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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Nutr.</journal-id>
<journal-title>Frontiers in Nutrition</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Nutr.</abbrev-journal-title>
<issn pub-type="epub">2296-861X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fnut.2022.1078201</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Nutrition</subject>
<subj-group>
<subject>Mini Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Microbial diversity of meat products under spoilage and its controlling approaches</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Zhu</surname> <given-names>Yanli</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/2022234/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Wang</surname> <given-names>Wei</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Li</surname> <given-names>Ming</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Zhang</surname> <given-names>Jiamin</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Ji</surname> <given-names>Lili</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Zhao</surname> <given-names>Zhiping</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1390540/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Zhang</surname> <given-names>Rui</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1700837/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Cai</surname> <given-names>Demin</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/867318/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Chen</surname> <given-names>Lin</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c002"><sup>&#x0002A;</sup></xref>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Key Lab of Meat Processing of Sichuan Province, Chengdu University</institution>, <addr-line>Chengdu</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>College of Animal Science and Technology, Yangzhou University</institution>, <addr-line>Yangzhou</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Tong Xing, Nanjing Agricultural University, China</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Huhu Wang, Nanjing Agricultural University, China; Jinxuan Cao, Beijing Technology and Business University, China</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Demin Cai <email>demincai&#x00040;yzu.edu.cn</email></corresp>
<corresp id="c002">Lin Chen <email>chenlin11222&#x00040;163.com</email></corresp>
<fn fn-type="other" id="fn001"><p>This article was submitted to Nutrition and Food Science Technology, a section of the journal Frontiers in Nutrition</p></fn></author-notes>
<pub-date pub-type="epub">
<day>01</day>
<month>12</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="collection">
<year>2022</year>
</pub-date>
<volume>9</volume>
<elocation-id>1078201</elocation-id>
<history>
<date date-type="received">
<day>24</day>
<month>10</month>
<year>2022</year>
</date>
<date date-type="accepted">
<day>17</day>
<month>11</month>
<year>2022</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2022 Zhu, Wang, Li, Zhang, Ji, Zhao, Zhang, Cai and Chen.</copyright-statement>
<copyright-year>2022</copyright-year>
<copyright-holder>Zhu, Wang, Li, Zhang, Ji, Zhao, Zhang, Cai and Chen</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license></permissions>
<abstract>
<p>Meat spoilage (MS) is a complex microbial ecological process involving multiple specific microbial interactions. MS is detrimental to people&#x00027;s health and leads to the waste of meat products which caused huge losses during production, storage, transportation, and marketing. A thorough understanding of microorganisms related to MS and their controlling approaches is a necessary prerequisite for delaying the occurrence of MS and developing new methods and strategies for meat product preservation. This mini-review summarizes the diversity of spoilage microorganisms in livestock, poultry, and fish meat, and the approaches to inhibit MS. This would facilitate the targeted development of technologies against MS, to extend meat&#x00027;s shelf life, and effectively diminish food waste and economic losses.</p></abstract>
<kwd-group>
<kwd>livestock</kwd>
<kwd>poultry</kwd>
<kwd>fish meat</kwd>
<kwd>microbial spoilage</kwd>
<kwd>bacterial community</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="81"/>
<page-count count="8"/>
<word-count count="6234"/>
</counts>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="s1">
<title>Introduction</title>
<p>According to a report by the Food and Agriculture Organization of the United Nations, one-third of food produced for human consumption is either spoiled or wasted (<xref ref-type="bibr" rid="B1">1</xref>). MS is defined as a change in color and the production of off-flavors, mucus, and exudates that result in unacceptable sensory and organoleptic properties. Parlapani confirms that the deterioration is caused by specific spoilage organisms that dominate and form metabolites that alter the organoleptic properties of the meat, making it unfit for consumption (<xref ref-type="bibr" rid="B2">2</xref>). Although the causes for meat deterioration vary, bacteria direct the process more than other factors such as endogenous enzymes. Meat is generally considered sterile before slaughter, but the environment during slaughter is not sterile, so some degree of microbial contamination may occur, leading to meat corruption (<xref ref-type="bibr" rid="B3">3</xref>). The sources of microbial contamination in this process can be summarized as both endogenous and exogenous. The microbiological quality of post-slaughter meat depends to a large extent on the type of meat, processing, distribution, and storage conditions. Contaminated slaughter equipment, personnel and environmental factors (e.g. water, air, and soil) can be cross-contaminated with spoilage-associated bacteria (<xref ref-type="bibr" rid="B4">4</xref>). After storage, various intrinsic and extrinsic factors affect the process of microbial MS, including oxygen demand, pH, temperature, and competing organisms (<xref ref-type="bibr" rid="B5">5</xref>). The diversity of these ecophysiological factors affects the dynamics of microbial growth, including microbial succession and microbiota composition, ultimately affecting the type and rate of MS. Several strategies have been proposed to preserve fresh products to overcome MS, including the addition of ingredients such as food preservatives, essential oils and storage under refrigerated conditions, and aeration packaging (<xref ref-type="bibr" rid="B6">6</xref>, <xref ref-type="bibr" rid="B7">7</xref>). Therefore, understanding the sources of spoilage microorganisms in meat, the diversity of microorganisms and measures to retard spoilage, and achieving accurate and effective inhibition of spoilage microorganisms is one of the common goals of meat industry sessions and academia.</p></sec>
<sec id="s2">
<title>Spoilage microbial diversity</title>
<sec>
<title>Major types of spoilage microorganisms in livestock meat</title>
<p>Not all bacteria cause spoilage of food, there is only an initial small group of microorganisms in meat, referred to as specific spoilage organisms (SSO) (<xref ref-type="bibr" rid="B8">8</xref>). In meat products, SSO metabolizes available substrates during storage, leading to changes in meat quality and odor (<xref ref-type="bibr" rid="B9">9</xref>). This section summarizes the common microorganisms and spoilage phenotypes associated with the spoilage of livestock meat (<xref ref-type="table" rid="T1">Table 1</xref>). A study showed that the dominant bacteria in the meatballs of the blown pack spoilage (BPS) group packed with 71.85% CO<sub>2</sub> were <italic>Klebsiella</italic> (46.05%) and <italic>Escherichia</italic> (39.96%). <italic>Klebsiella pneumoniae</italic> was the main strain causing BPS in meatballs due to its ability to pack swelling (<xref ref-type="bibr" rid="B26">26</xref>). Wang et al. (<xref ref-type="bibr" rid="B27">27</xref>) revealed that <italic>Proteobacteria, Firmicutes, Pseudomonas spp</italic>., <italic>Acinetobacter spp</italic>., <italic>Pantoea spp</italic>., <italic>Brochothrix spp</italic>., and <italic>Raoultella spp</italic>. were the main pathogenic and spoilage bacteria in chilled pork by culture-dependent and non-culture-dependent methods (<xref ref-type="bibr" rid="B27">27</xref>). The microbial composition of pork stored at&#x02212;2&#x000B0;C and 4&#x000B0;C showed a high degree of similarity, with <italic>Pseudomonads</italic> and <italic>Brochothrix</italic> being the dominant taxa. <italic>Acinetobacter spp</italic>., <italic>Myroides spp</italic>., and <italic>Kurthia spp</italic>. were markers for spoiled pork meat stored at 25&#x000B0;C (<xref ref-type="bibr" rid="B28">28</xref>). The current research results show that the abnormal growth of lactic acid bacteria, <italic>Micrococcaceae, Enterobacteriaceae</italic>, yeast, and mold plays a key role in the formation of dry cured ham odor defects, while the key putrefactive microorganisms of different types of ham are different (<xref ref-type="bibr" rid="B29">29</xref>, <xref ref-type="bibr" rid="B30">30</xref>). In Mianning ham, the dominant bacterial genus was <italic>Clostridium_sensu_stricto_</italic>2 (92.01%), and the dominant fungal genus was <italic>Aspergillus</italic> (84.27%) (<xref ref-type="bibr" rid="B31">31</xref>). The number of <italic>Enterobacteriaceae</italic> and <italic>Enterococcus</italic> in deteriorated ham was significantly higher than that in normal ham. High water content and low salt content lead to abnormal growth of <italic>Enterobacteriaceae</italic> and <italic>Enterococcus</italic> in deteriorated ham, leading to the deterioration of Jinhua ham (<xref ref-type="bibr" rid="B32">32</xref>, <xref ref-type="bibr" rid="B33">33</xref>). <italic>C. farmei CDC 2991&#x02013;81, B. cereus ATCC 14579</italic>, and <italic>E. faecalis ATCC 19433</italic> were the main spoilage microorganisms of Jinhua ham (<xref ref-type="bibr" rid="B34">34</xref>). <italic>C. sestertheticum</italic> was detected as the most abundant <italic>Clostridium spp</italic>. in vacuum packaging beef and other raw meats, associated with BPS (<xref ref-type="bibr" rid="B35">35</xref>). Li et al. (<xref ref-type="bibr" rid="B36">36</xref>) reported that total viable bacteria (8.75 log CFU/cm<sup>2</sup>) and Lactobacillus (3.20 log CFU/cm<sup>2</sup>) counts were higher on meat surfaces dry-aged for 19 days (<xref ref-type="bibr" rid="B36">36</xref>). The microbial communities of all samples evaluated in dry-aged beef contain <italic>Enterobacteriaceae</italic> and <italic>Pseudomonas</italic>, which are considered to be the major spoilers in dry-aged beef (<xref ref-type="bibr" rid="B13">13</xref>). In another study, beef and lamb samples from Europe, North and South America, and Oceania were investigated and <italic>Psychrophilic Clostridium spp</italic>. was found to be the most prevalent <italic>Clostridium</italic> (<xref ref-type="bibr" rid="B37">37</xref>).</p>
<table-wrap position="float" id="T1">
<label>Table 1</label>
<caption><p>List of bacterial groups associated with livestock and poultry MS.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>NO</bold>.</th>
<th valign="top" align="left"><bold>Bacteria genus</bold></th>
<th valign="top" align="left"><bold>Spoilage phenotype</bold></th>
<th valign="top" align="left"><bold>References</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left"><bold>Livestock</bold></td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">1</td>
<td valign="top" align="left">LAB</td>
<td valign="top" align="left">Slime and discoloration</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B8">8</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">2</td>
<td valign="top" align="left"><italic>Leuconostoc</italic></td>
<td valign="top" align="left">Slime, gas production and discoloration</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B9">9</xref>, <xref ref-type="bibr" rid="B10">10</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">3</td>
<td valign="top" align="left"><italic>Lactobacillus</italic></td>
<td valign="top" align="left">Slime</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B9">9</xref>, <xref ref-type="bibr" rid="B11">11</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">4</td>
<td valign="top" align="left"><italic>Serratia</italic></td>
<td valign="top" align="left">Discoloration</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B12">12</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">5</td>
<td valign="top" align="left"><italic>Weissella</italic></td>
<td valign="top" align="left">Slime and Discoloration</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B11">11</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">6</td>
<td valign="top" align="left"><italic>Enterobacteriales</italic></td>
<td valign="top" align="left">Slime and discoloration</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B13">13</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">7</td>
<td valign="top" align="left"><italic>Clostridium</italic></td>
<td valign="top" align="left">Blown pack spoilage</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B14">14</xref>, <xref ref-type="bibr" rid="B15">15</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">8</td>
<td valign="top" align="left"><italic>Pseudomonas</italic></td>
<td valign="top" align="left">Biofilm formation</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B16">16</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">9</td>
<td valign="top" align="left"><italic>Brochothrix</italic></td>
<td valign="top" align="left">Biofilm formation</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B17">17</xref>)</td>
</tr>
<tr>
<td valign="top" align="left"><bold>Poultry</bold></td>
<td/>
</tr>
<tr>
<td valign="top" align="left">1</td>
<td valign="top" align="left"><italic>Aeromonas</italic></td>
<td valign="top" align="left">Biofilm formation</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B19">19</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">2</td>
<td valign="top" align="left"><italic>Salmonell</italic></td>
<td valign="top" align="left">Unknown</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B20">20</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">3</td>
<td valign="top" align="left"><italic>Pseudomonas</italic></td>
<td valign="top" align="left">Slime formation and meat softening</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B21">21</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">4</td>
<td valign="top" align="left"><italic>Enterococcus</italic></td>
<td valign="top" align="left">Discoloration</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B22">22</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">5</td>
<td valign="top" align="left"><italic>Brochothrix</italic></td>
<td valign="top" align="left">Discoloration</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B41">41</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">6</td>
<td valign="top" align="left"><italic>Acinetobacter</italic></td>
<td valign="top" align="left">Biofilm formation</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B23">23</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">7</td>
<td valign="top" align="left"><italic>Shewanella</italic></td>
<td valign="top" align="left">Discoloration</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B24">24</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">8</td>
<td valign="top" align="left"><italic>Staphylococcus</italic></td>
<td valign="top" align="left">Acid production</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B25">25</xref>)</td>
</tr>
</tbody>
</table>
</table-wrap></sec>
<sec>
<title>Major types of spoilage microorganisms in poultry meat</title>
<p>There has been a steady increase in consumption and demand for poultry meat globally. Among poultry products, processed chicken meat is the most consumed (about 75% of total poultry meat), followed by turkey (about 25%) and duck meat (<xref ref-type="bibr" rid="B38">38</xref>). The bacterial community in poultry meat include pathogenic species such as <italic>Salmonella</italic> and <italic>Campylobacter</italic> (<xref ref-type="bibr" rid="B18">18</xref>). This section summarizes the common microorganisms and spoilage phenotypes associated with the spoilage of poultry meat (<xref ref-type="table" rid="T1">Table 1</xref>). When defining the dominant spoilage bacteria in the spoilage process of meat products based on the number of bacteria, <italic>Pseudomonas spp</italic>., <italic>Bacillus spp</italic>., <italic>Crude Typhimurium spp</italic>., <italic>Schwartzella spp</italic>., <italic>Aeromonas spp</italic>. are usually considered to be the dominant communities in cold meat and poultry packed under aerobic conditions (<xref ref-type="bibr" rid="B19">19</xref>). Poultry meat spoils quickly, even under refrigerated conditions. Wang et al. detected a significant increase of <italic>Clostridium</italic> perfringens over time in almost poultry samples stored aerobically under different refrigeration conditions. <italic>Pseudomonas fluorescens, Aeromonas salmonicida</italic>, and <italic>Serratia liquefaciens</italic> cause spoilage of poultry meat stored at 8&#x000B0;C for 4 days (<xref ref-type="bibr" rid="B20">20</xref>). Several new enterococci or lactic acid bacteria were also identified in poultry products, such as <italic>Viikkiensis enterococcus, Seigonensis enterococcus</italic>, and <italic>Heterofermentative lactic acid bacteria</italic> (<xref ref-type="bibr" rid="B39">39</xref>, <xref ref-type="bibr" rid="B40">40</xref>).</p>
<p>With the development of MS studies, it is more appropriate to determine the dominant spoilage organism by determining the spoilage capacity of bacterial isolates grown <italic>in situ</italic>. The main common <italic>Pseudomonas</italic> in poultry meat is <italic>Pseudomonas fragilis, Pseudomonas lundengensis</italic>, and <italic>Pseudomonas fluorescens</italic>. <italic>Pseudomonas fragilis, Pseudomonas fluorescens</italic>, and <italic>Pseudomonas aeruginosa</italic> produced slime on meat and its products during storage (<xref ref-type="bibr" rid="B41">41</xref>). Extracellular enzymes secreted by <italic>Pseudomonas aeruginosa</italic> have strong protease activity against myogenic fibronectin and myxomatosis protein. This helps bacteria penetrate the meat to obtain new sources of nutrients, increasing the formation of mucus and softening the meat (<xref ref-type="bibr" rid="B21">21</xref>). In addition, <italic>Serratia spp</italic>., <italic>Micrococcus spp</italic>., <italic>Serratia spp</italic>., and <italic>Brucella spp</italic>. were also associated with slime production and softening during MS (<xref ref-type="bibr" rid="B42">42</xref>).</p></sec>
<sec>
<title>Major types of spoilage microorganisms in fish meat</title>
<p>The increase in the global population has led to an increase in the consumption of fish and meat in various countries. It becomes highly susceptible to spoilage through a series of chemical reactions, under the action of microorganisms and enzymes due to its high water content and high pH (<xref ref-type="bibr" rid="B43">43</xref>). Similar to other meat, not all microorganisms in fish meat have the potential for corruption, except SSO. This section summarizes the common spoilage microorganisms associated with the spoilage of fish meat (<xref ref-type="table" rid="T2">Table 2</xref>).</p>
<table-wrap position="float" id="T2">
<label>Table 2</label>
<caption><p>List of bacterial groups associated with fish meat spoilage.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>NO</bold>.</th>
<th valign="top" align="left"><bold>Bacteria genus</bold></th>
<th valign="top" align="left"><bold>Fish meat</bold></th>
<th valign="top" align="left"><bold>References</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">1</td>
<td valign="top" align="left"><italic>Shewanella</italic></td>
<td valign="top" align="left">Raw lobster tails, whole lobster, salmon</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B44">44</xref>, <xref ref-type="bibr" rid="B45">45</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">2</td>
<td valign="top" align="left"><italic>Pseudomonas</italic></td>
<td valign="top" align="left">Raw lobster tails, whole lobster, salmon, carp</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B44">44</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">3</td>
<td valign="top" align="left"><italic>Photobacteriu</italic></td>
<td valign="top" align="left">Salmon</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B44">44</xref>, <xref ref-type="bibr" rid="B46">46</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">4</td>
<td valign="top" align="left"><italic>Staphylococcus</italic></td>
<td valign="top" align="left">Fresh shrimp</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B47">47</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">5</td>
<td valign="top" align="left"><italic>Psychrobacter</italic></td>
<td valign="top" align="left">Whole lobster, cod</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B48">48</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">6</td>
<td valign="top" align="left"><italic>Brochothrix</italic></td>
<td valign="top" align="left">Raw salmon, catfish, sea bass, sea bream</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B48">48</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">7</td>
<td valign="top" align="left"><italic>B.Thermospheracta</italic></td>
<td valign="top" align="left">Fresh shrimp</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B49">49</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">8</td>
<td valign="top" align="left"><italic>Serratia</italic></td>
<td valign="top" align="left">Oysters,fish, tropical shrimps</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B50">50</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">9</td>
<td valign="top" align="left"><italic>Salmonicida</italic></td>
<td valign="top" align="left">Shrimps, salmon, sea beam</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B51">51</xref>)</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>M&#x000F8;retr&#x000F8; et al. (<xref ref-type="bibr" rid="B44">44</xref>) found higher levels of <italic>Pseudomonas spp</italic>. and <italic>Salmonella spp</italic>. on industrially processed salmon filets with the methods of bacterial enumeration 16S rRNA analysis from seven processing plants. <italic>Salmonella spp</italic>. and <italic>Photobacterium spp</italic>. were found on salmon at the slaughter stage (<xref ref-type="bibr" rid="B44">44</xref>). The main microbiota of air-packaged (AP) and vacuum-packaged (VP) carp filets during storage were systematically identified by Zhang et al. (<xref ref-type="bibr" rid="B52">52</xref>) The results showed that <italic>Pseudomonas aeruginosa</italic> was the only microbiota found in spoiled AP carp, while <italic>Karnococcus</italic> were found mainly in VP samples (<xref ref-type="bibr" rid="B52">52</xref>). Characterization of some specific H<sub>2</sub>S-producing spoilage organisms isolated from raw tuna and swordfish by Serio et al. (<xref ref-type="bibr" rid="B45">45</xref>). Among them, <italic>Shewanella spp</italic>. can form biogenic amines, showing great corruption potential. <italic>Pseudomonas</italic> and <italic>Shewanella</italic> are two spoilage microorganisms of frozen fish meat preserved aerobically, while CO<sub>2</sub>-resistant <italic>Photobacterium phosphoreum</italic> is the main flora of fish meat packed under altered atmosphere conditions (<xref ref-type="bibr" rid="B46">46</xref>). <italic>Pseudomonas</italic> can inhibit each other in seafood matrices. Boziaris et al. (<xref ref-type="bibr" rid="B53">53</xref>) observed that <italic>Pseudomonas fluorescens</italic> outcompeted <italic>Pseudomonas spp</italic>. at increased storage temperatures and that <italic>Pseudomonas spp</italic>. could cause spoilage bacteria in raw salmon under aerobic conditions (<xref ref-type="bibr" rid="B53">53</xref>). <italic>Brochothrix thermosphacta</italic> produces caramel off-flavors (2,3-butanedione) in seafood under aerobic conditions. The genus <italic>Psychrobacter</italic> is a gram-negative, psychrophilic and aerobic bacterium found mainly in seafood and meat. Members of this category include <italic>Acinetobacter, Photosynthetic bacteria</italic> (<italic>Psb</italic>) <italic>cibatius, Psb. maritimus</italic> and <italic>Psb. proteolyticus</italic> are found in a variety of seafood, such as mackerel, anglerfish, lobster, oysters, and Atlantic cod (<xref ref-type="bibr" rid="B47">47</xref>). <italic>Psychrobacter</italic> species, especially <italic>Psb. immobilis</italic>, are able to break down lipids and hydrolyze amino acids, thus causing a slight ichthyological and musty odor.</p></sec></sec>
<sec id="s3">
<title>Common control approaches</title>
<sec>
<title>Packaging methods</title>
<p>Factors affecting the growth of microorganisms in meat include intrinsic factors (natural and added ingredients, pH, redox potential, and water activity), as well as extrinsic factors (storage temperature and packaging methods).</p>
<p>Modified atmospheric packaging (MAP) reported extending the shelf life of frozen meat (<xref ref-type="bibr" rid="B54">54</xref>). Luong et al. (<xref ref-type="bibr" rid="B55">55</xref>) showed that for fresh turkey sausage, a 2% (w/w) lactic acid formulation in combination with MAP (50% CO<sub>2</sub>-50% N<sub>2</sub>) significantly reduced acidification, off-flavors and prevented discoloration of the sausage from red to dark gray or brown. In pork sausages, MAP (70% O<sub>2</sub>-30% CO<sub>2</sub>) slightly reduces off-flavor perception (<xref ref-type="bibr" rid="B55">55</xref>). The decrease in the quality of meat during storage depends not only on the number of bacteria but also on the activity of bacterial metabolism. Proteases produce free amino acids which can be further metabolized by bacteria, resulting in off-flavors and mucus associated with spoilage. Previous studies have shown that a gas mixture of 30% CO<sub>2</sub> and 70% N<sub>2</sub> for MAP can extend the shelf life of frozen chicken (<xref ref-type="bibr" rid="B56">56</xref>). Meat stored under this MAP has a lower number of <italic>Pseudomonas spp</italic>. and is less likely to spoil than when stored in the air (<xref ref-type="bibr" rid="B57">57</xref>). Therefore, MAP may affect the growth as well as the metabolism of bacteria. Different packaging conditions affect the shelf life of carp and the growth of microorganisms. The shelf life of air-packed (AP) and vacuum-packed (VP) filets at 4&#x000B0;C is 8 days and 12 days, respectively, with the highest number of <italic>Pseudomonas aeruginosa</italic> in the AP sample and a relatively high level of lactic acid bacteria (LAB) in the VP sample. VP delays the increase in biogenic amine content compared to AP (<xref ref-type="bibr" rid="B52">52</xref>).</p>
<p>Dohlen et al. (<xref ref-type="bibr" rid="B58">58</xref>) studied the effect of novel antimicrobial packaging materials containing poly-[2-(tertbutylamino) methylstyrene] (poly-TBAMS) on the growth of typical spoilage and pathogenic bacteria present in meat. The results showed that gram-positive bacteria were more susceptible to poly(TBAMS) foil than gram-negative bacteria, and an increase of the antimicrobial activity with an increasing amount of poly(TBAMS) in the base polymer (<xref ref-type="bibr" rid="B58">58</xref>). Amna et al. (<xref ref-type="bibr" rid="B59">59</xref>) developed a new antimicrobial hybrid packaging pad consisting of biodegradable polyurethane. This type of packaging material was found to show effective antibacterial activity against <italic>Staphylococcus aureus</italic> and <italic>Salmonella typhimurium</italic> (<xref ref-type="bibr" rid="B59">59</xref>). Zeinab et al. (<xref ref-type="bibr" rid="B60">60</xref>) found that TiO<sub>2</sub> nanocomposites and irradiation at 3kGy maintained chemical, microbiological, and sensory properties for longer periods and extended the shelf life of fish filets in cold storage (<xref ref-type="bibr" rid="B60">60</xref>). It was shown that antibacterial polyvinyl alcohol films containing TiO<sub>2</sub> nanoparticles inhibited <italic>Shewanella spp</italic>., <italic>Pseudomonas putida</italic>, and <italic>Aeromonas hydrophila</italic>, and prolonged the shelf life of macroscopic rotenone by 1&#x02013;2 days (<xref ref-type="bibr" rid="B61">61</xref>).</p></sec>
<sec>
<title>Addition of antibacterial substances</title>
<p>Recently, the harmful effects associated with synthetic preservatives have led to a search for new alternatives in natural products. Commercially available polyphenols reduce primary and secondary lipid peroxidation levels, inhibit lipoxygenase activity, improve meat color stability, minimize degradation of salt-soluble myogenic fibrin and sulfhydryl groups, and retard bacterial growth (<xref ref-type="bibr" rid="B62">62</xref>). Essential oils (EOs) are secondary metabolites obtained from plants of Asteraceae, Lamiaceae, Lauraceae, Myrtaceae, Rutaceae, Umbelliferae, Zingiberaceae families, among others. Composed of a complex mixture of low molecular weight volatile compounds (<xref ref-type="bibr" rid="B63">63</xref>). These valuable substances can be obtained from different parts of the plant, such as bark, flowers, fruits, leaves, roots, and stems (<xref ref-type="bibr" rid="B64">64</xref>). This section summarizes the effects of common plant EOs on spoilage microorganisms in meat products and fish meat (<xref ref-type="table" rid="T3">Table 3</xref>).</p>
<table-wrap position="float" id="T3">
<label>Table 3</label>
<caption><p>List of common plant EOs effects on spoilage bacteria in meat products and fish meat.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>NO</bold>.</th>
<th valign="top" align="left"><bold>EOs</bold></th>
<th valign="top" align="left"><bold>Meat types</bold></th>
<th valign="top" align="left"><bold>Effects</bold></th>
<th valign="top" align="left"><bold>References</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">1</td>
<td valign="top" align="left">Sage EO</td>
<td valign="top" align="left">Fresh pork sausages</td>
<td valign="top" align="left">Inhibiting thermophilic aerobic bacterial.</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B65">65</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">2</td>
<td valign="top" align="left"><italic>Satureja montana L</italic>. EO</td>
<td valign="top" align="left">Fresh pork sausages</td>
<td valign="top" align="left">Reducing the number of thermophilic aerobic bacteria and <italic>Enterobacteriaceae</italic>.</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B66">66</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">3</td>
<td valign="top" align="left"><italic>Z.clinopodioides</italic> EO&#x0002B;nisin</td>
<td valign="top" align="left">Raw beef patty</td>
<td valign="top" align="left">Inhibiting the growth of Cryophilic, <italic>Enterobacteriaceae</italic>, and thermophilic bacteria as well as <italic>Staphylococcus aureus</italic> and <italic>Escherichia coli</italic> O157:H7.</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B67">67</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">4</td>
<td valign="top" align="left">Rosemary, sage, thyme, and clove Eos</td>
<td valign="top" align="left">Smoked rainbow trout</td>
<td valign="top" align="left">Extending the shelf life by 6-7 weeks.</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B68">68</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">5</td>
<td valign="top" align="left">Black pepper EO</td>
<td valign="top" align="left">Fresh pork</td>
<td valign="top" align="left">Deformation, depression, shrinkage, adhesion, and rupture of <italic>Escherichia coli</italic>; Inhibiting the growth of <italic>Pseudomonas</italic> and <italic>Enterobacteriaceae</italic>.</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B69">69</xref>, <xref ref-type="bibr" rid="B70">70</xref>)</td>
</tr>
<tr>
<td valign="top" align="left">6</td>
<td valign="top" align="left">Cinnamon EO</td>
<td valign="top" align="left">Fresh Italian style sausages</td>
<td valign="top" align="left">Inhibiting the growth of <italic>Enterobacteriaceae</italic>.</td>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B71">71</xref>)</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Thymol and carvacrol have inhibitory effects on <italic>Bacillus cereus, Pseudomonas aeruginosa</italic>, and <italic>Staphylococcus aureus</italic> (<xref ref-type="bibr" rid="B72">72</xref>). In contrast, Guimar&#x000E3;es et al. (<xref ref-type="bibr" rid="B73">73</xref>) observed that the free terpenes commonly found in essential oils have strong antibacterial activity against gram-negative bacteria (<xref ref-type="bibr" rid="B73">73</xref>). Sage EO as a preservative was demonstrated in meat products used as fresh pork sausages, suppressing aerobic thermophilic bacterial counts at the end of storage (4.8&#x02013;7.3%) (<xref ref-type="bibr" rid="B65">65</xref>). Sojic et al. (<xref ref-type="bibr" rid="B66">66</xref>) evaluated the antibacterial potential of <italic>Satureja montana L</italic>. EO in fresh pork sausage. Compared with the control group, adding <italic>Satureya montana L</italic>.EO can improve the microbial stability of the product, and reduce the total number of thermophilic aerobic bacteria (4.9-10.9%) and <italic>Enterobacteriaceae</italic> (7.1-19.6%) in sausage (<xref ref-type="bibr" rid="B66">66</xref>). Shahbazi et al. (<xref ref-type="bibr" rid="B67">67</xref>) found that both essential oils and lactobacillus peptides significantly (<italic>p</italic> &#x0003C; 0.05) affected the growth of Cryophilic, <italic>Enterobacteriaceae</italic>, and thermophilic bacteria as well as <italic>Staphylococcus aureus</italic> and <italic>Escherichia coli</italic> O157:H7 in raw beef patties, with the fastest decrease in the number of tested microorganisms in samples treated with 0.2% essential oil &#x0002B; 500 IU/g lactobacillus peptide (<xref ref-type="bibr" rid="B67">67</xref>).</p>
<p>For fish meat, MAP conditions favor the growth of anaerobic bacteria, which can produce toxins. Therefore, often in combination with other modalities (MAP, edible coatings and films, non-thermal sterilization, etc.) to enhance the effectiveness of natural preservatives (<xref ref-type="bibr" rid="B74">74</xref>). Yuan et al. (<xref ref-type="bibr" rid="B75">75</xref>) found that the total volatile alkaline nitrogen and total aerobic colony values of black spot shrimp treated with chitosan coating in combination with pomegranate peel extract (PPE) were lower than those of shrimp treated with chitosan coating or PPE alone, indicating a synergistic effect between chitosan coating and PPE (<xref ref-type="bibr" rid="B75">75</xref>). Emird et al. (<xref ref-type="bibr" rid="B68">68</xref>) found that rosemary, sage, thyme, and clove essential oils as natural antioxidants can be used with vacuum packaging to extend the shelf life of smoked rainbow trout by 6&#x02013;7 weeks (<xref ref-type="bibr" rid="B68">68</xref>). In a previous study, the effects of nanoemulsions based on commercial oils (sunflower, canola, corn, olive, soybean, and hazelnut oils) on the fatty acid compositions of farmed sea bass stored at 2 &#x000B1; 2&#x000B0;C was investigated. The results showed hazelnut group gave the highest polyunsaturated fatty acid content, followed by canola and soybean at the end of the storage period. These oils can be recommended for nanoemulsions as a preservative for fish (<xref ref-type="bibr" rid="B76">76</xref>).</p></sec>
<sec>
<title>Plasma sterilization</title>
<p>Reactive oxygen species (ROS) in atmospheric pressure cold plasma (APCP) act on gram-positive and gram-negative bacteria through different microbicidal mechanisms, and intracellular ROS levels increase in <italic>Listeria monocytogenes</italic> and <italic>Staphylococcus aureus</italic> with prolonged exposure to APCP, but with little damage to the cell wall (<xref ref-type="bibr" rid="B77">77</xref>). Exposure of <italic>Listeria monocytogenes</italic> and <italic>Staphylococcus aureus</italic> to APCP causes cell shrinkage, but little damage to the cell wall. In addition, intracellular ROS levels of <italic>Listeria monocytogenes</italic> and <italic>Staphylococcus aureus</italic> have been shown to increase with the exposure time of APCP (<xref ref-type="bibr" rid="B78">78</xref>). Dielectric barrier discharge (DBD) plasma is a source of plasma that generates ROS that can penetrate cell membranes and cause apoptosis through intracellular DNA damage. Previous studies have shown that the levels of <italic>Listeria monocytogenes</italic> in inoculated meat and meat products were reduced by 0.59&#x02013;6.52 Log CFU/g after DBD treatment (<xref ref-type="bibr" rid="B79">79</xref>).</p></sec>
<sec>
<title>Bacteriophage sterilization</title>
<p>Phages are considered promising new bioretention agents because they can efficiently and specifically lyse targeted bacteria. A cocktail of three phages effectively inhibited the growth of <italic>S. hiva</italic> in catfish filets and significantly improved the pH, total volatile basic nitrogen, and organoleptic value indices of the filets (<xref ref-type="bibr" rid="B80">80</xref>).</p></sec>
<sec>
<title>Low-dose irradiation</title>
<p>Low-dose irradiation is considered a common technique for keeping fish meat fresh. Dogruyol et al. reported that sous-vide filets could be irradiated (5.0 kGy) to extend their shelf life up to 8 weeks during refrigerated storage without any damage to the organoleptic and physicochemical properties of the filets (<xref ref-type="bibr" rid="B81">81</xref>).</p></sec></sec>
<sec sec-type="conclusions" id="s4">
<title>Conclusion</title>
<p>Microbial contamination of meat is the domain cause of losses during production, storage, and distribution, accounting for approximately 21% of total food losses. We review recent advances in research on microbial diversity causing spoilage of livestock, poultry, and fish meat and summarize measures to prevent MS. However, to achieve more accurate and effective control of spoilage microorganisms in meat, it is necessary to obtain more comprehensive and accurate information on the composition of microbial communities and the dynamic processes of their metabolism. By revealing specific interactions between various spoilage phenotypes during MS, we would achieve controllable product quality during the production, transportation, marketing, and storage of meat.</p></sec>
<sec id="s5">
<title>Author contributions</title>
<p>YZ and LC conceived and wrote the original draft. WW, LC, ML, JZ, RZ, LJ, ZZ, and DC reviewed, edited, and revised the manuscript. All authors approved the finalversion.</p></sec>
<sec sec-type="funding-information" id="s6">
<title>Funding</title>
<p>This work was supported by the National Modern Agricultural Industrial Technology System, Sichuan Innovation Team Construction Project (SCSZTD-2022-08-07), Liangshan Science and Technology Program (22ZDYF0249, 21CGZH0001), and the Natural Science Foundation of Jiangsu Province (BK20200932).</p></sec>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p></sec>
<sec sec-type="disclaimer" id="s7">
<title>Publisher&#x00027;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p></sec>
</body>
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