Please wait a minute...
Journal of Integrative Agriculture  2023, Vol. 22 Issue (5): 1514-1528    DOI: 10.1016/j.jia.2022.10.004
Animal Science · Veterinary Medicine Advanced Online Publication | Current Issue | Archive | Adv Search |
Molecular epidemiology, characterization of virulence factors and antibiotic-resistance profile of Streptococcus agalactiae isolated from dairy farms in China and Pakistan

Ambreen LEGHARI1, Shakeel Ahmed LAKHO2, Faiz Muhammad KHAND2, Khaliq ur Rehman BHUTTO3, Sameen Qayoom LONE1, Muhammad Tahir ALEEM1, Iqra BANO2, Muhammad Ali CHANDIO2, Jan Muhammad SHAH2, LIN Hui-xing1, FAN Hong-jie1, 4#

1 MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, P.R.China

2 Shaheed Benazir Bhutto University of Veterinary and Animal Sciences, Sakrand 67210, Pakistan

3 Central Veterinary Diagnostic Laboratory, Tando Jam 70050, Pakistan

4 Jiangsu Co-innovation Center for the Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, P.R.China

Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
摘要  

无乳链球菌是世界范围内引起奶牛乳房炎的最常见病原体之一。了解该菌的流行现状和毒力因子对于制定防治措施至关重要。本研究于2019-2021期间,从中国(n=558)和巴基斯坦(n=603)的多个奶牛场采集了1161份牛奶样本,并对其进行了无乳链球菌的分离鉴定。通过PCR检测分析了无乳链球菌的流行率、血清型、毒力基因和耐药基因。所有的分离菌株均具有溶血、生成生物被膜、细胞毒性、粘附并侵袭牛乳腺上皮细胞的特性。巴基斯坦地区由无乳链球菌引起的奶牛乳房炎的发病率显著高于中国。江苏省和信德省(Sindh)分别是中国和巴基斯坦地区无乳链球菌流行率最高的省份。血清型Ia型和II型的无乳链球菌在这两个国家的流行率均较高,而血清III型的无乳链球菌只在巴基斯坦发现。此外,无论是中国还是巴基斯坦,所有的无乳链球菌分离菌株均为PI-2b基因阳性,但PI-1和PI-2a基因均为阴性。所有的分离菌株都含有cfbcylEhylBfbsB毒力基因,而大多分离菌株无bibAribbca毒力基因。分离自中国的无乳链球菌均无bac和scp毒力基因,而分离自巴基斯坦的无乳链球菌均无cspA基因,同时两国的分离菌株中均未检测到spb1lmb毒力基因。分离自巴基斯坦的无乳链球菌,尤其是血清Ia型菌株,与分离自中国的菌株相比,具有更高的生物被膜形成、溶血、细胞毒性、粘附和侵袭能力。大多数分离菌株对四环素、红霉素和克林霉素具有耐药性,而ermAermBtetMtetO等耐药基因的存在也从基因水平验证了分离菌株的耐药性。上述研究结果为由无乳链球菌引起的奶牛乳房炎特异性防治措施的制定具有重要指导意义



Abstract  

Streptococcus agalactiae is one of the most common pathogens that cause bovine mastitis worldwide. Identifying pathogen prevalence and virulence factors is critical for developing prevention and control approaches. Herein, 1161 milk samples from various dairy farms in China (n=558) and Pakistan (n=603) were collected between 2019-2021 and were subjected to S. agalactiae isolation. Prevalence, serotyping, virulence genes, and antibiotic-resistant genes of S. agalactiae were evaluated by PCR assay. All isolates were characterized for haemolysis, biofilm production, cytotoxicity, adhesion, and invasion on bovine mammary epithelial cells. The prevalence of S. agalactiae-induced mastitis in cattle was found to be considerably higher in Pakistan than in China. Jiangsu and Sindh provinces had the highest area-wise prevalence in China and Pakistan, respectively. Serotypes Ia and II were prevalent in both countries, whereas serotype III was found only in Pakistan. Moreover, all isolates tested positive for PI-2b gene but negative for PI-1 and PI-2a genes. All isolates harboured cfb, cylE, hylB, and fbsB virulent genes, whereas many of them lacked bibA, rib and bca. However, the absence of bac and scp genes in Chinese isolates and cspA in Pakistani isolates was noted, while spb1 and lmb were not detected in isolates of both countries. Pakistani isolates, particularly serotype Ia-positive, had a considerably higher ability to produce biofilm, haemolysis, cytotoxicity, adhesion, and invasion than Chinese isolates. Most of the isolates were phenotypically resistant to tetracycline, erythromycin, and clindamycin and genotypic resistance was confirmed by the presence of ermA, ermB, tetM and tetO genes. Our study highlights the antimicrobial resistance profile and virulence-related factors contributing to the epidemiological spread of mastitis-causing S. agalactiae in China and Pakistan. The findings may facilitate future studies designed to develop improved treatment and control strategies against this pathogen. 

Keywords:  Streptococcus agalactiae         mastitis       epidemiology       virulence characterization       antibiotic resistance  
Received: 18 April 2022   Accepted: 09 September 2022
Fund: 

This study was supported by the National Key Research and Development Program of China (2021YFD1800400), the National Natural Science Foundation of China (31872480), the Jiangsu Agriculture Science and Technology Innovation Fund (CX(19)2020), and the Priority Academic Program Development of Jiangsu Higher Education Institutions, China (PAPD).

About author:  Ambreen LEGHARI, E-mail: 2018207075@njau.edu.cn; #Correspondence FAN Hong-jie, E-mail: fhj@njau.edu.cn

Cite this article: 

Ambreen LEGHARI, Shakeel Ahmed LAKHO, Faiz Muhammad KHAND, Khaliq ur Rehman BHUTTO, Sameen Qayoom LONE, Muhammad Tahir ALEEM, Iqra BANO, Muhammad Ali CHANDIO, Jan Muhammad SHAH, LIN Hui-xing, FAN Hong-jie. 2023. Molecular epidemiology, characterization of virulence factors and antibiotic-resistance profile of Streptococcus agalactiae isolated from dairy farms in China and Pakistan. Journal of Integrative Agriculture, 22(5): 1514-1528.

Ali M, Ahmad M, Muhammad K, Anjum A. 2011. Prevalence of sub clinical mastitis in dairy buffaloes of Punjab, Pakistan. Journal of Animal and Plant Sciences21, 477–480.

Ali T, Kamran, Raziq A, Wazir I, Ullah R, Shah P, Ali M I, Han B, Liu G. 2021. Prevalence of mastitis pathogens and antimicrobial susceptibility of isolates from cattle and buffaloes in northwest of Pakistan. Frontiers in Veterinary Science8, 746755–746755.

Ali T, Rahman A, Qureshi M S, Hussain M T, Khan M S, Uddin S, Iqbal M, Han B. 2014. Effect of management practices and animal age on incidence of mastitis in Nili Ravi buffaloes. Tropical Animal Health and Production46, 1279–1285.

Ali T, Rahman S U, Zhang L, Shahid M, Han D, Gao J, Zhang S, Ruegg P L, U Saddique, B Han. 2017. Characteristics and genetic diversity of multi-drug resistant extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli isolated from bovine mastitis. Oncotarget8, 90144–90163.

Andersen H J, Pedersen L H, Aarestrup F M, Chriél M. 2003. Evaluation of the surveillance program of Streptococcus agalactiae in Danish dairy herds. Journal of Dairy Science86, 1233–1239.

Bangar Y C, Singh B, Dohare A K, Verma M R. 2015. A systematic review and meta-analysis of prevalence of subclinical mastitis in dairy cows in India. Tropical Animal Health and Production47, 291–297.

Banno H, Kimura K, Tanaka Y, Sekizuka T, Kuroda M, Jin W, Wachino J I, Yamada K, Shibayama K, Arakawa Y. 2017. Analysis of multidrug resistant group B Streptococci with reduced penicillin susceptibility forming small, less hemolytic colonies. PLoS ONE12, e0183453.

Birhanu M, Leta S, Mamo G, Tesfaye S. 2017. Prevalence of bovine subclinical mastitis and isolation of its major causes in Bishoftu Town, Ethiopia. BMC Research Notes10, 767.

Bradley A J, Leach K A, Breen J E, Green L E, Green M J. 2007. Survey of the incidence and aetiology of mastitis on dairy farms in England and Wales. The Veterinary Record160, 253–257.

Burcham L R, Spencer B L, Keeler L R, Runft D L, Patras K A, Neely M N, Doran K S. 2019. Determinants of group B Streptococcal virulence potential amongst vaginal clinical isolates from pregnant women. PLoS ONE14, e0226699.

Carvalho-Castro G A, Silva J R, Paiva L V, Custódio D A C, Moreira R O, Mian G F, Prado I A, Chalfun-Junior A, Costa G M. 2017. Molecular epidemiology of Streptococcus agalactiae isolated from mastitis in Brazilian dairy herds. Brazilian Journal of Microbiology48, 551–559.

Cheng W N, Han S G. 2020. Bovine mastitis: risk factors, therapeutic strategies, and alternative treatments - A review. Asian–Australasian Journal of Animal Sciences33, 1699–1713.

Chohan L, Hollier L M, Bishop K, Kilpatrick C C. 2006. Patterns of antibiotic resistance among group B Streptococcus isolates: 2001–2004. Infectious Diseases in Obstetrics and Gynecology2006, 57492.

Costerton J W, Stewart P S, Greenberg E P. 1999. Bacterial biofilms: A common cause of persistent infections. Science284, 1318–1322.

Delannoy C M J, Crumlish M, Fontne M C, Pollock J, Foster G, Dagleish M P, Turnbull J F, Zadoks R N. 2013. Human Streptococcus agalactiae strains in aquatic mammals and fish. BMC Microbiology13, 41.

Dogan B, Schukken Y H, Santisteban C, Boor K J. 2005. Distribution of serotypes and antimicrobial resistance genes among Streptococcus agalactiae isolates from bovine and human hosts. Journal of Clinical Microbiology43, 5899–5906.

Duarte R S, Miranda O P, Bellei B C, Brito M A, Teixeira L M. 2004. Phenotypic and molecular characteristics of Streptococcus agalactiae isolates recovered from milk of dairy cows in Brazil. Journal of Clinical Microbiology42, 4214–4222.

El-Behiry A, Elsayed M, Marzouk E, Bathich Y. 2015. Detection of virulence genes in Staphylococcus aureus and Streptococcus agalactiae isolated from mastitis in the Middle East. Microbiology Research Journal International10, 1–9.

Erskine R, Walker R, Bolin C, Bartlett P, White D. 2002. Trends in antibacterial susceptibility of mastitis pathogens during a seven-year period. Journal of Dairy Science85, 1111–1118.

Gao J, Barkema H W, Zhang L, Liu G, Deng Z, Cai L, Shan R, Zhang S, Zou J, Kastelic J P, Han B. 2017. Incidence of clinical mastitis and distribution of pathogens on large Chinese dairy farms. Journal of Dairy Science100, 4797–4806.

Gao J, Yu F Q, Luo L P, He J Z, Hou R G, Zhang H Q, Li S M, Su J L, Han B. 2012. Antibiotic resistance of Streptococcus agalactiae from cows with mastitis. Veterinary Journal194, 423–424.

Gianneechini R, Concha C, Rivero R, Delucci I, López J M. 2002. Occurrence of clinical and sub-clinical mastitis in dairy herds in the west littoral region in Uruguay. Acta Veterinaria Scandinavica43, 221–230.

Gianneechini R E, Concha C, Franklin A. 2002. Antimicrobial susceptibility of udder pathogens isolated from dairy herds in the west littoral region of Uruguay. Acta Veterinaria Scandinavica43, 31–41.

Hassan A A, Abdulmawjood A, Yildirim A O, Fink K, Lämmler C, Schlenstedt R. 2000. Identification of Streptococci isolated from various sources by determination of cfb gene and other CAMP-factor genes. Canadian Journal of Microbiology46, 946–951.

He W, Ma S, Lei L, He J, Li X, Tao J, Wang X, Song S, Wang Y, Wang Y, Shen J, Cai C, Wu C. 2020. Prevalence, etiology, and economic impact of clinical mastitis on large dairy farms in China. Veterinary Microbiology242, 108570.

Herbert M A, Beveridge C J, Saunders N J. 2004. Bacterial virulence factors in neonatal sepsis: group B StreptococcusCurrent Opinion in Infectious Diseases17, 225–229.

Jain B, Tewari A, Bhandari B B, Jhala M K. 2012. Antibiotic resistance and virulence genes in Streptococcus agalactiae isolated from cases of bovine subclinical mastitis. Veterinarski Arhiv82, 423–432.

Jaramillo-Jaramillo A S, Cobo-Ángel C G, Moreno-Tolosa Y, Ceballos-Márquez A. 2018. Antimicrobial resistance of Streptococcus agalactiae of human and bovine origin. CES Medicina Veterinaria y Zootecnia13, 62–79. (in Spanish)

Kabelitz T, Aubry E, van Vorst K, Amon T, Fulde M. 2021. The role of Streptococcus spp. in bovine mastitis. Microorganisms9, 7.

Kannika K, Pisuttharachai D, Srisapoome P, Wongtavatchai J, Kondo H, Hirono I, Unajak S, Areechon N. 2017. Molecular serotyping, virulence gene profiling and pathogenicity of Streptococcus agalactiae isolated from tilapia farms in Thailand by multiplex PCR. Journal of Applied Microbiology122, 1497–1507.

Konto-Ghiorghi Y, Mairey E, Mallet A, Duménil G, Caliot E, Trieu-Cuot P, Dramsi S. 2009. Dual role for pilus in adherence to epithelial cells and biofilm formation in Streptococcus agalactiaePLoS Pathogens5, e1000422.

Leclercq S Y, Sullivan M J, Ipe D S, Smith J P, Cripps A W, Ulett G C. 2016. Pathogenesis of Streptococcus urinary tract infection depends on bacterial strain and β-hemolysin/cytolysin that mediates cytotoxicity, cytokine synthesis, inflammation and virulence. Scientific Reports6, 29000.

Leigh J A. 1999. Streptococcus uberis: A permanent barrier to the control of bovine mastitis? Veterinary Journal157, 225–238.

Li J P, Zhou H J, Yuan L, He T, Hu S H. 2009. Prevalence, genetic diversity, and antimicrobial susceptibility profiles of Staphylococcus aureus isolated from bovine mastitis in Zhejiang Province, China. Journal of Zhejiang University (Science B)10, 753–760.

Lindahl G, Stålhammar-Carlemalm M, Areschoug T. 2005. Surface proteins of Streptococcus agalactiae and related proteins in other bacterial pathogens. Clinical Microbiology Reviews18, 102–127.

Loch I M, Glenn K, Zadoks R N. 2005. Macrolide and lincosamide resistance genes of environmental Streptococci from bovine milk. Veterinary Microbiology111, 133–138.

Margarit I, Rinaudo C D, Galeotti C L, Maione D, Ghezzo C, Buttazzoni E, Rosini R, Runci Y, Mora M, Buccato S, Pagani M, Tresoldi E, Berardi A, Creti R, Baker C J, Telford J L, Grandi G. 2009. Preventing bacterial infections with pilus-based vaccines: The group B Streptococcus paradigm. The Journal of Infectious Diseases199, 108–115.

Meiri-Bendek I, Lipkin E, Friedmann A, Leitner G, Saran A, Friedman S, Kashi Y. 2002. A PCR-based method for the detection of Streptococcus agalactiae in milk. Journal of Dairy Science85, 1717–1723.

Merl K, Abdulmawjood A, Lämmler C, Zschöck M. 2003. Determination of epidemiological relationships of Streptococcus agalactiae isolated from bovine mastitis. FEMS Microbiology Letters226, 87–92.

Middleton J R, Timms L L, Bader G R, Lakritz J, Luby C D, Steevens B J. 2005. Effect of prepartum intramammary treatment with pirlimycin hydrochloride on prevalence of early first-lactation mastitis in dairy heifers. Journal of the American Veterinary Medical Association227, 1969–1974.

Nam H M, Lim S K, Kang H M, Kim J M, Moon J S, Jang K C, Joo Y S, Kang M I, Jung S C. 2009. Antimicrobial resistance of Streptococci isolated from mastitic bovine milk samples in Korea. Journal of Veterinary Diagnostic Investigation21, 698–701.

Oliver S P, Murinda S E. 2012. Antimicrobial resistance of mastitis pathogens. Veterinary Clinics of North America - Food Animal Practice28, 165–185.

Osterås O, Sølverød L, Reksen O. 2006. Milk culture results in a large Norwegian survey - Effects of season, parity, days in milk, resistance, and clustering. Journal of Dairy Science89, 1010–1023.

Pang M, Jiang J, Xie X, Wu Y, Dong Y, Kwok A H, Zhang W, Yao H, Lu C, Leung F C, Liu Y. 2015. Novel insights into the pathogenicity of epidemic Aeromonas hydrophila ST251 clones from comparative genomics. Scientific Reports5, 9833.

Pang M, Sun L, He T, Bao H, Zhang L, Zhou Y, Zhang H, Wei R, Liu Y, Wang R. 2017. Molecular and virulence characterization of highly prevalent Streptococcus agalactiae circulated in bovine dairy herds. Veterinary Research48, 65.

Papazafiri P, Avlonitis N, Angelou P, Calogeropoulou T, Koufaki M, Scoulica E, Fragiadaki I. 2005. Structure-activity relationships of antineoplastic ring-substituted ether phospholipid derivatives. Cancer Chemotherapy and Pharmacology56, 261–270.

Pereira U P, Mian G F, Oliveira I C, Benchetrit L C, Costa G M, Figueiredo H C. 2010. Genotyping of Streptococcus agalactiae strains isolated from fish, human and cattle and their virulence potential in Nile tilapia. Veterinary Microbiology140, 186–192.

Piepers S, Meulemeester L D, de Kruif A, Opsomer G, Barkema H W, Vliegher S D. 2007. Prevalence and distribution of mastitis pathogens in subclinically infected dairy cows in Flanders, Belgium. The Journal of Dairy Research74, 478–483.

Piepers S, Opsomer G, Barkema H, de Kruif A, Vliegher S D. 2010. Heifers infected with coagulase-negative Staphylococci in early lactation have fewer cases of clinical mastitis and higher milk production in their first lactation than noninfected heifers. Journal of Dairy Science93, 2014–2024.

Pinto T C, Costa N S, Souza A R V, Silva L G, Corrêa A B, Fernandes F G, Oliveira I C, Mattos M C, Rosado A S, Benchetrit L C. 2013. Distribution of serotypes and evaluation of antimicrobial susceptibility among human and bovine Streptococcus agalactiae strains isolated in Brazil between 1980 and 2006. The Brazilian Journal of Infectious Diseases17, 131–136.

Rajagopal L. 2009. Understanding the regulation of group B Streptococcal virulence factors. Future Microbiology4, 201–221.

Rato M G, Bexiga R, Florindo C, Cavaco L M, Vilela C L, Santos-Sanches I. 2013. Antimicrobial resistance and molecular epidemiology of Streptococci from bovine mastitis. Veterinary Microbiology161, 286–294.

Reyes J, Chaffer M, Rodriguez-Lecompte J C, Sánchez J, Zadoks R N, Robinson N, Cardona X, Ramírez N, Keefe G P. 2017. Short communication: Molecular epidemiology of Streptococcus agalactiae differs between countries. Journal of Dairy Science100, 9294–9297.

Romero J, Benavides E, Meza C. 2018. Assessing financial impacts of subclinical mastitis on Colombian dairy farms. Frontiers in Veterinary Science5, 273.

Rosini R, Margarit I. 2015. Biofilm formation by Streptococcus agalactiae: Influence of environmental conditions and implicated virulence factors. Frontiers in Cellular and Infection Microbiology5, 6.

Rosinski-Chupin I, Sauvage E, Mairey B, Mangenot S, Ma L, Cunha V D, Rusniok C, Bouchier C, Barbe V, Glaser P. 2013. Reductive evolution in Streptococcus agalactiae and the emergence of a host adapted lineage. BMC Genomics14, 252.

Rossitto P, Ruiz L, Kikuchi Y, Glenn K, Luiz K, Watts J, Cullor J S. 2002. Antibiotic susceptibility patterns for environmental Streptococci isolated from bovine mastitis in central California dairies. Journal of Dairy Science85, 132–138.

Roy R, Tiwari M, Donelli G, Tiwari V. 2018. Strategies for combating bacterial biofilms: A focus on anti-biofilm agents and their mechanisms of action. Virulence9, 522–554.

Rubens C E, Smith S, Hulse M, Chi E Y, van Belle G. 1992. Respiratory epithelial cell invasion by group B StreptococciInfection and Immunity60, 5157–5163.

Ruegg P L, Oliveira L, Jin W, Okwumabua O. 2015. Phenotypic antimicrobial susceptibility and occurrence of selected resistance genes in Gram-positive mastitis pathogens isolated from Wisconsin dairy cows. Journal of Dairy Science98, 4521–4534.

Sarker S C, Parvin M S, Rahman A K, Islam M T. 2013. Prevalence and risk factors of subclinical mastitis in lactating dairy cows in north and south regions of Bangladesh. Tropical Animal Health and Production45, 1171–1176.

Schmitt-van de Leemput E, Zadoks R. 2007. Genotypic and phenotypic detection of macrolide and lincosamide resistance in Streptococcus uberisJournal of Dairy Science90, 5089–5096.

Sharma P, Lata H, Arya D K, Kashyap A K, Kumar H, Dua M, Ali A, Johri A K. 2013. Role of pilus proteins in adherence and invasion of Streptococcus agalactiae to the lung and cervical epithelial cells. The Journal of Biological Chemistry288, 4023–4034.

Sharun K, Dhama K, Tiwari R, Gugjoo M B, Yatoo M I, Patel S K, Pathak M, Karthik K, Khurana S K, Singh R, Puvvala B, Amarpal, Singh R, Singh K P, Chaicumpa W. 2021. Advances in therapeutic and managemental approaches of bovine mastitis: A comprehensive review. Veterinary Quarterly41, 107–136.

Shome B R, Bhuvana M, Mitra S D, Krithiga N, Shome R, Velu D, Banerjee A, Barbuddhe S B, Prabhudas K, Rahman H. 2012. Molecular characterization of Streptococcus agalactiae and Streptococcus uberis isolates from bovine milk. Tropical Animal Health and Production44, 1981–1992.

Springman A C, Lacher D W, Waymire E A, Wengert S L, Singh P, Zadoks R N, Davies H D, Manning S D. 2014. Pilus distribution among lineages of group B Streptococcus: An evolutionary and clinical perspective. BMC Microbiology14, 159.

Sridhar S, Greenwood B, Head C, Plotkin S A, Sáfadi M A, Saha S, Taha M K, Tomori O, Gessner B D. 2015. Global incidence of serogroup B invasive meningococcal disease: A systematic review. The Lancet Infectious Diseases15, 1334–1346.

Szczypa K, Wilemska J, Hryniewicz W, Sitkiewicz I. 2013. Epidemiology of Streptococcus pyogenes infections, clonal structure population and antibiotic resistance. Postepy Mikrobiologii52, 223–232.

Sztachanska M, Baranski W, Janowski T, Pogorzelska J, Zdunczyk S. 2016. Prevalence and etiological agents of subclinical mastitis at the end of lactation in nine dairy herds in North-East Poland. Polish Journal of Veterinary Sciences19, 1.

Tenhagen B A, Köster G, Wallmann J, Heuwieser W. 2006. Prevalence of mastitis pathogens and their resistance against antimicrobial agents in dairy cows in Brandenburg, Germany. Journal of Dairy Science89, 2542–2551.

De Vliegher S, Fox L K, Piepers S, McDougall S, Barkema H W. 2012. Invited review: Mastitis in dairy heifers: Nature of the disease, potential impact, prevention, and control. Journal of Dairy Science95, 1025–1040.

Wilson D J, Gonzalez R N, Das H H. 1997. Bovine mastitis pathogens in New York and Pennsylvania: Prevalence and effects on somatic cell count and milk production. Journal of Dairy Science80, 2592–2598.

Yang Y, Liu Y, Ding Y, Yi L, Ma Z, Fan H, Lu C. 2013. Molecular characterization of Streptococcus agalactiae isolated from bovine mastitis in Eastern China. PLoS ONE8, e67755.

Yao K, Poulsen K, Maione D, Rinaudo C D, Baldassarri L, Telford J L, Sørensen U B S, Members D S G, Kilian M. 2013. Capsular gene typing of Streptococcus agalactiae compared to serotyping by latex agglutination. Journal of Clinical Microbiology51, 503–507.

Zhang X, Xu S, Wu Y, Wu C. 2005. Prevalence of bovine subclinical mastitis in Jinhua. Chinese Journal of Animal Science41, 37–38. (in Chinese)

Zhao X, Lacasse P. 2008. Mammary tissue damage during bovine mastitis: Causes and control. Journal of Animal Science86, 57–65.


[1] ZHAO Yu-qiang, TIAN Yan-li, WANG Li-min, GENG Guo-min, ZHAO Wen-jun, HU Bai-shi, ZHAO You-fu. Fire blight disease, a fast-approaching threat to apple and pear production in China[J]. >Journal of Integrative Agriculture, 2019, 18(4): 815-820.
[2] Sarne De Vliegher, Ian Ohnstad, Sofie Piepers. Management and prevention of mastitis: A multifactorial approach with a focus on milking, bedding and data-management[J]. >Journal of Integrative Agriculture, 2018, 17(06): 1214-1233.
[3] R V Chowda-Reddy, M Kirankumar, Susan E Seal, V Muniyappa, Girish B Val, M R Govindappa, John Colvin. Bemisia tabaci Phylogenetic Groups in India and the Relative Transmission Efficacy of Tomato leaf curl Bangalore virus by an Indigenous and an Exotic Population[J]. >Journal of Integrative Agriculture, 2012, 11(2): 235-248.
No Suggested Reading articles found!