Identification of Streptococcus agalactiae in western Cuba cattle milk affected by mastitis

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Dervel Felipe Díaz-Herrera
Dianys Remón-Díaz
Yamilka Riverón-Alemán
Ariel Ribot
Anel Ledesma-Rodríguez
Ailin Martínez-Vasallo
Odalys Uffo Reinoso

Abstract

Streptococcus agalactiae is one of the main agents causing mastitis in dairy cattle, with important implications for humans; whereby the diagnosis, control and prevention of this microorganism is fundamental to animal and human health as well for the economy. The objective of this work was to detect the presence of S. agalactiae in milk from cattle herds affected by mastitis. Five hundred and seventy-four samples of milk were collected from quarters affected with mastitis (840 production cattle of Siboney de Cuba, Holstein and Jersey breeds of 14 dairy farms in western Cuba). Bacteriological diagnosis was performed in all samples. DNA and PCR were extracted with primers that amplified a segment of the 16S-23S rRNA intergenic region, from colonies with morphological characteristics and biochemical tests indicative of S. agalactiae. The 43.45 % of animals showed symptoms of clinical or subclinical mastitis. In 57 samples (9.97 %), colonies characteristic of S. agalactiae were isolated, and 43 (75.43 %) were positive by PCR. Of the latter, 26 (60.46 %) corresponded to quarters with three crossings, 14 (32.55 %) to two crossings and 3 (6.97 %) to clinical rooms. S. agalactiae was isolated in eight dairy farms and the most affected breeds were Holstein and Siboney de Cuba. Strains of S. agalactiae were isolated and identified in mastitis-affected cows, indicating the need for programs to control mastitis caused by S. agalactiae to mitigate the effects caused by this microorganism on human-animal-environment interfaces.

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1.
Díaz-Herrera DF, Remón-Díaz D, Riverón-Alemán Y, Ribot A, Ledesma-Rodríguez A, Martínez-Vasallo A, Uffo Reinoso O. Identification of Streptococcus agalactiae in western Cuba cattle milk affected by mastitis. Rev. Salud Anim. [Internet]. 2019 Dec. 1 [cited 2024 Nov. 24];41(3). Available from: https://revistas.censa.edu.cu/index.php/RSA/article/view/1041
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ARTÍCULOS ORIGINALES

References

Jamali H, Barkema HW, Jacques M, Lavallée-Bourget EM, Malouin F, Saini V, et al. Invited review: Incidence, risk factors, and effects of clinical mastitis recurrence in dairy cows. J Dairy Sci. 2018;101(6):4729-4746. http://dx.doi.org/10.3168/jds.2017-13730

Ruiz Gil A, Peña Rodríguez J, Remón Díaz D. Mastitis bovina en Cuba. Artículo de revisión. Rev Prod Anim. 2016;28(2-3):39-50.

García F, Sánchez T, López O, Álvarez M. Prevalence of subclinical mastitis and associated microorganisms. Pastos y Forrajes. 2018;41(1):33-38.

Ramírez Vásquez N, Fernández-Silva JA, Palacio LG. Tasa de incidencia de mastitis clínica y susceptibilidad antibiótica de patógenos productores de mastitis en ganado lechero del norte de Antioquia, Colombia. Rev Med Vet (Bogotá). 2017;(36):75-87.

Carvalho-Castro GA, Silva JR, Paiva LV, Custódio DAC, Moreira RO, Mian GF, et al. Molecular epidemiology of Streptococcus agalactiae isolated from mastitis in Brazilian dairy herds. Brazilian J Microbiol. 2017;48:551-559.

Jørgensen HJ, Nordstoga AB, Sviland S, Zadoks RN, Sølverød L, Kvitle B, et al. Streptococcus agalactiae in the environment of bovine dairy herds - rewriting the textbooks?? Vet Microbiol. 2016;184:64-72. http://dx.doi.org/10.1016/j.vetmic.2015.12.014

Tomazi T, de Souza Filho AF, Heinemann MB, dos Santos MV. Molecular characterization and antimicrobial susceptibility pattern of Streptococcus agalactiae isolated from clinical mastitis in dairy cattle. PLOS ONE. 2018;13(6):e0199561. https://doi.org/10.1371/journal.pone.0199561

Cobo-a C, Sanchez J, Rodriguez-lecompte JC, Ceballos- A, Zadoks RN. Streptococcus agalactiae is not always an obligate intramammary pathogen: Molecular epidemiology of GBS from milk, feces and environment in Colombian dairy herds. PLOS ONE. 2018;13(12):e0208990. https://doi.org/10.1371/journal.pone.0208990.

Chen SL. Genomic insights into the distribution and evolution of group B streptococcus. Front Microbiol. 2019,1:1447.doi:10.3389/fmicb.2019.01447

Botelho ACN, Ferreira AFM, Fracalanzza SEL, Teixeira LM, Pinto TCA. A perspective on the potential zoonotic role of streptococcus agalactiae: Searching for a missing link in alternative transmission routes. Front Microbiol. 2018;9:1-5.

Ruegg PL. A 100-Year Review: Mastitis detection, management, and prevention. J Dairy Sci . 2017;100(12):10381-10397. http://dx.doi.org/10.3168/jds.2017-13023

Ahmadi M, Rohani SMR, Ayremlou N. Evaluation of Streptococcus agalactiae detection by PCR in Milk and its comparison to other microbiological methods. Iran J. Microbiol. 2009;1(4):28-31. http://ijm.tums.ac.ir/index.php/ijm/article/view/36

Phuektes P, Mansell PD, Browning GF. Multiplex polymerase chain reaction assay for simultaneous detection of Staphylococcus aureus and Streptococcal causes of bovine mastitis. J. Dairy Sci . 2001;84(5):1140-8. Available from: http://dx.doi.org/10.3168/jds.S0022-0302(01)74574-2

Alfonso D, Zanette J, Ruiz K, Peña J, González Y, Reinoso M. Situación de la mastitis subclínica y evaluación de los procesos lecheros en vaquerías de la provincia Villa Clara, Cuba. Rev Salud Anim. 2017;39(3):pp.9.

Ruiz AK, González D, Peña J. Situaciòn de la mastitis bovina en Cuba. Rev Electron Vet. 2012;13(12).

Castillo Duvergel Y, Miranda I. COMPAPROP: Sistema para comparación de proporciones múltiples. Rev Protección Veg. 2014;29(3):231-234.

Guo D, Xi Y, Wang S, Wang Z. Is a positive Christie-Atkinson-Munch-Peterson (CAMP) test sensitive enough for the identification of Streptococcus agalactiae? BMC Infect. Dis. 2019;19(7). https://doi.org/10.1186/s12879-018-3561-3

Perreten V, Vorlet-Fawer L, Slickers P, Ehricht R, Kuhnert P, Frey J. Microarray-based detection of 90 antibiotic resistance genes of gram-positive bacteria. J Clin Microbiol. 2005;43(5):2291-2302.

Ruiz AK, Peña J, González D, Ponce P. Prevalence, somatic cell count and etiology of bovine mastitis in Cuban herds from Mayabeque province using hand and machine milking. Rev. Salud Anim. 2014;36(1):7-13.

Relova D, Armenteros M, Capdevila JZ. Caracterización de la situación clínico-epizootiológica de la mastitis bovina en vacas primerizas Holstein de una lechería especializada. RedVet. 2008;IX(9).

Novoa, R. Evaluación epizootiológica y económica de la mastitis bovina en rebaños lecheros especializados de la provincia de Cienfuegos. (Tesis en Opción al Grado Científico de Máster en Ciencias, Especialidad de Medicina Preventiva Veterinaria(. Universidad Agraria de La Habana "Fructuoso Rodríguez Pérez", Cuba. 2003. p.116.

Novoa R, Armenteros M, Abeledo MA, Casanovas E, Valera R, Pulido CCJ. Clínica Y Subclínica Risk Factors Associated To Clinical and Subclinical Mastitis. Rev Salud Anim. 2005;27(2):84-88.

del Pilar Sánchez Bonilla M, Murillo NPG, Almanza IJP. Prevalence of bovine mastitis in the anaime canyon, a colombian dairy region, including etiology and antimicrobial resistance. Rev Investig Vet del Peru. 2018;29(1):226-239.

Lakew BT, Fayera T, Ali YM. Risk factors for bovine mastitis with the isolation and identification of Streptococcus agalactiae from farms in and around Haramaya district, eastern Ethiopia. Trop Anim Health Prod. 2019;51(6):1507-1513.

Armenteros M, Ponce P, Capdevila J, Zaldívar V, Hernández R. Prevalencia de mastitis en vacas lecheras de primer parto y patrón de sensibilidad de las bacterias aisladas en una lechería especializada. Rev Salud Anim. 2006;28(1):8-12.

Insua A. Evaluación epizootiològica de la mastitis bovina en cuatro vaquerias. RedVet. 2008;IX(7):1-9.

Cepero O, Camacho C, Castillo JC, Salado J. Conductividad Eléctrica y California Mastitis Test en la detección de la Mastitis Subclínicas. RedVet. 2005;VI:1-5

Santivañez CS, Gómez OE, Cárdenas LÁ, Escobedo MH, Bustinza RH, Peña J. Prevalencia y factores asociados a la mastitis subclínica bovina en los Andes peruanos. Vet Zootec. 2014;7(2):92-104.

Abdel-Shafy H, Bortfeldt RH, Reissmann M, Brockmann GA. Validating genome-wide associated signals for clinical mastitis in German Holstein cattle. Animal Genetics. 2018;49(1):82-85.

Kibebew K. Bovine Mastitis: A Review of Causes and Epidemiological Point of View. J Biol Agric Healthc. 2017;7(2):1-14.

Kirk J, Mellenberger R. Programa de control de mastitis para vacas lecheras infectadas con Streptococcus agalactiae. DAIREXNET (actualizado el 16 de Agosto de 2019; citado el 11 de Noviembre de 2019). Disponible en https://dairy-cattle.extension.org/

Soca PM, Suárez FYE, Soca PM, Pestano OM, Puron CA . Evaluación epizootiológica de la mastitis bovina en dos unidades ganaderas de la Empresa Pecuaria "El Cangre." REDVET Rev Electrónica Vet. 2005;VI(8):1-10.

Oltenacu PA, Broom DM. The impact of genetic selection for increased milk yield on the welfare of dairy cows. Anim Welf. 2010;19(S):39-49.

Wu J, Liu Y, Hu S, Zhou J. Development of a rapid PCR test for identification of Streptococcus agalactiae in milk samples collected on filter paper disks. Asian-Australasian J Anim Sci. 2008;21(1):124-130.

Denamiel G. Mastitis bovina: variaciones en la detección de ß-hemolisina y factor CAMP para la identificación. Rev Med Vet. (B Aires). 2013;94:24-27.

Zárate MS, Jordá VL, Pacheco MV, Fernández CL, Smayevsky J. Modified spot CAMP test: A rapid, inexpensive and accurate method for identification of group B streptococci. Rev Argent Microbiol. 2005;37(3):126-128.

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