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Mastitis in cattle due to Mycobacteroides abscessus - case report

[Mastite bovina por Mycobacteroides abscessus - relato de caso]

ABSTRACT

Mastitis is considered the main disease that affects dairy cattle worldwide, and it is caused mainly by Staphylococcus aureus and environmental Streptococcus spp. Eventually, nonconventional pathogens, as rapidly growing mycobacteria (RGM), may also cause chronic mastitis, which will not be responsive to antibiotic treatments. Diagnosis of mastitis caused by RGM is a difficult task, and most of time this agent may be misdiagnosed. Here we describe a case of clinical mastitis caused by the RGM Mycobacteroides abscessus in a cow from Southern Brazil, confirmed by microbiological and molecular characterization. Our results reinforce the necessity of a detailed laboratorial identification of the agent and to include this agent in differential diagnosis of chronical clinical mastitis nonresponsive to treatment.

Keywords:
RGM; rapidly growing mycobacteria; milk; bovine

RESUMO

A mastite é considerada uma das principais doenças que afetam rebanhos leiteiros ao redor do mundo e é causada principalmente por Staphylococcus aureus e Streptococcus spp. ambientais. Eventualmente, patógenos não convencionais, como Mycobacterium de crescimento rápido (RGM), podem também causar mastite crônica, a qual não respondera ao tratamento com antimicrobianos. O diagnóstico de mastite causada por RGM é uma tarefa difícil, e a maioria das vezes esse agente pode ser subdiagnosticado. Neste relato, descreveu-se um caso de mastite clínica em uma vaca, no sul do Brasil, causada por RGM Mycobacteroides abscessus, confirmado por caracterização microbiológica e molecular. Os resultados reforçam a necessidade de um diagnóstico laboratorial detalhado para a identificação do agente e a inclusão deste como diagnóstico diferencial no reconhecimento de mastite crônica não responsiva ao tratamento.

Palavras-chave:
RGM; Mycobacterium de crescimento rápido; leite; bovino

INTRODUCTION

Mastitis is an inflammation of the mammary gland, generally associated with intramammary infection. It is the main disease which affects dairy cattle worldwide, causing expressive economic losses to the dairy producer (Bradley, 2002BRADLEY, A.J. Bovine mastitis: an evolving disease. Vet. J., v.164, p.116-128, 2002.). Organisms such as bacteria, yeasts and algae have been described as causes of bovine mastitis, which is normally divided in clinical or subclinical manifestation, which have a negative impact in milk production and quality (Bradley, 2002).

The main pathogens causing mastitis worldwide are Staphylococcus aureus and environmental streptococci (Riekerink et al., 2008RIEKERINK, R.G.M.O.; BARKEMA, H.W.; KELTON, D.F.; SCHOLL, D.T. Incidence rate of clinical mastitis on Canadian dairy farms. J. Dairy Sci., v.91, p.1366-1377, 2008.). However, nonconventional pathogens may also cause chronic mastitis, which will not be responsive to antibiotic treatments. Some of those nonconventional pathogens include Prototheca spp. and environmental Mycobacterium sp. (or Mycobacteroides sp.) (Marques et al., 2008MARQUES, S.; SILVA, E.; KRAFT, C. et al. Bovine mastitis associated with Prototheca blaschkeae. J. Clin. Microbiol., v.46, p.1941-1945, 2008.; Machado et al., 2015MACHADO, G.; GRESSLER, T.L.; SIQUEIRA, F.M. et al. Bovine pyogranulomatous mastitis caused by Mycobacterium goodii. JMM Case Rep., v.2, p.1-4, 2015.).

Diagnosis of mastitis-causing rapidly growing mycobacteria (RGM) is a difficult task. Most of time, RGM species may be misdiagnosed due to their similarity with other conventional pathogens, such as Corynebacterium sp. At this point, the laboratory diagnosis of mastitis is of extreme importance, since it will be able to make the correct diagnosis and to perform the molecular identification/differentiation. Then, we describe a case of clinical mastitis in a cow due to RGM Mycobacteroides abscessus (formerly Mycobacterium abscessus) and its phenotypical and molecular characterization.

CASUISTRY

A Jersey cow, 4 years-old, from a small farm located in Southern Brazil, presented recurrent clinical mastitis nonresponsive to antibiotic treatment. The animal belonged to a small herd composed of four lactating cows which were manually milked. The affected cow had mastitis in previous lactation and was treated with antibiotic (systemic and intramammary therapy). As soon as the next lactation started, it was observed that the animal had pain in one quarter and the milk had a pinkish color, suggestive of blood. Immediately, the animal was treated with corticosteroid anti-inflammatory and parenteral antibiotic therapy composed by gentamicin and amoxicillin, followed by intramammary therapy with gentamicin. After those treatments, the owner started a homeopathic treatment using 12 drops of each, twice a day. The clinical signs disappeared, but the milk production remained reduced. To perform the identification of mastitis-causing agents, milk samples were aseptically collected from affected quarters and sent to laboratory to perform culture and antibiogram (SB 02/19 protocol). The milk sample for microbiological diagnosis was collected 25 days after the onset of clinical signs, which coincided with the period in which the antimicrobial and homeopathic treatment was performed. The milk sample was plated onto 5% sheep blood (BA) and MacConkey agar plates and incubated for 48h. Antimicrobial susceptibility assay was performed according to the routine protocol (CLSI, 2013).

RESULTS AND DISCUSSION

After 48h of sample inoculation, small, dry, and greyish colonies were observed only in BA plates. On Gram stain, the colonies looked like Gram-positive bacilli shaped, and didn’t color well. The isolate was non-motile, had fermentative metabolism of glucose, was positive in catalase, aesculin hydrolysis and indole tests, and negative to urease and oxidase enzymes. It was negative to hydrogen sulphide production and did not use citrate as a sole carbon source.

On antimicrobial susceptibility testing using disc-diffusion method, the isolate showed no inhibition halo to enrofloxacin (5µg), amoxicillin (10µg), penicillin (10µg), tetracycline (30µg), ampicillin (10µg), ceftiofur (30µg), sulfazotrim (25µg), cephalexin (30µg), doxycycline (30µg), ciprofloxacin (5µg) and cefepime (30µg), and showed a halo of inhibition for neomycin (30µg), amikacin (30µg) and gentamycin (10µg).

We suspected Mycobacterium sp. or Corynebacterium sp. according to the microbiological results, clinical signs, and laboratory findings. However, considering that Corynebacterium sp. normally is not a common cause of clinical mastitis and does not present a marked resistant profile in antimicrobial assays, identified colonies were submitted to PCR and nucleotide sequencing for 16s rDNA region (Lane, 1991LANE, D.J. 16S/23S rRNA sequencing. In: STACKEBRANDT, E.; GOODFELLOW, M. (Eds.). Nucleic acid techniques in bacterial systematics. New York: John Wiley & Sons, 1991. p.115-175.) and a duplex PCR for hsp65 gene of Mycobacterium species, which could differentiate between tuberculosis or non-tuberculosis (Kim et al., 2006KIM, H.J.; MUN, H.S.; KIM, H. et al. Differentiation of mycobacterial species by hsp65 duplex PCR followed by duplex-PCR-based restriction analysis and direct sequencing. J. Clin. Microbiol., v.44, p.3855-3862, 2006.). The isolate was positive in both PCR, and the amplicons were submitted to DNA sequencing and molecular analysis.

The average nucleotide identity of the amplicons was analyzed using the Basic Local Alignment Search Tool (BLAST). SB 02/19 presented higher nucleotide identity with Mycobacteroides abscessus in the 16S rDNA region (100% with CP065287.1) and hsp65 gene (99.27 to 100% with CP060408.1 and AP018436.1). Phylogenetic tree of 16S rDNA region was built in MEGA X software using the maximum likelihood method with 1,000 bootstrap replicates, using alignment of nucleotide sequences obtained from GenBank (Fig. 1). SB 02/19 clustered with M. abscessus and apart from another Mycobacterium spp. and Mycobacteroides spp.

Figure 1
Phylogenetic tree based on sequence of 16s rDNA region. The evolutionary history was inferred using maximum likelihood method with 1000 bootstrap replicates. The evolutionary distances were computed using the Tamura-3 parameter model and implemented by MEGA X. Values > 60% are shown. The SB 02/19 is identified with a black circle.

M. abscessus is a ubiquitous environmental organism and an opportunistic pathogen that can cause various diseases in humans and animals (Lunn et al., 2005LUNN, J.; MARTIN, P.; ZAKI, S.; MALIK, R. Pneumonia due to Mycobacterium abscessus in two domestic ferrets (Mustelo putorius furo). Aust. Vet. J., v.83, p.542-546, 2005.). The occurrence of infection caused by M. abscessus is extensively described in humans, especially in cases of infection of the surgical site and lung infection, being a major problem for people with cystic fibrosis (Jönsson et al., 2007JÖNSSON, B.E.; GILLJAM, M.; LINDBLAD, A. et al. Molecular epidemiology of Mycobacterium abscessus, with focus on cystic fibrosis. J. Clin. Microbiol., v.45, p.1497-1504, 2007.; Leão et al., 2010LEÃO, S.C.; VIANA-NIERO, C.; MATSUMOTO, C.K. et al. Epidemic of surgical-site infections by a single clone of rapidly growing mycobacteria in Brazil. Future Microbiol., v.5, p.971-980, 2010.). In animals, a range of different infections have been described in many species (Bercovier and Vincent, 2001BERCOVIER, H.; VINCENT, V. Mycobacterial infections in domestic and wild animals due to Mycobacterium marinum, M. fortuitum, M. chelonae, M. porcinum, M. farcinogenes, M. smegmatis, M. scrofulaceum, M. xenopi, M. kansasii, M. simiae and M. genavense. Rev. Sci. Techn.,v. 20, p.265-290, 2001.; Lunn et al., 2005).

M. abscessus causing mastitis in cattle is not a common pathogen described, but other RGM associated with mastitis cases have been described more frequently, as M. goodii (Machado et al., 2015MACHADO, G.; GRESSLER, T.L.; SIQUEIRA, F.M. et al. Bovine pyogranulomatous mastitis caused by Mycobacterium goodii. JMM Case Rep., v.2, p.1-4, 2015.) and M. elephantis (Ji et al., 2017JI, L.Y.; XU, D.L.; YIN, S.P. et al. First report in China on the identification and drug sensitivity of Mycobacterium elephantis isolated from the milk of a cow with mastitis. Biom. Environ. Sci., v.30, p.501-507, 2017.). Once it is an environmental organism, and according to the mastitis case related by Ji et al., 2017 caused by another Mycobacterium non-tuberculosis, we believe that in this case the mastitis started after a contamination from the environment, in an ascending route. M. abscessus probably entered the udder by contaminated materials, such as antibiotic cannula, reinforcing the need for using clean and sterile materials during mastitis treatment.

The presence of M. abscessus as well other non-tuberculous Mycobacterium in samples, such as milk, may be a big deal for disease control, once people and animals infected may have the agent but only develop the disease on an immune system failure (Jönsson et al., 2007JÖNSSON, B.E.; GILLJAM, M.; LINDBLAD, A. et al. Molecular epidemiology of Mycobacterium abscessus, with focus on cystic fibrosis. J. Clin. Microbiol., v.45, p.1497-1504, 2007.). In this case, the farmer reported that the cow had recurrent mastitis, which was treated before and regressed, but when a new lactation started the disease was manifested again.

CONCLUSIONS

Our findings showed that RGM species, as M. abscessus, should be also considered in the investigated of recurrent clinical mastitis, especially in cases that are not responsive to antibiotic treatment.

REFERENCES

  • BERCOVIER, H.; VINCENT, V. Mycobacterial infections in domestic and wild animals due to Mycobacterium marinum, M. fortuitum, M. chelonae, M. porcinum, M. farcinogenes, M. smegmatis, M. scrofulaceum, M. xenopi, M. kansasii, M. simiae and M. genavense. Rev. Sci. Techn.,v. 20, p.265-290, 2001.
  • BRADLEY, A.J. Bovine mastitis: an evolving disease. Vet. J., v.164, p.116-128, 2002.
  • Clinical and Laboratory Standards Institute (CLSI). Performance standards for antimicrobial disk and dilution susceptibility tests for bacteria isolated from animals. 4.ed., Wayne, Pennsylvania: NCCLS / CLSI, 2013.
  • JI, L.Y.; XU, D.L.; YIN, S.P. et al. First report in China on the identification and drug sensitivity of Mycobacterium elephantis isolated from the milk of a cow with mastitis. Biom. Environ. Sci., v.30, p.501-507, 2017.
  • JÖNSSON, B.E.; GILLJAM, M.; LINDBLAD, A. et al. Molecular epidemiology of Mycobacterium abscessus, with focus on cystic fibrosis. J. Clin. Microbiol., v.45, p.1497-1504, 2007.
  • KIM, H.J.; MUN, H.S.; KIM, H. et al. Differentiation of mycobacterial species by hsp65 duplex PCR followed by duplex-PCR-based restriction analysis and direct sequencing. J. Clin. Microbiol., v.44, p.3855-3862, 2006.
  • LANE, D.J. 16S/23S rRNA sequencing. In: STACKEBRANDT, E.; GOODFELLOW, M. (Eds.). Nucleic acid techniques in bacterial systematics. New York: John Wiley & Sons, 1991. p.115-175.
  • LEÃO, S.C.; VIANA-NIERO, C.; MATSUMOTO, C.K. et al. Epidemic of surgical-site infections by a single clone of rapidly growing mycobacteria in Brazil. Future Microbiol., v.5, p.971-980, 2010.
  • LUNN, J.; MARTIN, P.; ZAKI, S.; MALIK, R. Pneumonia due to Mycobacterium abscessus in two domestic ferrets (Mustelo putorius furo). Aust. Vet. J., v.83, p.542-546, 2005.
  • MACHADO, G.; GRESSLER, T.L.; SIQUEIRA, F.M. et al. Bovine pyogranulomatous mastitis caused by Mycobacterium goodii. JMM Case Rep., v.2, p.1-4, 2015.
  • MARQUES, S.; SILVA, E.; KRAFT, C. et al. Bovine mastitis associated with Prototheca blaschkeae. J. Clin. Microbiol., v.46, p.1941-1945, 2008.
  • RIEKERINK, R.G.M.O.; BARKEMA, H.W.; KELTON, D.F.; SCHOLL, D.T. Incidence rate of clinical mastitis on Canadian dairy farms. J. Dairy Sci., v.91, p.1366-1377, 2008.
  • FUNDING

    This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001, and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq).

Publication Dates

  • Publication in this collection
    17 Oct 2022
  • Date of issue
    Sep-Oct 2022

History

  • Received
    24 Feb 2022
  • Accepted
    24 June 2022
Universidade Federal de Minas Gerais, Escola de Veterinária Caixa Postal 567, 30123-970 Belo Horizonte MG - Brazil, Tel.: (55 31) 3409-2041, Tel.: (55 31) 3409-2042 - Belo Horizonte - MG - Brazil
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