSON et al., 1990AGERHOLM, J. S. et al. Diagnostic studies of abortion in Danish dairy herds. Journal of Veterinary Medicine Series A, v.44, n.1-10, p.551-558, 1997. Available from: <Available from: https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1439-0442.1997.tb01141.x >. Accessed: May, 25, 2020. doi: 10.1111/j.1439-0442.1997.tb01141.x.
https://onlinelibrary.wiley.com/doi/abs/...
; KIRKBRIDE, 1993KIRKBRIDE, C. A. Bacterial agents detected in a lo-year study of bovine abortions and stillbirths. Journal of Veterinary Diagnostic Investigation, v.5, n.1, p.64-68, 1993. Available from: <Available from: https://journals.sagepub.com/doi/pdf/10.1177/104063879300500114 >. Accessed: May, 25, 2020. doi: 10.1177/104063879300500114.
https://journals.sagepub.com/doi/pdf/10....
; CLOTHIER & ANDERSON, 2016CLOTHIER, K.; ANDERSON, M. Evaluation of bovine abortion cases and tissue suitability for identification of infectious agents in California diagnostic laboratory cases from 2007 to 2012. Theriogenology, v.85, n.5, p.933-938, 2016. Available from: <Available from: https://www.sciencedirect.com/science/article/abs/pii/S0093691X1500610X?via%3Dihub >. Accessed: May, 25, 2020. doi: 10.1016/j.theriogenology.2015.11.001.
https://www.sciencedirect.com/science/ar...
), and Oceania (REICHEL et al., 2018REICHEL, M. P. et al. Review of diagnostic procedures and approaches to infectious causes of reproductive failures of cattle in Australia and New Zealand. Frontiers in Veterinary Science, v.5, p.222, 2018. Available from: <Available from: https://www.frontiersin.org/articles/10.3389/fvets.2018.00222/full >. Accessed: May, 25, 2020. doi: 10.3389/fvets.2018.00222.
https://www.frontiersin.org/articles/10....
) with no previously reported cases in South America.

Necrotic, hemorrhagic and suppurated placentitis are often associated with Bacillus sp. infection. Bacillus sp.-induced fetal lesions include pneumonia, pericarditis, encephalitis, hepatitis, peritonitis, and inflammation of the thymus (LOGAN, 1988LOGAN, N. A. Bacillus species of medical and veterinary importance. Journal of medical microbiology, v.25, n.3, p.157-165, 1988. Available from: <Available from: https://www.microbiologyresearch.org/content/journal/jmm/10.1099/00222615-25-3-157 >. Accessed: May, 25, 2020. doi: 10.1099/00222615-25-3-157.
https://www.microbiologyresearch.org/con...
; KIRKBRIDE, 1993KIRKBRIDE, C. A. Bacterial agents detected in a lo-year study of bovine abortions and stillbirths. Journal of Veterinary Diagnostic Investigation, v.5, n.1, p.64-68, 1993. Available from: <Available from: https://journals.sagepub.com/doi/pdf/10.1177/104063879300500114 >. Accessed: May, 25, 2020. doi: 10.1177/104063879300500114.
https://journals.sagepub.com/doi/pdf/10....
). Silage is considered an important source of contamination for cattle; although, Bacillus sp. is widely distributed in nature (LOGAN, 1988LOGAN, N. A. Bacillus species of medical and veterinary importance. Journal of medical microbiology, v.25, n.3, p.157-165, 1988. Available from: <Available from: https://www.microbiologyresearch.org/content/journal/jmm/10.1099/00222615-25-3-157 >. Accessed: May, 25, 2020. doi: 10.1099/00222615-25-3-157.
https://www.microbiologyresearch.org/con...
).

This report described for the first time in Brazil a bovine abortion in the final third of pregnancy caused by Bacillus cereus. A five-year-old Holstein cow, at 32 weeks of gestation, developed apathy, anorexia and pyrexia (41.5 °C). During physical examination, the cow was not in labor and on rectal palpation the fetus was in an eutopic position with no movement. Antibiotic therapy (penicillin 10,000 IU/Kg and gentamicin 160 mg/kg) was administered every 48 hours in association with anti-inflammatory therapy (phenylbutazone OF 20%, 12 mL) daily. Twenty-four hours later, the cow presented external decubitus and fetal expulsion.

Male fetus with a crown-rump length of 57 cm was expelled with the fragments of the fetal membranes and a large amount of purulent, fetid and bloody fluid. A few hours after fetal expulsion, clinical condition of the cow worsened, progressing to death. Blood samples from the cow were collected for hemogram, and samples of the aminiotic fluid from the intrauterine retained placenta were collected for cytology and bacterial isolation. At necropsy, the cow presented an accumulation of fibrinopurulent necrotizing exudate covering the caruncles within the uterus and fetal membranes thickened with pyosanguinolent exudate. Fragments of the placentome were collected for histopathological examination. Necropsy examination of the stillborn was not performed.

The cow had leukocytosis with left deviation. The cytological examination of the aminiotic fluid in the panotic stained smears revealed numerous red blood cells and degenerate neutrophils, some of which with high numbers of elongated bacillary microbial structures often sporulated. Gram stained smears demonstrated numerous Gram-positive elongated rods with central endospore, compatible with microorganisms of the genus Bacillus both extracellular or within the cytoplasm of macrophages (Figure 1A).

Figure 1
(A) Cytology of amniotic fluid. Numerous Gram-positive rods mostly associated with macrophages. Gram staining. (B) Cross section of a bovine placentome fixed in 10% formalin, B. cereus-induced abortion. Chorionic surface covered with a yellowish fibrinopurulent exudate (arrow) and multifocal areas of hemorrhage (arrowheads). (C-D) Bovine placenta, B. cereus-induced abortion. Fibrinous and necrotizing placentitis with mild multifocal neutrophilic inflammatory infiltrate, and bacterial colony. Hematoxylin and eosin, 100X and 400X. (E) Gram-positive rods extra and intracytoplasmic. Good-Pasture, 600x.

Samples of the placentome were referred to the pathology service at the Veterinary School of the Universidade Federal de Minas Gerais (UFMG, Belo Horizonte, Brazil). Grossly, cross sections of fixed fragments of placenta had multifocal to coalescing hemorrhage, particularly at the arcade region (caruncular surface and bases of the chorionic villi), and accumulation of fibrinopurulent exudate (Figure 1B).

Microscopically, there was a moderate multifocal neutrophilic inflammatory infiltrate in the placenta with necrosis, accumulation of fibrin, and myriad of Gram-positive bacterial colonies, in the form of rods, with both extracellular and intracellular localization in trophoblastic cells. Macrophages containing brown pigments were observed with multifocal distribution. Morphological diagnosis of fibrinonecrotizing placentitis with intralesional Gram-positive bacteria was established (Figure 1C-E).

The etiological diagnosis of placentitis by B. cereus was confirmed by bacterial isolation, which included aerobic and anaerobic protocols. Bacteria were isolated when 5 mL of the aminiotic fluid was heated at 62 °C for 15 minutes, subsequently, plated on sheep blood 5% agar, and incubated at 37 °C for 24-48 hours. Beta hemolytic, irregular, large and matte colonies were submitted to biochemical tests in order to identify the microbial species. The isolates were motility+, catalase+, oxidase-, urease-, citrate+, gelatin+, nitrates reduction+, voges proskauer+, lecithinase+, esculin hydrolysis+. Results were validated according to the taxonomic key of the ABIS ONLINE software (https://www.tgw1916.net/bacteria_logare.html) with an accuracy of 99%. Additionally, when the isolates were cultured in serum agar and incubated with 10% CO2 there was formation of capsule. Cultures in brain heart infusion broth were sent to the Aquacen laboratory (UFMG Veterinary School), where the bacterium was identified as B. cereus by the MALDI-TOF (Matrix Associated Laser Desorption-Ionization - Time of Flight) mass spectrometry as previously described (ASSIS et al., 2017ASSIS, G. B. N. et al. Use of MALDI-TOF mass spectrometry for the fast identification of gram-positive fish pathogens. Frontiers in Microbiology, v.8, p.1-12, 2017. Available from: <Available from: https://www.frontiersin.org/articles/10.3389/fmicb.2017.01492/full >. Accessed: May, 25, 2020. doi: 10.3389/fmicb.2017.01492.
https://www.frontiersin.org/articles/10....
).

In addition, other important pathogens associated with bovine abortion or placentitis were investigated by PCR with DNA templates extracted from formalin-fixed placental samples. DNA extraction was performed according to SILVA et al., 2009SILVA, T. M. A., et al. Etiologic diagnosis of bovine infections abortion by PCR. Ciência Rural, v.39, n.9, p.2563-2570, 2009. Available from: <Available from: https://www.scielo.br/pdf/cr/v39n9/a401cr1871.pdf >. Accessed: Oct. 30, 2020. doi: 10.1590/S0103-84782009000900028.
https://www.scielo.br/pdf/cr/v39n9/a401c...
and PCR reactions performed as previously described for Brucella sp. Leptospira sp., Neospora caninum (SILVA et al., 2009SILVA, T. M. A., et al. Etiologic diagnosis of bovine infections abortion by PCR. Ciência Rural, v.39, n.9, p.2563-2570, 2009. Available from: <Available from: https://www.scielo.br/pdf/cr/v39n9/a401cr1871.pdf >. Accessed: Oct. 30, 2020. doi: 10.1590/S0103-84782009000900028.
https://www.scielo.br/pdf/cr/v39n9/a401c...
), Listeria monocytogenes (BUBERT et al., 1999BUBERT, A. et al. Detection and differentiation of Listeria spp. by a single reaction based on multiplex PCR. Applied and Environmental Microbiology, v.65, n.10, p.4688-4692, 1999. Available from: <Available from: https://aem.asm.org/content/aem/65/10/4688.full.pdf >. Accessed: Oct. 30, 2020. doi: 10.1128/AEM.65.10.4688-4692.1999.
https://aem.asm.org/content/aem/65/10/46...
), and Herpesvirus Bovine Type 1 (VAN ENGELENBURG, et al., 1993VAN ENGELENBURG, F. A. C.; et al. Development of a rapid and sensitive polymerase chain reaction of bovine herpesvirus type 1 in bovine semen. Journal of Clinical Microbiology, v.31, p.3129- 3135, 1993. Available from: <Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC266363/pdf/jcm00024-0065.pdf >. Accessed: Oct. 30, 2020.
https://www.ncbi.nlm.nih.gov/pmc/article...
). The quality of the extracted DNA was confirmed by the positive PCR reaction for amplification of the bovine α- actin gene (SILVA et al., 2009). Negative and positive controls were included in each reaction. The etiological diagnosis of placentitis by B. cereus in this case was confirmed by bacterial isolation from aminiotic fluid collected directly from the uterine cavity and specific identification by a comprehensive biochemical panel and MALDI-TOF mass spectrometry. Fibrinopurulent placentitis was the probable cause of the clinical changes presented by the cow, which were associated with abortion followed by maternal death.

The cow in this report was approximately at eight months of pregnancy with clinical signs of pyrexia, apathy and anorexia, and absence of fetal movement. Therefore, in this case, fetal death preceded fetal expulsion as reported in previously described cases (SCHUH & WEINSTOCK, 1985SCHUH, J.; WEINSTOCK, D. Bovine abortion caused by Bacillus cereus. Journal of the American Veterinary Medical Association, v.187, n.10, p.1047-1048, 1985.). B. cereus-induced abortion followed by death of the cow has not been previously described; although, cases of gangrenous mastitis due to B. cereus infection are often lethal due to toxemia (SCHIEFER et al., 1976SCHIEFER, B. et al. Pathology of Bacillus cereus mastitis in dairy cows. The Canadian Veterinary Journal, v.17, n.9, p.239-243, 1976. Available from: <Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1697321/pdf/canvetj00394-0029.pdf >. Accessed: May, 25, 2020.
https://www.ncbi.nlm.nih.gov/pmc/article...
).

In cases of abortion in domestic animals caused by Bacillus spp. that the pathogen may be isolated from vaginal swabs, placenta, fetal abomasal contents, heart, liver, lung, bronchial and mediastinum lymph nodes of aborted fetuses (LOGAN et al., 1988LOGAN, N. A. Bacillus species of medical and veterinary importance. Journal of medical microbiology, v.25, n.3, p.157-165, 1988. Available from: <Available from: https://www.microbiologyresearch.org/content/journal/jmm/10.1099/00222615-25-3-157 >. Accessed: May, 25, 2020. doi: 10.1099/00222615-25-3-157.
https://www.microbiologyresearch.org/con...
). In this case, B. cereus was isolated from aminiotic fluid while fetal membranes were still within the uterus, which minimized environmental contamination.

JOHNSON et al. (1994JOHNSON, C. T.; et al. The bovine placentome in bacterial and mycotic abortions. The Veterinary record, v.134, n.11, p.263-266, 1994. Available from: <Available from: https://veterinaryrecord.bmj.com/content/134/11/263 >. Accessed: May, 25, 2020. doi: 10.1136/vr.134.11.263.
https://veterinaryrecord.bmj.com/content...
) considered placentome a good tissue to obtain the definitive etiological diagnosis because it allows associating isolation with necrotic placentitis lesion, which may allow a conclusive diagnosis even without access to fetal tissues. There is evidence of abortion with necrotic placentitis by B. cereus without fetal injury, even if there is bacterial colonization in the fetus (SCHUH & WEINSTOCK, 1985SCHUH, J.; WEINSTOCK, D. Bovine abortion caused by Bacillus cereus. Journal of the American Veterinary Medical Association, v.187, n.10, p.1047-1048, 1985.). In this report, the fetus was not available and the only tissue sent for hispathological examination was a placentome, which along with microbiological examination of the aminiotic fluid supported a conclusive diagnosis of necrotic placentitis with intralesional Gram-positive bacteria (Bacillus cereus).

Considering that B. cereus is an ubiquitous microorganism, isolation of the bacteria by itself is not sufficient for a conclusive diagnosis since the isolated bacterium may be an environmental contaminant. The diagnosis of bovine abortion by B. cereus is usually based on the pure culture of the microorganism isolated from placenta and/or fetus, with presence of microorganisms within microscopic lesions, and the absence of other agents known to cause abortion in cattle (SCHUH & WEINSTOCK, 1985SCHUH, J.; WEINSTOCK, D. Bovine abortion caused by Bacillus cereus. Journal of the American Veterinary Medical Association, v.187, n.10, p.1047-1048, 1985.). In this case, no other infectious agent was isolated on microbiological examination or detected by PCR. Furthermore, the visualization of phagocytosed Gram-positive bacteria by macrophages present in the amniotic fluid indicates that this agent was not an environmental contaminant, but it was present within the uterus prior to fetal expulsion and it was associated with the intrauterine inflammatory reaction.

The pathogenesis of B. cereus-induced abortion is unknown; although, B. cereus secretes several enzymatic or lytic exotoxins, including phospholipases, hemolysins, pore-forming enterotoxins, and cytotoxin K (LOGAN, 1988LOGAN, N. A. Bacillus species of medical and veterinary importance. Journal of medical microbiology, v.25, n.3, p.157-165, 1988. Available from: <Available from: https://www.microbiologyresearch.org/content/journal/jmm/10.1099/00222615-25-3-157 >. Accessed: May, 25, 2020. doi: 10.1099/00222615-25-3-157.
https://www.microbiologyresearch.org/con...
, BOTTONE, 2010BOTTONE, E. J. Bacillus cereus, a volatile human pathogen. Clinical Microbiology Reviews, v.23, n.2, p.382-398, 2010. Available from: <Available from: https://cmr.asm.org/content/cmr/23/2/382.full.pdf >. Accessed: May, 25, 2020. doi: 10.1128/CMR.00073-09.
https://cmr.asm.org/content/cmr/23/2/382...
). According to SCHUH & WEINSTOCK (1985SCHUH, J.; WEINSTOCK, D. Bovine abortion caused by Bacillus cereus. Journal of the American Veterinary Medical Association, v.187, n.10, p.1047-1048, 1985.), one of the consequences of toxins produced by B. cereus is a necrotizing placentitis followed by death and fetal expulsion before fetal injury or even colonization of fetal tissues by B. cereus (SCHUH & WEINSTOCK, 1985SCHUH, J.; WEINSTOCK, D. Bovine abortion caused by Bacillus cereus. Journal of the American Veterinary Medical Association, v.187, n.10, p.1047-1048, 1985.). Studies suggested that bovine abortions caused by B. cereus may be associated to virus-induced immunosuppression as occurs in cases of bovine viral diarrhea virus infection (SCHUH & WEINSTOCK,1985SCHUH, J.; WEINSTOCK, D. Bovine abortion caused by Bacillus cereus. Journal of the American Veterinary Medical Association, v.187, n.10, p.1047-1048, 1985.; KIRKBRIDE, 1993KIRKBRIDE, C. A. Bacterial agents detected in a lo-year study of bovine abortions and stillbirths. Journal of Veterinary Diagnostic Investigation, v.5, n.1, p.64-68, 1993. Available from: <Available from: https://journals.sagepub.com/doi/pdf/10.1177/104063879300500114 >. Accessed: May, 25, 2020. doi: 10.1177/104063879300500114.
https://journals.sagepub.com/doi/pdf/10....
). In conclusion; although, it is an opportunistic agent, B. cereus should be considered in the differential diagnosis of sporadic infectious bovine abortion in the country.

ACKNOWLEDGMENTS:

This work has financial support of Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brasil - Finance code 001. CEVR are supported by CAPES and HCPF, RLS and TAP are supported by CNPq.

REFERENCES

  • CR-2020-0553.R2

BIOETHICS AND BIOSSECURITY COMMITTEE APPROVAL

  • We authors of the article entitled “Necrotizing placentitis in a cow caused by Bacillus cereus” declared, for all due purposes, the project that gave rise to the present data of the same has not been submitted for evaluation to Ethics Committee of the Universidade Federal de Minas Gerais”, but we are aware of the content of the Brazilian resolutions of the National Council for Control of Animal Experimentation - CONCEA “http://www.mct.gov.br/index.php/content/view/310553.html” if it involves animals. Thus, the authors assume full responsibility for the presented data and are available for possible questions, should they be required by the competent authorities.

Publication Dates

  • Publication in this collection
    29 Mar 2021
  • Date of issue
    2021

History

  • Received
    10 June 2020
  • Accepted
    17 Nov 2020
  • Reviewed
    26 Jan 2021
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