Mastitis is a condition in which the mammary tissue becomes inflamed. Changes in color and the appearance of clots, as well as increases in cell counts in the milk, are all indicators of inflammation. Mastitis is a common occurrence in cows as a result of inframammary infections. The present study aimed to find out how often nontuberculous mycobacteria (NTM) mastitis occurs and how hp65 affects Interleukin (IL) 6 concentrations. The findings of the Modified Whiteside Test (MWT) on the milk samples from 70 cows, 50 sheep, and 30 goats revealed that 82.9%, 76.7%, and 46.7% of milk samples from cows, sheep, and goats were positive, respectively. This test demonstrated a range of positive milk sample MWT reactions, and the difference among the current positivity score results was statistically significant (P<0.05). The presence of NTM in analyzed milk samples from cows and sheep was confirmed by hsp65-based polymerase chain reaction (PCR) and gene sequencing, with significant differences (P<0.05) in 71.4% and 20% of milk samples from cows and sheep, respectively. The PCR detection of the NTM hsp65 gene in fecal samples from cows, sheep, and goats indicated that cows (80%) had the highest proportion of NTM hsp65 gene amplification, followed by goats (70%), while sheep fecal samples had the lowest amount (22%). The difference among the positive NTM hsp65-based PCR was statistically significant (P<0.05). The phylogenetic tree and sequence analysis of the hsp65 gene revealed two novel variant NTM hsp65 genes that were deposited in Gene Bank (GenBank acc. LC636294 and LC636295). The current examined NTM Hsp65 Mycobacterium sequences which were included in the Mycobacterium avium clade in the currently produced tree ELISA detection of IL6 concentration in cow's milk revealed that IL-6 concentration in mastitis milk was varied. The mean of IL-6 concentration in cow's mastitis milk with MWT scores (+++ve) and mean of IL6 concentration in each MWT scores (++ve), MWT scores (+ve), and -ve MWT cow's milk had a highly significant difference (P<0.001). |
- Faria S, Joao I, Jordao L. General overview on nontuberculous mycobacteria, biofilms, and human infection. J Pathog. 2015;2015.
- Brandt M, Haeussermann A, Hartung E. Invited review: Technical solutions for analysis of milk constituents and abnormal milk. J Dairy Sci. 2010;93(2):427-36.
- Bradley AJ. Bovine mastitis: an evolving disease. Vet J. 2002;164(2):116-28.
- Halasa T, Huijps K, Østerås O, Hogeveen H. Economic effects of bovine mastitis and mastitis management: A review. Vet Q. 2007;29(1):18-31.
- Duarte CM, Freitas PP, Bexiga R. Technological advances in bovine mastitis diagnosis: an overview. J Vet Diagn Invest. 2015;27(6):665-72.
- Bannerman D. Pathogen-dependent induction of cytokines and other soluble inflammatory mediators during intramammary infection of dairy cows. J Anim Sci. 2009;87(3):10-25.
- Sharma SK, Upadhyay V. Non-tuberculous mycobacteria: a disease beyond TB and preparedness in India. Expert Rev Respir Med. 2021;15(7):949-58.
- Kawther K, Fawziah A, Rasha M. Association of polymorphisms in slc11a1 gene with autoimmunity caused by Mycobacterium avium subspecies paratuberculosis (MAP) in cattle. Basra J Vet Res. 2019;18(1).
- Al-Mussawi AA. Isolation and Identification of Mycobacterium chelonae from Human Sputum among Suspected Pulmonary Tuberculosis Infections in Basra-Iraq. Am J Infect Dis. 2014;2(6):145-8.
- Al-Sulami AA, Al-Taee A, Hasan ZA. Frequency of rapid growing mycobacteria among tuberculosis suspected patients in Basra-Iraq. Biol Med. 2016;8(4):1.
- Nasr Esfahani B, Rezaei Yazdi H, Moghim S, Ghasemian Safaei H, Zarkesh Esfahani H. Rapid and accurate identification of Mycobacterium tuberculosis complex and common non-tuberculous mycobacteria by multiplex real-time PCR targeting different housekeeping genes. Curr Microbiol. 2012;65(5):493-9.
- Bae J, Park S-B, Kim J-H, Kang MR, Lee KE, Kim S, et al. Comparison of the Three Molecular Diagnostic Assays for Molecular Identification of Mycobacterium tuberculosis and Nontuberculous Mycobacteria Species in Sputum Samples. Biomed Sci Lett. 2020;26(3):170-8.
- Sumiyah R, Deepti N, Mudit C, Sharma N. Identification of non-tuberculous mycobacteria in faeces of cattle and buffaloes using polymerase chain reaction-restriction fragment length polymorphism analysis. Haryana Vet. 2017;56(1):87-91.
- Schiller I, Oesch B, Vordermeier H, Palmer M, Harris B, Orloski K, et al. Bovine tuberculosis: a review of current and emerging diagnostic techniques in view of their relevance for disease control and eradication. Transbound Emerg Dis. 2010;57(4):205-20.
- Poyntz HC, Stylianou E, Griffiths KL, Marsay L, Checkley AM, McShane H. Non-tuberculous mycobacteria have diverse effects on BCG efficacy against Mycobacterium tuberculosis. Tuberculosis. 2014;94(3):226-37.
- Kahir MA, Islam MM, Rahman A, Nahar A, Rahman MS, Son H-J. Prevalence and risk factors of subclinical bovine mastitis in some dairy farms of Sylhet district of Bangladesh. Korean J Vet Serv. 2008;31(4):497-504.
- Telenti A, Marchesi F, Balz M, Bally F, Böttger E, Bodmer T. Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis. J Clin Microbiol. 1993;31(2):175-8.
- Zhang Z, Schwartz S, Wagner L, Miller W. A greedy algorithm for aligning DNA sequences. J Comput Biol. 2000;7(1-2):203-14.
- Drummond WK, Kasperbauer SH. Nontuberculous mycobacteria: epidemiology and the impact on pulmonary and cardiac disease. Thorac Surg Clin. 2019;29(1):59-64.
- Siqueira FM, Lopes CE, Snell GG, Gomes MJP. Identification of Mycobacterium smegmatis in bovine Mastitis. Acta Sci Vet. 2016;44:1-4.
- Escobar-Escamilla N, Ramirez-Gonzalez JE, Gonzalez-Villa M, Torres-Mazadiego P, Mandujano-Martinez A, Barron-Rivera C, et al. Hsp65 phylogenetic assay for molecular diagnosis of nontuberculous mycobacteria isolated in Mexico. Arch Med Res. 2014;45(1):90-7.
- Franco MMJ, Paes AC, Ribeiro MG, de Figueiredo Pantoja JC, Santos ACB, Miyata M, et al. Occurrence of mycobacteria in bovine milk samples from both individual and collective bulk tanks at farms and informal markets in the southeast region of Sao Paulo, Brazil. BMC Vet Res. 2013;9(1):1-8.
- Machado G, Gressler LT, Siqueira FM, Balzan C, Brum JS, De Vargas AC. Bovine pyogranulomatous mastitis caused by Mycobacterium goodii. JMM Case Rep. 2015;2(1):e004150.
- Jayasumana M, Galappaththi T, Pushpakumara P, Gamage C, Smith N, Jinadasa H. Screening milk for bovine tuberculosis in dairy farms in Central Province, Sri Lanka. Trop Agric Res. 2018.
- Alzaidi KKJ. Exploring The Role of Mycobacterium aviumsubspecies paratuberculosis in the Pathogenesis of Autoimmunity in Animals and Human: University of Basrah; 2018.
- Leão CCF. Molecular tools in the diagnostic and epidemiology of infections caused by members of Mycobacterium avium complex. 2015.
- de Zwaan R, van Ingen J, van Soolingen D. Utility of rpoB gene sequencing for identification of nontuberculous mycobacteria in the Netherlands. J Clin Microbiol. 2014;52(7):2544-51.
- Joao I, Cristovao P, Antunes L, Nunes B, Jordao L. Identification of nontuberculous mycobacteria by partial gene sequencing and public databases. Int J Mycobacteriol. 2014;3(2):144-51.
- Eckersall P, Young F, McComb C, Hogarth C, Safi S, Fitzpatrick J, et al. Acute phase proteins in serum and milk from dairy cows with clinical mastitis. Vet Record. 2001;148(2):35-41.
- Sakemi Y, Tamura Y, Hagiwara K. Interleukin-6 in quarter milk as a further prediction marker for bovine subclinical mastitis. J Dairy Res. 2011;78(1):118-21.
- Nayan V, Phulia, S. K., Bhardwaj, A., Jerome, A. and Singh, D. Transcripts of interleukins in mastitis affected and oxytocin administered buffaloes: Clinical significance and prognostic value. J Biotechnol Biomat. 2012.
- Bayoumi MA, Amer IH, Mansour MA, Handousa SA. Comparative evaluation of Interleukin-6, somatic cell count and electrical conductivity as predictive tools for subclinical mastitis in dairy Buffaloes. Jpn J Vet Res. 2016;64(2):155-60.
|